THP-1人单核细胞白血病传代细胞活性强|送STR图谱

"THP-1人单核细胞白血病传代细胞活性强|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：该细胞从一名１岁的患有急性单核细胞性白血病的男孩的外周血中分离建立。该细胞可以吞噬乳胶颗粒和激活的红细胞，细胞膜和胞浆内均没有免疫球蛋白，表达C３R和FcR；可受佛波酯TPA诱导向单核系方向分化；可作为转染宿主。
N-2a 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：详见产品说明;相关产品有：SUDHL16 Cells、B16-BL6 Cells、NCI.H226 Cells
C-6 Cells;背景说明：胶质细胞株C６是由Benda等用N-nitrosomethylurea诱导的大鼠胶质瘤克隆，并经过一系列的体外培养和动物传代交替后建成的。 当细胞从低密度生长到满瓶时，S-１００产量增加１０倍。;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：MRC9 Cells、JIMT Cells、GM-637 Cells
Human fetal lung fibroblast 1 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：成纤维细胞样;相关产品有：OCI AML3 Cells、LC-1 sq Cells、WM239 Cells
接收细胞相关问题：如不能在收到细胞后及时操作细胞，２５及离心管发货的细胞将可以消毒后在３７度过夜，血清发货的细胞在室温下静置１-２天(注意不要放冰箱)，干冰发货的可以在确认干冰未完全升华时将细胞直接放回或者-８０度冰箱，若干冰完全升华，请即刻复苏细胞。２５瓶及离心管在培养箱平衡是为了让细胞尽快适应培养箱环境，同时使部分因运输导致脱落的细胞贴壁，此步骤非常必要。２５瓶如果在显微镜下可以看到部分不贴壁的细胞，可以收集上清后离心(１２００rpm，５min)后，将沉淀用新的培养基重悬后接种至新的培养瓶或皿中。部分细胞在运输过程中，由于不断震荡及环境不适，可能导致细胞破碎死亡，从而使培养基中漂浮很多细胞碎片及颗粒状物质。这种情况下，平衡后，贴壁细胞用PBS洗两遍再加新的培养基培养或者传代至新瓶中培养即可；悬浮细胞可以离心(１０００rpm，３min)收集细胞，并用PBS重悬后再离心一次，再用新的培养基重悬并接种细胞。
THP-1人单核细胞白血病传代细胞活性强|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
BALL1 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：悬浮生长;形态特性：淋巴母细胞;相关产品有：Wien 133 Cells、HEH2 Cells、UCLA-SO-M21 Cells
TSU-Pr1 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：H1568 Cells、COLO-829 Cells、R.K.13 Cells
HEK 293-EBNA Cells;背景说明：详见相关文献介绍;传代方法：１：４-１：１０传代；每周２次。;生长特性：贴壁生长;形态特性：上皮细胞样;相关产品有：HIT clone T15 Cells、NCIH211 Cells、SUM-52-PE Cells
MCF 10A Cells;背景说明：乳腺；上皮细胞；自发永生；女性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：OCI-Ly01 Cells、HBdSMC Cells、University of Michigan-Renal Carcinoma-2 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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THP-1人单核细胞白血病传代细胞活性强|送STR图谱
形态特性：淋巴母细胞样
淋巴母细胞(lymphoblast)是一类未成熟的淋巴细胞，通常在淋巴组织的发育过程中出现。它们在淋巴瘤和白血病的病理过程中扮演重要角色。淋巴母细胞是淋巴细胞的前体细胞，处于从造血干细胞向成熟淋巴细胞分化的过程中。它们可以来源于T细胞或B细胞。根据来源不同，淋巴母细胞可分为T细胞淋巴母细胞和B细胞淋巴母细胞。
CCK-81 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：H6c7 Cells、MA-c Cells、Mouse Colon 38 Cells
293-EBNA1 Cells;背景说明：详见相关文献介绍;传代方法：１：４-１：１０传代；每周２次。;生长特性：贴壁生长;形态特性：上皮细胞样;相关产品有：NS-1-Ag4-1 Cells、RAW264.7 Cells、Blotchy fibroblast-11 Cells
CHO-S 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：OPM-2 Cells、NTera2 cl.D1 Cells、KMB17 Cells
HOK Cells;背景说明：口腔角质 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：T98 G Cells、HSC-2 Cells、SW962 Cells
H-64 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：IOSE-80 Cells、RDES Cells、HPASMC Cells
MIMVEC Cells;背景说明：肠粘膜微血管；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;相关产品有：A2780 Cells、CCLP1 Cells、SW-780 Cells
SVOG Cells;背景说明：卵巢；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;相关产品有：Panc-1-P Cells、HCC94 Cells、B10BR Cells
WM 115 Cells;背景说明：黑色素瘤；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;相关产品有：FU-OV-1 Cells、N-2a Cells、BT325 Cells
SNU-119 Cells;背景说明：卵巢癌；女性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：HL7702 Cells、IBRS2 Cells、PaCa2 Cells
Abcam HEK293 TUBB2B KO Cells(拥有STR基因鉴定图谱)
AG0880 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line KST264 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line XB865 Cells(拥有STR基因鉴定图谱)
BRC-37 Cells(拥有STR基因鉴定图谱)
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COLO 16 Cells(拥有STR基因鉴定图谱)
DA03856 Cells(拥有STR基因鉴定图谱)
DA05034 Cells(拥有STR基因鉴定图谱)
G4-2 Cells(拥有STR基因鉴定图谱)
FUOV1 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：COLO320 DM Cells、MonoMac 6 Cells、MNNGHOS Cells
Sf21 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-251_MG Cells、NHRF Cells、HT-3 Cells
SK-ChA-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：CHL Cells、PC-3 Cells、TOV-112D Cells
IMR32 Cells;背景说明：该细胞是１９６７年４月由NicholsWW,LeeJ和DwightS建立，来源于一名１３月龄白人男婴腹部肿块，临床诊断为神经母细胞瘤，伴有极少部位的类器官样分化。;传代方法：１：２传代;生长特性：贴壁生长;形态特性：存在两种细胞类型，小的神经母细胞样细胞和大的透明成纤维样细胞;相关产品有：Tu686 Cells、TE8 Cells、266 Bl Cells
H719 Cells;背景说明：小细胞肺癌；骨髓转移；女性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：半贴壁;形态特性：详见产品说明;相关产品有：CAL-78 Cells、MV411 Cells、HuT 78 Cells
LN229 Cells;背景说明：详见相关文献介绍;传代方法：１：４-１：６传代；每周换液２-３次;生长特性：贴壁生长;形态特性：上皮细胞;相关产品有：Hs 870.T Cells、H647ell Cells、Swiss3T3 Cells
H-1568 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：详见产品说明;相关产品有：HKC Cells、Me Wo Cells、NP69SV40T Cells
NuTu-19 Cells;背景说明：卵巢癌;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：SUP-B15 Cells、WI 38 Cells、Tb 1-Lu Cells
IB-RS-2 Cells;背景说明：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;相关产品有：CNE Cells、RIMEC Cells、MDA-MB-435-S Cells
HO1-N1 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：SU-DHL-8 Cells、Dakiki Cells、YH-13 Cells
OV-1063 Cells;背景说明：卵巢上皮细胞癌;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：C127 Cells、SKMES1 Cells、HCT-15 Cells
NPC-039 Cells;背景说明：鼻咽癌;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：MCF 7B Cells、PE/CA-PJ-34 Cells、Sp2/O-Ag14 Cells
OCI/AML2 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：BrCL18 Cells、CORL26 Cells、MDA415 Cells
15C12 Cells(拥有STR基因鉴定图谱)
C8D1A Cells;背景说明：该永生化细胞系源自出生８天小鼠小脑组织，由B Pessac, D Trisler建立。该细胞具有小神经胶质细胞特征。该细胞为GFAP阳性细胞，除此之外，没有检测到其它神经胶质神经元或小神经胶质细胞的分子标记。;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：NCIH1930 Cells、HELA-GFP Cells、Dunn LM8 Cells
THP-1人单核细胞白血病传代细胞活性强|送STR图谱
hTERT RPE1 Cells;背景说明：视网膜色素上皮；hTERT永生；女性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：RPMI-8226 Cells、MHCC97-H Cells、H-2108 Cells
HPAF-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：L Wnt-3A Cells、NCI-H2107 Cells、HMC3 Cells
HEL 92.1.7 Cells;背景说明：详见相关文献介绍;传代方法：每周２-３次。;生长特性：悬浮生长;形态特性：成淋巴细胞;相关产品有：MA104 Cells、MSTO-211 H Cells、T-24 Cells
G402 Cells;背景说明：详见相关文献介绍;传代方法：１：２-１：６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：MOLP2 Cells、TE353.SK Cells、PANC403 Cells
SK-Col-1 Cells;背景说明：该细胞来源于结直肠病人的转移性腹水。;传代方法：１：２-１：３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：H-1838 Cells、NIE-115 Cells、TYK-nu Cells
OC-3-VGH 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：SUDHL-6 Cells、PJ34 Cells、SUD-4 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：HCT GEO Cells、MESSADX5 Cells、PM6 Cells
GM23382 Cells(拥有STR基因鉴定图谱)
HAP1 MTCH1 (-) 3 Cells(拥有STR基因鉴定图谱)
NCI-H187 Cells;背景说明：经典小细胞肺癌；胸腔积液转移；男性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：悬浮;形态特性：详见产品说明;相关产品有：RCK8 Cells、Y 1 Cells、HEK-293H Cells
Doubling time: ~50 hours (ATCC). 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：OV1/P Cells、HFL Cells、RBSMC Cells
NCI-H1781 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：253JBV Cells、NHEK Cells、ESC-410 Cells
H-250 Cells;背景说明：小细胞肺癌；男性;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：H520 Cells、Functional Liver Cell-7 Cells、OUMS-27 Cells
NCTC clone 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：MDAMB157 Cells、SU-DHL-1 Cells、CCD19Lu Cells
LUDLU-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：HOP62 Cells、SY5Y Cells、NCIH1734 Cells
MAC1 Cells;背景说明：皮肤T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：MuM-2B Cells、HCC-1428 Cells、SACC-LM Cells
NCI-H2066 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：聚团悬浮;相关产品有：Panc_08_13 Cells、Hs606T Cells、3T3 Cells
HQ00870 Cells(拥有STR基因鉴定图谱)
KE-6 Cells(拥有STR基因鉴定图谱)
MHHi006-A Cells(拥有STR基因鉴定图谱)
NLGIP-5876 Cells(拥有STR基因鉴定图谱)
RBL182T Cells(拥有STR基因鉴定图谱)
Ubigene HeLa SLC12A4 KO Cells(拥有STR基因鉴定图谱)
XP42RO-hTERT Cells(拥有STR基因鉴定图谱)
HCT116-SLC25A38-KO-c11 Cells(拥有STR基因鉴定图谱)
B16-F10 Cells;背景说明：B１６-F１０是B１６-F０的亚系。;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：Sp2/mIL-6 Cells、HEK293-A Cells、EU-4 Cells
HTR-8 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：NCI-H2330 Cells、MDA-157 Cells、V 79 Cells
MES-13 Cells;背景说明：肾小球系膜；SV４０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;相关产品有：OSK-1 Cells、CTLL(2) Cells、Calu3 Cells
IEC-18 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：McA-RH7777 Cells、CTV1 Cells、Kit 225 Cells
Chang liver 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：COS-7 Cells、IB-RS2 Cells、L-6TG Cells
Chang liver 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：COS-7 Cells、IB-RS2 Cells、L-6TG Cells
Bronchial Epithelium transformed with Ad12-SV40 2B Cells;背景说明：从一位非癌个体的正常人支气管上皮病理切片分离出上皮细胞。这些细胞用腺病毒１２-SV４０病毒杂交病毒感染并克隆。DEAS-２B细胞保留了对血清反应进行鳞关分化的能力，并有用于筛选诱导或影响分化及致癌的化学或生物制剂。细胞角蛋白及SV４０抗原染色阳性。;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：上皮细胞样;相关产品有：QBC(939) Cells、JB 6 Cells、HIT T15 Cells
PBMC Cells;背景说明：外周血单核 Cells;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：kms 11 Cells、LLC-MK-2 Cells、526-mel Cells
SW-579 Cells;背景说明：在裸鼠中成瘤(产生三级恶性纺锤状巨细胞瘤)。 ;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：OCI/AML3 Cells、M-G63 Cells、MAVER Cells
MDA330 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：Pt K2 Cells、PG [Human lung carcinoma] Cells、ROS-17/2.8 Cells
CHO-ori Cells;背景说明：１９５７年，PuckTT从成年中国仓鼠卵巢的活检组织建立了CHO细胞；广泛用于生物制品的表达。;传代方法：１：３传代，３-４天换液一次;生长特性：贴壁生长;形态特性：上皮样;相关产品有：FL 62891 Cells、X63-Ag 8.6.5.3 Cells、HCASMC Cells
CL1.0 Cells;背景说明：肺癌；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：COR-L 105 Cells、M14-MEL Cells、MMAc-Serum Free Cells
U138 Cells;背景说明：星形细胞瘤；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：EJ-1 Cells、SW-1353 Cells、EC-9706 Cells
C3H-10T1/2 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：MUTZ-3 Cells、ATN1 Cells、Hs 281.T Cells
AG06814-J Cells;背景说明：LeonardHayflick建系；有限传代细胞系；寿命为５０±１０代（倍增时间２４h）；来自妊娠３个月的正常胚胎肺组织。该细胞系是第一个用于人制备的人二倍体细胞；培养基中添加TNFα可以加快细胞生长。;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：成纤维细胞样;相关产品有：BAC1.2F5 Cells、Pt K2 Cells、LWnt-3A Cells
STAN272i-726C4 Cells(拥有STR基因鉴定图谱)
NCI-H2030 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：上皮细胞样;相关产品有：TK+/- (clone 3.7.2C) Cells、H-2591 Cells、BIU-87/Adr Cells
H1975 Cells;背景说明：这株细胞于１９８８年七月建株。组织提供者是一位非吸烟人士。;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：上皮细胞样;相关产品有：GM0637 Cells、Spodoptera frugiperda clone 9 Cells、Human Epidermoid carcinoma #2 Cells
HuT 78 Cells;背景说明：皮肤；T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：LS 174T Cells、SKMEL3 Cells、ST Cells
RFL 6 Cells;背景说明：胚肺；成纤维细胞；SD大鼠;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：BT 325 Cells、HEC1-A Cells、SUM52 Cells
NOR-10 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：ROS-17/2.8 Cells、H146 Cells、SKNFI Cells
IHH Cells;背景说明：肝;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：HS5 Cells、Jurkat-E6 Cells、LPC-H12 Cells
FRTL-5 Cells;背景说明：甲状腺；自发永生；Fischer;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-675-T Cells、P3X63Ag8.653 Cells、SO-RB50 Cells
H-292 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：上皮样;相关产品有：WEHI164 Cells、PC3M Cells、NCI-H-128 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；
P3J.HR1K Cells;背景说明：详见相关文献介绍;传代方法：每２-３天换液;生长特性：悬浮生长 ;形态特性：淋巴母细胞样;相关产品有：H-510A Cells、B16BL6 Cells、SUSM1 Cells
LU165 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：WIL2-S Cells、HCCC-9810 Cells、TI-73 Cells
Ej138 Cells;背景说明：膀胱癌；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：Hi5 Cells、H-87 Cells、NK10a Cells
IFRS1 Cells;背景说明：雪旺 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：SNU-423 Cells、MDA 231-LM2-4175 Cells、OVCAR 4 Cells
U-343-MG 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：PANC-10-05 Cells、AR4-2J Cells、A-704 Cells
253J-BV Cells;背景说明：膀胱癌；淋巴结转移；男性;传代方法：１：２-１：３传代；每周换液２-３次。;生长特性：贴壁;形态特性：详见产品说明;相关产品有：RC-K8 Cells、GTL 16 Cells、MIA PaCa-2 Cells
BayGenomics ES cell line RRR242 Cells(拥有STR基因鉴定图谱)
BayGenomics ES cell line YHD217 Cells(拥有STR基因鉴定图谱)
HT26 Cells(拥有STR基因鉴定图谱)
PCRP-HHEX-1D3 Cells(拥有STR基因鉴定图谱)
THP-1人单核细胞白血病传代细胞活性强|送STR图谱
ERC-18M Cells(拥有STR基因鉴定图谱)
HPS2733 Cells(拥有STR基因鉴定图谱)
"    "PubMed=2985879; DOI=10.1016/0145-2126(85)90084-0
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cell lines -- 1 carboxylic esterase.
Leuk. Res. 9:209-229(1985)

PubMed=3159941; DOI=10.1016/0145-2126(85)90134-1
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cell lines -- III Beta-hexosaminidase (E.C. 3.2.1.30).
Leuk. Res. 9:549-559(1985)

PubMed=3874327; DOI=10.1016/0145-2126(85)90133-x
Drexler H.G., Gaedicke G., Minowada J.
Isoenzyme studies in human leukemia-lymphoma cells lines -- II. Acid phosphatase.
Leuk. Res. 9:537-548(1985)

PubMed=2633408; DOI=10.1620/tjem.159.299
Saijo Y., Kumano N., Tokue Y., Satoh K., Oizumi K., Motomiya M.
Characterization of resistance to VP-16 in human leukemic cell line.
Tohoku J. Exp. Med. 159:299-306(1989)

PubMed=1915666; DOI=10.1016/0014-4827(91)90482-A
Limouse M., Manie S., Konstantinova I., Ferrua B., Schaffar L.
Inhibition of phorbol ester-induced cell activation in microgravity.
Exp. Cell Res. 197:82-86(1991)

PubMed=1571549; DOI=10.1182/blood.V79.9.2378.2378
Sugimoto K., Toyoshima H., Sakai R., Miyagawa K., Hagiwara K., Ishikawa F., Takaku F., Yazaki Y., Hirai H.
Frequent mutations in the p53 gene in human myeloid leukemia cell lines.
Blood 79:2378-2383(1992)

PubMed=8558913
Morita S., Tsuchiya S., Fujie H., Itano M., Ohashi Y., Minegishi M., Imaizumi M., Endo M., Takano N., Konno T.
Cell surface c-kit receptors in human leukemia cell lines and pediatric leukemia: selective preservation of c-kit expression on megakaryoblastic cell lines during adaptation to in vitro culture.
Leukemia 10:102-105(1996)

PubMed=9290701; DOI=10.1002/(SICI)1098-2744(199708)19:4<243::AID-MC5>3.0.CO;2-D
Jia L.-Q., Osada M., Ishioka C., Gamo M., Ikawa S., Suzuki T., Shimodaira H., Niitani T., Kudo T., Akiyama M., Kimura N., Matsuo M., Mizusawa H., Tanaka N., Koyama H., Namba M., Kanamaru R., Kuroki T.
Screening the p53 status of human cell lines using a yeast functional assay.
Mol. Carcinog. 19:243-253(1997)

PubMed=9379676; DOI=10.1016/S0145-2126(97)00036-2
Sheng X.-M., Kawamura M., Ohnishi H., Ida K., Hanada R., Kojima S., Kobayashi M., Bessho F., Yanagisawa M., Hayashi Y.
Mutations of the RAS genes in childhood acute myeloid leukemia, myelodysplastic syndrome and juvenile chronic myelocytic leukemia.
Leuk. Res. 21:697-701(1997)

PubMed=9510473; DOI=10.1111/j.1349-7006.1998.tb00476.x; PMCID=PMC5921588
Hosoya N., Hangaishi A., Ogawa S., Miyagawa K., Mitani K., Yazaki Y., Hirai H.
Frameshift mutations of the hMSH6 gene in human leukemia cell lines.
Jpn. J. Cancer Res. 89:33-39(1998)

PubMed=9738977; DOI=10.1111/j.1349-7006.1998.tb03275.x; PMCID=PMC5921886
Takizawa J., Suzuki R., Kuroda H., Utsunomiya A., Kagami Y., Joh T., Aizawa Y., Ueda R., Seto M.
Expression of the TCL1 gene at 14q32 in B-cell malignancies but not in adult T-cell leukemia.
Jpn. J. Cancer Res. 89:712-718(1998)

PubMed=10223614; DOI=10.1620/tjem.186.99
Tominaga T., Suzuki M., Saeki H., Matsuno S., Tachibana T., Kudo T.
Establishment of an activated macrophage cell line, A-THP-1, and its properties.
Tohoku J. Exp. Med. 186:99-119(1998)

PubMed=10739008; DOI=10.1016/S0145-2126(99)00182-4
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines.
Leuk. Res. 24:255-262(2000)

PubMed=11066077; DOI=10.1002/1098-2264(2000)9999:9999<::AID-GCC1040>3.0.CO;2-Z
Odero M.D., Zeleznik-Le N.J., Chinwalla V., Rowley J.D.
Cytogenetic and molecular analysis of the acute monocytic leukemia cell line THP-1 with an MLL-AF9 translocation.
Genes Chromosomes Cancer 29:333-338(2000)

DOI=10.1016/B978-0-12-221970-2.50457-5
Drexler H.G.
The leukemia-lymphoma cell line factsbook.
(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001)

PubMed=11226526; DOI=10.1016/S0145-2126(00)00121-1
Inoue K., Kohno T., Takakura S., Hayashi Y., Mizoguchi H., Yokota J.
Corrigendum to: Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines Leukemia Research 24 (2000), 255-262.
Leuk. Res. 25:275-278(2001)

PubMed=11414198; DOI=10.1007/s004320000207
Lahm H., Andre S., Hoeflich A., Fischer J.R., Sordat B., Kaltner H., Wolf E., Gabius H.-J.
Comprehensive galectin fingerprinting in a panel of 61 human tumor cell lines by RT-PCR and its implications for diagnostic and therapeutic procedures.
J. Cancer Res. Clin. Oncol. 127:375-386(2001)

PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)

PubMed=12068308; DOI=10.1038/nature00766
Davies H.R., Bignell G.R., Cox C., Stephens P.J., Edkins S., Clegg S., Teague J.W., Woffendin H., Garnett M.J., Bottomley W., Davis N., Dicks E., Ewing R., Floyd Y., Gray K., Hall S., Hawes R., Hughes J., Kosmidou V., Menzies A., Mould C., Parker A., Stevens C., Watt S., Hooper S., Wilson R., Jayatilake H., Gusterson B.A., Cooper C.S., Shipley J.M., Hargrave D., Pritchard-Jones K., Maitland N.J., Chenevix-Trench G., Riggins G.J., Bigner D.D., Palmieri G., Cossu A., Flanagan A.M., Nicholson A., Ho J.W.C., Leung S.Y., Yuen S.T., Weber B.L., Seigler H.F., Darrow T.L., Paterson H.F., Marais R., Marshall C.J., Wooster R., Stratton M.R., Futreal P.A.
Mutations of the BRAF gene in human cancer.
Nature 417:949-954(2002)

PubMed=14504097; DOI=10.1182/blood-2003-02-0418
Taketani T., Taki T., Sugita K., Furuichi Y., Ishii E., Hanada R., Tsuchida M., Sugita K., Ida K., Hayashi Y.
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy.
Blood 103:1085-1088(2004)

PubMed=14671638; DOI=10.1038/sj.leu.2403236
Drexler H.G., Quentmeier H., MacLeod R.A.F.
Malignant hematopoietic cell lines: in vitro models for the study of MLL gene alterations.
Leukemia 18:227-232(2004)

PubMed=15843827; DOI=10.1038/sj.leu.2403749
Andersson A., Eden P., Lindgren D., Nilsson J., Lassen C., Heldrup J., Fontes M., Borg A., Mitelman F., Johansson B., Hoglund M., Fioretos T.
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations.
Leukemia 19:1042-1050(2005)

PubMed=16311011; DOI=10.1016/j.tiv.2005.10.012
Ashikaga T., Yoshida Y., Hirota M., Yoneyama K., Itagaki H., Sakaguchi H., Miyazawa M., Ito Y., Suzuki H., Toyoda H.
Development of an in vitro skin sensitization test using human cell lines: the human Cell Line Activation Test (h-CLAT). I. Optimization of the h-CLAT protocol.
Toxicol. In Vitro 20:767-773(2006)

PubMed=16337770; DOI=10.1016/j.tiv.2005.10.014
Sakaguchi H., Ashikaga T., Miyazawa M., Yoshida Y., Ito Y., Yoneyama K., Hirota M., Itagaki H., Toyoda H., Suzuki H.
Development of an in vitro skin sensitization test using human cell lines; human Cell Line Activation Test (h-CLAT). II. An inter-laboratory study of the h-CLAT.
Toxicol. In Vitro 20:774-784(2006)

PubMed=16408098; DOI=10.1038/sj.leu.2404081
Quentmeier H., MacLeod R.A.F., Zaborski M., Drexler H.G.
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.
Leukemia 20:471-476(2006)

PubMed=19220422; DOI=10.1111/j.1600-0609.2009.01211.x
Kamihira S., Terada C., Sasaki D., Yanagihara K., Tsukasaki K., Hasegawa H., Yamada Y.
Aberrant p53 protein expression and function in a panel of hematopoietic cell lines with different p53 mutations.
Eur. J. Haematol. 82:301-307(2009)

PubMed=19377474; DOI=10.1038/ng.375; PMCID=PMC6711855
Suzuki H., Forrest A.R.R., van Nimwegen E., Daub C.O., Balwierz P.J., Irvine K.M., Lassmann T., Ravasi T., Hasegawa Y., de Hoon M.J.L., Katayama S., Schroder K., Carninci P., Tomaru Y., Kanamori-Katayama M., Kubosaki A., Akalin A., Ando Y., Arner E., Asada M., Asahara H., Bailey T., Bajic V.B., Bauer D., Beckhouse A.G., Bertin N., Bjorkegren J., Brombacher F., Bulger E., Chalk A.M., Chiba J., Cloonan N., Dawe A., Dostie J., Engstrom P.G., Essack M., Faulkner G.J., Fink J.L., Fredman D., Fujimori K., Furuno M., Gojobori T., Gough J., Grimmond S.M., Gustafsson M., Hashimoto M., Hashimoto T., Hatakeyama M., Heinzel S., Hide W.A., Hofmann O., Hornquist M., Huminiecki L., Ikeo K., Imamoto N., Inoue S., Inoue Y., Ishihara R., Iwayanagi T., Jacobsen A., Kaur M., Kawaji H., Kerr M.C., Kimura R., Kimura S., Kimura Y., Kitano H., Koga H., Kojima T., Kondo S., Konno T., Krogh A., Kruger A., Kumar A., Lenhard B., Lennartsson A., Lindow M., Lizio M., MacPherson C., Maeda N., Maher C.A., Maqungo M., Mar J., Matigian N.A., Matsuda H., Mattick J.S., Meier S., Miyamoto S., Miyamoto-Sato E., Nakabayashi K., Nakachi Y., Nakano M., Nygaard S., Okayama T., Okazaki Y., Okuda-Yabukami H., Orlando V., Otomo J., Pachkov M., Petrovsky N., Plessy C., Quackenbush J., Radovanovic A., Rehli M., Saito R., Sandelin A., Schmeier S., Schonbach C., Schwartz A.S., Semple C.A., Sera M., Severin J., Shirahige K., Simons C., St Laurent G., Suzuki M., Suzuki T., Sweet M.J., Taft R.J., Takeda S., Takenaka Y., Tan K., Taylor M.S., Teasdale R.D., Tegner J., Teichmann S.A., Valen E., Wahlestedt C., Waki K., Waterhouse A., Wells C.A., Winther O., Wu L., Yamaguchi K., Yanagawa H., Yasuda J., Zavolan M., Hume D.A., Arakawa T., Fukuda S., Imamura K., Kai C., Kaiho A., Kawashima T., Kawazu C., Kitazume Y., Kojima M., Miura H., Murakami K., Murata M., Ninomiya N., Nishiyori H., Noma S., Ogawa C., Sano T., Simon C., Tagami M., Takahashi Y., Kawai J., Hayashizaki Y.
FANTOM Consortium
Riken Omics Science Center
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line.
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