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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:
22RV1人前列腺癌传代细胞活性强|送STR图谱
- 规格:
1*10(6)Cellls/瓶
"22RV1人前列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:22RV1是来自异种移植(在阉割引起前列腺癌衰退又在其父亲的雄性激素信赖型CWR22嫁接后复发的小鼠中连续传代)的人前列腺癌上皮细胞系。此细胞系表达前列腺特异抗原。二羟基睾丸脂酮轻微刺激细胞生长,经westernblot检测溶解产物与抗雄性激素受体抗体起免疫反应。EGF刺激细胞生长,但TGFβ-1不能抑制细胞生长。该细胞在裸鼠中成瘤。
MDA MB 453 Cells;背景说明:该细胞系由CailleauR在1976年从一名48岁的患有转移性乳腺癌的白人女性的心包渗出液中分离建立的。该细胞表达FGF的受体。;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:上皮样;多角形;相关产品有:M-G63 Cells、T47D:A Cells、C32-mel Cells
C41 Cells;背景说明:宫颈鳞癌;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:详见产品说明书;相关产品有:HEK293-A Cells、C2A Cells、EMT6 Cells
PTK1 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:UPCISCC154 Cells、CHP 100 Cells、GLRK 13 Cells
细胞接收操作说明:请仔细阅读本操作说明及相应的细胞说明书。本公司细胞发货有四种形式:25培养瓶(一般是贴壁细胞使用,悬浮细胞也可以)、离心管(悬浮细胞使用多,当然,有些公司也会用这种离心管形式发贴壁细胞,但是,长期经验来说,贴壁细胞容易发生形态变化,估计是细胞培养空间狭小,血清不足导致(Zui主要是怕运输延误导致这些情况发生),个人不建议用离心管形式发贴壁细胞)及干冰(冻存细胞用,主要是冬天天气冷,温度低于4℃的地方,都要考虑冻存细胞)。25培养瓶:是用25细胞培养瓶直接发货的形式。收到细胞后,拆开包装25培养瓶的自封袋,不拆封口膜,表面喷75%酒精消毒后显微镜观察细胞状态(有条件可以拍下此时细胞照片)。将细胞放入37度培养箱平衡两小时以上,再处理细胞。首先将25中培养基取出装HAO备用,如细胞密度GAO于80%,可以直接消化传代,相反则加入5-6ml培养基放回培养箱继续培养即可。离心管:是用15ml离心管发货的形式,只用于悬浮细胞发货。收到细胞后消毒处理及将细胞放入37度培养箱平衡两小时以上,再处理细胞。首先将25中培养基取出装HAO备用(如果实验室没有25培养瓶,可以暂时75培养瓶,加入10-15ml培养基,建议10ml培养基,也可以使用175培养瓶,加入50-60ml培养基,培养瓶越大,需要的培养基越多。当然如果刚接收到细胞密度不够的话,ZuiHAO不用大瓶子,先用小瓶子养起来再换大的,不然会长得很慢,严重的,会导致细胞死亡等危险),平衡完成后,离心(1000rpm,3min)收集细胞,弃上清,用新的培养基重悬细胞并接种至培养瓶或皿中,放回培养箱继续培养。干冰:是用本公司冻存冻存细胞后,直接用干冰将冻存的细胞冷冻发货的形式。收到细胞后按照细胞复苏的步骤操作即可。
22RV1人前列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
H-661 Cells;背景说明:该细胞1982年建系,源自一位患有大细胞肺癌的男性的胸腔积液。该细胞角蛋白、波形蛋白阳性。;传代方法:1:3—1:5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:PCI-4M Cells、MKN7 Cells、HCC1359 Cells
NBL-1 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:详见产品说明书;相关产品有:LC-1 sq Cells、Highly Aggressively Proliferating Immortalized Cells、KU19-19 Cells
SW1222 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HRA 19 Cells、Normal Rat Kidney-49F Cells、HCC941122 Cells
QGP1 Cells;背景说明:胰腺癌;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:详见产品说明书;相关产品有:NCI-H220 Cells、MT-2J Cells、LS-180 Cells
细胞接收后的操作流程与注意事项:1)如果细胞为贴壁细胞,而收到时呈悬浮或者部分悬浮的状态,请将悬浮的细胞即时离心,加15%血清的完全培养基到新的培养皿/瓶继续培养3天;同时原培养瓶中剩下的贴壁细胞更换为15%血清的完全培养基培养3天。3天后若原瓶或者新瓶中的细胞都没有出现增值而是继续脱落死亡,请及时联系实验室技术人员会跟进解决;2)贴壁细胞生长缓慢;适当提GAO血清浓度(ZuiGAO不能超过20%),或可根据该细胞生长密度,考虑胰酶消化后,转移到新的培养瓶继续培养;3)生长不均:贴壁细胞若出现分布不均,成岛状生长,可将细胞进行消化,重悬打散细胞,加入新鲜培养基进行培养。
┈订┈购┈热┈线:1┈5┈8┈0┈0┈5┈7┈6┈8┈6┈7【微信同号】┈Q┈Q:3┈3┈0┈7┈2┈0┈4┈2┈7┈1;
22RV1人前列腺癌传代细胞活性强|送STR图谱
形态特性:上皮细胞样
准确判断胰酶消化是否完成,首先,观察细胞形态变化是判断胰酶消化程度的重要依据。在加入胰酶后,随着消化的进行,原本贴壁生长的细胞会逐渐变圆。当大部分细胞呈现出圆形,且细胞之间的连接变得松散时,说明消化正在进行中。如果细胞完全脱离培养瓶底部,变成单个的圆形细胞悬浮在消化液中,这通常是消化完成的一个重要标志。此时,在显微镜下观察,细胞应该是圆润、饱满且边界清晰的。其次,可以通过轻轻拍打培养瓶或轻轻晃动培养板来辅助判断。如果细胞很容易从瓶底或板底脱落并在液体中悬浮,说明消化程度可能已经比较合适。但要注意动作要轻柔,避免过度剧烈的晃动对细胞造成损伤。另外,消化时间也是一个参考因素。一般来说,在开始消化时,可以先根据经验设定一个大致的消化时间,然后在这个时间点前后密切观察细胞的状态。如果消化时间过长,可能会导致细胞受损,影响细胞的活性和功能;而消化时间过短,则可能导致细胞没有完全分离,影响传代效果。还可以通过观察消化液的浑浊程度来判断。在消化开始时,消化液通常是比较澄清的。随着消化的进行,当细胞逐渐脱落进入消化液中,消化液会变得浑浊。当浑浊度达到一定程度,且细胞形态也符合消化完成的特征时,可以认为消化好了。总之,在细胞传代用胰酶消化时,需要综合考虑细胞形态变化、拍打或晃动的反应、消化时间以及消化液的浑浊程度等多个因素,来准确判断消化是否完成。
BEP2D Cells;背景说明:支气管;上皮细胞;HPV18转化;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:详见产品说明书;相关产品有:HuT102 Cells、HFL-I Cells、LS-1034 Cells
RWPE1 Cells;背景说明:肿瘤抑制基因: p53 + [PubMed: 9214605] pRB + [PubMed: 9214605] 一位正常男性前列腺组织切片的周围区域的上皮细胞用单拷贝的人乳头瘤病毒的18(HPV-18)进行转化,建立了RWPE-1 (ATCC CRL-11609) 细胞株 [PubMed: 9214605]. 在三维Matrigel培养时,在雄激素作用下,RWPE-1细胞形成腺胞并向培养基中分泌PSA。[PubMed: 11170142]. 当与Matrigel或基质细胞混合注射雄性裸鼠时,RWPE-1细胞也能形成腺胞[PubMed: 11304724] 并产生PSA。 来源于RWPE-1的细胞再用Kirstin鼠类肿瘤病毒转染Ki-ras基因,建立了能成瘤的RWPE-2细胞株(ATCC CRL-11610) [PubMed: 9214605] 和 RWPE2-W99 (ATCC CRL-2853) 细胞株。 另外,用N--N-(MNU)处理RWPE-1,建立了一系列模拟前列腺癌进程中不同时期的成瘤细胞株。 它们是 WPE1-NA22 (ATCC CRL-2849), WPE1-NB14 (ATCC CRL-2850, WPE1-NB11 (ATCC CRL-2851) 和 WPE1-NB26 (ATCC CRL-2852) 细胞株。 据提供者报道,RWPE-1 细胞株(ATCC CRL-11609)经过检测,乙肝、丙肝、都呈阴性。;传代方法:1:3传代,2-3天传一代。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:Walker-256 Cells、mIMCD3 Cells、P3-X63-Ag8.653 Cells
HCGC Cells;背景说明:小脑;颗粒 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:详见产品说明书;相关产品有:BC3H-1 Cells、PG-BE1 Cells、OCUM-1 Cells
ABE8.1/2 Cells;背景说明:淋巴瘤;BALB/c;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:详见产品说明书;相关产品有:Bovine ENDometrial cells Cells、RC-K8 Cells、FL 62891 Cells
SN12C Cells;背景说明:详见相关文献介绍;传代方法:2x10^4 cells/ml;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:H727 Cells、D283-MED Cells、TJ905 Cells
PTK2 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:JIII Cells、OVCAR3 Cells、MDA-MB-435 S Cells
HRVEC Cells;背景说明:视网膜微血管;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:详见产品说明书;相关产品有:CCK-81 Cells、COLO_320DM Cells、L-6 Cells
H2198 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:Malme3M Cells、NK10a Cells、TB-1 Lu Cells
1.1B4 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:4传代;每周2-3次。;生长特性:贴壁生长;形态特性:上皮样;多角形 ;相关产品有:LN-18 Cells、GM637A Cells、Human Kidney-2 Cells
77RD40 Cells(拥有STR基因鉴定图谱)
Abcam MCF-7 DNMT3B KO Cells(拥有STR基因鉴定图谱)
ASUi004-A Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRN197 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YHA254 Cells(拥有STR基因鉴定图谱)
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CC-11 Cells(拥有STR基因鉴定图谱)
DA00926 Cells(拥有STR基因鉴定图谱)
DA05959 Cells(拥有STR基因鉴定图谱)
GM00344 Cells(拥有STR基因鉴定图谱)
NCTC 3960 Cells;背景说明:黑色素瘤;雄性;DBA;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:详见产品说明书;相关产品有:MD Anderson-Metastatic Breast-157 Cells、HOS/MNNG Cells、JAR Cells
HCC-1419 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:上皮样;相关产品有:Adeno 293 Cells、MCFs Cells、INS-1E Cells
OCI-LY-1 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:详见产品说明书;相关产品有:Hs 445 Cells、L6 Cells、SMMC7721 Cells
L-363 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:H2342 Cells、MCF-7 Cells、SK ES 01 Cells
HEK-293FT Cells;背景说明:该细胞稳定表达SV40大T抗原,并且促进最适病毒产物的产生。;传代方法:1:2传代;生长特性:悬浮生长;形态特性:圆形;相关产品有:B16F10 Cells、Jiyoye(P-2003) Cells、High 5 Cells
LICCF Cells;背景说明:肝内胆管癌;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:详见产品说明书;相关产品有:Emory University-3 Cells、DB Cells、EJ1 Cells
H-2052 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:SUM149-PT Cells、SCL II Cells、Hs 863.T Cells
C127 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:M 1 Cells、PTK 1 Cells、TE6 Cells
J-82 Cells;背景说明:电子显微镜下未观察到桥粒但观察到数目不同的粗面内质网和突出微丝。 含ras (H-ras)癌基因。;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:293EBNA Cells、MDA-175 Cells、NCI-H2172 Cells
BL2141 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:CAL148 Cells、MOVAS-1 Cells、PL 45 Cells
U-343 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:详见产品说明书;相关产品有:P3HR1-BL Cells、HCCC9810 Cells、786-0 Cells
AML12 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:详见产品说明书;相关产品有:MC-3T3-E1 Cells、PIG3 Cells、Panc-08.13 Cells
NTera2/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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:PK13 Cells、LOUNH91 Cells、HEK293A Cells
295D2 Cells(拥有STR基因鉴定图谱)
Hs600T Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:详见产品说明书;相关产品有:SNK1 Cells、Hs832T Cells、U20-S Cells
22RV1人前列腺癌传代细胞活性强|送STR图谱
Panc_03_27 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:A2780/Taxol Cells、Strain KB Cells、GP293 Cells
C-28I2 Cells;背景说明:软骨;SV40转化;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:详见产品说明书;相关产品有:RPPVEC Cells、H-1650 Cells、NCI-H1993 Cells
MDA-MB435 Cells;背景说明:乳腺癌;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:详见产品说明书;相关产品有:BHK-21 Cells、Me-Wo Cells、NCI-H1238 Cells
NRK 49F Cells;背景说明:肾;成纤维细胞;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:详见产品说明书;相关产品有:MCA205 Cells、YAC-1 Cells、T-CAM2 Cells
SACC83 Cells;背景说明:涎腺腺样囊性癌;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:详见产品说明书;相关产品有:BMSCs(mBMSCs) Cells、MLMA Cells、SF17 Cells
AML-2 Cells;背景说明:急性髓系白血病;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:详见产品说明书;相关产品有:OCI-Ly7 Cells、NCI-H1755 Cells、C-28I2 Cells
PTK 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:Medical Research Council cell strain-9 Cells、SKRC-42 Cells、SHI-1 Cells
HAP1 ATF5 (-) 1 Cells(拥有STR基因鉴定图谱)
HAP1 SLC46A3 (-) 1 Cells(拥有STR基因鉴定图谱)
FRO 81-2 Cells;背景说明:未分化甲状腺癌;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:详见产品说明书;相关产品有:hTERT-RPE1 Cells、Ect1/E6E7 Cells、IMCD3 Cells
MUS-M1 Cells;背景说明:小肠;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:详见产品说明书;相关产品有:KE-37 Cells、PCI-4M Cells、BNCL2 Cells
DC2.4 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:详见产品说明书;相关产品有:Psi-2-DAP Cells、PK136 Cells、HNSC Cells
SKMEL2 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:多边形的;相关产品有:Tca-83 Cells、SW1353 Cells、GM04679 Cells
Anip-973 Cells;背景说明:肺腺癌;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:详见产品说明书;相关产品有:D 407 Cells、HR-8348 Cells、RKOE6 Cells
AR4IP 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:D341 Med Cells、IEC 6 Cells、SUDHL-16 Cells
SKMel-5 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6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:WC00097 Cells、Hepatoma-22 Cells、HL-1 Cells
ARH-77 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:悬浮生长;形态特性:淋巴母细胞样 ;相关产品有:RFL-6 Cells、NCI-N87 Cells、HEK/EBNA Cells
iBMK Atg5-/- 7.2B9 Cells(拥有STR基因鉴定图谱)
Lis13_Alport2 Cells(拥有STR基因鉴定图谱)
NCCIT-R Cells(拥有STR基因鉴定图谱)
PathHunter CHO-K1 DRD3 beta-arrestin Cells(拥有STR基因鉴定图谱)
S12-27IIb Cells(拥有STR基因鉴定图谱)
Ubigene HCT 116 CFLAR KO Cells(拥有STR基因鉴定图谱)
VRISGi001-A Cells(拥有STR基因鉴定图谱)
HG01806 Cells(拥有STR基因鉴定图谱)
PC 61 5.3 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:NE1-E6E7 Cells、ST2 Cells、HT 1197 Cells
JEG-3 Cells;背景说明:这是一株超三倍体人类细胞株;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:H-295R Cells、GM02131A Cells、Shadyside Hospital Pittsburgh-77 Cells
SW1222 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HRA 19 Cells、Normal Rat Kidney-49F Cells、HCC941122 Cells
CAL 33 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HO1-N1 Cells、HOP 92 Cells、KM932 Cells
SU-DHL2 Cells;背景说明:弥漫性大细胞淋巴瘤;胸腔积液转移;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:详见产品说明书;相关产品有:HCoEpiC Cells、Oka-C1 Cells、TMD8 Cells
HD11 Cells;背景说明:巨噬 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:详见产品说明书;相关产品有:GM05887 Cells、RPMI-6666 Cells、SKNDZ Cells
TALL1 Cells;背景说明:该细胞源于一名复发T-ALL(急性T淋巴细胞性白血病)的儿童的外周血;具有很强的细胞毒性,体内体外实验中都能破坏肿瘤细胞;IL-2可使细胞更好地生长;α/β TCR阳性,γ/δ TCR阴性;可产生IFNγ、TNF-α和GM-CSF。;传代方法:维持细胞密度在4×105-1×106 cells/ml之间,2-3天换液1次 ;生长特性:悬浮生长;形态特性:淋巴母细胞;相关产品有:VERO76 Cells、293-H Cells、SHZ-88 Cells
SKML-28 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:8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:CT26.CL25 Cells、TE32 Cells、PG13 Cells
ETCC007 Cells;背景说明:原位导管癌;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:详见产品说明书;相关产品有:VP303 Cells、Panc 08.13 Cells、RCS Cells
CEM Cells;背景说明:G.E. Foley 等人建立了类淋巴母细胞细胞株CCRF-CEM。 细胞是1964年11月从一位四岁白人女性急性淋巴细胞白血病患者的外周血白血球衣中得到。此细胞系从香港收集而来。;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:淋巴母细胞样;相关产品有:Stanford University-Diffuse Histiocytic Lymphoma-4 Cells、HEK-293H Cells、H740 Cells
HCT 15 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:COV 434 Cells、NCIH2170 Cells、MSTO211H Cells
HD-LM-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:详见产品说明书;相关产品有:EOC 20 Cells、GM04679 Cells、FU-MMT-1 Cells
IGROV 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HDF-a Cells、NCI-Hut 125 Cells、OLN-93 Cells
H2170 Cells;背景说明:该细胞1989年建系,源自一位患有肺鳞状细胞癌的男性,该患者不吸烟;传代方法:1:3—1:6传代,3—5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:MBdSMC Cells、IM95 Cells、MADB 106 Cells
MNNGHOS Cells;背景说明:骨肉瘤;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:详见产品说明书;相关产品有:BIC1 Cells、V 79 Cells、H28 Cells
TK-160 Cells(拥有STR基因鉴定图谱)
HN 4 Cells;背景说明:喉鳞癌;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:详见产品说明书;相关产品有:NTERA2 Cells、EFM-192A Cells、NCI-H1915 Cells
3T3-L1 Cells;背景说明:3T3-L1是从3T3细胞(Swissalbino)中经克隆分离得到的连续传代的亚系。该细胞从快速分裂到汇合和接触性抑制状态经历了前脂肪细胞到脂肪样细胞的转变。该细胞鼠痘病毒阴性;可产生甘油三酯,高浓度血清可增强细胞内脂肪堆积。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:NS1-Ag 4/1 Cells、LTEP-a2 Cells、CCD1112Sk Cells
LAN-5 Cells;背景说明:神经母细胞瘤;骨髓转移;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:详见产品说明书;相关产品有:GA-10 Cells、HCC941122 Cells、HEM-L Cells
WEHI-164 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HSC 3 Cells、3T3(A31) Cells、PC-3M-1E8 Cells
HTh 74 Cells;背景说明:未分化甲状腺癌;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:详见产品说明书;相关产品有:MDA-MB-415 Cells、GM00637 Cells、IOSE-Mar Cells
MDA231-LM2-4175 Cells;背景说明:乳腺癌;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:详见产品说明书;相关产品有:CSQT-2 Cells、Leukemia L1210 Cells、HCT-FET Cells
Buffalo Rat Liver-3A 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:VMRCLCD Cells、Hs940.T Cells、Verda reno Cells
C-Li-7 Cells;背景说明:人肝癌细胞株。这株细胞从裸鼠体外移植瘤中建立。;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明书;相关产品有:SW-780 Cells、SJSA1 Cells、KU 812F Cells
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THC-8307 Cells;背景说明:高分化结肠癌;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:详见产品说明书;相关产品有:LS 123 Cells、SW-403 Cells、Medical Research Council cell strain-9 Cells
HSAS3 Cells;背景说明:皮肤;成纤维 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:详见产品说明书;相关产品有:PE/CA-PJ-34 Cells、CCK81 Cells、Hs445 Cells
MHH-CALL2 Cells;背景说明:急性B淋巴细胞白血病;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:详见产品说明书;相关产品有:D-283MED Cells、NTERA2 Cells、SG231 Cells
NCI-H226 Cells;背景说明:1980年分离建立。;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:Doubling time: ~50 hours (ATCC). Cells、ZR-75-30 Cells、CNE Cells
MA-104 Cells;背景说明:胚肾;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:详见产品说明书;相关产品有:6-10B Cells、SUNE 1 Cells、NCI H2106 Cells
BC3H1 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:H-596 Cells、B 95.8 Cells、HEC-151 Cells
BayGenomics ES cell line RRR557 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YTA062 Cells(拥有STR基因鉴定图谱)
HyCyte LL/2 (LLC1)-Luc Cells(拥有STR基因鉴定图谱)
PCRP-KLF7-1C11 Cells(拥有STR基因鉴定图谱)
22RV1人前列腺癌传代细胞活性强|送STR图谱
GoH3 Cells(拥有STR基因鉴定图谱)
HPSI0115i-zuer_1 Cells(拥有STR基因鉴定图谱)
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Characterization of fibroblast-free CWR-R1ca castration-recurrent prostate cancer cell line.
Prostate 76:1067-1077(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=28145883; DOI=10.18632/oncotarget.14850; PMCID=PMC5386661
Nouri M., Caradec J., Lubik A.A., Li N., Hollier B.G., Takhar M., Altimirano-Dimas M., Chen M.-Q., Roshan-Moniri M., Butler M., Lehman M., Bishop J.L., Truong S., Huang S.-C., Cochrane D.R., Cox M., Collins C., Gleave M.E., Erho N., Alshalafa M., Davicioni E., Nelson C., Gregory-Evans C.Y., Karnes R.J., Jenkins R.B., Klein E.A., Buttyan R.
Therapy-induced developmental reprogramming of prostate cancer cells and acquired therapy resistance.
Oncotarget 8:18949-18967(2017)
PubMed=28928128; DOI=10.1158/0008-5472.CAN-17-0320; PMCID=PMC5654612
Van Etten J.L., Nyquist M.D., Li Y.-M., Yang R.-D., Ho Y., Johnson R., Ondigi O., Voytas D.F., Henzler C., Dehm S.M.
Targeting a single alternative polyadenylation site coordinately blocks expression of androgen receptor mRNA splice variants in prostate cancer.
Cancer Res. 77:5228-5235(2017)
PubMed=30629668; DOI=10.1371/journal.pone.0210404; PMCID=PMC6328144
Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.
Screening human cell lines for viral infections applying RNA-Seq data analysis.
PLoS ONE 14:E0210404-E0210404(2019)
PubMed=30787054; DOI=10.1158/1055-9965.EPI-18-1132; PMCID=PMC6548687
Hooker S.E. Jr., Woods-Burnham L., Bathina M., Lloyd S., Gorjala P., Mitra R., Nonn L., Kimbro K.S., Kittles R.A.
Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines.
Cancer Epidemiol. Biomarkers Prev. 28:1003-1009(2019)
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)
PubMed=30971826; DOI=10.1038/s41586-019-1103-9
Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.
Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.
Nature 568:511-516(2019)
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Kounatidou E., Nakjang S., McCracken S.R.C., Dehm S.M., Robson C.N., Jones D., Gaughan L.
A novel CRISPR-engineered prostate cancer cell line defines the AR-V transcriptome and identifies PARP inhibitor sensitivities.
Nucleic Acids Res. 47:5634-5647(2019)
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Ghandi M., Huang F.W., Jane-Valbuena J., Kryukov G.V., Lo C.C., McDonald E.R. 3rd, Barretina J.G., Gelfand E.T., Bielski C.M., Li H.-X., Hu K., Andreev-Drakhlin A.Y., Kim J., Hess J.M., Haas B.J., Aguet F., Weir B.A., Rothberg M.V., Paolella B.R., Lawrence M.S., Akbani R., Lu Y.-L., Tiv H.L., Gokhale P.C., de Weck A., Mansour A.A., Oh C., Shih J., Hadi K., Rosen Y., Bistline J., Venkatesan K., Reddy A., Sonkin D., Liu M., Lehar J., Korn J.M., Porter D.A., Jones M.D., Golji J., Caponigro G., Taylor J.E., Dunning C.M., Creech A.L., Warren A.C., McFarland J.M., Zamanighomi M., Kauffmann A., Stransky N., Imielinski M., Maruvka Y.E., Cherniack A.D., Tsherniak A., Vazquez F., Jaffe J.D., Lane A.A., Weinstock D.M., Johannessen C.M., Morrissey M.P., Stegmeier F., Schlegel R., Hahn W.C., Getz G., Mills G.B., Boehm J.S., Golub T.R., Garraway L.A., Sellers W.R.
Next-generation characterization of the Cancer Cell Line Encyclopedia.
Nature 569:503-508(2019)
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Yu K., Chen B., Aran D., Charalel J., Yau C., Wolf D.M., van 't Veer L.J., Butte A.J., Goldstein T., Sirota M.
Comprehensive transcriptomic analysis of cell lines as models of primary tumors across 22 tumor types.
Nat. Commun. 10:3574.1-3574.11(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:22RV1是来自异种移植(在阉割引起前列腺癌衰退又在其父亲的雄性激素信赖型CWR22嫁接后复发的小鼠中连续传代)的人前列腺癌上皮细胞系。此细胞系表达前列腺特异抗原。二羟基睾丸脂酮轻微刺激细胞生长,经westernblot检测溶解产物与抗雄性激素受体抗体起免疫反应。EGF刺激细胞生长,但TGFβ-1不能抑制细胞生长。该细胞在裸鼠中成瘤。
MDA MB 453 Cells;背景说明:该细胞系由CailleauR在1976年从一名48岁的患有转移性乳腺癌的白人女性的心包渗出液中分离建立的。该细胞表达FGF的受体。;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:上皮样;多角形;相关产品有:M-G63 Cells、T47D:A Cells、C32-mel Cells
C41 Cells;背景说明:宫颈鳞癌;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:详见产品说明书;相关产品有:HEK293-A Cells、C2A Cells、EMT6 Cells
PTK1 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:UPCISCC154 Cells、CHP 100 Cells、GLRK 13 Cells
细胞接收操作说明:请仔细阅读本操作说明及相应的细胞说明书。本公司细胞发货有四种形式:25培养瓶(一般是贴壁细胞使用,悬浮细胞也可以)、离心管(悬浮细胞使用多,当然,有些公司也会用这种离心管形式发贴壁细胞,但是,长期经验来说,贴壁细胞容易发生形态变化,估计是细胞培养空间狭小,血清不足导致(Zui主要是怕运输延误导致这些情况发生),个人不建议用离心管形式发贴壁细胞)及干冰(冻存细胞用,主要是冬天天气冷,温度低于4℃的地方,都要考虑冻存细胞)。25培养瓶:是用25细胞培养瓶直接发货的形式。收到细胞后,拆开包装25培养瓶的自封袋,不拆封口膜,表面喷75%酒精消毒后显微镜观察细胞状态(有条件可以拍下此时细胞照片)。将细胞放入37度培养箱平衡两小时以上,再处理细胞。首先将25中培养基取出装HAO备用,如细胞密度GAO于80%,可以直接消化传代,相反则加入5-6ml培养基放回培养箱继续培养即可。离心管:是用15ml离心管发货的形式,只用于悬浮细胞发货。收到细胞后消毒处理及将细胞放入37度培养箱平衡两小时以上,再处理细胞。首先将25中培养基取出装HAO备用(如果实验室没有25培养瓶,可以暂时75培养瓶,加入10-15ml培养基,建议10ml培养基,也可以使用175培养瓶,加入50-60ml培养基,培养瓶越大,需要的培养基越多。当然如果刚接收到细胞密度不够的话,ZuiHAO不用大瓶子,先用小瓶子养起来再换大的,不然会长得很慢,严重的,会导致细胞死亡等危险),平衡完成后,离心(1000rpm,3min)收集细胞,弃上清,用新的培养基重悬细胞并接种至培养瓶或皿中,放回培养箱继续培养。干冰:是用本公司冻存冻存细胞后,直接用干冰将冻存的细胞冷冻发货的形式。收到细胞后按照细胞复苏的步骤操作即可。
22RV1人前列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
H-661 Cells;背景说明:该细胞1982年建系,源自一位患有大细胞肺癌的男性的胸腔积液。该细胞角蛋白、波形蛋白阳性。;传代方法:1:3—1:5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:PCI-4M Cells、MKN7 Cells、HCC1359 Cells
NBL-1 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:详见产品说明书;相关产品有:LC-1 sq Cells、Highly Aggressively Proliferating Immortalized Cells、KU19-19 Cells
SW1222 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HRA 19 Cells、Normal Rat Kidney-49F Cells、HCC941122 Cells
QGP1 Cells;背景说明:胰腺癌;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:详见产品说明书;相关产品有:NCI-H220 Cells、MT-2J Cells、LS-180 Cells
细胞接收后的操作流程与注意事项:1)如果细胞为贴壁细胞,而收到时呈悬浮或者部分悬浮的状态,请将悬浮的细胞即时离心,加15%血清的完全培养基到新的培养皿/瓶继续培养3天;同时原培养瓶中剩下的贴壁细胞更换为15%血清的完全培养基培养3天。3天后若原瓶或者新瓶中的细胞都没有出现增值而是继续脱落死亡,请及时联系实验室技术人员会跟进解决;2)贴壁细胞生长缓慢;适当提GAO血清浓度(ZuiGAO不能超过20%),或可根据该细胞生长密度,考虑胰酶消化后,转移到新的培养瓶继续培养;3)生长不均:贴壁细胞若出现分布不均,成岛状生长,可将细胞进行消化,重悬打散细胞,加入新鲜培养基进行培养。
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22RV1人前列腺癌传代细胞活性强|送STR图谱
形态特性:上皮细胞样
准确判断胰酶消化是否完成,首先,观察细胞形态变化是判断胰酶消化程度的重要依据。在加入胰酶后,随着消化的进行,原本贴壁生长的细胞会逐渐变圆。当大部分细胞呈现出圆形,且细胞之间的连接变得松散时,说明消化正在进行中。如果细胞完全脱离培养瓶底部,变成单个的圆形细胞悬浮在消化液中,这通常是消化完成的一个重要标志。此时,在显微镜下观察,细胞应该是圆润、饱满且边界清晰的。其次,可以通过轻轻拍打培养瓶或轻轻晃动培养板来辅助判断。如果细胞很容易从瓶底或板底脱落并在液体中悬浮,说明消化程度可能已经比较合适。但要注意动作要轻柔,避免过度剧烈的晃动对细胞造成损伤。另外,消化时间也是一个参考因素。一般来说,在开始消化时,可以先根据经验设定一个大致的消化时间,然后在这个时间点前后密切观察细胞的状态。如果消化时间过长,可能会导致细胞受损,影响细胞的活性和功能;而消化时间过短,则可能导致细胞没有完全分离,影响传代效果。还可以通过观察消化液的浑浊程度来判断。在消化开始时,消化液通常是比较澄清的。随着消化的进行,当细胞逐渐脱落进入消化液中,消化液会变得浑浊。当浑浊度达到一定程度,且细胞形态也符合消化完成的特征时,可以认为消化好了。总之,在细胞传代用胰酶消化时,需要综合考虑细胞形态变化、拍打或晃动的反应、消化时间以及消化液的浑浊程度等多个因素,来准确判断消化是否完成。
BEP2D Cells;背景说明:支气管;上皮细胞;HPV18转化;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:详见产品说明书;相关产品有:HuT102 Cells、HFL-I Cells、LS-1034 Cells
RWPE1 Cells;背景说明:肿瘤抑制基因: p53 + [PubMed: 9214605] pRB + [PubMed: 9214605] 一位正常男性前列腺组织切片的周围区域的上皮细胞用单拷贝的人乳头瘤病毒的18(HPV-18)进行转化,建立了RWPE-1 (ATCC CRL-11609) 细胞株 [PubMed: 9214605]. 在三维Matrigel培养时,在雄激素作用下,RWPE-1细胞形成腺胞并向培养基中分泌PSA。[PubMed: 11170142]. 当与Matrigel或基质细胞混合注射雄性裸鼠时,RWPE-1细胞也能形成腺胞[PubMed: 11304724] 并产生PSA。 来源于RWPE-1的细胞再用Kirstin鼠类肿瘤病毒转染Ki-ras基因,建立了能成瘤的RWPE-2细胞株(ATCC CRL-11610) [PubMed: 9214605] 和 RWPE2-W99 (ATCC CRL-2853) 细胞株。 另外,用N--N-(MNU)处理RWPE-1,建立了一系列模拟前列腺癌进程中不同时期的成瘤细胞株。 它们是 WPE1-NA22 (ATCC CRL-2849), WPE1-NB14 (ATCC CRL-2850, WPE1-NB11 (ATCC CRL-2851) 和 WPE1-NB26 (ATCC CRL-2852) 细胞株。 据提供者报道,RWPE-1 细胞株(ATCC CRL-11609)经过检测,乙肝、丙肝、都呈阴性。;传代方法:1:3传代,2-3天传一代。;生长特性:贴壁生长;形态特性:上皮细胞;相关产品有:Walker-256 Cells、mIMCD3 Cells、P3-X63-Ag8.653 Cells
HCGC Cells;背景说明:小脑;颗粒 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:详见产品说明书;相关产品有:BC3H-1 Cells、PG-BE1 Cells、OCUM-1 Cells
ABE8.1/2 Cells;背景说明:淋巴瘤;BALB/c;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:详见产品说明书;相关产品有:Bovine ENDometrial cells Cells、RC-K8 Cells、FL 62891 Cells
SN12C Cells;背景说明:详见相关文献介绍;传代方法:2x10^4 cells/ml;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:H727 Cells、D283-MED Cells、TJ905 Cells
PTK2 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:JIII Cells、OVCAR3 Cells、MDA-MB-435 S Cells
HRVEC Cells;背景说明:视网膜微血管;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:详见产品说明书;相关产品有:CCK-81 Cells、COLO_320DM Cells、L-6 Cells
H2198 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:Malme3M Cells、NK10a Cells、TB-1 Lu Cells
1.1B4 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:4传代;每周2-3次。;生长特性:贴壁生长;形态特性:上皮样;多角形 ;相关产品有:LN-18 Cells、GM637A Cells、Human Kidney-2 Cells
77RD40 Cells(拥有STR基因鉴定图谱)
Abcam MCF-7 DNMT3B KO Cells(拥有STR基因鉴定图谱)
ASUi004-A Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRN197 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YHA254 Cells(拥有STR基因鉴定图谱)
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CC-11 Cells(拥有STR基因鉴定图谱)
DA00926 Cells(拥有STR基因鉴定图谱)
DA05959 Cells(拥有STR基因鉴定图谱)
GM00344 Cells(拥有STR基因鉴定图谱)
NCTC 3960 Cells;背景说明:黑色素瘤;雄性;DBA;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:详见产品说明书;相关产品有:MD Anderson-Metastatic Breast-157 Cells、HOS/MNNG Cells、JAR Cells
HCC-1419 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:上皮样;相关产品有:Adeno 293 Cells、MCFs Cells、INS-1E Cells
OCI-LY-1 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:详见产品说明书;相关产品有:Hs 445 Cells、L6 Cells、SMMC7721 Cells
L-363 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:H2342 Cells、MCF-7 Cells、SK ES 01 Cells
HEK-293FT Cells;背景说明:该细胞稳定表达SV40大T抗原,并且促进最适病毒产物的产生。;传代方法:1:2传代;生长特性:悬浮生长;形态特性:圆形;相关产品有:B16F10 Cells、Jiyoye(P-2003) Cells、High 5 Cells
LICCF Cells;背景说明:肝内胆管癌;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:详见产品说明书;相关产品有:Emory University-3 Cells、DB Cells、EJ1 Cells
H-2052 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:SUM149-PT Cells、SCL II Cells、Hs 863.T Cells
C127 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:M 1 Cells、PTK 1 Cells、TE6 Cells
J-82 Cells;背景说明:电子显微镜下未观察到桥粒但观察到数目不同的粗面内质网和突出微丝。 含ras (H-ras)癌基因。;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:293EBNA Cells、MDA-175 Cells、NCI-H2172 Cells
BL2141 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:CAL148 Cells、MOVAS-1 Cells、PL 45 Cells
U-343 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:详见产品说明书;相关产品有:P3HR1-BL Cells、HCCC9810 Cells、786-0 Cells
AML12 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:详见产品说明书;相关产品有:MC-3T3-E1 Cells、PIG3 Cells、Panc-08.13 Cells
NTera2/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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:PK13 Cells、LOUNH91 Cells、HEK293A Cells
295D2 Cells(拥有STR基因鉴定图谱)
Hs600T Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:3传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:详见产品说明书;相关产品有:SNK1 Cells、Hs832T Cells、U20-S Cells
22RV1人前列腺癌传代细胞活性强|送STR图谱
Panc_03_27 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:A2780/Taxol Cells、Strain KB Cells、GP293 Cells
C-28I2 Cells;背景说明:软骨;SV40转化;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:详见产品说明书;相关产品有:RPPVEC Cells、H-1650 Cells、NCI-H1993 Cells
MDA-MB435 Cells;背景说明:乳腺癌;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:详见产品说明书;相关产品有:BHK-21 Cells、Me-Wo Cells、NCI-H1238 Cells
NRK 49F Cells;背景说明:肾;成纤维细胞;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:详见产品说明书;相关产品有:MCA205 Cells、YAC-1 Cells、T-CAM2 Cells
SACC83 Cells;背景说明:涎腺腺样囊性癌;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:详见产品说明书;相关产品有:BMSCs(mBMSCs) Cells、MLMA Cells、SF17 Cells
AML-2 Cells;背景说明:急性髓系白血病;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:详见产品说明书;相关产品有:OCI-Ly7 Cells、NCI-H1755 Cells、C-28I2 Cells
PTK 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:Medical Research Council cell strain-9 Cells、SKRC-42 Cells、SHI-1 Cells
HAP1 ATF5 (-) 1 Cells(拥有STR基因鉴定图谱)
HAP1 SLC46A3 (-) 1 Cells(拥有STR基因鉴定图谱)
FRO 81-2 Cells;背景说明:未分化甲状腺癌;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:详见产品说明书;相关产品有:hTERT-RPE1 Cells、Ect1/E6E7 Cells、IMCD3 Cells
MUS-M1 Cells;背景说明:小肠;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:详见产品说明书;相关产品有:KE-37 Cells、PCI-4M Cells、BNCL2 Cells
DC2.4 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:详见产品说明书;相关产品有:Psi-2-DAP Cells、PK136 Cells、HNSC Cells
SKMEL2 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:多边形的;相关产品有:Tca-83 Cells、SW1353 Cells、GM04679 Cells
Anip-973 Cells;背景说明:肺腺癌;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:详见产品说明书;相关产品有:D 407 Cells、HR-8348 Cells、RKOE6 Cells
AR4IP 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:D341 Med Cells、IEC 6 Cells、SUDHL-16 Cells
SKMel-5 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:6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:WC00097 Cells、Hepatoma-22 Cells、HL-1 Cells
ARH-77 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:悬浮生长;形态特性:淋巴母细胞样 ;相关产品有:RFL-6 Cells、NCI-N87 Cells、HEK/EBNA Cells
iBMK Atg5-/- 7.2B9 Cells(拥有STR基因鉴定图谱)
Lis13_Alport2 Cells(拥有STR基因鉴定图谱)
NCCIT-R Cells(拥有STR基因鉴定图谱)
PathHunter CHO-K1 DRD3 beta-arrestin Cells(拥有STR基因鉴定图谱)
S12-27IIb Cells(拥有STR基因鉴定图谱)
Ubigene HCT 116 CFLAR KO Cells(拥有STR基因鉴定图谱)
VRISGi001-A Cells(拥有STR基因鉴定图谱)
HG01806 Cells(拥有STR基因鉴定图谱)
PC 61 5.3 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:NE1-E6E7 Cells、ST2 Cells、HT 1197 Cells
JEG-3 Cells;背景说明:这是一株超三倍体人类细胞株;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:H-295R Cells、GM02131A Cells、Shadyside Hospital Pittsburgh-77 Cells
SW1222 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HRA 19 Cells、Normal Rat Kidney-49F Cells、HCC941122 Cells
CAL 33 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HO1-N1 Cells、HOP 92 Cells、KM932 Cells
SU-DHL2 Cells;背景说明:弥漫性大细胞淋巴瘤;胸腔积液转移;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:详见产品说明书;相关产品有:HCoEpiC Cells、Oka-C1 Cells、TMD8 Cells
HD11 Cells;背景说明:巨噬 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:详见产品说明书;相关产品有:GM05887 Cells、RPMI-6666 Cells、SKNDZ Cells
TALL1 Cells;背景说明:该细胞源于一名复发T-ALL(急性T淋巴细胞性白血病)的儿童的外周血;具有很强的细胞毒性,体内体外实验中都能破坏肿瘤细胞;IL-2可使细胞更好地生长;α/β TCR阳性,γ/δ TCR阴性;可产生IFNγ、TNF-α和GM-CSF。;传代方法:维持细胞密度在4×105-1×106 cells/ml之间,2-3天换液1次 ;生长特性:悬浮生长;形态特性:淋巴母细胞;相关产品有:VERO76 Cells、293-H Cells、SHZ-88 Cells
SKML-28 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:8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:CT26.CL25 Cells、TE32 Cells、PG13 Cells
ETCC007 Cells;背景说明:原位导管癌;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:详见产品说明书;相关产品有:VP303 Cells、Panc 08.13 Cells、RCS Cells
CEM Cells;背景说明:G.E. Foley 等人建立了类淋巴母细胞细胞株CCRF-CEM。 细胞是1964年11月从一位四岁白人女性急性淋巴细胞白血病患者的外周血白血球衣中得到。此细胞系从香港收集而来。;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:淋巴母细胞样;相关产品有:Stanford University-Diffuse Histiocytic Lymphoma-4 Cells、HEK-293H Cells、H740 Cells
HCT 15 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:COV 434 Cells、NCIH2170 Cells、MSTO211H Cells
HD-LM-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:详见产品说明书;相关产品有:EOC 20 Cells、GM04679 Cells、FU-MMT-1 Cells
IGROV 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HDF-a Cells、NCI-Hut 125 Cells、OLN-93 Cells
H2170 Cells;背景说明:该细胞1989年建系,源自一位患有肺鳞状细胞癌的男性,该患者不吸烟;传代方法:1:3—1:6传代,3—5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:MBdSMC Cells、IM95 Cells、MADB 106 Cells
MNNGHOS Cells;背景说明:骨肉瘤;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:详见产品说明书;相关产品有:BIC1 Cells、V 79 Cells、H28 Cells
TK-160 Cells(拥有STR基因鉴定图谱)
HN 4 Cells;背景说明:喉鳞癌;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:详见产品说明书;相关产品有:NTERA2 Cells、EFM-192A Cells、NCI-H1915 Cells
3T3-L1 Cells;背景说明:3T3-L1是从3T3细胞(Swissalbino)中经克隆分离得到的连续传代的亚系。该细胞从快速分裂到汇合和接触性抑制状态经历了前脂肪细胞到脂肪样细胞的转变。该细胞鼠痘病毒阴性;可产生甘油三酯,高浓度血清可增强细胞内脂肪堆积。;传代方法:1:2传代;生长特性:贴壁生长;形态特性:成纤维细胞样;相关产品有:NS1-Ag 4/1 Cells、LTEP-a2 Cells、CCD1112Sk Cells
LAN-5 Cells;背景说明:神经母细胞瘤;骨髓转移;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:详见产品说明书;相关产品有:GA-10 Cells、HCC941122 Cells、HEM-L Cells
WEHI-164 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:HSC 3 Cells、3T3(A31) Cells、PC-3M-1E8 Cells
HTh 74 Cells;背景说明:未分化甲状腺癌;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:详见产品说明书;相关产品有:MDA-MB-415 Cells、GM00637 Cells、IOSE-Mar Cells
MDA231-LM2-4175 Cells;背景说明:乳腺癌;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:详见产品说明书;相关产品有:CSQT-2 Cells、Leukemia L1210 Cells、HCT-FET Cells
Buffalo Rat Liver-3A 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:VMRCLCD Cells、Hs940.T Cells、Verda reno Cells
C-Li-7 Cells;背景说明:人肝癌细胞株。这株细胞从裸鼠体外移植瘤中建立。;传代方法:1:2传代;生长特性:贴壁生长 ;形态特性:详见产品说明书;相关产品有:SW-780 Cells、SJSA1 Cells、KU 812F Cells
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THC-8307 Cells;背景说明:高分化结肠癌;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:详见产品说明书;相关产品有:LS 123 Cells、SW-403 Cells、Medical Research Council cell strain-9 Cells
HSAS3 Cells;背景说明:皮肤;成纤维 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:详见产品说明书;相关产品有:PE/CA-PJ-34 Cells、CCK81 Cells、Hs445 Cells
MHH-CALL2 Cells;背景说明:急性B淋巴细胞白血病;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:详见产品说明书;相关产品有:D-283MED Cells、NTERA2 Cells、SG231 Cells
NCI-H226 Cells;背景说明:1980年分离建立。;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:Doubling time: ~50 hours (ATCC). Cells、ZR-75-30 Cells、CNE Cells
MA-104 Cells;背景说明:胚肾;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:详见产品说明书;相关产品有:6-10B Cells、SUNE 1 Cells、NCI H2106 Cells
BC3H1 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,详见产品说明书部分;形态特性:详见产品说明书;相关产品有:H-596 Cells、B 95.8 Cells、HEC-151 Cells
BayGenomics ES cell line RRR557 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YTA062 Cells(拥有STR基因鉴定图谱)
HyCyte LL/2 (LLC1)-Luc Cells(拥有STR基因鉴定图谱)
PCRP-KLF7-1C11 Cells(拥有STR基因鉴定图谱)
22RV1人前列腺癌传代细胞活性强|送STR图谱
GoH3 Cells(拥有STR基因鉴定图谱)
HPSI0115i-zuer_1 Cells(拥有STR基因鉴定图谱)
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PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.
Cancer Res. 70:2158-2164(2010)
PubMed=21248069; DOI=10.1158/0008-5472.CAN-10-1998; PMCID=PMC3059379
Li Y.-M., Alsagabi M., Fan D.-H., Bova G.S., Tewfik A.H., Dehm S.M.
Intragenic rearrangement and altered RNA splicing of the androgen receptor in a cell-based model of prostate cancer progression.
Cancer Res. 71:2108-2117(2011)
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)
DOI=10.5897/IJBMBR2013.0154
Iloki Assanga S.B., Gil-Salido A.A., Lewis Lujan L.M., de Jesus Rosas-Durazo A., Acosta-Silva A.L., Rivera-Castaneda E.G., Rubio-Pino J.L.
Cell growth curves for different cell lines and their relationship with biological activities.
Int. J. Biotechnol. Mol. Biol. Res. 4:60-70(2013)
PubMed=23117885; DOI=10.1158/0008-5472.CAN-12-3630; PMCID=PMC3549016
Li Y.-M., Chan S.-C., Brand L.J., Hwang T.H., Silverstein K.A.T., Dehm S.M.
Androgen receptor splice variants mediate enzalutamide resistance in castration-resistant prostate cancer cell lines.
Cancer Res. 73:483-489(2013)
PubMed=23671654; DOI=10.1371/journal.pone.0063056; PMCID=PMC3646030
Lu Y.-H., Soong T.D., Elemento O.
A novel approach for characterizing microsatellite instability in cancer cells.
PLoS ONE 8:E63056-E63056(2013)
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=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=27271795; DOI=10.1002/pros.23190
Shourideh M., DePriest A., Mohler J.L., Wilson E.M., Koochekpour S.
Characterization of fibroblast-free CWR-R1ca castration-recurrent prostate cancer cell line.
Prostate 76:1067-1077(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=28145883; DOI=10.18632/oncotarget.14850; PMCID=PMC5386661
Nouri M., Caradec J., Lubik A.A., Li N., Hollier B.G., Takhar M., Altimirano-Dimas M., Chen M.-Q., Roshan-Moniri M., Butler M., Lehman M., Bishop J.L., Truong S., Huang S.-C., Cochrane D.R., Cox M., Collins C., Gleave M.E., Erho N., Alshalafa M., Davicioni E., Nelson C., Gregory-Evans C.Y., Karnes R.J., Jenkins R.B., Klein E.A., Buttyan R.
Therapy-induced developmental reprogramming of prostate cancer cells and acquired therapy resistance.
Oncotarget 8:18949-18967(2017)
PubMed=28928128; DOI=10.1158/0008-5472.CAN-17-0320; PMCID=PMC5654612
Van Etten J.L., Nyquist M.D., Li Y.-M., Yang R.-D., Ho Y., Johnson R., Ondigi O., Voytas D.F., Henzler C., Dehm S.M.
Targeting a single alternative polyadenylation site coordinately blocks expression of androgen receptor mRNA splice variants in prostate cancer.
Cancer Res. 77:5228-5235(2017)
PubMed=30629668; DOI=10.1371/journal.pone.0210404; PMCID=PMC6328144
Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.
Screening human cell lines for viral infections applying RNA-Seq data analysis.
PLoS ONE 14:E0210404-E0210404(2019)
PubMed=30787054; DOI=10.1158/1055-9965.EPI-18-1132; PMCID=PMC6548687
Hooker S.E. Jr., Woods-Burnham L., Bathina M., Lloyd S., Gorjala P., Mitra R., Nonn L., Kimbro K.S., Kittles R.A.
Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines.
Cancer Epidemiol. Biomarkers Prev. 28:1003-1009(2019)
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)
PubMed=30971826; DOI=10.1038/s41586-019-1103-9
Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.
Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.
Nature 568:511-516(2019)
PubMed=31006810; DOI=10.1093/nar/gkz286; PMCID=PMC6582326
Kounatidou E., Nakjang S., McCracken S.R.C., Dehm S.M., Robson C.N., Jones D., Gaughan L.
A novel CRISPR-engineered prostate cancer cell line defines the AR-V transcriptome and identifies PARP inhibitor sensitivities.
Nucleic Acids Res. 47:5634-5647(2019)
PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
Ghandi M., Huang F.W., Jane-Valbuena J., Kryukov G.V., Lo C.C., McDonald E.R. 3rd, Barretina J.G., Gelfand E.T., Bielski C.M., Li H.-X., Hu K., Andreev-Drakhlin A.Y., Kim J., Hess J.M., Haas B.J., Aguet F., Weir B.A., Rothberg M.V., Paolella B.R., Lawrence M.S., Akbani R., Lu Y.-L., Tiv H.L., Gokhale P.C., de Weck A., Mansour A.A., Oh C., Shih J., Hadi K., Rosen Y., Bistline J., Venkatesan K., Reddy A., Sonkin D., Liu M., Lehar J., Korn J.M., Porter D.A., Jones M.D., Golji J., Caponigro G., Taylor J.E., Dunning C.M., Creech A.L., Warren A.C., McFarland J.M., Zamanighomi M., Kauffmann A., Stransky N., Imielinski M., Maruvka Y.E., Cherniack A.D., Tsherniak A., Vazquez F., Jaffe J.D., Lane A.A., Weinstock D.M., Johannessen C.M., Morrissey M.P., Stegmeier F., Schlegel R., Hahn W.C., Getz G., Mills G.B., Boehm J.S., Golub T.R., Garraway L.A., Sellers W.R.
Next-generation characterization of the Cancer Cell Line Encyclopedia.
Nature 569:503-508(2019)
PubMed=31395879; DOI=10.1038/s41467-019-11415-2; PMCID=PMC6687785
Yu K., Chen B., Aran D., Charalel J., Yau C., Wolf D.M., van 't Veer L.J., Butte A.J., Goldstein T., Sirota M.
Comprehensive transcriptomic analysis of cell lines as models of primary tumors across 22 tumor types.
Nat. Commun. 10:3574.1-3574.11(2019)"
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文献和实验该产品被引用文献
"PubMed=14518030; DOI=10.1002/pros.10291
van Bokhoven A., Caires A., Di Maria M., Schulte A.P., Lucia M.S., Nordeen S.K., Miller G.J., Varella-Garcia M.
Spectral karyotype (SKY) analysis of human prostate carcinoma cell lines.
Prostate 57:226-244(2003)
CLPUB00698
van Bokhoven A.
Models for prostate cancer. Molecular characterization and critical appraisal of human prostate carcinoma cell lines.
Thesis PhD (2004); Katholieke Universiteit Nijmegen; Nijmegen; Netherlands
PubMed=15486987; DOI=10.1002/pros.20158
Zhao H.-J., Kim Y., Wang P., Lapointe J., Tibshirani R., Pollack J.R., Brooks J.D.
Genome-wide characterization of gene expression variations and DNA copy number changes in prostate cancer cell lines.
Prostate 63:187-197(2005)
PubMed=19403664; DOI=10.1128/JVI.00546-09; PMCID=PMC2704771
Knouf E.C., Metzger M.J., Mitchell P.S., Arroyo J.D., Chevillet J.R., Tewari M., Miller A.D.
Multiple integrated copies and high-level production of the human retrovirus XMRV (xenotropic murine leukemia virus-related virus) from 22Rv1 prostate carcinoma cells.
J. Virol. 83:7353-7356(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=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.
Cancer Res. 70:2158-2164(2010)
PubMed=21248069; DOI=10.1158/0008-5472.CAN-10-1998; PMCID=PMC3059379
Li Y.-M., Alsagabi M., Fan D.-H., Bova G.S., Tewfik A.H., Dehm S.M.
Intragenic rearrangement and altered RNA splicing of the androgen receptor in a cell-based model of prostate cancer progression.
Cancer Res. 71:2108-2117(2011)
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)
DOI=10.5897/IJBMBR2013.0154
Iloki Assanga S.B., Gil-Salido A.A., Lewis Lujan L.M., de Jesus Rosas-Durazo A., Acosta-Silva A.L., Rivera-Castaneda E.G., Rubio-Pino J.L.
Cell growth curves for different cell lines and their relationship with biological activities.
Int. J. Biotechnol. Mol. Biol. Res. 4:60-70(2013)
PubMed=23117885; DOI=10.1158/0008-5472.CAN-12-3630; PMCID=PMC3549016
Li Y.-M., Chan S.-C., Brand L.J., Hwang T.H., Silverstein K.A.T., Dehm S.M.
Androgen receptor splice variants mediate enzalutamide resistance in castration-resistant prostate cancer cell lines.
Cancer Res. 73:483-489(2013)
PubMed=23671654; DOI=10.1371/journal.pone.0063056; PMCID=PMC3646030
Lu Y.-H., Soong T.D., Elemento O.
A novel approach for characterizing microsatellite instability in cancer cells.
PLoS ONE 8:E63056-E63056(2013)
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=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=27271795; DOI=10.1002/pros.23190
Shourideh M., DePriest A., Mohler J.L., Wilson E.M., Koochekpour S.
Characterization of fibroblast-free CWR-R1ca castration-recurrent prostate cancer cell line.
Prostate 76:1067-1077(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=28145883; DOI=10.18632/oncotarget.14850; PMCID=PMC5386661
Nouri M., Caradec J., Lubik A.A., Li N., Hollier B.G., Takhar M., Altimirano-Dimas M., Chen M.-Q., Roshan-Moniri M., Butler M., Lehman M., Bishop J.L., Truong S., Huang S.-C., Cochrane D.R., Cox M., Collins C., Gleave M.E., Erho N., Alshalafa M., Davicioni E., Nelson C., Gregory-Evans C.Y., Karnes R.J., Jenkins R.B., Klein E.A., Buttyan R.
Therapy-induced developmental reprogramming of prostate cancer cells and acquired therapy resistance.
Oncotarget 8:18949-18967(2017)
PubMed=28928128; DOI=10.1158/0008-5472.CAN-17-0320; PMCID=PMC5654612
Van Etten J.L., Nyquist M.D., Li Y.-M., Yang R.-D., Ho Y., Johnson R., Ondigi O., Voytas D.F., Henzler C., Dehm S.M.
Targeting a single alternative polyadenylation site coordinately blocks expression of androgen receptor mRNA splice variants in prostate cancer.
Cancer Res. 77:5228-5235(2017)
PubMed=30629668; DOI=10.1371/journal.pone.0210404; PMCID=PMC6328144
Uphoff C.C., Pommerenke C., Denkmann S.A., Drexler H.G.
Screening human cell lines for viral infections applying RNA-Seq data analysis.
PLoS ONE 14:E0210404-E0210404(2019)
PubMed=30787054; DOI=10.1158/1055-9965.EPI-18-1132; PMCID=PMC6548687
Hooker S.E. Jr., Woods-Burnham L., Bathina M., Lloyd S., Gorjala P., Mitra R., Nonn L., Kimbro K.S., Kittles R.A.
Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines.
Cancer Epidemiol. Biomarkers Prev. 28:1003-1009(2019)
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)
PubMed=30971826; DOI=10.1038/s41586-019-1103-9
Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.
Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.
Nature 568:511-516(2019)
PubMed=31006810; DOI=10.1093/nar/gkz286; PMCID=PMC6582326
Kounatidou E., Nakjang S., McCracken S.R.C., Dehm S.M., Robson C.N., Jones D., Gaughan L.
A novel CRISPR-engineered prostate cancer cell line defines the AR-V transcriptome and identifies PARP inhibitor sensitivities.
Nucleic Acids Res. 47:5634-5647(2019)
PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
Ghandi M., Huang F.W., Jane-Valbuena J., Kryukov G.V., Lo C.C., McDonald E.R. 3rd, Barretina J.G., Gelfand E.T., Bielski C.M., Li H.-X., Hu K., Andreev-Drakhlin A.Y., Kim J., Hess J.M., Haas B.J., Aguet F., Weir B.A., Rothberg M.V., Paolella B.R., Lawrence M.S., Akbani R., Lu Y.-L., Tiv H.L., Gokhale P.C., de Weck A., Mansour A.A., Oh C., Shih J., Hadi K., Rosen Y., Bistline J., Venkatesan K., Reddy A., Sonkin D., Liu M., Lehar J., Korn J.M., Porter D.A., Jones M.D., Golji J., Caponigro G., Taylor J.E., Dunning C.M., Creech A.L., Warren A.C., McFarland J.M., Zamanighomi M., Kauffmann A., Stransky N., Imielinski M., Maruvka Y.E., Cherniack A.D., Tsherniak A., Vazquez F., Jaffe J.D., Lane A.A., Weinstock D.M., Johannessen C.M., Morrissey M.P., Stegmeier F., Schlegel R., Hahn W.C., Getz G., Mills G.B., Boehm J.S., Golub T.R., Garraway L.A., Sellers W.R.
Next-generation characterization of the Cancer Cell Line Encyclopedia.
Nature 569:503-508(2019)
PubMed=31395879; DOI=10.1038/s41467-019-11415-2; PMCID=PMC6687785
Yu K., Chen B., Aran D., Charalel J., Yau C., Wolf D.M., van 't Veer L.J., Butte A.J., Goldstein T., Sirota M.
Comprehensive transcriptomic analysis of cell lines as models of primary tumors across 22 tumor types.
Nat. Commun. 10:3574.1-3574.11(2019)"
van Bokhoven A., Caires A., Di Maria M., Schulte A.P., Lucia M.S., Nordeen S.K., Miller G.J., Varella-Garcia M.
Spectral karyotype (SKY) analysis of human prostate carcinoma cell lines.
Prostate 57:226-244(2003)
CLPUB00698
van Bokhoven A.
Models for prostate cancer. Molecular characterization and critical appraisal of human prostate carcinoma cell lines.
Thesis PhD (2004); Katholieke Universiteit Nijmegen; Nijmegen; Netherlands
PubMed=15486987; DOI=10.1002/pros.20158
Zhao H.-J., Kim Y., Wang P., Lapointe J., Tibshirani R., Pollack J.R., Brooks J.D.
Genome-wide characterization of gene expression variations and DNA copy number changes in prostate cancer cell lines.
Prostate 63:187-197(2005)
PubMed=19403664; DOI=10.1128/JVI.00546-09; PMCID=PMC2704771
Knouf E.C., Metzger M.J., Mitchell P.S., Arroyo J.D., Chevillet J.R., Tewari M., Miller A.D.
Multiple integrated copies and high-level production of the human retrovirus XMRV (xenotropic murine leukemia virus-related virus) from 22Rv1 prostate carcinoma cells.
J. Virol. 83:7353-7356(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=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.
Cancer Res. 70:2158-2164(2010)
PubMed=21248069; DOI=10.1158/0008-5472.CAN-10-1998; PMCID=PMC3059379
Li Y.-M., Alsagabi M., Fan D.-H., Bova G.S., Tewfik A.H., Dehm S.M.
Intragenic rearrangement and altered RNA splicing of the androgen receptor in a cell-based model of prostate cancer progression.
Cancer Res. 71:2108-2117(2011)
PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027
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