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- 详细信息
- 文献和实验
- 技术资料
- 品系:
详见细胞说明资料
- 细胞类型:
详见细胞说明资料
- 肿瘤类型:
详见细胞说明资料
- 供应商:
上海冠导生物工程有限公司
- 库存:
≥100瓶
- 生长状态:
详见细胞说明资料
- 年限:
详见细胞说明资料
- 运输方式:
常温运输【复苏细胞】或干冰运输【冻存细胞】
- 器官来源:
详见细胞说明资料
- 是否是肿瘤细胞:
详见细胞说明资料
- 细胞形态:
详见细胞说明资料
- 免疫类型:
详见细胞说明资料
- 物种来源:
详见细胞说明资料
- 相关疾病:
详见细胞说明资料
- 组织来源:
详见细胞说明资料
- 英文名:
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
- 规格:
1*10(6)Cellls/瓶
"CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
传代方法:1:2-1:4(首次传代建议1:2)
生长特性:贴壁生长
换液频率:每周2-3次
背景资料:是一种人胰腺导管腺癌(Pancreatic Ductal Adenocarcinoma, PDAC)细胞系,建自26岁白人男性囊性纤维变性(CF)的肝转移灶,该患者合并有囊肿性纤维化。CFPAC-1细胞表达囊性纤维变性跨膜调节因子(CFTR),CFPAC-1细胞形态为上皮细胞样且顶端微绒毛极化。CFPAC-1细胞表达胰腺管细胞特征性的细胞角蛋白和癌胚抗原。
GFP-Olig2 Cells;背景说明:胚胎干细胞;129X1/SvJ;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:hTERT-RPE Cells、AML 12 Cells、NCIH1618 Cells
RPE1 Cells;背景说明:视网膜色素上皮;hTERT永生;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:WM 266-4 Cells、H-2195 Cells、CCD-112 CoN Cells
HPAF-II/CD18 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:MSC Cells、GM-346 Cells、SUP-B15 Cells
养了几年细胞,说一点自己培养细胞方面的看法:1)培养细胞前,可以看看细胞点说明,包括细胞正常生长的状态图、传代、培养基的类型等;2)不同细胞生长周期不同,有的生长很快,比如说-MB-231,传代的时候取离心悬的十分之一就已经足够了,有的又是别慢,等的人心焦,B474就是,传代是一分二,复苏起始的时候两周多才能长满,所以就要在培养细胞的过程中多多摸索了;3)对于娇弱的细胞,就得细心呵护了,胰酶消化不能过久,吹得时候要轻柔,离心时候也要注意转速和时间,每天都要去看一下细胞,肉眼观察培养基状况、显微镜下观察细胞生长状况;4)冻存细胞复苏后第二天ZuiHAO更换一次培养基;5)培养箱隔一段时间彻底用酒精棉擦洗一次;6)养细胞Zui大的教训:不能偷懒!细胞虐我千百遍,我待细胞如初恋。1)不管买的细胞、惠赠的细胞,刚拿到手赶紧做两件事:检测是否有支原体污染; 迅速扩增冻存;2)发现有污染迅速处理掉,别是当你养了很多种细胞时; 细菌污染,真菌污染很容易发现,支原体污染的话,细胞会长的慢,买个支原体检测的ki定期检测一下;3)传代细胞日常的值日清洁是必须的,此外还要定期熏蒸;4)细胞的传代一定要规律,保持相同的confluency和传代时间间隔,不要随心所欲或者拖延;5)注意个人卫生。
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
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产品包装形式:复苏细胞:T25培养瓶(一瓶)或冻存细胞:1ml冻存管(两支)
来源说明:细胞主要来源ATCC、DSMZ等细胞库
物种来源:Human\Mouse\Rat\Others
Calu-3 Cells;背景说明:该细胞是从一名25岁的白人男性肺腺癌患者的胸水中分离建立的;该患者曾使用过环磷酰胺、博来霉素、阿霉素进行治疗。该细胞接种至裸鼠可成瘤;可作转染宿主。;传代方法:消化20分钟。1:2。5-6天长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H-378 Cells、OP-9 Cells、Hs 611.T Cells
SupB15WT Cells;背景说明:详见相关文献介绍;传代方法:1:2传代。3天内可长满。;生长特性:悬浮生长;形态特性:淋巴母细胞;相关产品有:H-1944 Cells、IGROV 1 Cells、ME 180 Cells
SNU-638 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:Hu-P-T4 Cells、VeroC1008 Cells、Anip[973] Cells
EA. hy 926 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:SUM190PT Cells、THLE-2 Cells、AU 565 Cells
细胞常规培养传代流程(请严格遵照无菌操作):1)吸出原培养瓶中的培养基,PBS缓冲润洗细胞两次,加2-3ml 0.25%胰酶进行消化细胞(注意把握消化时间,通常控制在1-2min);2)镜下观察消化情况,在细胞边缘缩小,贴壁松动时(不建议消化到细胞漂浮)去掉胰酶,加6-8ml完全培养基,轻轻吹打细胞层,尽量把细胞层吹落,吹散;3)取部分细胞悬转移到新的培养皿/瓶中,添加适当的完全培养基,把细胞悬打匀,于培养箱中培养;4)注意培养基PH值变化情况,定期换(每周2-3次),待细胞密度达到80%以后重复1项操作或者冻存;别注意:(如使用公共实验室或者初次接触细胞培养,建议添加双抗培养)1)收到细胞后请尽快更换为含15%血清的新鲜培养基,如因殊情况需要继续使用原瓶,请在原瓶培养基中额外添加10%的血清,(原瓶培养基的继续使用时间Zui长不宜超过72小时);2)贴壁细胞收到当天切忌立刻消化,请将细胞换后放置培养箱孵育到第二天再做消化传代,请YOU先选择直径6cm的培养皿进行传代培养;3)如签收时出现培养瓶壁破裂,漏等情况请及时做HAO照片记录并联系实验室。
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CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
形态特性:上皮细胞样
在细胞传代过程中,离心操作后的上清液处理是一个关键步骤,而关于是用移液枪吸走还是直接倒掉上清液,需要综合多方面因素来考量。使用移液枪吸走上清液具有一定的优势。移液枪能够较为精准地控制吸取的量和速度,可以地减少对细胞沉淀的扰动。可以根据实际情况尽可能地吸净上清液,减少残留血清或培养基成分对后续细胞培养的潜在影响,比如残留的血清可能会改变新培养基的营养成分比例或带来一些未知的生长因子干扰。然而,直接倒掉上清液也并非不可行。在处理一些细胞数量较多、细胞耐受性较好且对实验精度要求并非极高的细胞传代时,直接倒掉上清液能够提高操作效率,节省时间。但这种方式存在一定风险,直接倾倒时较难控制力度和角度,如果操作不慎,容易使细胞沉淀随着上清液一起流出,导致细胞损失,而且可能会因液体快速流下冲击细胞沉淀造成细胞的物理性损伤。在实际的细胞传代操作中,应根据细胞的特性、实验的要求以及个人的操作熟练程度来选择合适的上清液处理方式。对于新手或者处理珍贵细胞系时,建议优先采用移液枪吸走的方式,以保障细胞的活性和传代的成功率。而在积累了丰富经验且对实验条件有充分把握的情况下,可以根据具体情况灵活运用直接倒掉上清液的方法,在保证实验质量的同时提高工作效率。
Baby Hamster Kidney from litter No. 21 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代,每周换液1-2次。;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:PCI-4B Cells、KATO III Cells、GFP-Olig2 Cells
SKMEL24 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:4传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:星形的;相关产品有:32D clone 3 Cells、UMNSAH/DF-1 Cells、RGC6 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
TE354.T Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明;相关产品有:S.B. Cells、HCC44 Cells、RS1 Cells
COLO 320 HSR Cells;背景说明:该细胞1984年建系,源自一位33岁患有大肠腺癌男性经5-fu治疗后的腹水。;传代方法:1:2传代。3天内可长满。;生长特性:半贴壁生长;形态特性:详见产品说明;相关产品有:DR2R1610 Cells、E0771 Cells、H-498 Cells
NCIH1618 Cells;背景说明:详见相关文献介绍;传代方法:3-4天换液1次。;生长特性:悬浮生长;形态特性:详见产品说明;相关产品有:CFSC-2G Cells、LAN1 Cells、KP-N-YN Cells
OCI-LY-3 Cells;背景说明:弥漫大B淋巴瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:MEC-1 Cells、SKml2 Cells、HIT Cells
CHO/dhFr- Cells;背景说明:该细胞为二叶酸还原酶缺陷型;培养基中没有HT(次黄嘌呤-胸腺嘧啶)时,该细胞会死亡;培养基中加入甲喋呤可以防止对该药物具有低抵抗性的回变细胞的生长;可作转染宿主。;传代方法:消化3-5分钟。1:2。3天内可长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:MDBK Cells、NOK Cells、HT 115 Cells
Intestinal Porcine Epithelial Cell line-J2 Cells;背景说明:小肠;上皮细胞;自发永生;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:B10BR Cells、C-33A Cells、HuH 6 Cells
Abcam A-549 NRP1 KO Cells(拥有STR基因鉴定图谱)
ABS-9 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line CSH003 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRU401 Cells(拥有STR基因鉴定图谱)
BB88 Cells(拥有STR基因鉴定图谱)
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CHO-glyA Cells(拥有STR基因鉴定图谱)
DA02517 Cells(拥有STR基因鉴定图谱)
DA05596 Cells(拥有STR基因鉴定图谱)
GIBHe013-A Cells(拥有STR基因鉴定图谱)
SNU407 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:NCI-BL6 Cells、SNU251 Cells、OVCAR.4 Cells
JJN3 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:DrG Cells、SK-RC 39 Cells、MiaPaca.2 Cells
TM3 Cells;背景说明:TM3细胞在LH作用下cAMP产量升高,但对促卵泡激素没有响应。对LH的响应持续时间与血清批次有关。在LH存在下,细胞可以代谢胆固醇。检测发现鼠痘病毒阴性。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HRCEC Cells、NS653 Cells、HSC-1 Cells
H2052 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:K-562 Cells、P560 Cells、L cells (TK-) Cells
3T3 Cells;背景说明:3T3细胞株是1962年Todaro G和Green H从分离的瑞士小鼠胚胎中建立的;该细胞的生长受接触性抑制,汇合状态的单层细胞密度为40000个细胞/平方厘米;检测结果显示该细胞鼠痘病毒阴性;在中生长较好,在某些玻璃表面上可能状态不佳;细胞生长饱和时其密度可以达到约50000 cells/cm2。;传代方法:1:3传代;3-4天1次。;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:Me-Wo Cells、WERIRb1 Cells、Line 207 Cells
Ca Ski Cells;背景说明:这株细胞是从小肠肠系膜转移灶的细胞中建立的。 据报道,它含有完整的HPV-16(每个细胞大约600个拷贝)和HPV-18相关序列。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:Tb 1 Lu (NBL-12) Cells、University of Michigan-Urothelial Carcinoma-14 Cells、D-407 Cells
HUASMC Cells;背景说明:脐动脉平滑肌;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:HC11 Cells、SKLU01 Cells、hTERT-HME1 Cells
TR 146 Cells;背景说明:食管鳞癌;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:SW1222 Cells、SNB19 Cells、KM H-2 Cells
BC-022 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:EL-4 Cells、COLO 206F Cells、RPMI-7666 Cells
Vero 76 clone E6 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:EFO 27 Cells、HMCB Cells、PaTu-8988s Cells
NCI-H2141 Cells;背景说明:详见相关文献介绍;传代方法:3-4天换液1次。;生长特性:悬浮生长;形态特性:聚团悬浮;相关产品有:KTA-7 Cells、Ca9-22 Cells、BIC-1 Cells
HS852.T Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:HEL-299 Cells、NCIH1915 Cells、Fetal Rhesus Kidney-4 Cells
VM-CUB-1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:BT-483 Cells、SF-126 Cells、AU565 Cells
2.43 Cells(拥有STR基因鉴定图谱)
L 428 Cells;背景说明:霍奇金淋巴瘤;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:SNU475 Cells、HCC-1833 Cells、QGP1 Cells
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
ACC-3 Cells;背景说明:Acc-3细胞源自一位49岁男性的腺样囊性癌。能表达角蛋白。;传代方法:消化3-5分钟。1:2。3天内可长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:4T1-LUC Cells、HRA 19 Cells、SUM-149 Cells
SK UT 1 Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:12传代,2天换液1次。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:SNU216 Cells、HD11 Cells、MN60 Cells
L-5178-Y Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:Clone 929 Cells、MD Anderson-Metastatic Breast-330 Cells、GM03569D Cells
SKNBE-1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:SKOV-433 Cells、BC3H-1 Cells、JS1 Cells
NCIH2122 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:4传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:淋巴母细胞;相关产品有:LN-382 Cells、OVTOKO Cells、NCIH1581 Cells
H-446 Cells;背景说明:该细胞是1982年由CarneyD和GazdarAF等从一位小细胞肺癌患者的胸腔积液中建立的。细胞的原始形态并不具有小细胞肺癌特征。这个细胞株是小细胞肺癌的生化和形态学上的变种,表达神经元特有的烯醇酶和脑型肌酸激酶同工酶;左旋多巴脱羧酶、蚕素、抗利尿激素、催产素或胃泌激素释放肽未达到可检测水平。与正常细胞相比,该细胞c-mycDNA序列扩增约20倍,RNA增加15倍。最初传代培养基用含有5%FBS的RPMI1640,另外添加10nM化可的松、0.005mg/ml胰岛素、0.01mg/ml转铁;传代方法:1:2传代;生长特性:贴壁/悬浮生长,混合;形态特性:上皮样;相关产品有:U251-MG Cells、Hs 888.T Cells、A9(Hamprecht) Cells
3T3F442A Cells;背景说明:脂肪前体细胞;雄性;Swiss albino;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Microbiological Associates-104 Cells、JB-6 Cl 30 Cells、NWA Cells
GM10650 Cells(拥有STR基因鉴定图谱)
HAP1 CD81 (-) 2 Cells(拥有STR基因鉴定图谱)
CMT-93 Cells;背景说明:结肠癌;C57BL/ICRF;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Bac1 2F5 Cells、D341MD Cells、H1105 Cells
253J-Bladder-V Cells;背景说明:膀胱癌;淋巴结转移;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:LA 4 Cells、KMST-6 Cells、PAI Cells
MKN1 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:MDCK2 Cells、KLN-205 Cells、Ly3 Cells
Metastatic Variant 522 Cells;背景说明:肺腺癌;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:ZR-75-30 Cells、MV3 Cells、MKN-74 Cells
C1R Cells;背景说明:B细胞;EBV转染;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:HEK-293 Cells、UMNSAH-DF1 Cells、NOR 10 Cells
JROECL33 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:LS-411N Cells、HEK AD293 Cells、OCI-AML5 Cells
D283-MED Cells;背景说明:详见相关文献介绍;传代方法:每周换液2-3次。;生长特性:悬浮细胞的多细胞聚集体,和一些贴壁 Cells;形态特性:上皮细胞;相关产品有:MBVP Cells、CAL 78 Cells、WM115-mel Cells
ONS76 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:TCam 2 Cells、He-La Cells、MG63 Cells
HG03899 Cells(拥有STR基因鉴定图谱)
IM Cells(拥有STR基因鉴定图谱)
LTEP-sm Cells(拥有STR基因鉴定图谱)
ND01457 Cells(拥有STR基因鉴定图谱)
PCC3 Cells(拥有STR基因鉴定图谱)
Ubigene HeLa WRN KO Cells(拥有STR基因鉴定图谱)
XPL1KM Cells(拥有STR基因鉴定图谱)
HG01965 Cells(拥有STR基因鉴定图谱)
K1 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明;相关产品有:McCoy B Cells、PLA-802 Cells、PNEC30 Cells
Madison lung Cells;背景说明:肺癌;BALB/c;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:WEHI-279 Cells、CFPAC-1 Cells、K 562 Cells
NFS-60 Cells;背景说明:详见相关文献介绍;传代方法:1:3传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:Hs-600-T Cells、MeSoTheliOma-211H Cells、293 H Cells
NTERA-2/D1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:RM-1 Cells、H-520 Cells、MAVER-1 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
SK-OV-433 Cells;背景说明:卵巢癌;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:KYSE-450 Cells、WIL2S Cells、DMS 273 Cells
SC1 Cells;背景说明:胚胎;自发永生;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:H-1105 Cells、3AO Cells、RH30SJ Cells
NR 8383 Cells;背景说明:NR8383(正常大鼠,1983年8月3日)来源于肺灌洗时的正常大鼠肺泡巨噬细胞。细胞在gerbil肺细胞连续培养液存在下培养了大约8-9个月。随后,不再需要外源生长因子。通过有限稀释法从单个细胞克隆并亚克隆NR8383细胞,并三次用软琼脂亚克隆。细胞表现出巨噬细胞的特性,吞噬酵母多糖和铜绿,非特异性脂酶活性,Fc受体,氧化降解;分泌IL-1,TNFbeta和IL-6,可重复地响应外源生长因子。NR8383细胞响应博莱霉素,分泌TGFbeta前体。在博莱霉素刺激下,TGFbe;传代方法:1:2传代;生长特性:半贴壁生长;形态特性:巨噬细胞;相关产品有:RH-30 Cells、SF 539 Cells、PLC8024 Cells
RD-ES Cells;背景说明:详见相关文献介绍;传代方法:1:8传代:每周换液2-3次;生长特性:贴壁和悬浮混合;形态特性:上皮样;相关产品有:BSC1 Cells、H-810 Cells、OCI-AML-4 Cells
Bovine ENDometrial cells Cells;背景说明:子宫内膜;上皮细胞;雌性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:N9 Cells、MDA-MB-134-VI Cells、CF Pac1 Cells
brain-derived Endothelial cells.3 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:NH-6 Cells、RPMI 7951 Cells、OCI-Ly 3 Cells
EA.hy 926 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:RAMSCs Cells、SKMel-5 Cells、HEI-193 Cells
HDLM-2 Cells;背景说明:霍奇金淋巴瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:MHCC-97 Cells、D407 Cells、H2106 Cells
H28 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代,每周换液2-3次;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:H1618 Cells、HOK Cells、V79-GalK1 Cells
SCRP2307i Cells(拥有STR基因鉴定图谱)
PLMVEC Cells;背景说明:肺微血管;内皮 Cells;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:JB6 clone 30, subclone 7b Cells、HTh-74 Cells、L(TK-) Cells
LS123 Cells;背景说明:详见相关文献介绍;传代方法:1:4—1:8传代,每周换液2—3次;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HS-68 Cells、A-172 MG Cells、HSMC Cells
HGMC Cells;背景说明:肾小球系膜;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:MFE 296 Cells、DSL-6A/C1 Cells、OVCAR-8 Cells
HT 1376 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:PG-4(S+L-) Cells、Panc-327 Cells、NCIH1993 Cells
Hs 611.T Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;每周换液2-3次。;生长特性:混合型;形态特性:淋巴母细胞样;相关产品有:PE/CA-PJ34 (clone C12) Cells、P3/X63-Ag8 Cells、HPAF/CD18 Cells
SKNBE(1) Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:WERI-Rb 1 Cells、HCC-1588 Cells、NBL_S Cells
JKT1 Cells;背景说明:精原瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Hi-5 Cells、PC3M-1E8 Cells、CAL 120 Cells
U373 Cells;背景说明:胶质瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:ASPC1 Cells、BIC1 Cells、Y-79 Cells
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NCIH1734 Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:SUDHL-1 Cells、NCI-H1395 Cells、SW-403 Cells
RFL6 Cells;背景说明:胚肺;成纤维细胞;SD大鼠;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:HT-1197 Cells、AML-2 Cells、M619 Cells
Panc2_03 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H-1836 Cells、SW620 Cells、Mahlavu Cells
rHSC-99 Cells;背景说明:肝星状 Cells;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:624 Cells、PANC 203 Cells、MCMEC Cells
253J-BV Cells;背景说明:膀胱癌;淋巴结转移;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:RC-K8 Cells、GTL 16 Cells、MIA PaCa-2 Cells
NCIH1355 Cells;背景说明:详见相关文献介绍;传代方法:每周换液2次。;生长特性:悬浮生长;形态特性:详见产品说明;相关产品有:HSC1 Cells、MOLM16 Cells、beta-TC6 Cells
BayGenomics ES cell line RRI359 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line XH819 Cells(拥有STR基因鉴定图谱)
F45J Cells(拥有STR基因鉴定图谱)
ND23 Cells(拥有STR基因鉴定图谱)
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
v6.5 Eapp-K1 Cells(拥有STR基因鉴定图谱)
MCF-10AGFP Cells(拥有STR基因鉴定图谱)
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Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.
Pancreas 29:193-203(2004)
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Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.
Established cell lines used in cystic fibrosis research.
J. Cyst. Fibros. 3:191-196(2004)
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Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
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Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.
Cancer Sci. 99:986-994(2008)
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Yamada M., Fujii K., Koyama K., Hirohashi S., Kondo T.
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Distribution of characteristic mutations in native ductal adenocarcinoma of the pancreas and pancreatic cancer cell lines.
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PubMed=25167228; DOI=10.1038/bjc.2014.475; PMCID=PMC4453732
Hamidi H., Lu M., Chau K., Anderson L., Fejzo M.S., Ginther C., Linnartz R., Zubel A., Slamon D.J., Finn R.S.
KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.
Br. J. Cancer 111:1788-1801(2014)
PubMed=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652
Cowley G.S., Weir B.A., Vazquez F., Tamayo P., Scott J.A., Rusin S., East-Seletsky A., Ali L.D., Gerath W.F.J., Pantel S.E., Lizotte P.H., Jiang G.-Z., Hsiao J., Tsherniak A., Dwinell E., Aoyama S., Okamoto M., Harrington W., Gelfand E.T., Green T.M., Tomko M.J., Gopal S., Wong T.C., Li H.-B., Howell S., Stransky N., Liefeld T., Jang D., Bistline J., Meyers B.H., Armstrong S.A., Anderson K.C., Stegmaier K., Reich M., Pellman D., Boehm J.S., Mesirov J.P., Golub T.R., Root D.E., Hahn W.C.
Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.
Sci. Data 1:140035-140035(2014)
PubMed=25485619; DOI=10.1038/nbt.3080
Klijn C., Durinck S., Stawiski E.W., Haverty P.M., Jiang Z.-S., Liu H.-B., Degenhardt J., Mayba O., Gnad F., Liu J.-F., Pau G., Reeder J., Cao Y., Mukhyala K., Selvaraj S.K., Yu M.-M., Zynda G.J., Brauer M.J., Wu T.D., Gentleman R.C., Manning G., Yauch R.L., Bourgon R., Stokoe D., Modrusan Z., Neve R.M., de Sauvage F.J., Settleman J., Seshagiri S., Zhang Z.-M.
A comprehensive transcriptional portrait of human cancer cell lines.
Nat. Biotechnol. 33:306-312(2015)
PubMed=25877200; DOI=10.1038/nature14397
Yu M., Selvaraj S.K., Liang-Chu M.M.Y., Aghajani S., Busse M., Yuan J., Lee G., Peale F.V., Klijn C., Bourgon R., Kaminker J.S., Neve R.M.
A resource for cell line authentication, annotation and quality control.
Nature 520:307-311(2015)
PubMed=26216984; DOI=10.1073/pnas.1501605112; PMCID=PMC4538616
Daemen A., Peterson D., Sahu N., McCord R., Du X.-N., Liu B., Kowanetz K., Hong R., Moffat J., Gao M., Boudreau A., Mroue R., Corson L., O'Brien T., Qing J., Sampath D., Merchant M., Yauch R.L., Manning G., Settleman J., Hatzivassiliou G., Evangelista M.
Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.
Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(2015)
PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
Scholtalbers J., Boegel S., Bukur T., Byl M., Goerges S., Sorn P., Loewer M., Sahin U., Castle J.C.
TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.
Genome Med. 7:118.1-118.7(2015)
PubMed=27259358; DOI=10.1074/mcp.M116.058313; PMCID=PMC4974343
Humphrey E.S., Su S.-P., Nagrial A.M., Hochgrafe F., Pajic M., Lehrbach G.M., Parton R.G., Yap A.S., Horvath L.G., Chang D.K., Biankin A.V., Wu J.-M., Daly R.J.
Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.
Mol. Cell. Proteomics 15:2671-2685(2016)
PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)
PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.
Characterization of human cancer cell lines by reverse-phase protein arrays.
Cancer Cell 31:225-239(2017)
PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.
An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
Cancer Res. 79:1263-1273(2019)"
传代方法:1:2-1:4(首次传代建议1:2)
生长特性:贴壁生长
换液频率:每周2-3次
背景资料:是一种人胰腺导管腺癌(Pancreatic Ductal Adenocarcinoma, PDAC)细胞系,建自26岁白人男性囊性纤维变性(CF)的肝转移灶,该患者合并有囊肿性纤维化。CFPAC-1细胞表达囊性纤维变性跨膜调节因子(CFTR),CFPAC-1细胞形态为上皮细胞样且顶端微绒毛极化。CFPAC-1细胞表达胰腺管细胞特征性的细胞角蛋白和癌胚抗原。
GFP-Olig2 Cells;背景说明:胚胎干细胞;129X1/SvJ;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:hTERT-RPE Cells、AML 12 Cells、NCIH1618 Cells
RPE1 Cells;背景说明:视网膜色素上皮;hTERT永生;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:WM 266-4 Cells、H-2195 Cells、CCD-112 CoN Cells
HPAF-II/CD18 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:MSC Cells、GM-346 Cells、SUP-B15 Cells
养了几年细胞,说一点自己培养细胞方面的看法:1)培养细胞前,可以看看细胞点说明,包括细胞正常生长的状态图、传代、培养基的类型等;2)不同细胞生长周期不同,有的生长很快,比如说-MB-231,传代的时候取离心悬的十分之一就已经足够了,有的又是别慢,等的人心焦,B474就是,传代是一分二,复苏起始的时候两周多才能长满,所以就要在培养细胞的过程中多多摸索了;3)对于娇弱的细胞,就得细心呵护了,胰酶消化不能过久,吹得时候要轻柔,离心时候也要注意转速和时间,每天都要去看一下细胞,肉眼观察培养基状况、显微镜下观察细胞生长状况;4)冻存细胞复苏后第二天ZuiHAO更换一次培养基;5)培养箱隔一段时间彻底用酒精棉擦洗一次;6)养细胞Zui大的教训:不能偷懒!细胞虐我千百遍,我待细胞如初恋。1)不管买的细胞、惠赠的细胞,刚拿到手赶紧做两件事:检测是否有支原体污染; 迅速扩增冻存;2)发现有污染迅速处理掉,别是当你养了很多种细胞时; 细菌污染,真菌污染很容易发现,支原体污染的话,细胞会长的慢,买个支原体检测的ki定期检测一下;3)传代细胞日常的值日清洁是必须的,此外还要定期熏蒸;4)细胞的传代一定要规律,保持相同的confluency和传代时间间隔,不要随心所欲或者拖延;5)注意个人卫生。
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
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产品包装形式:复苏细胞:T25培养瓶(一瓶)或冻存细胞:1ml冻存管(两支)
来源说明:细胞主要来源ATCC、DSMZ等细胞库
物种来源:Human\Mouse\Rat\Others
Calu-3 Cells;背景说明:该细胞是从一名25岁的白人男性肺腺癌患者的胸水中分离建立的;该患者曾使用过环磷酰胺、博来霉素、阿霉素进行治疗。该细胞接种至裸鼠可成瘤;可作转染宿主。;传代方法:消化20分钟。1:2。5-6天长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H-378 Cells、OP-9 Cells、Hs 611.T Cells
SupB15WT Cells;背景说明:详见相关文献介绍;传代方法:1:2传代。3天内可长满。;生长特性:悬浮生长;形态特性:淋巴母细胞;相关产品有:H-1944 Cells、IGROV 1 Cells、ME 180 Cells
SNU-638 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:Hu-P-T4 Cells、VeroC1008 Cells、Anip[973] Cells
EA. hy 926 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:SUM190PT Cells、THLE-2 Cells、AU 565 Cells
细胞常规培养传代流程(请严格遵照无菌操作):1)吸出原培养瓶中的培养基,PBS缓冲润洗细胞两次,加2-3ml 0.25%胰酶进行消化细胞(注意把握消化时间,通常控制在1-2min);2)镜下观察消化情况,在细胞边缘缩小,贴壁松动时(不建议消化到细胞漂浮)去掉胰酶,加6-8ml完全培养基,轻轻吹打细胞层,尽量把细胞层吹落,吹散;3)取部分细胞悬转移到新的培养皿/瓶中,添加适当的完全培养基,把细胞悬打匀,于培养箱中培养;4)注意培养基PH值变化情况,定期换(每周2-3次),待细胞密度达到80%以后重复1项操作或者冻存;别注意:(如使用公共实验室或者初次接触细胞培养,建议添加双抗培养)1)收到细胞后请尽快更换为含15%血清的新鲜培养基,如因殊情况需要继续使用原瓶,请在原瓶培养基中额外添加10%的血清,(原瓶培养基的继续使用时间Zui长不宜超过72小时);2)贴壁细胞收到当天切忌立刻消化,请将细胞换后放置培养箱孵育到第二天再做消化传代,请YOU先选择直径6cm的培养皿进行传代培养;3)如签收时出现培养瓶壁破裂,漏等情况请及时做HAO照片记录并联系实验室。
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CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
形态特性:上皮细胞样
在细胞传代过程中,离心操作后的上清液处理是一个关键步骤,而关于是用移液枪吸走还是直接倒掉上清液,需要综合多方面因素来考量。使用移液枪吸走上清液具有一定的优势。移液枪能够较为精准地控制吸取的量和速度,可以地减少对细胞沉淀的扰动。可以根据实际情况尽可能地吸净上清液,减少残留血清或培养基成分对后续细胞培养的潜在影响,比如残留的血清可能会改变新培养基的营养成分比例或带来一些未知的生长因子干扰。然而,直接倒掉上清液也并非不可行。在处理一些细胞数量较多、细胞耐受性较好且对实验精度要求并非极高的细胞传代时,直接倒掉上清液能够提高操作效率,节省时间。但这种方式存在一定风险,直接倾倒时较难控制力度和角度,如果操作不慎,容易使细胞沉淀随着上清液一起流出,导致细胞损失,而且可能会因液体快速流下冲击细胞沉淀造成细胞的物理性损伤。在实际的细胞传代操作中,应根据细胞的特性、实验的要求以及个人的操作熟练程度来选择合适的上清液处理方式。对于新手或者处理珍贵细胞系时,建议优先采用移液枪吸走的方式,以保障细胞的活性和传代的成功率。而在积累了丰富经验且对实验条件有充分把握的情况下,可以根据具体情况灵活运用直接倒掉上清液的方法,在保证实验质量的同时提高工作效率。
Baby Hamster Kidney from litter No. 21 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代,每周换液1-2次。;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:PCI-4B Cells、KATO III Cells、GFP-Olig2 Cells
SKMEL24 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:4传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:星形的;相关产品有:32D clone 3 Cells、UMNSAH/DF-1 Cells、RGC6 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
TE354.T Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明;相关产品有:S.B. Cells、HCC44 Cells、RS1 Cells
COLO 320 HSR Cells;背景说明:该细胞1984年建系,源自一位33岁患有大肠腺癌男性经5-fu治疗后的腹水。;传代方法:1:2传代。3天内可长满。;生长特性:半贴壁生长;形态特性:详见产品说明;相关产品有:DR2R1610 Cells、E0771 Cells、H-498 Cells
NCIH1618 Cells;背景说明:详见相关文献介绍;传代方法:3-4天换液1次。;生长特性:悬浮生长;形态特性:详见产品说明;相关产品有:CFSC-2G Cells、LAN1 Cells、KP-N-YN Cells
OCI-LY-3 Cells;背景说明:弥漫大B淋巴瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:MEC-1 Cells、SKml2 Cells、HIT Cells
CHO/dhFr- Cells;背景说明:该细胞为二叶酸还原酶缺陷型;培养基中没有HT(次黄嘌呤-胸腺嘧啶)时,该细胞会死亡;培养基中加入甲喋呤可以防止对该药物具有低抵抗性的回变细胞的生长;可作转染宿主。;传代方法:消化3-5分钟。1:2。3天内可长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:MDBK Cells、NOK Cells、HT 115 Cells
Intestinal Porcine Epithelial Cell line-J2 Cells;背景说明:小肠;上皮细胞;自发永生;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:B10BR Cells、C-33A Cells、HuH 6 Cells
Abcam A-549 NRP1 KO Cells(拥有STR基因鉴定图谱)
ABS-9 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line CSH003 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRU401 Cells(拥有STR基因鉴定图谱)
BB88 Cells(拥有STR基因鉴定图谱)
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CHO-glyA Cells(拥有STR基因鉴定图谱)
DA02517 Cells(拥有STR基因鉴定图谱)
DA05596 Cells(拥有STR基因鉴定图谱)
GIBHe013-A Cells(拥有STR基因鉴定图谱)
SNU407 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:NCI-BL6 Cells、SNU251 Cells、OVCAR.4 Cells
JJN3 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:DrG Cells、SK-RC 39 Cells、MiaPaca.2 Cells
TM3 Cells;背景说明:TM3细胞在LH作用下cAMP产量升高,但对促卵泡激素没有响应。对LH的响应持续时间与血清批次有关。在LH存在下,细胞可以代谢胆固醇。检测发现鼠痘病毒阴性。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HRCEC Cells、NS653 Cells、HSC-1 Cells
H2052 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:K-562 Cells、P560 Cells、L cells (TK-) Cells
3T3 Cells;背景说明:3T3细胞株是1962年Todaro G和Green H从分离的瑞士小鼠胚胎中建立的;该细胞的生长受接触性抑制,汇合状态的单层细胞密度为40000个细胞/平方厘米;检测结果显示该细胞鼠痘病毒阴性;在中生长较好,在某些玻璃表面上可能状态不佳;细胞生长饱和时其密度可以达到约50000 cells/cm2。;传代方法:1:3传代;3-4天1次。;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:Me-Wo Cells、WERIRb1 Cells、Line 207 Cells
Ca Ski Cells;背景说明:这株细胞是从小肠肠系膜转移灶的细胞中建立的。 据报道,它含有完整的HPV-16(每个细胞大约600个拷贝)和HPV-18相关序列。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:Tb 1 Lu (NBL-12) Cells、University of Michigan-Urothelial Carcinoma-14 Cells、D-407 Cells
HUASMC Cells;背景说明:脐动脉平滑肌;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:HC11 Cells、SKLU01 Cells、hTERT-HME1 Cells
TR 146 Cells;背景说明:食管鳞癌;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:SW1222 Cells、SNB19 Cells、KM H-2 Cells
BC-022 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:EL-4 Cells、COLO 206F Cells、RPMI-7666 Cells
Vero 76 clone E6 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:EFO 27 Cells、HMCB Cells、PaTu-8988s Cells
NCI-H2141 Cells;背景说明:详见相关文献介绍;传代方法:3-4天换液1次。;生长特性:悬浮生长;形态特性:聚团悬浮;相关产品有:KTA-7 Cells、Ca9-22 Cells、BIC-1 Cells
HS852.T Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:HEL-299 Cells、NCIH1915 Cells、Fetal Rhesus Kidney-4 Cells
VM-CUB-1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:BT-483 Cells、SF-126 Cells、AU565 Cells
2.43 Cells(拥有STR基因鉴定图谱)
L 428 Cells;背景说明:霍奇金淋巴瘤;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:SNU475 Cells、HCC-1833 Cells、QGP1 Cells
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
ACC-3 Cells;背景说明:Acc-3细胞源自一位49岁男性的腺样囊性癌。能表达角蛋白。;传代方法:消化3-5分钟。1:2。3天内可长满。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:4T1-LUC Cells、HRA 19 Cells、SUM-149 Cells
SK UT 1 Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:12传代,2天换液1次。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:SNU216 Cells、HD11 Cells、MN60 Cells
L-5178-Y Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:Clone 929 Cells、MD Anderson-Metastatic Breast-330 Cells、GM03569D Cells
SKNBE-1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:SKOV-433 Cells、BC3H-1 Cells、JS1 Cells
NCIH2122 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:4传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:淋巴母细胞;相关产品有:LN-382 Cells、OVTOKO Cells、NCIH1581 Cells
H-446 Cells;背景说明:该细胞是1982年由CarneyD和GazdarAF等从一位小细胞肺癌患者的胸腔积液中建立的。细胞的原始形态并不具有小细胞肺癌特征。这个细胞株是小细胞肺癌的生化和形态学上的变种,表达神经元特有的烯醇酶和脑型肌酸激酶同工酶;左旋多巴脱羧酶、蚕素、抗利尿激素、催产素或胃泌激素释放肽未达到可检测水平。与正常细胞相比,该细胞c-mycDNA序列扩增约20倍,RNA增加15倍。最初传代培养基用含有5%FBS的RPMI1640,另外添加10nM化可的松、0.005mg/ml胰岛素、0.01mg/ml转铁;传代方法:1:2传代;生长特性:贴壁/悬浮生长,混合;形态特性:上皮样;相关产品有:U251-MG Cells、Hs 888.T Cells、A9(Hamprecht) Cells
3T3F442A Cells;背景说明:脂肪前体细胞;雄性;Swiss albino;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Microbiological Associates-104 Cells、JB-6 Cl 30 Cells、NWA Cells
GM10650 Cells(拥有STR基因鉴定图谱)
HAP1 CD81 (-) 2 Cells(拥有STR基因鉴定图谱)
CMT-93 Cells;背景说明:结肠癌;C57BL/ICRF;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Bac1 2F5 Cells、D341MD Cells、H1105 Cells
253J-Bladder-V Cells;背景说明:膀胱癌;淋巴结转移;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:LA 4 Cells、KMST-6 Cells、PAI Cells
MKN1 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:MDCK2 Cells、KLN-205 Cells、Ly3 Cells
Metastatic Variant 522 Cells;背景说明:肺腺癌;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:ZR-75-30 Cells、MV3 Cells、MKN-74 Cells
C1R Cells;背景说明:B细胞;EBV转染;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:HEK-293 Cells、UMNSAH-DF1 Cells、NOR 10 Cells
JROECL33 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:LS-411N Cells、HEK AD293 Cells、OCI-AML5 Cells
D283-MED Cells;背景说明:详见相关文献介绍;传代方法:每周换液2-3次。;生长特性:悬浮细胞的多细胞聚集体,和一些贴壁 Cells;形态特性:上皮细胞;相关产品有:MBVP Cells、CAL 78 Cells、WM115-mel Cells
ONS76 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:TCam 2 Cells、He-La Cells、MG63 Cells
HG03899 Cells(拥有STR基因鉴定图谱)
IM Cells(拥有STR基因鉴定图谱)
LTEP-sm Cells(拥有STR基因鉴定图谱)
ND01457 Cells(拥有STR基因鉴定图谱)
PCC3 Cells(拥有STR基因鉴定图谱)
Ubigene HeLa WRN KO Cells(拥有STR基因鉴定图谱)
XPL1KM Cells(拥有STR基因鉴定图谱)
HG01965 Cells(拥有STR基因鉴定图谱)
K1 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明;相关产品有:McCoy B Cells、PLA-802 Cells、PNEC30 Cells
Madison lung Cells;背景说明:肺癌;BALB/c;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:WEHI-279 Cells、CFPAC-1 Cells、K 562 Cells
NFS-60 Cells;背景说明:详见相关文献介绍;传代方法:1:3传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:Hs-600-T Cells、MeSoTheliOma-211H Cells、293 H Cells
NTERA-2/D1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:RM-1 Cells、H-520 Cells、MAVER-1 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
BpRcl Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代;每周换液2-3次。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:HTR-8/SV neo Cells、NCI-H508 Cells、ARH 77 Cells
SK-OV-433 Cells;背景说明:卵巢癌;女性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:KYSE-450 Cells、WIL2S Cells、DMS 273 Cells
SC1 Cells;背景说明:胚胎;自发永生;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:H-1105 Cells、3AO Cells、RH30SJ Cells
NR 8383 Cells;背景说明:NR8383(正常大鼠,1983年8月3日)来源于肺灌洗时的正常大鼠肺泡巨噬细胞。细胞在gerbil肺细胞连续培养液存在下培养了大约8-9个月。随后,不再需要外源生长因子。通过有限稀释法从单个细胞克隆并亚克隆NR8383细胞,并三次用软琼脂亚克隆。细胞表现出巨噬细胞的特性,吞噬酵母多糖和铜绿,非特异性脂酶活性,Fc受体,氧化降解;分泌IL-1,TNFbeta和IL-6,可重复地响应外源生长因子。NR8383细胞响应博莱霉素,分泌TGFbeta前体。在博莱霉素刺激下,TGFbe;传代方法:1:2传代;生长特性:半贴壁生长;形态特性:巨噬细胞;相关产品有:RH-30 Cells、SF 539 Cells、PLC8024 Cells
RD-ES Cells;背景说明:详见相关文献介绍;传代方法:1:8传代:每周换液2-3次;生长特性:贴壁和悬浮混合;形态特性:上皮样;相关产品有:BSC1 Cells、H-810 Cells、OCI-AML-4 Cells
Bovine ENDometrial cells Cells;背景说明:子宫内膜;上皮细胞;雌性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:N9 Cells、MDA-MB-134-VI Cells、CF Pac1 Cells
brain-derived Endothelial cells.3 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:NH-6 Cells、RPMI 7951 Cells、OCI-Ly 3 Cells
EA.hy 926 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:RAMSCs Cells、SKMel-5 Cells、HEI-193 Cells
HDLM-2 Cells;背景说明:霍奇金淋巴瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:悬浮;形态特性:详见产品说明;相关产品有:MHCC-97 Cells、D407 Cells、H2106 Cells
H28 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代,每周换液2-3次;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:H1618 Cells、HOK Cells、V79-GalK1 Cells
SCRP2307i Cells(拥有STR基因鉴定图谱)
PLMVEC Cells;背景说明:肺微血管;内皮 Cells;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:JB6 clone 30, subclone 7b Cells、HTh-74 Cells、L(TK-) Cells
LS123 Cells;背景说明:详见相关文献介绍;传代方法:1:4—1:8传代,每周换液2—3次;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HS-68 Cells、A-172 MG Cells、HSMC Cells
HGMC Cells;背景说明:肾小球系膜;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:MFE 296 Cells、DSL-6A/C1 Cells、OVCAR-8 Cells
HT 1376 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:详见产品说明;相关产品有:PG-4(S+L-) Cells、Panc-327 Cells、NCIH1993 Cells
Hs 611.T Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;每周换液2-3次。;生长特性:混合型;形态特性:淋巴母细胞样;相关产品有:PE/CA-PJ34 (clone C12) Cells、P3/X63-Ag8 Cells、HPAF/CD18 Cells
SKNBE(1) Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁或悬浮,详见产品说明部分;形态特性:详见产品说明;相关产品有:WERI-Rb 1 Cells、HCC-1588 Cells、NBL_S Cells
JKT1 Cells;背景说明:精原瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:Hi-5 Cells、PC3M-1E8 Cells、CAL 120 Cells
U373 Cells;背景说明:胶质瘤;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:ASPC1 Cells、BIC1 Cells、Y-79 Cells
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NCIH1734 Cells;背景说明:详见相关文献介绍;传代方法:1:4-1:6传代。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:SUDHL-1 Cells、NCI-H1395 Cells、SW-403 Cells
RFL6 Cells;背景说明:胚肺;成纤维细胞;SD大鼠;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:HT-1197 Cells、AML-2 Cells、M619 Cells
Panc2_03 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H-1836 Cells、SW620 Cells、Mahlavu Cells
rHSC-99 Cells;背景说明:肝星状 Cells;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:624 Cells、PANC 203 Cells、MCMEC Cells
253J-BV Cells;背景说明:膀胱癌;淋巴结转移;男性;传代方法:1:2-1:3传代;每周换液2-3次。;生长特性:贴壁;形态特性:详见产品说明;相关产品有:RC-K8 Cells、GTL 16 Cells、MIA PaCa-2 Cells
NCIH1355 Cells;背景说明:详见相关文献介绍;传代方法:每周换液2次。;生长特性:悬浮生长;形态特性:详见产品说明;相关产品有:HSC1 Cells、MOLM16 Cells、beta-TC6 Cells
BayGenomics ES cell line RRI359 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line XH819 Cells(拥有STR基因鉴定图谱)
F45J Cells(拥有STR基因鉴定图谱)
ND23 Cells(拥有STR基因鉴定图谱)
CFPAC-1人胰腺癌传代细胞活性强|送STR图谱
v6.5 Eapp-K1 Cells(拥有STR基因鉴定图谱)
MCF-10AGFP Cells(拥有STR基因鉴定图谱)
" "PubMed=11169959; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1049>3.0.CO;2-C
Sirivatanauksorn V., Sirivatanauksorn Y., Gorman P.A., Davidson J.M., Sheer D., Moore P.S., Scarpa A., Edwards P.A.W., Lemoine N.R.
Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.
Int. J. Cancer 91:350-358(2001)
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Moore P.S., Sipos B., Orlandini S., Sorio C., Real F.X., Lemoine N.R., Gress T.M., Bassi C., Kloppel G., Kalthoff H., Ungefroren H., Lohr J.-M., Scarpa A.
Genetic profile of 22 pancreatic carcinoma cell lines. Analysis of K-ras, p53, p16 and DPC4/Smad4.
Virchows Arch. 439:798-802(2001)
PubMed=12800145; DOI=10.1002/gcc.10218
Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.
Genes Chromosomes Cancer 37:333-345(2003)
PubMed=14695172
Iacobuzio-Donahue C.A., Ashfaq R., Maitra A., Adsay N.V., Shen-Ong G.L.-C., Berg K., Hollingsworth M.A., Cameron J.L., Yeo C.J., Kern S.E., Goggins M.G., Hruban R.H.
Highly expressed genes in pancreatic ductal adenocarcinomas: a comprehensive characterization and comparison of the transcription profiles obtained from three major technologies.
Cancer Res. 63:8614-8622(2003)
PubMed=15126341; DOI=10.1158/0008-5472.CAN-03-3159
Heidenblad M., Schoenmakers E.F.P.M., Jonson T., Gorunova L., Veltman J.A., van Kessel A.G., Hoglund M.
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
Cancer Res. 64:3052-3059(2004)
PubMed=15367885; DOI=10.1097/00006676-200410000-00004
Loukopoulos P., Kanetaka K., Takamura M., Shibata T., Sakamoto M., Hirohashi S.
Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.
Pancreas 29:193-203(2004)
PubMed=15463957; DOI=10.1016/j.jcf.2004.05.040
Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.
Established cell lines used in cystic fibrosis research.
J. Cyst. Fibros. 3:191-196(2004)
PubMed=15688027; DOI=10.1038/sj.onc.1208383
Heidenblad M., Lindgren D., Veltman J.A., Jonson T., Mahlamaki E.H., Gorunova L., van Kessel A.G., Schoenmakers E.F.P.M., Hoglund M.
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
Oncogene 24:1794-1801(2005)
PubMed=16912165; DOI=10.1158/0008-5472.CAN-06-0721
Calhoun E.S., Hucl T., Gallmeier E., West K.M., Arking D.E., Maitra A., Iacobuzio-Donahue C.A., Chakravarti A., Hruban R.H., Kern S.E.
Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
Cancer Res. 66:7920-7928(2006)
PubMed=18380791; DOI=10.1111/j.1349-7006.2008.00779.x; PMCID=PMC11158928
Suzuki A., Shibata T., Shimada Y., Murakami Y., Horii A., Shiratori K., Hirohashi S., Inazawa J., Imoto I.
Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.
Cancer Sci. 99:986-994(2008)
DOI=10.4172/jpb.1000057
Yamada M., Fujii K., Koyama K., Hirohashi S., Kondo T.
The proteomic profile of pancreatic cancer cell lines corresponding to carcinogenesis and metastasis.
J. Proteomics Bioinformatics 2:1-18(2009)
PubMed=19077451; DOI=10.1159/000178871
Harada T., Chelala C., Crnogorac-Jurcevic T., Lemoine N.R.
Genome-wide analysis of pancreatic cancer using microarray-based techniques.
Pancreatology 9:13-24(2009)
PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113
Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.
Signatures of mutation and selection in the cancer genome.
Nature 463:893-898(2010)
PubMed=20418756; DOI=10.1097/MPA.0b013e3181c15963; PMCID=PMC2860631
Deer E.L., Gonzalez-Hernandez J., Coursen J.D., Shea J.E., Ngatia J.G., Scaife C.L., Firpo M.A., Mulvihill S.J.
Phenotype and genotype of pancreatic cancer cell lines.
Pancreas 39:425-435(2010)
PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027
Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature 483:603-607(2012)
PubMed=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396
Marcotte R., Brown K.R., Suarez Saiz F.J., Sayad A., Karamboulas K., Krzyzanowski P.M., Sircoulomb F., Medrano M., Fedyshyn Y., Koh J.L.-Y., van Dyk D., Fedyshyn B., Luhova M., Brito G.C., Vizeacoumar F.J., Vizeacoumar F.S., Datti A., Kasimer D., Buzina A., Mero P., Misquitta C., Normand J., Haider M., Ketela T., Wrana J.L., Rottapel R., Neel B.G., Moffat J.
Essential gene profiles in breast, pancreatic, and ovarian cancer cells.
Cancer Discov. 2:172-189(2012)
DOI=10.4172/2324-9293.1000104
Wagenhauser M.U., Ruckert F., Niedergethmann M., Grutzmann R., Saeger H.-D.
Distribution of characteristic mutations in native ductal adenocarcinoma of the pancreas and pancreatic cancer cell lines.
Cell Biol. Res. Ther. 2:1000104.1-1000104.5(2013)
PubMed=25167228; DOI=10.1038/bjc.2014.475; PMCID=PMC4453732
Hamidi H., Lu M., Chau K., Anderson L., Fejzo M.S., Ginther C., Linnartz R., Zubel A., Slamon D.J., Finn R.S.
KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.
Br. J. Cancer 111:1788-1801(2014)
PubMed=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652
Cowley G.S., Weir B.A., Vazquez F., Tamayo P., Scott J.A., Rusin S., East-Seletsky A., Ali L.D., Gerath W.F.J., Pantel S.E., Lizotte P.H., Jiang G.-Z., Hsiao J., Tsherniak A., Dwinell E., Aoyama S., Okamoto M., Harrington W., Gelfand E.T., Green T.M., Tomko M.J., Gopal S., Wong T.C., Li H.-B., Howell S., Stransky N., Liefeld T., Jang D., Bistline J., Meyers B.H., Armstrong S.A., Anderson K.C., Stegmaier K., Reich M., Pellman D., Boehm J.S., Mesirov J.P., Golub T.R., Root D.E., Hahn W.C.
Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.
Sci. Data 1:140035-140035(2014)
PubMed=25485619; DOI=10.1038/nbt.3080
Klijn C., Durinck S., Stawiski E.W., Haverty P.M., Jiang Z.-S., Liu H.-B., Degenhardt J., Mayba O., Gnad F., Liu J.-F., Pau G., Reeder J., Cao Y., Mukhyala K., Selvaraj S.K., Yu M.-M., Zynda G.J., Brauer M.J., Wu T.D., Gentleman R.C., Manning G., Yauch R.L., Bourgon R., Stokoe D., Modrusan Z., Neve R.M., de Sauvage F.J., Settleman J., Seshagiri S., Zhang Z.-M.
A comprehensive transcriptional portrait of human cancer cell lines.
Nat. Biotechnol. 33:306-312(2015)
PubMed=25877200; DOI=10.1038/nature14397
Yu M., Selvaraj S.K., Liang-Chu M.M.Y., Aghajani S., Busse M., Yuan J., Lee G., Peale F.V., Klijn C., Bourgon R., Kaminker J.S., Neve R.M.
A resource for cell line authentication, annotation and quality control.
Nature 520:307-311(2015)
PubMed=26216984; DOI=10.1073/pnas.1501605112; PMCID=PMC4538616
Daemen A., Peterson D., Sahu N., McCord R., Du X.-N., Liu B., Kowanetz K., Hong R., Moffat J., Gao M., Boudreau A., Mroue R., Corson L., O'Brien T., Qing J., Sampath D., Merchant M., Yauch R.L., Manning G., Settleman J., Hatzivassiliou G., Evangelista M.
Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.
Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(2015)
PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
Scholtalbers J., Boegel S., Bukur T., Byl M., Goerges S., Sorn P., Loewer M., Sahin U., Castle J.C.
TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.
Genome Med. 7:118.1-118.7(2015)
PubMed=27259358; DOI=10.1074/mcp.M116.058313; PMCID=PMC4974343
Humphrey E.S., Su S.-P., Nagrial A.M., Hochgrafe F., Pajic M., Lehrbach G.M., Parton R.G., Yap A.S., Horvath L.G., Chang D.K., Biankin A.V., Wu J.-M., Daly R.J.
Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.
Mol. Cell. Proteomics 15:2671-2685(2016)
PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)
PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.
Characterization of human cancer cell lines by reverse-phase protein arrays.
Cancer Cell 31:225-239(2017)
PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.
An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
Cancer Res. 79:1263-1273(2019)"
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文献和实验该产品被引用文献
"PubMed=11169959; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1049>3.0.CO;2-C
Sirivatanauksorn V., Sirivatanauksorn Y., Gorman P.A., Davidson J.M., Sheer D., Moore P.S., Scarpa A., Edwards P.A.W., Lemoine N.R.
Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.
Int. J. Cancer 91:350-358(2001)
PubMed=11787853; DOI=10.1007/s004280100474
Moore P.S., Sipos B., Orlandini S., Sorio C., Real F.X., Lemoine N.R., Gress T.M., Bassi C., Kloppel G., Kalthoff H., Ungefroren H., Lohr J.-M., Scarpa A.
Genetic profile of 22 pancreatic carcinoma cell lines. Analysis of K-ras, p53, p16 and DPC4/Smad4.
Virchows Arch. 439:798-802(2001)
PubMed=12800145; DOI=10.1002/gcc.10218
Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.
Genes Chromosomes Cancer 37:333-345(2003)
PubMed=14695172
Iacobuzio-Donahue C.A., Ashfaq R., Maitra A., Adsay N.V., Shen-Ong G.L.-C., Berg K., Hollingsworth M.A., Cameron J.L., Yeo C.J., Kern S.E., Goggins M.G., Hruban R.H.
Highly expressed genes in pancreatic ductal adenocarcinomas: a comprehensive characterization and comparison of the transcription profiles obtained from three major technologies.
Cancer Res. 63:8614-8622(2003)
PubMed=15126341; DOI=10.1158/0008-5472.CAN-03-3159
Heidenblad M., Schoenmakers E.F.P.M., Jonson T., Gorunova L., Veltman J.A., van Kessel A.G., Hoglund M.
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
Cancer Res. 64:3052-3059(2004)
PubMed=15367885; DOI=10.1097/00006676-200410000-00004
Loukopoulos P., Kanetaka K., Takamura M., Shibata T., Sakamoto M., Hirohashi S.
Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.
Pancreas 29:193-203(2004)
PubMed=15463957; DOI=10.1016/j.jcf.2004.05.040
Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.
Established cell lines used in cystic fibrosis research.
J. Cyst. Fibros. 3:191-196(2004)
PubMed=15688027; DOI=10.1038/sj.onc.1208383
Heidenblad M., Lindgren D., Veltman J.A., Jonson T., Mahlamaki E.H., Gorunova L., van Kessel A.G., Schoenmakers E.F.P.M., Hoglund M.
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
Oncogene 24:1794-1801(2005)
PubMed=16912165; DOI=10.1158/0008-5472.CAN-06-0721
Calhoun E.S., Hucl T., Gallmeier E., West K.M., Arking D.E., Maitra A., Iacobuzio-Donahue C.A., Chakravarti A., Hruban R.H., Kern S.E.
Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
Cancer Res. 66:7920-7928(2006)
PubMed=18380791; DOI=10.1111/j.1349-7006.2008.00779.x; PMCID=PMC11158928
Suzuki A., Shibata T., Shimada Y., Murakami Y., Horii A., Shiratori K., Hirohashi S., Inazawa J., Imoto I.
Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.
Cancer Sci. 99:986-994(2008)
DOI=10.4172/jpb.1000057
Yamada M., Fujii K., Koyama K., Hirohashi S., Kondo T.
The proteomic profile of pancreatic cancer cell lines corresponding to carcinogenesis and metastasis.
J. Proteomics Bioinformatics 2:1-18(2009)
PubMed=19077451; DOI=10.1159/000178871
Harada T., Chelala C., Crnogorac-Jurcevic T., Lemoine N.R.
Genome-wide analysis of pancreatic cancer using microarray-based techniques.
Pancreatology 9:13-24(2009)
PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113
Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.
Signatures of mutation and selection in the cancer genome.
Nature 463:893-898(2010)
PubMed=20418756; DOI=10.1097/MPA.0b013e3181c15963; PMCID=PMC2860631
Deer E.L., Gonzalez-Hernandez J., Coursen J.D., Shea J.E., Ngatia J.G., Scaife C.L., Firpo M.A., Mulvihill S.J.
Phenotype and genotype of pancreatic cancer cell lines.
Pancreas 39:425-435(2010)
PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027
Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature 483:603-607(2012)
PubMed=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396
Marcotte R., Brown K.R., Suarez Saiz F.J., Sayad A., Karamboulas K., Krzyzanowski P.M., Sircoulomb F., Medrano M., Fedyshyn Y., Koh J.L.-Y., van Dyk D., Fedyshyn B., Luhova M., Brito G.C., Vizeacoumar F.J., Vizeacoumar F.S., Datti A., Kasimer D., Buzina A., Mero P., Misquitta C., Normand J., Haider M., Ketela T., Wrana J.L., Rottapel R., Neel B.G., Moffat J.
Essential gene profiles in breast, pancreatic, and ovarian cancer cells.
Cancer Discov. 2:172-189(2012)
DOI=10.4172/2324-9293.1000104
Wagenhauser M.U., Ruckert F., Niedergethmann M., Grutzmann R., Saeger H.-D.
Distribution of characteristic mutations in native ductal adenocarcinoma of the pancreas and pancreatic cancer cell lines.
Cell Biol. Res. Ther. 2:1000104.1-1000104.5(2013)
PubMed=25167228; DOI=10.1038/bjc.2014.475; PMCID=PMC4453732
Hamidi H., Lu M., Chau K., Anderson L., Fejzo M.S., Ginther C., Linnartz R., Zubel A., Slamon D.J., Finn R.S.
KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.
Br. J. Cancer 111:1788-1801(2014)
PubMed=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652
Cowley G.S., Weir B.A., Vazquez F., Tamayo P., Scott J.A., Rusin S., East-Seletsky A., Ali L.D., Gerath W.F.J., Pantel S.E., Lizotte P.H., Jiang G.-Z., Hsiao J., Tsherniak A., Dwinell E., Aoyama S., Okamoto M., Harrington W., Gelfand E.T., Green T.M., Tomko M.J., Gopal S., Wong T.C., Li H.-B., Howell S., Stransky N., Liefeld T., Jang D., Bistline J., Meyers B.H., Armstrong S.A., Anderson K.C., Stegmaier K., Reich M., Pellman D., Boehm J.S., Mesirov J.P., Golub T.R., Root D.E., Hahn W.C.
Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.
Sci. Data 1:140035-140035(2014)
PubMed=25485619; DOI=10.1038/nbt.3080
Klijn C., Durinck S., Stawiski E.W., Haverty P.M., Jiang Z.-S., Liu H.-B., Degenhardt J., Mayba O., Gnad F., Liu J.-F., Pau G., Reeder J., Cao Y., Mukhyala K., Selvaraj S.K., Yu M.-M., Zynda G.J., Brauer M.J., Wu T.D., Gentleman R.C., Manning G., Yauch R.L., Bourgon R., Stokoe D., Modrusan Z., Neve R.M., de Sauvage F.J., Settleman J., Seshagiri S., Zhang Z.-M.
A comprehensive transcriptional portrait of human cancer cell lines.
Nat. Biotechnol. 33:306-312(2015)
PubMed=25877200; DOI=10.1038/nature14397
Yu M., Selvaraj S.K., Liang-Chu M.M.Y., Aghajani S., Busse M., Yuan J., Lee G., Peale F.V., Klijn C., Bourgon R., Kaminker J.S., Neve R.M.
A resource for cell line authentication, annotation and quality control.
Nature 520:307-311(2015)
PubMed=26216984; DOI=10.1073/pnas.1501605112; PMCID=PMC4538616
Daemen A., Peterson D., Sahu N., McCord R., Du X.-N., Liu B., Kowanetz K., Hong R., Moffat J., Gao M., Boudreau A., Mroue R., Corson L., O'Brien T., Qing J., Sampath D., Merchant M., Yauch R.L., Manning G., Settleman J., Hatzivassiliou G., Evangelista M.
Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.
Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(2015)
PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
Scholtalbers J., Boegel S., Bukur T., Byl M., Goerges S., Sorn P., Loewer M., Sahin U., Castle J.C.
TCLP: an online cancer cell line catalogue integrating HLA type, predicted neo-epitopes, virus and gene expression.
Genome Med. 7:118.1-118.7(2015)
PubMed=27259358; DOI=10.1074/mcp.M116.058313; PMCID=PMC4974343
Humphrey E.S., Su S.-P., Nagrial A.M., Hochgrafe F., Pajic M., Lehrbach G.M., Parton R.G., Yap A.S., Horvath L.G., Chang D.K., Biankin A.V., Wu J.-M., Daly R.J.
Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.
Mol. Cell. Proteomics 15:2671-2685(2016)
PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)
PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.
Characterization of human cancer cell lines by reverse-phase protein arrays.
Cancer Cell 31:225-239(2017)
PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.
An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
Cancer Res. 79:1263-1273(2019)"
Sirivatanauksorn V., Sirivatanauksorn Y., Gorman P.A., Davidson J.M., Sheer D., Moore P.S., Scarpa A., Edwards P.A.W., Lemoine N.R.
Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.
Int. J. Cancer 91:350-358(2001)
PubMed=11787853; DOI=10.1007/s004280100474
Moore P.S., Sipos B., Orlandini S., Sorio C., Real F.X., Lemoine N.R., Gress T.M., Bassi C., Kloppel G., Kalthoff H., Ungefroren H., Lohr J.-M., Scarpa A.
Genetic profile of 22 pancreatic carcinoma cell lines. Analysis of K-ras, p53, p16 and DPC4/Smad4.
Virchows Arch. 439:798-802(2001)
PubMed=12800145; DOI=10.1002/gcc.10218
Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.
Genes Chromosomes Cancer 37:333-345(2003)
PubMed=14695172
Iacobuzio-Donahue C.A., Ashfaq R., Maitra A., Adsay N.V., Shen-Ong G.L.-C., Berg K., Hollingsworth M.A., Cameron J.L., Yeo C.J., Kern S.E., Goggins M.G., Hruban R.H.
Highly expressed genes in pancreatic ductal adenocarcinomas: a comprehensive characterization and comparison of the transcription profiles obtained from three major technologies.
Cancer Res. 63:8614-8622(2003)
PubMed=15126341; DOI=10.1158/0008-5472.CAN-03-3159
Heidenblad M., Schoenmakers E.F.P.M., Jonson T., Gorunova L., Veltman J.A., van Kessel A.G., Hoglund M.
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
Cancer Res. 64:3052-3059(2004)
PubMed=15367885; DOI=10.1097/00006676-200410000-00004
Loukopoulos P., Kanetaka K., Takamura M., Shibata T., Sakamoto M., Hirohashi S.
Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.
Pancreas 29:193-203(2004)
PubMed=15463957; DOI=10.1016/j.jcf.2004.05.040
Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.
Established cell lines used in cystic fibrosis research.
J. Cyst. Fibros. 3:191-196(2004)
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