Raji人Burkitt's淋巴瘤传代细胞活性强|送STR图

"Raji人Burkitt's淋巴瘤传代细胞活性强|送STR图谱
传代方法：1:2-1:4(首次传代建议1:2)
生长特性：悬浮生长
换液频率：每周2-3次
背景资料：Raji细胞由PulvertaftRJV于１９６３年从一位１１岁黑人男孩的左上颌骨的Burkitt淋巴瘤中分离建立的，是第一个人类造血系统的连续传代细胞，为B细胞起源。该细胞中含有EBV，需要在二级生物安全柜中操作；可作转染宿主。
SPDC-CCL141 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：成纤维母细胞样;相关产品有：CCC-HEH-2 Cells、CHP-126 Cells、LTEP a2 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;相关产品有：D 407 Cells、HR-8348 Cells、RKOE6 Cells
CCRF/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：M-1 Cells、PL 5 Cells、DHBE 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。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。
Raji人Burkitt's淋巴瘤传代细胞活性强|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
KU-19-19 Cells;背景说明：膀胱癌；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：MM1.S Cells、SK-NEP-1 Cells、HT Cells
JB6 Cl 30-7b 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：T-ALL-1 Cells、Jurkat-77 Cells、NCI-H2030 Cells
Renal Proximal Tubule Epithelial Cells/TERT-immortalized 1 Cells;背景说明：肾；近端小管上皮；HGNC-TERT转化；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：NCI-H-69 Cells、WI38 Cells、H-292 Cells
CMT 167 Cells;背景说明：肺腺癌；雌性；C５７BL/ICRF-a(t);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：LLC-PK(1) Cells、VERO76 Cells、RL95-2 Cells
造成实验室细胞污染常见情况总结：细胞培养中Zui常见污染的是细菌、真菌和支原体污染。细胞一旦污染，大多数较难处理。那么，哪些情况我们不注意的话就会造成细胞污染呢？我们根据常见细胞培养实验分析总结下。【违规操作】１)为节省时间，有人已经用超净台四个多小时，不开紫外灭菌３０min,酒精擦拭后直接开始试验；２)器材或者溶很久没用，未检测是否污染而直接使用；离心管多次使用，枪头为了方便交叉使用；３)超净台不点酒精灯；点了酒精灯放在右上角，而你在左下角做试验；４)不带手套，徒手操作；５)细胞培养间配备枪式移器、手术器械、离心机、冰箱等专用仪器设备以及专用的实验服和拖鞋，未定期消毒。专用物品被带出传代细胞使用。培养细胞过程中使用的所有实验用具，如移管、一次性枪头、一次性塑料离心管、冻存管等未按要求灭菌使用(通常需１２１°CGAO压灭菌２０分钟后３７％烤干备用)。超净台和桌面，东西太多太乱：超净台不是储物箱，什么培养皿、各种规格的板子、枪头就不要堆在超净台！这样就会有许多紫外线顾不到的卫生死角。传代细胞其他的桌面，切忌东西堆积如山，不要将酒精棉球、标签纸、牛皮纸买来后全部堆在传代细胞！一不小心“飘”进你的细胞培养板里，细胞就会养的不HAO，啥时候死了都不知道！【培养箱太久没清洁】细胞污染了，并非直接扔了培养皿就不管了，首先你还得看看这个恒温培养箱里其他培养皿或孔板里的细胞是否污染，如果有而且HAO几个板子都有类似的污染块，那很可能是培养箱中的水或者空气污染了，得给培养箱做个大扫除，重新酒精消毒，照紫外；孵箱里的水，水没了要记得加，还得记得十天半个月的就用酒精擦擦托盘。【传代细胞人多口杂，难管理】在传代细胞这种卫生要求GAO，人多了，不确定因素多了，难以保证试验在无菌条件下操作。出入试验室，实验服当风衣穿，不扣纽扣，不戴，就容易造成细胞污染；超净台做实验时，喜欢说话聊着做试验，要是还不带口罩，里面就有很多细菌等着去攻击你的细胞呢！
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Raji人Burkitt's淋巴瘤传代细胞活性强|送STR图谱
形态特性：淋巴母细胞样
关于细胞株是否都能一直传代，答案是否定的。细胞系分为有限细胞系与连续细胞系两类。有限细胞系就像一位有着既定行程的行者，其传代之旅存在明确的终点。以正常的人体肝细胞系为例，在体外培养时，它大约能传代20-30次。随着传代次数的递增，细胞内部仿佛一台精密仪器的零件逐渐磨损老化。端粒酶活性降低，端粒不断缩短，染色体结构开始不稳定，基因表达也出现异常。同时，细胞的代谢速率减缓，对营养物质的摄取和利用效率大打折扣，有害物质的积累却日益增多，最终导致细胞停止分裂，走向生命的尽头。而连续细胞系则像是拥有无限活力的长跑健将，具有较强的传代能力。如Hela细胞系，自1951年从Henrietta Lacks女士的宫颈癌组织中分离出来后，便在全球生物实验室中“大放异彩”，至今已传代无数次。它能持续分裂得益于其特殊的遗传变异，使其染色体端粒能够维持稳定长度，并且细胞内的一些关键信号通路持续激活，促进细胞增殖。但这并不意味着它的传代毫无风险与限制。在漫长的传代过程中，它可能会发生新的基因突变、染色体易位等变异事件，从而改变细胞的生物学特性，如细胞形态、生长速度、对药物的敏感性等。
3T3-L1 ad 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：D-283 Med Cells、Hs 819.T Cells、H2009 Cells
DMS 273 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：AN-3 Cells、OCI-Ly7 Cells、Hs940-T Cells
HCC9204 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：BEL 7402 Cells、RKO_AS45 Cells、Roswell Park Memorial Institute 7666 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，详见产品说明部分;形态特性：详见产品说明;相关产品有：WEHI 3B Cells、MDCK.2 Cells、LU451 Cells
OCI-Ly1 Cells;背景说明：弥漫大B淋巴瘤；男性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：悬浮;形态特性：详见产品说明;相关产品有：THPI Cells、Mahlavu Cells、HCC1500 Cells
FLS Cells;背景说明：滑膜;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：Hs68 Cells、PC10 Cells、SNU484 Cells
MADB-106 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：MNNG/HOS Clone F-5 Cells、MUTZ-1 Cells、Caov-3 Cells
293F 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；悬浮生长;形态特性：上皮细胞样;相关产品有：NCIH1876 Cells、T_T_ Cells、MV4;11 Cells
CMT-93 Cells;背景说明：结肠癌；C５７BL/ICRF;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：Bac1 2F5 Cells、D341MD Cells、H1105 Cells
3T3.T4.CXCR4 Cells(拥有STR基因鉴定图谱)
Abcam Jurkat EPHX1 KO Cells(拥有STR基因鉴定图谱)
ALC [Mouse ameloblast] Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line RRJ555 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line XK542 Cells(拥有STR基因鉴定图谱)
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CaBa31 Cells(拥有STR基因鉴定图谱)
DA00410 Cells(拥有STR基因鉴定图谱)
DAE100A Cells(拥有STR基因鉴定图谱)
GM01353 Cells(拥有STR基因鉴定图谱)
SUM-102 Cells;背景说明：乳腺癌；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：H-1651 Cells、NRK 49F Cells、SKN-AS Cells
HBL1 Cells;背景说明：弥漫大B淋巴瘤；男性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：悬浮;形态特性：详见产品说明;相关产品有：U2-OS Cells、VSMC Cells、D324 Cells
SK-ES1 Cells;背景说明：详见相关文献介绍;传代方法：１：２-１：５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：上皮样;相关产品有：HS-5 Cells、PSN1 Cells、PFSK1 Cells
H-1436 Cells;背景说明：详见相关文献介绍;传代方法：随细胞的密度而增加;生长特性：悬浮生长;形态特性：详见产品说明;相关产品有：PNT1/A Cells、SUM-52-PE Cells、Hca-F Cells
OV 2008 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;相关产品有：FOXNY Cells、HFF-1 Cells、NCI-H78 Cells
X63-Ag8-653 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：CemT4 Cells、C-4-I Cells、NCIH1155 Cells
HO-8910 PM Cells;背景说明：高转移卵巢癌 Cells;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：CL-40 Cells、H-2227 Cells、NCI-H345 Cells
CL11 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：HuH6 Cells、P3-X63.Ag8.653 Cells、HL7702 Cells
HCC0366 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：MCF/Adr Cells、RN-c Cells、NTC200 Cells
HOP-62 Cells;背景说明：肺癌；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：LK2 Cells、HUTU80 Cells、T24 Cells
COLO 678 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：OVCA-432 Cells、NCIH295R Cells、Panc-1-P Cells
SupB15W Cells;背景说明：详见相关文献介绍;传代方法：１：２传代。３天内可长满。;生长特性：悬浮生长;形态特性：淋巴母细胞;相关产品有：SNU387 Cells、EOMA Cells、COLO-16 Cells
GMK,BSC-1 Cells;背景说明：详见相关文献介绍;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁或悬浮，详见产品说明部分;形态特性：详见产品说明;相关产品有：TE 85 ClF-5 Cells、HEK-AD293 Cells、HARA-B Cells
368B1-5 Cells(拥有STR基因鉴定图谱)
Mevo Cells;背景说明：详见相关文献介绍;传代方法：１：３-１：５传代，２-３天换液１次。;生长特性：混合生长;形态特性：成纤维细胞;相关产品有：Sci-1 Cells、BxPC-3 Cells、MDA2B Cells
Raji人Burkitt's淋巴瘤传代细胞活性强|送STR图谱
EAC-E2G8 Cells;背景说明：腹水瘤;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：半贴壁;形态特性：详见产品说明;相关产品有：OVCAR3 Cells、TM-3 Cells、A9 (Hamprecht) Cells
NIH:OVCAR-4 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：HTori:3 Cells、HLE-B3 Cells、ECC-1 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：JROECL 19 Cells、624 Cells、HNE2 Cells
Strain L-929 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：LED-WiDr Cells、H1915 Cells、MT-4 Cells
KLM1 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：EU-4 Cells、ESC-410 Cells、NCIH2110 Cells
KLM1 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：EU-4 Cells、ESC-410 Cells、NCIH2110 Cells
6-T CEM 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：1.1B4 Cells、TR146 Cells、Walker256 Cells
GM24374 Cells(拥有STR基因鉴定图谱)
HAP1 NLRC5 (-) 1 Cells(拥有STR基因鉴定图谱)
HUASMC Cells;背景说明：脐动脉平滑肌;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：HC11 Cells、SKLU01 Cells、hTERT-HME1 Cells
HTori:3 Cells;背景说明：甲状腺；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;相关产品有：KBM-7/Hap8 Cells、H4-II-E Cells、SCC7 Cells
MESSA Cells;背景说明：详见相关文献介绍;传代方法：１：６-１：８传代；每周２-３次。;生长特性：贴壁生长;形态特性：成纤维细胞样　;相关产品有：M109 Cells、KYSE-70 Cells、L1210 Cells
MC3T3-E 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：SK-RC-42 Cells、LNCaP Cells、FLC7 Cells
Hs895T 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：成纤维细胞;相关产品有：Roswell Park Memorial Institute 7951 Cells、SK-N-AS Cells、MOLP2 Cells
LMH Cells;背景说明：肝癌；雄性;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：SAOS 2 Cells、Madin-Darby Canine Kidney Cells、NCI-H920 Cells
SNUC2B 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：PaTu 8988 S Cells、H-727 Cells、C-28/I2 Cells
118MG Cells;背景说明：注意： 据报道来自不同个体的胶质母细胞瘤细胞株U-１１８ MG (HTB-１５) 和 U-１３８ MG (HTB-１６)有着一致的VNTR和相近的STR模式。 U-１１８ MG 和 U-１３８ MG细胞遗传学上很相似并有至少六个衍生标记染色体。 这是１９６６年至１９６９年间J. Ponten和同事从恶性神经胶质瘤中构建的细胞株中的一株(其它包括ATCC HTB-１４和 ATCC HTB-１６ and ATCC HTB-１７)。 １９８７年用BM-Cycline培养６周去除了支原体污染。 ;传代方法： 消化３-５分钟。１：２传代。３天内可长满。;生长特性：贴壁生长;形态特性：混合型;相关产品有：SUP-B1 Cells、Detroit 562 Cells、LM1 Cells
HRA-19a1.1 Alpha2 F Cells(拥有STR基因鉴定图谱)
KKU-M139/GEM Cells(拥有STR基因鉴定图谱)
ML-DmBG6 Cells(拥有STR基因鉴定图谱)
NRCAN-LL-41 Cells(拥有STR基因鉴定图谱)
RECC-CU66 Cells(拥有STR基因鉴定图谱)
UCD-Dm-mei-41-1 Cells(拥有STR基因鉴定图谱)
ZJUCHi002-A Cells(拥有STR基因鉴定图谱)
HBL-10 Cells(拥有STR基因鉴定图谱)
HANK-1 Cells;背景说明：NK/T细胞淋巴瘤；女性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：悬浮;形态特性：详见产品说明;相关产品有：HPAF-II/CD18 Cells、Hs274T Cells、NCI-H1618 Cells
SUP-B15 Cells;背景说明：详见相关文献介绍;传代方法：１：２传代。３天内可长满。;生长特性：悬浮生长;形态特性：淋巴母细胞;相关产品有：NK-92.05 Cells、PC-3M 2B4 Cells、Hs 742.T Cells
293T Cells;背景说明：２９３细胞株插入SV４０T-抗原的温度敏感基因后产生的高转染效率的衍生株称为２９３T。;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：CMT-64 Cells、HL-60 clone15 Cells、SMA560 Cells
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;相关产品有：SNK1 Cells、Hs832T Cells、U20-S Cells
HCoEpiC Cells;背景说明：结肠上皮 Cells;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：P36 Cells、C8D1A Cells、HONE-1 Cells
HCoEpiC Cells;背景说明：结肠上皮 Cells;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：P36 Cells、C8D1A Cells、HONE-1 Cells
SKO3 Cells;背景说明：SK-OV-３由G.Trempe和L.J.Old在１９７３年从卵巢肿瘤病人的腹水分离得到。 此细胞对肿瘤坏死因子和几种细胞毒性药物包括白喉毒素、顺铂和阿霉素均耐受。 在裸鼠中致瘤，且形成与卵巢原位癌一致的中度分化的腺癌。;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：上皮细胞样;相关产品有：143 B Cells、NCIH460 Cells、CV-1 in Origin Simian-7 Cells
HuP-T4 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：LAN-6 Cells、OCI/AML-2 Cells、EL4 Cells
HCC1833 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：HBL-100 Cells、NGEC Cells、HUT-125 Cells
DAN-G 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：aNK Cells、MC 3T3-E1 Cells、Ramos-2G6-4C10 Cells
HCCLM6 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：LM3 Cells、639 V Cells、Capan 2 Cells
HCS-2/8 Cells;背景说明：软骨肉瘤；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：293 c18 Cells、PVEC Cells、GM03570 Cells
NE1-E6E7 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：SNU668 Cells、H-1105 Cells、MOLT 4 Cells
NCIH2110 Cells;背景说明：详见相关文献介绍;传代方法：１：３-１：６传代，每周换液２-３次;生长特性：贴壁或悬浮，详见产品说明部分;形态特性：上皮细胞;相关产品有：CL1.0 Cells、SK-N-BE(1) Cells、LA 4 Cells
HM1900 Cells;背景说明：小胶质 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：Hs 636.T Cells、RFL6 Cells、Immortal Pig Intestinal-2I Cells
STBCi058-B Cells(拥有STR基因鉴定图谱)
ME180 Cells;背景说明：这株细胞来源于一个细胞集落不规则没有显著角质化的侵染性鳞状细胞癌。 单层培养的细胞间可以观察到带状连接，也注意到有细胞质张力丝。 １９７０年发现支原体污染并去除。 肿瘤坏死因子(TNF)α抑制ME-１８０的生长。 这株细胞含有人乳头瘤病毒(HPV)DNA，与HPV-３９的同源性高于HPV-１８。;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：PNT1-a Cells、L78 Cells、Fetal Human Colon Cells
Pa14C 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：DLD 1 Cells、HL7702 Cells、RPMI no. 8226 Cells
KAT-5 Cells;背景说明：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;相关产品有：NCIH2030 Cells、NCIH1993 Cells、CMT93 Cells
BMSCs（mBMSCs） 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：U-2OS Cells、Cloudman S91 melanoma Cells、BALB/3T3 (clone A31) Cells
bEnd.3[BEND3] 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：H1819 Cells、FL83B Cells、BC3 H1 Cells
EM-3 Cells;背景说明：髓系白血病；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：WERI-Rb-1 Cells、SUP T1 Cells、CNE-2 Cells
NCI-H358 Cells;背景说明：１９８１年从一位开始化疗之前的患者的肿瘤组织中分离建株。超微结构研究表明细胞质中有Clara细胞的特征结构细胞表达主要的肺表面结合蛋白SP-A的蛋白和RNA。不表达SP-B和SP-C。他们在软琼脂中的克隆形成效率为０.８３%。;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：OCI Ly3 Cells、3T3F442A Cells、WPMY1 Cells
MC3T3-L1 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：成纤维细胞样;相关产品有：C-Li-7 Cells、BV2 Cells、MES-SA-Dx5 Cells
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HT 1080.T Cells;背景说明：该细胞源自一名３５岁患有纤维肉瘤的白人男性的结缔组织；ras＋。;传代方法：１：４-１：８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：SK-Hep1 Cells、HANK Cells、HFL Cells
JVM2 Cells;背景说明：该细胞是 J.V.Melo从一位６３岁患有套细胞淋巴瘤白人女性外周血中分离建立的，经EBV介导获得永生化，该细胞表达p１６和细胞周期蛋白D２,低水平表达细胞周期蛋白D１。;传代方法：１：３传代,２-３天传一代;生长特性：悬浮生长;形态特性：淋巴母细胞样;相关产品有：YES-2 Cells、H2198 Cells、SK-MES Cells
C12 Cells;背景说明：该细胞株是YaffeD,SaxelO建立的小鼠成肌细胞系的亚株。该细胞分化较快，可形成能收缩的微管，产生特异的肌肉蛋白。在骨形态形成蛋白（BMP-２）的作用下，该细胞可由成肌细胞分化为成骨细胞。检测发现该细胞鼠痘病毒阴性。;传代方法：１：２传代;生长特性：贴壁生长;形态特性：成纤维细胞样；梭形;相关产品有：DLM8 Cells、Hs 274.T Cells、Capan 2 Cells
H2444 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次。;生长特性：贴壁生长;形态特性：上皮样;相关产品有：H1437 Cells、U266 B1 Cells、C4-2B Cells
Tb 1-Lu Cells;背景说明：肺;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、BT-474 Cells、P3HR1-BL Cells
DMS-273 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：McA-RH7777 Cells、H2172 Cells、143B TK- Cells
BayGenomics ES cell line CSI799 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line SYA144 Cells(拥有STR基因鉴定图谱)
CBL63 Cells(拥有STR基因鉴定图谱)
LuNm03 Cells(拥有STR基因鉴定图谱)
Raji人Burkitt's淋巴瘤传代细胞活性强|送STR图谱
RAW-ASC Cells(拥有STR基因鉴定图谱)
RNK-9 Cells(拥有STR基因鉴定图谱)
"    "PubMed=4894370; DOI=10.1002/1097-0142(196908)24:2<211::AID-CNCR2820240202>3.0.CO;2-3
Southam C.M., Burchenal J.H., Clarkson B.D. Sr., Tanzi A., Mackey R., McComb V.
Heterotransplantability of human cell lines derived from leukemia and lymphomas into immunologically tolerant rats.
Cancer 24:211-222(1969)

DOI=10.1007/BF02618370
Stulberg C.S., Coriell L.L., Kniazeff A.J., Shannon J.E.
The animal cell culture collection.
In Vitro 5:1-16(1970)

PubMed=4321017; DOI=10.1002/ijc.2910060315
Durr F.E., Monroe J.H., Schmitter R., Traul K.A., Hirshaut Y.
Studies on the infectivity and cytopathology of Epstein-Barr virus in human lymphoblastoid cells.
Int. J. Cancer 6:436-449(1970)

PubMed=4321974
Maurer B.A., Imamura T., Wilbert S.M.
Incidence of EB virus-containing cells in primary and secondary clones of several Burkitt lymphoma cell lines.
Cancer Res. 30:2870-2875(1970)

PubMed=4325933; DOI=10.1093/jnci/46.6.1243
Pearson G.R., Henle G.S., Henle W.
Production of antigens associated with Epstein-Barr virus in experimentally infected lymphoblastoid cell lines.
J. Natl. Cancer Inst. 46:1243-1250(1971)

PubMed=4122458; DOI=10.1002/ijc.2910100108
Klein G., Dombos L., Gothoskar B.
Sensitivity of Epstein-Barr virus (EBV) producer and non-producer human lymphoblastoid cell lines to superinfection with EB-virus.
Int. J. Cancer 10:44-57(1972)

PubMed=4347031; DOI=10.1093/jnci/48.1.87
Hewetson J.F., Gothoskar B., Klein G.
Radioiodine-labeled antibody test for the detection of membrane antigens associated with Epstein-Barr virus.
J. Natl. Cancer Inst. 48:87-94(1972)

PubMed=4550511; DOI=10.1073/pnas.69.1.78; PMCID=PMC427548
Hampar B., Derge J.G., Martos L.M., Walker J.L.
Synthesis of Epstein-Barr virus after activation of the viral genome in a 'virus-negative' human lymphoblastoid cell (Raji) made resistant to 5-bromodeoxyuridine.
Proc. Natl. Acad. Sci. U.S.A. 69:78-82(1972)

PubMed=4364259; DOI=10.1002/ijc.2910110210
Klein G., Dombos L.
Relationship between the sensitivity of EBV-carrying lymphoblastoid lines to superinfection and the inducibility of the resident viral genome.
Int. J. Cancer 11:327-337(1973)

PubMed=4736620; DOI=10.1111/j.1469-1809.1973.tb00588.x
Povey S., Gardiner S.E., Watson B., Mowbray S., Harris H., Arthur E., Steel C.M., Blenkinsop C., Evans H.J.
Genetic studies on human lymphoblastoid lines: isozyme analysis on cell lines from forty-one different individuals and on mutants produced following exposure to a chemical mutagen.
Ann. Hum. Genet. 36:247-266(1973)

PubMed=4366935
Minowada J., Nonoyama M., Moore G.E., Rauch A.M., Pagano J.S.
The presence of the Epstein-Barr viral genome in human lymphoblastoid B-cell lines and its absence in a myeloma cell line.
Cancer Res. 34:1898-1903(1974)

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Hutt L.M., Huang Y.-T., Dascomb H.E., Pagano J.S.
Enhanced destruction of lymphoid cell lines by peripheral blood leukocytes taken from patients with acute infectious mononucleosis.
J. Immunol. 115:243-248(1975)

PubMed=170370; DOI=10.1099/0022-1317-28-2-207
Adams A., Strander H., Cantell K.
Sensitivity of the Epstein-Barr virus transformed human lymphoid cell lines to interferon.
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