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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:
A172人胶质母细胞瘤传代细胞活性强|送STR图谱
- 规格:
1*10(6)Cellls/瓶
"A172人胶质母细胞瘤传代细胞活性强|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:A172细胞在半固体培养基中可形成克隆;A172细胞在免疫抑制小鼠中不成瘤。最初分离自一名患者的胶质母细胞瘤组织,在培养中表现出典型的胶质瘤细胞形态,如多形性、核异型性、高核质比等。
NCI-H1930 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:TCC Sup Cells、Hs695 Cells、NCI-H1793 Cells
DU4475 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,多细胞聚集;形态特性:上皮细胞样;相关产品有:LNCaP Cells、MT-4 Cells、KTC1 Cells
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:Reuber H-35 Cells、LP-1 Cells、NCI-Hut 125 Cells
解冻细胞常见实验问题分析及推荐解决方法:在解冻冻存细胞时,发现会出现存活率低、大量细胞碎片及生长缓慢等问题,究竟是什么原因导致,我们该怎么进行解决?以下是国内外细胞培养专家针对解冻细胞实验问题,总结的一些解决方案!出现低存活率的可能原因及推荐解决方案如下:1)解冻过程中细胞裂解,推荐的解决方案:可预期到一定量的细胞死亡,因此细胞的浓度应足够GAO,考虑到这一损失。起始浓度为1*10(6)至1*10(7)细胞/毫升;2)解冻过程中的问题,推荐的解决方案:在-70℃至-80℃下保存冷冻的培养物,保存时间为1-5天,但这不是保存的方法。在37℃充分解冻后应立即开始培养;3)对冷冻过敏,推荐的解决方案:A.完全或部分更换培养基,减少培养基中冷冻的量。在24小时后更换培养体可全部去除冷冻。B.留出更多时间供培养物恢复。有时细胞需要几周时间才能形成单层或密集的悬浮物,取决于冷冻时细胞的年龄或传代次数或在生长阶段中的位置。冷冻的Zui佳条件在对数期;4)被冷冻的原种细胞的年龄或冷冻时培养物的年龄,推荐的解决方案:解冻Zui近冷冻的细胞。细胞处于冷冻状态的时间越长,存活率越低。检查冷冻细胞的时间和方法。在冷冻时细胞应处于对数期。
A172人胶质母细胞瘤传代细胞活性强|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
HR-8348 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:MV(4;11) Cells、NCI-H441 Cells、PLC/PRF5 Cells
COLO 357 Cells;背景说明:胰腺癌;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:MB-49 Cells、PC 61-5-3 Cells、AR42J Cells
COLO-16 Cells;背景说明:皮肤鳞癌;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;相关产品有:OUMS27 Cells、P3-X63-Ag8.653 Cells、SW900 Cells
10RGB 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:OCM1A Cells、TKB-1 Cells、CEM-T4 Cells
细胞冻存的步骤:1)选择处于对数生长期的细胞,在冻存前一天ZuiHAO换。将多个培养瓶中的细胞培养去掉,用0.25% 胰蛋白酶消化。适时去掉胰蛋白酶,加入少量新培养。用吸管吸取培养反复吹打瓶壁上的细胞,使其成为均匀分散的细胞悬。悬浮生产细胞则不要消化处理。然后将细胞收集于离心管中离心(1000r/min,10分钟);2)去上清,加入含20%小牛血清的完全培养基,于4℃预冷15分钟后,逐滴加入已无菌的DMSO或甘油,用吸管轻轻吹打使细胞均匀,细胞浓度为5×106~1×107/mL之间。(冻存培养的配置是不是一定要用小牛血清呢?答案是不一定的,具体要看培养的细胞类型来选择;3)将分装上述细胞悬于2ml冻存管中,每管0.25ml。冻存管要将盖子盖紧,并标记HAO细胞名称和冻存日期,同时作HAO登记(日期、细胞种类及代次、冻存支数);4)将装HAO细胞的冻存管放到冻存盒中,-80℃冰箱过夜。;如果有程序降温器(放在-80℃冰箱过夜,放入罐)ZuiHAO;或者可以在4℃,2h;然后转到-20℃,2h;-80℃,2h;放入罐;5)细胞冻存在中可以长期保存,但为妥善起见,冻存半年后,ZuiHAO取出一只冻存管细胞复苏培养,观察生长情况,然后再继续冻存。
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A172人胶质母细胞瘤传代细胞活性强|送STR图谱
形态特性:上皮细胞样
在实验室细胞培养过程中,细胞聚集是一个常见的问题,它可能会影响细胞的正常生长、实验结果的准确性等诸多方面。为了防止细胞聚集,科研人员通常会采用多种有效的方法。首先,合适的细胞培养容器表面处理至关重要。许多细胞培养瓶和培养皿会经过特殊的表面处理,例如用亲水性的聚合物涂层。减少细胞之间因为吸附在同一位置而聚集的可能性。酶处理也是常用的手段之一。在细胞消化传代过程中,使用适量的胰蛋白酶等酶试剂。胰蛋白酶能够分解细胞间的连接蛋白,使细胞彼此分离。但是,酶的浓度和处理时间需要严格把控。如果酶浓度过高或者处理时间过长,虽然细胞能够很好地分散,但可能会对细胞造成损伤,影响细胞的活性。以常见的哺乳动物细胞为例,一般使用0.25%的胰蛋白酶,在37℃下处理1-3分钟,就可以有效地将细胞分散开,同时又能保证细胞的健康状态。添加合适的试剂也是防止细胞聚集的有效策略。一些抗聚集剂如四乙酸(EDTA)被广泛使用。EDTA能够螯合细胞培养液中的钙、镁离子,而这些离子是细胞间连接所依赖的重要成分。当它们被螯合后,细胞间的连接就会变弱,从而减少聚集。在细胞培养过程中,轻柔的操作也不容忽视。无论是在细胞的接种、换液还是转移过程中,避免剧烈摇晃或吹打。通过这些综合的方法,实验室能够更好地防止细胞聚集,为细胞系培养实验的成功提供保障。
MOVAS-1 Cells;背景说明:主动脉平滑肌;SV40转化;C57BL/6;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:Human Liver-7702 Cells、NCI-H460 Cells、WM266 Cells
NCIH1155 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:悬浮生长;形态特性:上皮细胞;相关产品有:LS 1034 Cells、IEC18 Cells、Opossum Kidney Cells
Panc-813 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:IA-LM Cells、PCI:SG-231 Cells、OE-19 Cells
LIXC-002 Cells;背景说明:详见相关文献介绍;传代方法:1:3传代,3-4天传1次;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:B4G12 Cells、MRC9 Cells、M059J Cells
Mouse INsulinoma 6 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:U251MG Cells、H1436 Cells、WI38 Cells
SBC-3 Cells;背景说明:小细胞肺癌;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;相关产品有:HCC4006 Cells、NCIH716 Cells、RM-1 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;相关产品有:D-283MED Cells、W133 Cells、BE(2)-C Cells
HCC0827 Cells;背景说明:这株细胞建于1994年三月。这株肺腺癌在EGFR酪酸激酶区域有一个获得性突变(E746-A750缺失)。患者在25岁到26岁时每个月抽1包烟。在诊断前12年不再抽烟。;传代方法:消化5分钟。1:2。4-5天长满。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:RPMI-8402 Cells、3 LL Cells、IBRS-2 Cells
A2780/Taxol 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:RT112 Cells、OVMANA Cells、HSC/mHSC Cells
Abcam A-549 LGALS3 KO Cells(拥有STR基因鉴定图谱)
Abcam U-87MG RAB39B KO Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line CSG153 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRT582 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YTC531 Cells(拥有STR基因鉴定图谱)
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CHO PBj gp130 Cells(拥有STR基因鉴定图谱)
DA02383 Cells(拥有STR基因鉴定图谱)
ESSA2 Cells(拥有STR基因鉴定图谱)
GM07259 Cells(拥有STR基因鉴定图谱)
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、D 407 Cells、UCLA SO M21 Cells
HCC-2935 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:746T Cells、MOLT4 Cells、253JBV Cells
SKLMS1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:5传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:成纤维细胞;相关产品有:SCLC-21H Cells、PLA 802 Cells、L5178Y TK+/-3.7.2c 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,详见产品说明部分;形态特性:详见产品说明;相关产品有:T9 Cells、OC 316 Cells、NS-20Y Cells
MDAMB157 Cells;背景说明:该细胞源自一位患有乳腺髓样癌的44岁黑人女性,表达WNT7B癌基因,细胞与细胞边界处有细胞桥粒、微绒毛、张力细丝。;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:MRC-V Cells、H-596 Cells、no-11 Cells
JC Cells;背景说明:乳腺癌;雌性;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:NCI H157 Cells、THEECs Cells、MDCKII-WT Cells
COLO357 Cells;背景说明:胰腺癌;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:NCI-H810 Cells、WM-239-A Cells、Anip-973 Cells
OVCAR.3 Cells;背景说明:该细胞1982年由T.C. Hamilton等建系,源自一位60卵巢腺癌的腹水,是卵巢癌抗药性研究的模型。;传代方法:1:2—1:4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:Vero C1008 Cells、SKNEP1 Cells、Madin Darby Canine Kidney Cells
HS-294T 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:混合星状和多边形;相关产品有:HF-91 Cells、Hep 2 Cells、LIXC002 Cells
H69C Cells;背景说明:详见相关文献介绍;传代方法:1:2—1:4传代,每周换液2次;生长特性:悬浮生长,聚团;形态特性:聚团悬浮;相关产品有:H522 Cells、MEF (CF-1) Cells、Jurkat E6-1 Cells
MRC 5 Cells;背景说明:MRC-5细胞系来自14周龄男性胎儿的正常肺组织,该细胞老化前能传代42~46个倍增时间。;传代方法:1:2-1:5传代;每周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:BE2-C Cells、PE CA PJ34 Cells、RC-4B Cells
NCI-H1373 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:4传代;2-3天换液1次。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HLMVEC Cells、Colon 38 Cells、RIN Cl-5F Cells
HCC-1937 Cells;背景说明:这株细胞1995年10月13日最初来源于原发性导管癌, 用了11.5个月建株。肿瘤分类为TNM IIB期, 3级。BRCA1分析表明这株细胞是BRCA1 5382C突变纯合的, 而来源于同一病人的类淋巴母细胞细胞株在这个突变位点上是杂合的。 另两个家庭成员也有这个突变; 一个同卵双生姐妹也患有乳腺癌。这株细胞有一个后天的TP53突变, 而其野生型等位基因丢失; 一个PTEN基因的后天的纯合缺失, 以及多个与乳腺癌发病机理相关的位点上发生的杂合突变。这株细胞Her2-neu和p53表达都呈阴性。;传代方法:1:2传代;4-5天传代一次。;生长特性:贴壁生长;形态特性:上皮样;多角形;相关产品有:RBMEC Cells、OE21 Cells、MDAMB330 Cells
APB5 Cells(拥有STR基因鉴定图谱)
WEHI3 Cells;背景说明:白血病;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;相关产品有:Hs294T Cells、RPMI-7951 Cells、SGC7901/DDP Cells
A172人胶质母细胞瘤传代细胞活性强|送STR图谱
K-562 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:GFP-Olig2 Cells、Colo205 Cells、H3255 Cells
SK Mel 24 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:Earle's L cells Cells、SNK-6 Cells、Mono Mac 6 Cells
U343 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:HEK AD293 Cells、FO [Mouse myeloma] Cells、SKNBE(2) Cells
LS-411 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;每周2次;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H1693 Cells、MC3T3-E1 Subclone 14 Cells、OVCA433_Bast Cells
HCC-1833 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:Menschliche Und Tierische Zellkulture-1 Cells、Panc 5.04 Cells、HOCF Cells
P-36 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:HCT_116 Cells、Chinese Hamster Ovary Cells、VM-CUB-1 Cells
HONE-1 Cells;背景说明:鼻咽癌;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;相关产品有:PG-4 S+L- Cells、GM05372E Cells、H1522 Cells
GM09639 Cells(拥有STR基因鉴定图谱)
HAP1 AXIN1 (-) 4 Cells(拥有STR基因鉴定图谱)
OV1-P 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:H740 Cells、SK-ChA-1 Cells、UPCI:SCC154 Cells
HS-940-T 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:成纤维细胞;相关产品有:Hs940-T Cells、WILL-2 Cells、HSF2 Cells
MC-CAR Cells;背景说明:B淋巴;EBV转化;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:NSH Cells、SKLU1 Cells、BE2M17 Cells
LM6 Cells;背景说明:肝癌;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:NFS 60 Cells、NCI-H735 Cells、P30-OHKUBO Cells
FRhK-4 Cells;背景说明:胚胎;肾;自发永生;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:IEC-18 Cells、EA hy 926 Cells、WEHI-164 Cells
HCC1395 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:贴壁生长;形态特性:上皮样;相关产品有:COLO-829 Cells、3T6 Cells、Human Fetal Thymocyte-8810 Cells
OCI-AML-3 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;相关产品有:HS-294T Cells、MHCC-97 Cells、UMUC3 Cells
108CC15 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:OAW 42 Cells、BHP10-3 Cells、RT 112 Cells
HG03077 Cells(拥有STR基因鉴定图谱)
iBMK W2.3.1-5 Cells(拥有STR基因鉴定图谱)
LL/2-mNIS-Puro Cells(拥有STR基因鉴定图谱)
NCI-BL2347 Cells(拥有STR基因鉴定图谱)
PathHunter CHO-K1 GPR84 beta-arrestin Cells(拥有STR基因鉴定图谱)
Ubigene A-549 FZD3 KO Cells(拥有STR基因鉴定图谱)
UPCI-SCC-044 Cells(拥有STR基因鉴定图谱)
HAP1 TFG (-) 2 Cells(拥有STR基因鉴定图谱)
MILE SVEN1 Cells;背景说明:MS1是1994年建株的胰岛内皮细胞株。原代培养的胰岛内皮细胞用抗G418的温度敏感型SV40大T抗原(tsA-58-3)转染。抗性克隆用克隆环分离,并筛选吸收dil-Ac-LDL的。这株细胞保留了内皮细胞的许多特性,如吸收乙酰化LDL和表达八因子相关抗原及BEGF受体。;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:详见产品说明;相关产品有:3T3-A31 Cells、HuH7 Cells、IFRS1 Cells
SK_N_BE2C 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;相关产品有:MSTO-211 H Cells、NCI-H865 Cells、NCIH2126 Cells
LM6 Cells;背景说明:肝癌;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:NFS 60 Cells、NCI-H735 Cells、P30-OHKUBO Cells
DHL10 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;形态特性:淋巴母细胞;相关产品有:H1793 Cells、TB-1 Lu Cells、32D CL3 Cells
PC-9/GR 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:PC 61-5-3 Cells、NCI-H2172 Cells、MDA MB 134VI Cells
PC-9/GR 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:PC 61-5-3 Cells、NCI-H2172 Cells、MDA MB 134VI Cells
HCC1171 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:Wistar Institute-38 Cells、MiaPaCa-2 Cells、DSL-6A/C1 Cells
769-P Cells;背景说明:该细胞系1975年建系,源自一位63岁白人女性的初期透明细胞腺癌组织,细胞呈圆形且边界不清,核浆比大,有微绒毛及桥粒。该细胞可在软琼脂上生长。 ;传代方法:1:4—1:12传代,2—3天换液一次;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:143B Cells、MA 104 Cells、RBE Cells
Hs-606-T 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天换液一次;生长特性:贴壁生长;形态特性:成纤维细胞;相关产品有:SKES1 Cells、NCIH1838 Cells、LP-1 Cells
RPMI 8226/S Cells;背景说明:来源于一位61岁的男性浆细胞瘤患者;可产生免疫球蛋白轻链,未检测到重链。;传代方法:按1:2传代,5-6小时可以看到细胞分裂;生长特性:悬浮生长;形态特性:淋巴母细胞样;相关产品有:AC16 [Human hybrid] Cells、NCIH1650 Cells、PANC-1 Cells
PC9 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:CNE1 Cells、HME-1 Cells、SU-DHL-6 Cells
PCI-4B Cells;背景说明:喉鳞癌;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:GDM-1 Cells、NUGC4 Cells、HUT125 Cells
HCC0078 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:HT144 Cells、OVCAR-4 Cells、HRCEC Cells
AD-293 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:C4-2 Bone metastatic Cells、KYSE 150 KYSE150 Kyse150 KY150
Cells、Hs 888Lu Cells
KY-270 Cells;背景说明:详见相关文献介绍;传代方法:1:5传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:B78 Cells、H1688 Cells、COV362 Cells
S2R+-spin-GFP-2 Cells(拥有STR基因鉴定图谱)
C166 Cells;背景说明:血管内皮;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:MD Anderson-Metastatic Breast-175-VIII Cells、NCI-SNU-601 Cells、NCI-H847 Cells
CAL-39 Cells;背景说明:外阴鳞癌细胞;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:B16 subline B78 Cells、EA.hy 926 Cells、MC-3T3-E1 Cells
SKNO-1 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;相关产品有:HEC-151 Cells、IEC-18 Cells、C32 [Human melanoma] Cells
Swiss-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:H-1688 Cells、Capan2 Cells、HCC1395 Cells
RMS1598 Cells;背景说明:详见相关文献介绍;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:成纤维细胞;相关产品有:NCIH1355 Cells、T2 Cells、Ramos 1 Cells
Mc Coy Cells;背景说明: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;相关产品有:FHs74 Int Cells、526 Cells、KASUMI1 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
NCM356 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:MDCK II Cells、REC1 Cells、AK Cells
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OCI/AML3 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;相关产品有:hRMECs Cells、Fetal Bovine Heart Endothelial Cells、PC.3 Cells
LN 382 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:SK-N-FI Cells、H146 Cells、NTera2 cl.D1 Cells
MIA-Pa-Ca-2 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:451-LU Cells、WISH Cells、H676 Cells
EAhy926 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:Hs.27 Cells、HANK-1 Cells、mREC Cells
MDCC MSB1 Cells;背景说明:淋巴瘤;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:SKCO 1 Cells、18G3.cl 1 Cells、HEK 293-EBNA Cells
RCC4 Cells;背景说明:肾透明细胞癌;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;相关产品有:H522 Cells、IOSE-Van Cells、H510 Cells
BayGenomics ES cell line CSH598 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRZ260 Cells(拥有STR基因鉴定图谱)
BoMaMa-J2imm Casp1-/- Cells(拥有STR基因鉴定图谱)
KUM10 Cells(拥有STR基因鉴定图谱)
A172人胶质母细胞瘤传代细胞活性强|送STR图谱
PGL3 Cells(拥有STR基因鉴定图谱)
PMab-117 Cells(拥有STR基因鉴定图谱)
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p53-defective tumors with a functional apoptosome-mediated pathway: a new therapeutic target.
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Cancer Sci. 96:676-683(2005)
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Lee J., Kotliarova S., Kotliarov Y., Li A.-G., Su Q., Donin N.M., Pastorino S., Purow B.W., Christopher N., Zhang W., Park J.K., Fine H.A.
Tumor stem cells derived from glioblastomas cultured in bFGF and EGF more closely mirror the phenotype and genotype of primary tumors than do serum-cultured cell lines.
Cancer Cell 9:391-403(2006)
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Azari S., Ahmadi N., Jeddi-Tehrani M., Shokri F.
Profiling and authentication of human cell lines using short tandem repeat (STR) loci: report from the National Cell Bank of Iran.
Biologicals 35:195-202(2007)
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Rieger J., Frank B., Weller M., Wick W.
Mechanisms of resistance of human glioma cells to Apo2 ligand/TNF-related apoptosis-inducing ligand.
Cell. Physiol. Biochem. 20:23-34(2007)
PubMed=19365568; DOI=10.1371/journal.pone.0005209; PMCID=PMC2666263
Bax D.A., Little S.E., Gaspar N., Perryman L., Marshall L., Viana-Pereira M., Jones T.A., Williams R.D., Grigoriadis A., Vassal G., Workman P., Sheer D., Reis R.M., Pearson A.D.J., Hargrave D., Jones C.
Molecular and phenotypic characterisation of paediatric glioma cell lines as models for preclinical drug development.
PLoS ONE 4:E5209-E5209(2009)
PubMed=19435942; DOI=10.1215/15228517-2009-025; PMCID=PMC2743214
Ichimura K., Pearson D.M., Kocialkowski S., Backlund L.M., Chan R., Jones D.T.W., Collins V.P.
IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas.
Neuro-oncol. 11:341-347(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=21406405; DOI=10.1158/0008-5472.CAN-10-3112
Grzmil M., Morin P. Jr., Lino M.M., Merlo A., Frank S., Wang Y.-H., Moncayo G., Hemmings B.A.
MAP kinase-interacting kinase 1 regulates SMAD2-dependent TGF-beta signaling pathway in human glioblastoma.
Cancer Res. 71:2392-2402(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)
PubMed=22570425; DOI=10.1093/neuonc/nos072; PMCID=PMC3367844
Bady P., Diserens A.-C., Castella V., Kalt S., Heinimann K., Hamou M.-F., Delorenzi M., Hegi M.E.
DNA fingerprinting of glioma cell lines and considerations on similarity measurements.
Neuro-oncol. 14:701-711(2012)
PubMed=23637631; DOI=10.1371/journal.pgen.1003464; PMCID=PMC3636093
Giacomini C.P., Sun S., Varma S., Shain A.H., Giacomini M.M., Balagtas J.M.S., Sweeney R.T., Lai E., Del Vecchio C.A., Forster A.D., Clarke N., Montgomery K.D., Zhu S., Wong A.J., van de Rijn M., West R.B., Pollack J.R.
Breakpoint analysis of transcriptional and genomic profiles uncovers novel gene fusions spanning multiple human cancer types.
PLoS Genet. 9:E1003464-E1003464(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=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=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=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=30188626; DOI=10.1134/S1990519X16050072
Kiseleva L.N., Kartashev A.V., Vartanyan N.L., Pinevich A.A., Samoylovich M.P.
Characteristics of A172 and T98G cell lines.
Tsitologiia 58:349-355(2016)
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=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)"
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:A172细胞在半固体培养基中可形成克隆;A172细胞在免疫抑制小鼠中不成瘤。最初分离自一名患者的胶质母细胞瘤组织,在培养中表现出典型的胶质瘤细胞形态,如多形性、核异型性、高核质比等。
NCI-H1930 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:TCC Sup Cells、Hs695 Cells、NCI-H1793 Cells
DU4475 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,多细胞聚集;形态特性:上皮细胞样;相关产品有:LNCaP Cells、MT-4 Cells、KTC1 Cells
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:Reuber H-35 Cells、LP-1 Cells、NCI-Hut 125 Cells
解冻细胞常见实验问题分析及推荐解决方法:在解冻冻存细胞时,发现会出现存活率低、大量细胞碎片及生长缓慢等问题,究竟是什么原因导致,我们该怎么进行解决?以下是国内外细胞培养专家针对解冻细胞实验问题,总结的一些解决方案!出现低存活率的可能原因及推荐解决方案如下:1)解冻过程中细胞裂解,推荐的解决方案:可预期到一定量的细胞死亡,因此细胞的浓度应足够GAO,考虑到这一损失。起始浓度为1*10(6)至1*10(7)细胞/毫升;2)解冻过程中的问题,推荐的解决方案:在-70℃至-80℃下保存冷冻的培养物,保存时间为1-5天,但这不是保存的方法。在37℃充分解冻后应立即开始培养;3)对冷冻过敏,推荐的解决方案:A.完全或部分更换培养基,减少培养基中冷冻的量。在24小时后更换培养体可全部去除冷冻。B.留出更多时间供培养物恢复。有时细胞需要几周时间才能形成单层或密集的悬浮物,取决于冷冻时细胞的年龄或传代次数或在生长阶段中的位置。冷冻的Zui佳条件在对数期;4)被冷冻的原种细胞的年龄或冷冻时培养物的年龄,推荐的解决方案:解冻Zui近冷冻的细胞。细胞处于冷冻状态的时间越长,存活率越低。检查冷冻细胞的时间和方法。在冷冻时细胞应处于对数期。
A172人胶质母细胞瘤传代细胞活性强|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
HR-8348 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:MV(4;11) Cells、NCI-H441 Cells、PLC/PRF5 Cells
COLO 357 Cells;背景说明:胰腺癌;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:MB-49 Cells、PC 61-5-3 Cells、AR42J Cells
COLO-16 Cells;背景说明:皮肤鳞癌;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;相关产品有:OUMS27 Cells、P3-X63-Ag8.653 Cells、SW900 Cells
10RGB 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:OCM1A Cells、TKB-1 Cells、CEM-T4 Cells
细胞冻存的步骤:1)选择处于对数生长期的细胞,在冻存前一天ZuiHAO换。将多个培养瓶中的细胞培养去掉,用0.25% 胰蛋白酶消化。适时去掉胰蛋白酶,加入少量新培养。用吸管吸取培养反复吹打瓶壁上的细胞,使其成为均匀分散的细胞悬。悬浮生产细胞则不要消化处理。然后将细胞收集于离心管中离心(1000r/min,10分钟);2)去上清,加入含20%小牛血清的完全培养基,于4℃预冷15分钟后,逐滴加入已无菌的DMSO或甘油,用吸管轻轻吹打使细胞均匀,细胞浓度为5×106~1×107/mL之间。(冻存培养的配置是不是一定要用小牛血清呢?答案是不一定的,具体要看培养的细胞类型来选择;3)将分装上述细胞悬于2ml冻存管中,每管0.25ml。冻存管要将盖子盖紧,并标记HAO细胞名称和冻存日期,同时作HAO登记(日期、细胞种类及代次、冻存支数);4)将装HAO细胞的冻存管放到冻存盒中,-80℃冰箱过夜。;如果有程序降温器(放在-80℃冰箱过夜,放入罐)ZuiHAO;或者可以在4℃,2h;然后转到-20℃,2h;-80℃,2h;放入罐;5)细胞冻存在中可以长期保存,但为妥善起见,冻存半年后,ZuiHAO取出一只冻存管细胞复苏培养,观察生长情况,然后再继续冻存。
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A172人胶质母细胞瘤传代细胞活性强|送STR图谱
形态特性:上皮细胞样
在实验室细胞培养过程中,细胞聚集是一个常见的问题,它可能会影响细胞的正常生长、实验结果的准确性等诸多方面。为了防止细胞聚集,科研人员通常会采用多种有效的方法。首先,合适的细胞培养容器表面处理至关重要。许多细胞培养瓶和培养皿会经过特殊的表面处理,例如用亲水性的聚合物涂层。减少细胞之间因为吸附在同一位置而聚集的可能性。酶处理也是常用的手段之一。在细胞消化传代过程中,使用适量的胰蛋白酶等酶试剂。胰蛋白酶能够分解细胞间的连接蛋白,使细胞彼此分离。但是,酶的浓度和处理时间需要严格把控。如果酶浓度过高或者处理时间过长,虽然细胞能够很好地分散,但可能会对细胞造成损伤,影响细胞的活性。以常见的哺乳动物细胞为例,一般使用0.25%的胰蛋白酶,在37℃下处理1-3分钟,就可以有效地将细胞分散开,同时又能保证细胞的健康状态。添加合适的试剂也是防止细胞聚集的有效策略。一些抗聚集剂如四乙酸(EDTA)被广泛使用。EDTA能够螯合细胞培养液中的钙、镁离子,而这些离子是细胞间连接所依赖的重要成分。当它们被螯合后,细胞间的连接就会变弱,从而减少聚集。在细胞培养过程中,轻柔的操作也不容忽视。无论是在细胞的接种、换液还是转移过程中,避免剧烈摇晃或吹打。通过这些综合的方法,实验室能够更好地防止细胞聚集,为细胞系培养实验的成功提供保障。
MOVAS-1 Cells;背景说明:主动脉平滑肌;SV40转化;C57BL/6;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:Human Liver-7702 Cells、NCI-H460 Cells、WM266 Cells
NCIH1155 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:悬浮生长;形态特性:上皮细胞;相关产品有:LS 1034 Cells、IEC18 Cells、Opossum Kidney Cells
Panc-813 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:IA-LM Cells、PCI:SG-231 Cells、OE-19 Cells
LIXC-002 Cells;背景说明:详见相关文献介绍;传代方法:1:3传代,3-4天传1次;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:B4G12 Cells、MRC9 Cells、M059J Cells
Mouse INsulinoma 6 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:U251MG Cells、H1436 Cells、WI38 Cells
SBC-3 Cells;背景说明:小细胞肺癌;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;相关产品有:HCC4006 Cells、NCIH716 Cells、RM-1 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;相关产品有:D-283MED Cells、W133 Cells、BE(2)-C Cells
HCC0827 Cells;背景说明:这株细胞建于1994年三月。这株肺腺癌在EGFR酪酸激酶区域有一个获得性突变(E746-A750缺失)。患者在25岁到26岁时每个月抽1包烟。在诊断前12年不再抽烟。;传代方法:消化5分钟。1:2。4-5天长满。;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:RPMI-8402 Cells、3 LL Cells、IBRS-2 Cells
A2780/Taxol 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:RT112 Cells、OVMANA Cells、HSC/mHSC Cells
Abcam A-549 LGALS3 KO Cells(拥有STR基因鉴定图谱)
Abcam U-87MG RAB39B KO Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line CSG153 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRT582 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YTC531 Cells(拥有STR基因鉴定图谱)
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CHO PBj gp130 Cells(拥有STR基因鉴定图谱)
DA02383 Cells(拥有STR基因鉴定图谱)
ESSA2 Cells(拥有STR基因鉴定图谱)
GM07259 Cells(拥有STR基因鉴定图谱)
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、D 407 Cells、UCLA SO M21 Cells
HCC-2935 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:746T Cells、MOLT4 Cells、253JBV Cells
SKLMS1 Cells;背景说明:详见相关文献介绍;传代方法:1:2-1:5传代,2-3天换液1次。;生长特性:贴壁生长;形态特性:成纤维细胞;相关产品有:SCLC-21H Cells、PLA 802 Cells、L5178Y TK+/-3.7.2c 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,详见产品说明部分;形态特性:详见产品说明;相关产品有:T9 Cells、OC 316 Cells、NS-20Y Cells
MDAMB157 Cells;背景说明:该细胞源自一位患有乳腺髓样癌的44岁黑人女性,表达WNT7B癌基因,细胞与细胞边界处有细胞桥粒、微绒毛、张力细丝。;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:MRC-V Cells、H-596 Cells、no-11 Cells
JC Cells;背景说明:乳腺癌;雌性;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:NCI H157 Cells、THEECs Cells、MDCKII-WT Cells
COLO357 Cells;背景说明:胰腺癌;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:NCI-H810 Cells、WM-239-A Cells、Anip-973 Cells
OVCAR.3 Cells;背景说明:该细胞1982年由T.C. Hamilton等建系,源自一位60卵巢腺癌的腹水,是卵巢癌抗药性研究的模型。;传代方法:1:2—1:4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:Vero C1008 Cells、SKNEP1 Cells、Madin Darby Canine Kidney Cells
HS-294T 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:混合星状和多边形;相关产品有:HF-91 Cells、Hep 2 Cells、LIXC002 Cells
H69C Cells;背景说明:详见相关文献介绍;传代方法:1:2—1:4传代,每周换液2次;生长特性:悬浮生长,聚团;形态特性:聚团悬浮;相关产品有:H522 Cells、MEF (CF-1) Cells、Jurkat E6-1 Cells
MRC 5 Cells;背景说明:MRC-5细胞系来自14周龄男性胎儿的正常肺组织,该细胞老化前能传代42~46个倍增时间。;传代方法:1:2-1:5传代;每周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:BE2-C Cells、PE CA PJ34 Cells、RC-4B Cells
NCI-H1373 Cells;背景说明:详见相关文献介绍;传代方法:1:3-1:4传代;2-3天换液1次。;生长特性:贴壁生长;形态特性:上皮样;相关产品有:HLMVEC Cells、Colon 38 Cells、RIN Cl-5F Cells
HCC-1937 Cells;背景说明:这株细胞1995年10月13日最初来源于原发性导管癌, 用了11.5个月建株。肿瘤分类为TNM IIB期, 3级。BRCA1分析表明这株细胞是BRCA1 5382C突变纯合的, 而来源于同一病人的类淋巴母细胞细胞株在这个突变位点上是杂合的。 另两个家庭成员也有这个突变; 一个同卵双生姐妹也患有乳腺癌。这株细胞有一个后天的TP53突变, 而其野生型等位基因丢失; 一个PTEN基因的后天的纯合缺失, 以及多个与乳腺癌发病机理相关的位点上发生的杂合突变。这株细胞Her2-neu和p53表达都呈阴性。;传代方法:1:2传代;4-5天传代一次。;生长特性:贴壁生长;形态特性:上皮样;多角形;相关产品有:RBMEC Cells、OE21 Cells、MDAMB330 Cells
APB5 Cells(拥有STR基因鉴定图谱)
WEHI3 Cells;背景说明:白血病;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;相关产品有:Hs294T Cells、RPMI-7951 Cells、SGC7901/DDP Cells
A172人胶质母细胞瘤传代细胞活性强|送STR图谱
K-562 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:GFP-Olig2 Cells、Colo205 Cells、H3255 Cells
SK Mel 24 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:Earle's L cells Cells、SNK-6 Cells、Mono Mac 6 Cells
U343 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:HEK AD293 Cells、FO [Mouse myeloma] Cells、SKNBE(2) Cells
LS-411 Cells;背景说明:详见相关文献介绍;传代方法:1:2传代;每周2次;生长特性:贴壁生长;形态特性:上皮样;相关产品有:H1693 Cells、MC3T3-E1 Subclone 14 Cells、OVCA433_Bast Cells
HCC-1833 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:Menschliche Und Tierische Zellkulture-1 Cells、Panc 5.04 Cells、HOCF Cells
P-36 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:HCT_116 Cells、Chinese Hamster Ovary Cells、VM-CUB-1 Cells
HONE-1 Cells;背景说明:鼻咽癌;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;相关产品有:PG-4 S+L- Cells、GM05372E Cells、H1522 Cells
GM09639 Cells(拥有STR基因鉴定图谱)
HAP1 AXIN1 (-) 4 Cells(拥有STR基因鉴定图谱)
OV1-P 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:H740 Cells、SK-ChA-1 Cells、UPCI:SCC154 Cells
HS-940-T 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:成纤维细胞;相关产品有:Hs940-T Cells、WILL-2 Cells、HSF2 Cells
MC-CAR Cells;背景说明:B淋巴;EBV转化;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:NSH Cells、SKLU1 Cells、BE2M17 Cells
LM6 Cells;背景说明:肝癌;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:NFS 60 Cells、NCI-H735 Cells、P30-OHKUBO Cells
FRhK-4 Cells;背景说明:胚胎;肾;自发永生;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:IEC-18 Cells、EA hy 926 Cells、WEHI-164 Cells
HCC1395 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:贴壁生长;形态特性:上皮样;相关产品有:COLO-829 Cells、3T6 Cells、Human Fetal Thymocyte-8810 Cells
OCI-AML-3 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;相关产品有:HS-294T Cells、MHCC-97 Cells、UMUC3 Cells
108CC15 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:OAW 42 Cells、BHP10-3 Cells、RT 112 Cells
HG03077 Cells(拥有STR基因鉴定图谱)
iBMK W2.3.1-5 Cells(拥有STR基因鉴定图谱)
LL/2-mNIS-Puro Cells(拥有STR基因鉴定图谱)
NCI-BL2347 Cells(拥有STR基因鉴定图谱)
PathHunter CHO-K1 GPR84 beta-arrestin Cells(拥有STR基因鉴定图谱)
Ubigene A-549 FZD3 KO Cells(拥有STR基因鉴定图谱)
UPCI-SCC-044 Cells(拥有STR基因鉴定图谱)
HAP1 TFG (-) 2 Cells(拥有STR基因鉴定图谱)
MILE SVEN1 Cells;背景说明:MS1是1994年建株的胰岛内皮细胞株。原代培养的胰岛内皮细胞用抗G418的温度敏感型SV40大T抗原(tsA-58-3)转染。抗性克隆用克隆环分离,并筛选吸收dil-Ac-LDL的。这株细胞保留了内皮细胞的许多特性,如吸收乙酰化LDL和表达八因子相关抗原及BEGF受体。;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:详见产品说明;相关产品有:3T3-A31 Cells、HuH7 Cells、IFRS1 Cells
SK_N_BE2C 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;相关产品有:MSTO-211 H Cells、NCI-H865 Cells、NCIH2126 Cells
LM6 Cells;背景说明:肝癌;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:NFS 60 Cells、NCI-H735 Cells、P30-OHKUBO Cells
DHL10 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;形态特性:淋巴母细胞;相关产品有:H1793 Cells、TB-1 Lu Cells、32D CL3 Cells
PC-9/GR 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:PC 61-5-3 Cells、NCI-H2172 Cells、MDA MB 134VI Cells
PC-9/GR 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:PC 61-5-3 Cells、NCI-H2172 Cells、MDA MB 134VI Cells
HCC1171 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:Wistar Institute-38 Cells、MiaPaCa-2 Cells、DSL-6A/C1 Cells
769-P Cells;背景说明:该细胞系1975年建系,源自一位63岁白人女性的初期透明细胞腺癌组织,细胞呈圆形且边界不清,核浆比大,有微绒毛及桥粒。该细胞可在软琼脂上生长。 ;传代方法:1:4—1:12传代,2—3天换液一次;生长特性:贴壁生长;形态特性:上皮细胞样;相关产品有:143B Cells、MA 104 Cells、RBE Cells
Hs-606-T 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天换液一次;生长特性:贴壁生长;形态特性:成纤维细胞;相关产品有:SKES1 Cells、NCIH1838 Cells、LP-1 Cells
RPMI 8226/S Cells;背景说明:来源于一位61岁的男性浆细胞瘤患者;可产生免疫球蛋白轻链,未检测到重链。;传代方法:按1:2传代,5-6小时可以看到细胞分裂;生长特性:悬浮生长;形态特性:淋巴母细胞样;相关产品有:AC16 [Human hybrid] Cells、NCIH1650 Cells、PANC-1 Cells
PC9 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:CNE1 Cells、HME-1 Cells、SU-DHL-6 Cells
PCI-4B Cells;背景说明:喉鳞癌;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:GDM-1 Cells、NUGC4 Cells、HUT125 Cells
HCC0078 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:HT144 Cells、OVCAR-4 Cells、HRCEC Cells
AD-293 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:C4-2 Bone metastatic Cells、KYSE 150 KYSE150 Kyse150 KY150
Cells、Hs 888Lu Cells
KY-270 Cells;背景说明:详见相关文献介绍;传代方法:1:5传代;生长特性:贴壁生长;形态特性:上皮样;相关产品有:B78 Cells、H1688 Cells、COV362 Cells
S2R+-spin-GFP-2 Cells(拥有STR基因鉴定图谱)
C166 Cells;背景说明:血管内皮;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:MD Anderson-Metastatic Breast-175-VIII Cells、NCI-SNU-601 Cells、NCI-H847 Cells
CAL-39 Cells;背景说明:外阴鳞癌细胞;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:B16 subline B78 Cells、EA.hy 926 Cells、MC-3T3-E1 Cells
SKNO-1 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;相关产品有:HEC-151 Cells、IEC-18 Cells、C32 [Human melanoma] Cells
Swiss-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:H-1688 Cells、Capan2 Cells、HCC1395 Cells
RMS1598 Cells;背景说明:详见相关文献介绍;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:成纤维细胞;相关产品有:NCIH1355 Cells、T2 Cells、Ramos 1 Cells
Mc Coy Cells;背景说明: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;相关产品有:FHs74 Int Cells、526 Cells、KASUMI1 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
NCM356 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:MDCK II Cells、REC1 Cells、AK Cells
┈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;
OCI/AML3 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;相关产品有:hRMECs Cells、Fetal Bovine Heart Endothelial Cells、PC.3 Cells
LN 382 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:SK-N-FI Cells、H146 Cells、NTera2 cl.D1 Cells
MIA-Pa-Ca-2 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:451-LU Cells、WISH Cells、H676 Cells
EAhy926 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:Hs.27 Cells、HANK-1 Cells、mREC Cells
MDCC MSB1 Cells;背景说明:淋巴瘤;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:SKCO 1 Cells、18G3.cl 1 Cells、HEK 293-EBNA Cells
RCC4 Cells;背景说明:肾透明细胞癌;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;相关产品有:H522 Cells、IOSE-Van Cells、H510 Cells
BayGenomics ES cell line CSH598 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRZ260 Cells(拥有STR基因鉴定图谱)
BoMaMa-J2imm Casp1-/- Cells(拥有STR基因鉴定图谱)
KUM10 Cells(拥有STR基因鉴定图谱)
A172人胶质母细胞瘤传代细胞活性强|送STR图谱
PGL3 Cells(拥有STR基因鉴定图谱)
PMab-117 Cells(拥有STR基因鉴定图谱)
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Todaro G.J., De Larco J.E.
Growth factors produced by sarcoma virus-transformed cells.
Cancer Res. 38:4147-4154(1978)
PubMed=450131; DOI=10.1038/279797a0
Day R.S. 3rd, Ziolkowski C.H.J.
Human brain tumour cell strains with deficient host-cell reactivation of N-methyl-N'-nitro-N-nitrosoguanidine-damaged adenovirus 5.
Nature 279:797-799(1979)
PubMed=6256643; DOI=10.1038/288724a0
Day R.S. 3rd, Ziolkowski C.H.J., Scudiero D.A., Meyer S.A., Lubiniecki A.S., Girardi A.J., Galloway S.M., Bynum G.D.
Defective repair of alkylated DNA by human tumour and SV40-transformed human cell strains.
Nature 288:724-727(1980)
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Bigner D.D., Bigner S.H., Ponten J., Westermark B., Mahaley M.S. Jr., Ruoslahti E., Herschman H.R., Eng L.F., Wikstrand C.J.
Heterogeneity of genotypic and phenotypic characteristics of fifteen permanent cell lines derived from human gliomas.
J. Neuropathol. Exp. Neurol. 40:201-229(1981)
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Westin E.H., Gallo R.C., Arya S.K., Eva A., Souza L.M., Baluda M.A., Aaronson S.A., Wong-Staal F.
Differential expression of the amv gene in human hematopoietic cells.
Proc. Natl. Acad. Sci. U.S.A. 79:2194-2198(1982)
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Dracopoli N.C., Fogh J.
Polymorphic enzyme analysis of cultured human tumor cell lines.
J. Natl. Cancer Inst. 70:469-476(1983)
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Bigner S.H., Mark J., Bigner D.D.
Chromosomal composition of four permanent cultured cell lines derived from human gliomas.
Cancer Genet. Cytogenet. 10:335-349(1983)
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Yarosh D.B., Foote R.S., Mitra S., Day R.S. 3rd
Repair of O6-methylguanine in DNA by demethylation is lacking in Mer- human tumor cell strains.
Carcinogenesis 4:199-205(1983)
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Cell 166:740-754(2016)
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Next-generation characterization of the Cancer Cell Line Encyclopedia.
Nature 569:503-508(2019)"
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文献和实验该产品被引用文献
"PubMed=212188
Todaro G.J., De Larco J.E.
Growth factors produced by sarcoma virus-transformed cells.
Cancer Res. 38:4147-4154(1978)
PubMed=450131; DOI=10.1038/279797a0
Day R.S. 3rd, Ziolkowski C.H.J.
Human brain tumour cell strains with deficient host-cell reactivation of N-methyl-N'-nitro-N-nitrosoguanidine-damaged adenovirus 5.
Nature 279:797-799(1979)
PubMed=6256643; DOI=10.1038/288724a0
Day R.S. 3rd, Ziolkowski C.H.J., Scudiero D.A., Meyer S.A., Lubiniecki A.S., Girardi A.J., Galloway S.M., Bynum G.D.
Defective repair of alkylated DNA by human tumour and SV40-transformed human cell strains.
Nature 288:724-727(1980)
PubMed=6260907; DOI=10.1097/00005072-198105000-00001
Bigner D.D., Bigner S.H., Ponten J., Westermark B., Mahaley M.S. Jr., Ruoslahti E., Herschman H.R., Eng L.F., Wikstrand C.J.
Heterogeneity of genotypic and phenotypic characteristics of fifteen permanent cell lines derived from human gliomas.
J. Neuropathol. Exp. Neurol. 40:201-229(1981)
PubMed=6954533; DOI=10.1073/pnas.79.7.2194; PMCID=PMC346157
Westin E.H., Gallo R.C., Arya S.K., Eva A., Souza L.M., Baluda M.A., Aaronson S.A., Wong-Staal F.
Differential expression of the amv gene in human hematopoietic cells.
Proc. Natl. Acad. Sci. U.S.A. 79:2194-2198(1982)
PubMed=6220172
Dracopoli N.C., Fogh J.
Polymorphic enzyme analysis of cultured human tumor cell lines.
J. Natl. Cancer Inst. 70:469-476(1983)
PubMed=6652614; DOI=10.1016/0165-4608(83)90091-2
Bigner S.H., Mark J., Bigner D.D.
Chromosomal composition of four permanent cultured cell lines derived from human gliomas.
Cancer Genet. Cytogenet. 10:335-349(1983)
PubMed=6825208; DOI=10.1093/carcin/4.2.199
Yarosh D.B., Foote R.S., Mitra S., Day R.S. 3rd
Repair of O6-methylguanine in DNA by demethylation is lacking in Mer- human tumor cell strains.
Carcinogenesis 4:199-205(1983)
PubMed=3518877; DOI=10.3109/07357908609038260
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