"HCC1954人乳腺導(dǎo)管癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

傳代比例：1:2-1:4(首次傳代建議1:2)

生長(zhǎng)特性：貼壁生長(zhǎng)

公司細(xì)胞系培養(yǎng)穩(wěn)定、耐活、復(fù)蘇好，提供人源、鼠源、兔源、豬源等不同組織如肺、氣管、支氣管、甲狀腺、胰腺、垂體、腎上腺、扁桃體、胸腺、腎、膀胱、輸尿管、前列腺、心臟、血管等細(xì)胞系。全程提供細(xì)胞系組織來(lái)源、生長(zhǎng)特性、細(xì)胞形態(tài)、背景資料、培養(yǎng)條件、凍存條件、參考文獻(xiàn)、運(yùn)輸方式等產(chǎn)品信息及技術(shù)服務(wù)。

換液周期：每周2-3次

BALB/3T3 (clone A31) Cells;背景說(shuō)明：胚胎；成纖維；自發(fā)永生；雄性；BALB/c;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：OVCAR5細(xì)胞、MUTZ3細(xì)胞、BNL CL2細(xì)胞

UO-31 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代；２-３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：Human Kidney-2細(xì)胞、PC2細(xì)胞、MC-3T3細(xì)胞

TT Cells;背景說(shuō)明：TT細(xì)胞由LeongSS等，自一位７７歲白人女性甲狀腺髓樣癌患者的穿刺活檢樣本中建立。TT細(xì)胞持續(xù)產(chǎn)生高水平的降血素和CEA。更換培養(yǎng)基后２４h和７２h，在培養(yǎng)基中檢測(cè)到的免疫活性的降血素濃度分別為３９００pg/１０６個(gè)細(xì)胞和７７００pg/１０６個(gè)細(xì)胞。７２小時(shí)后CEA積累濃度超過(guò)２７ng/１０６個(gè)細(xì)胞；該細(xì)胞最初是在RPMI１６４０培養(yǎng)液中培養(yǎng)，可產(chǎn)生神經(jīng)肽，但還不知道在F１２培養(yǎng)液中培養(yǎng)是否會(huì)產(chǎn)生。;傳代方法：１：３-１：４傳代，每周換液２次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：IEC 6細(xì)胞、no.11細(xì)胞、GM04154B細(xì)胞

HCC1954人乳腺導(dǎo)管癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：詳見相關(guān)文獻(xiàn)介紹

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線：1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q：3┈1┈8┈0┈8┈0┈7┈3┈2┈4；

貼壁細(xì)胞的傳代培養(yǎng)，詳細(xì)步驟如下：首先倒掉培養(yǎng)基，在這一步驟可以收集一些細(xì)胞上清做支原體檢測(cè)；加入胰蛋白酶，一般T25是加2mL，蓋好瓶蓋，搖晃T25培養(yǎng)瓶，使胰蛋白酶均勻覆蓋在細(xì)胞表面，放入培養(yǎng)箱2-3min，期間可在顯微鏡下觀察，看到大部分細(xì)胞變圓，即可放入超凈臺(tái)，加入2倍的完全培養(yǎng)基，這里就是加4mL培養(yǎng)基，終止消化；將含有胰蛋白酶，細(xì)胞和培養(yǎng)基一起轉(zhuǎn)移到離心管中，1000rpm/3min離心，去掉上清；新鮮的完全培養(yǎng)基重懸，根據(jù)細(xì)胞的生長(zhǎng)特性和后續(xù)的實(shí)驗(yàn)需求進(jìn)行傳代，比如我養(yǎng)的Hepa1-6就長(zhǎng)的比較快，不是著急用的話，我就會(huì)按1E6個(gè)細(xì)胞/T75培養(yǎng)瓶進(jìn)行傳代；但如果后兩天要用，就會(huì)適當(dāng)多傳一點(diǎn)；還可通過(guò)顯微鏡計(jì)數(shù)后，直接用于細(xì)胞鋪板，繼續(xù)后續(xù)的實(shí)驗(yàn)。

產(chǎn)品包裝：復(fù)蘇發(fā)貨：T25培養(yǎng)瓶(一瓶)或凍存發(fā)貨：1ml凍存管(兩支)

來(lái)源說(shuō)明：細(xì)胞主要來(lái)源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫(kù)

HCC1954人乳腺導(dǎo)管癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來(lái)源：人源、鼠源等其它物種來(lái)源

U251MG Cells;背景說(shuō)明：U-２５１ MG分離至一位患者的膠質(zhì)母細(xì)胞瘤組織。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：3AO細(xì)胞、Cattle chondrocytes細(xì)胞、MCF10A細(xì)胞

Bac1 2F5 Cells;背景說(shuō)明：巨噬細(xì)胞；SV４０轉(zhuǎn)化；BALB/c x A.CA;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：X63Ag8.653細(xì)胞、PanC1細(xì)胞、Hu-P-T4細(xì)胞

OV 1063 Cells;背景說(shuō)明：卵巢上皮細(xì)胞癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Pt K2 (NBL-5)細(xì)胞、B6Tert-1細(xì)胞、RL細(xì)胞

RSC96 Cells;背景說(shuō)明：雪旺細(xì)胞；自發(fā)永生;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：PG [Human lung carcinoma]細(xì)胞、H-322細(xì)胞、Y 1細(xì)胞

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線：1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q：3┈1┈8┈0┈8┈0┈7┈3┈2┈4；

形態(tài)特性：上皮細(xì)胞樣

細(xì)胞株(系)的使用，為醫(yī)學(xué)研究和測(cè)試工作帶來(lái)了大的方便。但細(xì)胞的傳代是有限制的，長(zhǎng)期連續(xù)傳代的細(xì)胞，不僅消耗大量的人力和物力，而且細(xì)胞的生長(zhǎng)與形態(tài)等會(huì)有一定退變或轉(zhuǎn)化，因而細(xì)胞失去原有的遺傳性，有時(shí)還會(huì)由于細(xì)胞污染而造成傳代中斷，種子丟失。因此，在實(shí)際工作中常需凍存一定數(shù)量的細(xì)胞，以備替換使用。細(xì)胞冷凍與復(fù)蘇是細(xì)胞培養(yǎng) 室的常規(guī)工作和通用技術(shù)。目前，細(xì)胞凍存Zui常用的技術(shù)是冷凍保存法，主要采用加適量保護(hù)劑的緩慢冷凍法凍存細(xì)胞。細(xì)胞在不加任何保護(hù)劑的情況下直接冷凍，細(xì)胞內(nèi)外的水分會(huì)很快形成冰晶，從而引起一系列不良反應(yīng)。如細(xì)胞脫水使局部電解質(zhì)濃度增GAO，pH值改變，部分蛋白質(zhì)由于上述原因而變性，引起細(xì)胞內(nèi)部空間結(jié)構(gòu)紊亂，溶酶體膜由此遭到損傷而釋放出溶酶體酶，使細(xì)胞內(nèi)結(jié)構(gòu)成分造成破壞，線粒體腫脹，功能丟失，并造成能量代謝障礙。胞膜上的類脂蛋白復(fù)合體也易破壞引起細(xì)胞膜通透性的改變，使細(xì)胞內(nèi)容物丟失。如果細(xì)胞內(nèi)冰晶形成較多，隨冷凍溫度的降低，冰晶體積膨脹造成細(xì)胞核DNA空間構(gòu)型發(fā)生不可逆的損傷，而致細(xì)胞死亡。因此，細(xì)胞冷凍技術(shù)的關(guān)鍵是盡可能地減少細(xì)胞內(nèi)水分，減少細(xì)胞內(nèi)冰晶的形成。采用甘油或二甲基亞砜作保護(hù)劑，這兩種物質(zhì)分子量小，溶解度大，易穿透細(xì)胞，可以使冰點(diǎn)下降，提GAO細(xì)胞膜對(duì)水的通透性，且對(duì)細(xì)胞無(wú)明顯毒性。慢速冷凍方法又可使細(xì)胞內(nèi)的水分滲出細(xì)胞外，減少胞內(nèi)形成冰結(jié)晶的機(jī)會(huì)，從而減少冰晶對(duì)細(xì)胞的損傷。

UCLA-SO-M20 Cells;背景說(shuō)明：黑色素瘤;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：HCC-2935細(xì)胞、Henrietta Lacks cells細(xì)胞、BC-3H-1細(xì)胞

Kobe university Oral Squamous Cell culture-2 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：２.２ x １０^４ cells/ml ;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：SHEE細(xì)胞、NCI-H660細(xì)胞、NS-1-Ag4-1細(xì)胞

RCC 786-O Cells;背景說(shuō)明：該細(xì)胞源自一位原發(fā)性腎透明細(xì)胞癌患者。該細(xì)胞有微絨毛和橋粒，能在軟瓊脂上生長(zhǎng)。此細(xì)胞生成一種PTH（甲狀旁腺素）樣的多肽，與乳癌和肺癌中生成的肽相似，其N端序列與PTH相似，具有PTH樣活性，分子量為６０００D。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：IM95細(xì)胞、NCI-H1869細(xì)胞、T-84細(xì)胞

NCI H82 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：５傳代，每周換液２-３次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：SP2/0 Ag-14細(xì)胞、SNU668細(xì)胞、Clone Y-1細(xì)胞

RH-30 Cells;背景說(shuō)明：肺泡橫紋肌肉瘤；骨髓轉(zhuǎn)移;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：IAR-20細(xì)胞、SK-N-BE2C細(xì)胞、CMT 93細(xì)胞

TCam 2 Cells;背景說(shuō)明：睪丸精原細(xì)胞瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：COLO-320-HSR細(xì)胞、OCI-Ly 7細(xì)胞、LNT-229細(xì)胞

HEL-1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SCC 4細(xì)胞、Adeno-293細(xì)胞、H2052細(xì)胞

NCI-H1836 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２-３次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：GRSL細(xì)胞、WM 266-4細(xì)胞、Jurkat 77細(xì)胞

NCI-SNU-C2B Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：X63-Ag8細(xì)胞、SUM 52細(xì)胞、GL261細(xì)胞

SKMES Cells;背景說(shuō)明：源于一位６５歲患有肺鱗狀細(xì)胞癌的白人男性，自轉(zhuǎn)移性胸腔積液分離而來(lái)。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：THLE2細(xì)胞、HcerEpic細(xì)胞、hFOB1.19細(xì)胞

T98 Cells;背景說(shuō)明：膠質(zhì)瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SUPB-15細(xì)胞、CF PAC-1細(xì)胞、MV-4-11細(xì)胞

H-1954 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：OV 1063細(xì)胞、ZR75_1細(xì)胞、C-Lu65細(xì)胞

C3H/10T1/2 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：JIMT-1細(xì)胞、SF763細(xì)胞、RTMC細(xì)胞

NCI-SNU-C1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每３-５天換液。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：SH-SY5Y細(xì)胞、HeLa S3細(xì)胞、PC-9/GR細(xì)胞

NCIH2291 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：４傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：Mouse Colon 38細(xì)胞、WB F344細(xì)胞、KE37細(xì)胞

ZR75_1 Cells;背景說(shuō)明：該細(xì)胞產(chǎn)生高水平的黏液素MUC-１ mRNA，低水平的MUC-２ mRNA，但不表達(dá)MUC-３基因；表達(dá)雌激素受體。;傳代方法：１：４-１：６傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：AML193細(xì)胞、CCC-ESF-1細(xì)胞、RPMI 2650細(xì)胞

ME-1 [Human leukemia] Cells;背景說(shuō)明：急性髓系白血?。荒行?傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Murine Thymic Epithelial Cell line 1細(xì)胞、U373MG細(xì)胞、NCIH2591細(xì)胞

49B2 Cells(提供STR鑒定圖譜)

Abcam Jurkat TPD52 KO Cells(提供STR鑒定圖譜)

AME-hTERT Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRK198 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XL785 Cells(提供STR鑒定圖譜)

CaHo-50 Cells(提供STR鑒定圖譜)

DA00554 Cells(提供STR鑒定圖譜)

DA06543 Cells(提供STR鑒定圖譜)

GM01166 Cells(提供STR鑒定圖譜)

HMC Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：CEM-CCRF (CAMR)細(xì)胞、624 MEL細(xì)胞、GM2132細(xì)胞

HCC1954人乳腺導(dǎo)管癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

A7r5 Cells;背景說(shuō)明：培養(yǎng)到穩(wěn)定期后細(xì)胞表現(xiàn)出長(zhǎng)高的肌激酶和肌酸激酶活性(CPK)。 細(xì)胞分裂終止后合成骨肉型CPK。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：SKCol1細(xì)胞、HuH6細(xì)胞、NCI-H64細(xì)胞

NTERA-2 cl.D1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：GM02219細(xì)胞、HMC3細(xì)胞、B16/F1細(xì)胞

BC-023 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：PL5細(xì)胞、COLO320HSR細(xì)胞、Gingival carcinoma Neck Metastasis細(xì)胞

U-251 Cells;背景說(shuō)明：U-２５１ MG分離至一位患者的膠質(zhì)母細(xì)胞瘤組織。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：Hs 606細(xì)胞、293E細(xì)胞、CT26-clone 25細(xì)胞

LS123 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４—１：８?jìng)鞔?，每周換液２—３次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：HS-68細(xì)胞、A-172 MG細(xì)胞、HSMC細(xì)胞

338.11.5 Cells(提供STR鑒定圖譜)

MLTC-1 Cells;背景說(shuō)明：睪丸間質(zhì)瘤;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：MV3細(xì)胞、HemECs細(xì)胞、SK N SH細(xì)胞

Hs 636 T Cells;背景說(shuō)明：宮頸鱗癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SNG-M細(xì)胞、Hs.27細(xì)胞、A-101D細(xì)胞

H3255_DA Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng)　;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：HCS2/8細(xì)胞、KPL-4細(xì)胞、OCI Ly3細(xì)胞

HCC-1937 Cells;背景說(shuō)明：這株細(xì)胞１９９５年１０月１３日最初來(lái)源于原發(fā)性導(dǎo)管癌, 用了１１.５個(gè)月建株。腫瘤分類為TNM IIB期, ３級(jí)。BRCA１分析表明這株細(xì)胞是BRCA１ ５３８２C突變純合的, 而來(lái)源于同一病人的類淋巴母細(xì)胞細(xì)胞株在這個(gè)突變位點(diǎn)上是雜合的。 另兩個(gè)家庭成員也有這個(gè)突變; 一個(gè)同卵雙生姐妹也患有乳腺癌。這株細(xì)胞有一個(gè)后天的TP５３突變, 而其野生型等位基因丟失; 一個(gè)PTEN基因的后天的純合缺失, 以及多個(gè)與乳腺癌發(fā)病機(jī)理相關(guān)的位點(diǎn)上發(fā)生的雜合突變。這株細(xì)胞Her２-neu和p５３表達(dá)都呈陰性。;傳代方法：１：２傳代；４-５天傳代一次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣；多角形;相關(guān)產(chǎn)品有：RBMEC細(xì)胞、OE21細(xì)胞、MDAMB330細(xì)胞

H1819 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：HEL細(xì)胞、NCI-H446細(xì)胞、NCI-H1395細(xì)胞

Laboratory of Allergic Diseases 2 Cells;背景說(shuō)明：肥大 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SU-DHL-1細(xì)胞、Hep 3B2_1-7細(xì)胞、GM-215細(xì)胞

OCILY7 Cells;背景說(shuō)明：彌漫大B淋巴瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SNU-520細(xì)胞、PT-67細(xì)胞、Hs839T細(xì)胞

FDC-P1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：２-３天換液１次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：CMT-93細(xì)胞、NCTC clone 929細(xì)胞、COLO 829細(xì)胞

GM12569 Cells(提供STR鑒定圖譜)

HAP1 EPOR (-) 1 Cells(提供STR鑒定圖譜)

NCIH841 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３—１：５傳代，;生長(zhǎng)特性：混合型生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：C33-A細(xì)胞、HARAB細(xì)胞、NCI-SNU-761細(xì)胞

NCI-H2085 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代 ;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：L-6細(xì)胞、H-7721細(xì)胞、HT55細(xì)胞

SF 763 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：GM2131細(xì)胞、RD細(xì)胞、HT-29細(xì)胞

OSRC2 Cells;背景說(shuō)明：來(lái)源于日本人的腎臟腫瘤細(xì)胞。 可以移植到裸鼠。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：GL261細(xì)胞、Hep 3B2.1-7細(xì)胞、CA-OV-3細(xì)胞

R1610 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：H510細(xì)胞、Murine Thymic Epithelial Cell line 1細(xì)胞、HUT 28細(xì)胞

HBZY1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：VeroE6細(xì)胞、Mac-1細(xì)胞、LS 174T細(xì)胞

MAntle cell VERona-1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：５傳代；２-３天換液１次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：CORL88細(xì)胞、PASMCS細(xì)胞、Tu686細(xì)胞

Hut292 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：８?jìng)鞔唬?３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：H650細(xì)胞、GM3569細(xì)胞、H-841細(xì)胞

HiPS-RIKEN-1B Cells(提供STR鑒定圖譜)

iPS MS1 Cells(提供STR鑒定圖譜)

MB-MK Cells(提供STR鑒定圖譜)

ND10525 Cells(提供STR鑒定圖譜)

PL-29018 Cells(提供STR鑒定圖譜)

Ubigene HeLa RUVBL1 KO Cells(提供STR鑒定圖譜)

XP3OS(SVT) Cells(提供STR鑒定圖譜)

HE50 Cells(提供STR鑒定圖譜)

SKBR-3 Cells;背景說(shuō)明：這株細(xì)胞源自胸水。沒有病毒顆粒。亞顯微結(jié)構(gòu)特征包括微絲和橋粒，肝糖原顆粒，大溶酶體，成束的細(xì)胞質(zhì)纖絲。SK-BR-３細(xì)胞株過(guò)表達(dá)HER２/c-erb-２基因產(chǎn)物。;傳代方法：消化３-５分鐘，１：２,３天內(nèi)可長(zhǎng)滿;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：RPMI 1846細(xì)胞、NCIH2085細(xì)胞、RT-BM-1細(xì)胞

Mv 1 Lu Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Sf-21細(xì)胞、C4-1細(xì)胞、RL-65細(xì)胞

AZ 521 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４傳代;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：A72細(xì)胞、H1651細(xì)胞、U-343-MG細(xì)胞

HN4 Cells;背景說(shuō)明：喉鱗癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：LA4細(xì)胞、MDA361細(xì)胞、H-1618細(xì)胞

KYSE-50 Cells;背景說(shuō)明：食管鱗癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Hs604T細(xì)胞、Calu 3細(xì)胞、SW 620細(xì)胞

NCIH1105 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２-３次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：ST 486細(xì)胞、CT26.WT細(xì)胞、H-1299細(xì)胞

Leukemic 1210 Cells;背景說(shuō)明：該細(xì)胞源于用０.２%甲基膽蒽（溶解）涂抹雌性小鼠的皮膚誘發(fā)的腫瘤，鼠痘病毒陰性。;傳代方法：１：２傳代;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：NCI-H2108細(xì)胞、H-1693細(xì)胞、Co320細(xì)胞

870 Cells;背景說(shuō)明：兒童急性髓系白血病;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：H1650細(xì)胞、BTI-Tn5B14細(xì)胞、EFO 27細(xì)胞

End1/E6E7 Cells;背景說(shuō)明：子宮內(nèi)膜；女性；HPV１６轉(zhuǎn)化;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Vero E6細(xì)胞、HECCL-1細(xì)胞、H1869細(xì)胞

SUDHL-4 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：NCI H345細(xì)胞、NW-MEL-38細(xì)胞、H-676B細(xì)胞

NCIH1373 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：４傳代；２-３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：H774細(xì)胞、BAR-T細(xì)胞、OVTOKO細(xì)胞

NCI-H146 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：６傳代，每周換液２-３次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：B16-F10細(xì)胞、HCC1143細(xì)胞、DLD-1細(xì)胞

Vero Cells;背景說(shuō)明：Vero細(xì)胞株是日本千葉大學(xué)的YasumuraY和KawakitaY從正常成年非洲綠猴的腎臟組織中分離建立的。該細(xì)胞常作為轉(zhuǎn)染宿主，用于支原體的檢測(cè)。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：H3255細(xì)胞、A-375SM細(xì)胞、32D.3細(xì)胞

D407 RPE Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng)　;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：NCI H508細(xì)胞、SuDHL 10細(xì)胞、GM05384細(xì)胞

Karpas299 Cells;背景說(shuō)明：間變性大細(xì)胞淋巴瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：DAN-G細(xì)胞、PL-11細(xì)胞、MDAPCa2b細(xì)胞

Sg4 Cells(提供STR鑒定圖譜)

COLO824 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：U87MG細(xì)胞、G422細(xì)胞、H146細(xì)胞

IGROV-1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：G361細(xì)胞、PC-9/GR細(xì)胞、RPE-1細(xì)胞

H1792 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：８?jìng)鞔?生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：IM9細(xì)胞、Caco-2BBe細(xì)胞、MRC-V細(xì)胞

NCIH748 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：３-４天換液１次。;生長(zhǎng)特性：懸浮生長(zhǎng) ;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：A375S2細(xì)胞、Central Adrenergic TH-expressing a細(xì)胞、SUDHL-10細(xì)胞

H2.35 Cells;背景說(shuō)明：肝；SV４０轉(zhuǎn)化；雌性；BALB/c;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：LNT-229細(xì)胞、CCD1112Sk細(xì)胞、Karpas 299細(xì)胞

T47-D Cells;背景說(shuō)明：浸潤(rùn)性導(dǎo)管癌；胸腔積液轉(zhuǎn)移；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：L 1210細(xì)胞、EFM-19細(xì)胞、CAL 33細(xì)胞

HCC1954人乳腺導(dǎo)管癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

SK-NSH Cells;背景說(shuō)明：SK-N-SH細(xì)胞系由J.L.Bieder建系，它與SK-N-MC所不同的是倍增時(shí)間較長(zhǎng)且多巴胺-β-羥基酶水平較高。 SK-N-SH在細(xì)胞介導(dǎo)的細(xì)胞毒性試驗(yàn)中用作靶細(xì)胞系。;傳代方法：１：２傳代;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：COV-362細(xì)胞、HCC 38細(xì)胞、C4-1細(xì)胞

Neuro2a Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代；２-３天換液１次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：DKMG細(xì)胞、IPAM-WT細(xì)胞、H-1651細(xì)胞

H64 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：EC109細(xì)胞、NCI H82細(xì)胞、PLC PRF 5細(xì)胞

KP2 Cells;背景說(shuō)明：胰腺癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Hs832.Tc細(xì)胞、9L細(xì)胞、Tu 212細(xì)胞

HBZY1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：VeroE6細(xì)胞、NCI-H838細(xì)胞、293GP細(xì)胞

NPA87 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：DU 145細(xì)胞、HEK-293-EBNA細(xì)胞、SK-NMC細(xì)胞

MOLT 4 Cells;背景說(shuō)明：MOLT-４與MOLT-３來(lái)源于一名１９歲的男性急性淋巴細(xì)胞性白血病的復(fù)發(fā)患者，該患者前期接受過(guò)多種藥物聯(lián)合化療。MOLT-４細(xì)胞系為T淋巴細(xì)胞起源，p５３基因的第２４８位密碼子有一個(gè)G→A突變，不表達(dá)p５３，不表達(dá)免疫球蛋白或EB病毒；可產(chǎn)生高水平的末端脫氧核糖轉(zhuǎn)移酶；表達(dá)CD１(４９%),CD２(３５%),CD３A(２６%)B(３３%)C(３４%),CD４(５５%),CD５(７２%),CD６(２２%),CD７(７７%)。;傳代方法：１：２傳代;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞樣；圓形;相關(guān)產(chǎn)品有：HS 1.Tes細(xì)胞、HEI-193細(xì)胞、CAL62細(xì)胞

HRCEC Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：MIA Paca2細(xì)胞、PE/CA-PJ34細(xì)胞、NUGC-2細(xì)胞

BayGenomics ES cell line RRK006 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XL004 Cells(提供STR鑒定圖譜)

G5B1 Cells(提供STR鑒定圖譜)

NS20Y-BU-7 Cells(提供STR鑒定圖譜)

Y1-Forsk-10r-6 Cells(提供STR鑒定圖譜)

McNRAS2 Cells(提供STR鑒定圖譜)

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Neve R.M., Chin K., Fridlyand J., Yeh J., Baehner F.L., Fevr T., Clark L., Bayani N., Coppe J.-P., Tong F., Speed T., Spellman P.T., DeVries S., Lapuk A., Wang N.J., Kuo W.-L., Stilwell J.L., Pinkel D., Albertson D.G., Waldman F.M., McCormick F., Dickson R.B., Johnson M.D., Lippman M.E., Ethier S.P., Gazdar A.F., Gray J.W.

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes.

Cancer Cell 10:515-527(2006)

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Wood L.D., Parsons D.W., Jones S., Lin J., Sjoblom T., Leary R.J., Shen D., Boca S.M., Barber T.D., Ptak J., Silliman N., Szabo S., Dezso Z., Ustyanksky V., Nikolskaya T., Nikolsky Y., Karchin R., Wilson P.A., Kaminker J.S., Zhang Z.-M., Croshaw R., Willis J.E., Dawson D., Shipitsin M., Willson J.K.V., Sukumar S., Polyak K., Park B.H., Pethiyagoda C.L., Pant P.V.K., Ballinger D.G., Sparks A.B., Hartigan J., Smith D.R., Suh E., Papadopoulos N., Buckhaults P., Markowitz S.D., Parmigiani G., Kinzler K.W., Velculescu V.E., Vogelstein B.

The genomic landscapes of human breast and colorectal cancers.

Science 318:1108-1113(2007)

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Kao J., Salari K., Bocanegra M., Choi Y.-L., Girard L., Gandhi J., Kwei K.A., Hernandez-Boussard T., Wang P., Gazdar A.F., Minna J.D., Pollack J.R.

Molecular profiling of breast cancer cell lines defines relevant tumor models and provides a resource for cancer gene discovery.

PLoS ONE 4:E6146-E6146(2009)

PubMed=20070913; DOI=10.1186/1471-2407-10-15; PMCID=PMC2836299

Tsuji K., Kawauchi S., Saito S., Furuya T., Ikemoto K., Nakao M., Yamamoto S., Oka M., Hirano T., Sasaki K.

Breast cancer cell lines carry cell line-specific genomic alterations that are distinct from aberrations in breast cancer tissues: comparison of the CGH profiles between cancer cell lines and primary cancer tissues.

BMC Cancer 10:15.1-15.10(2010)

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=21378333

Ford C.H.J., Al-Bader M., Al-Ayadhi B., Francis I.

Reassessment of estrogen receptor expression in human breast cancer cell lines.

Anticancer Res. 31:521-527(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=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396

Marcotte R., Brown K.R., Suarez Saiz F.J., Sayad A., Karamboulas K., Krzyzanowski P.M., Sircoulomb F., Medrano M., Fedyshyn Y., Koh J.L.-Y., van Dyk D., Fedyshyn B., Luhova M., Brito G.C., Vizeacoumar F.J., Vizeacoumar F.S., Datti A., Kasimer D., Buzina A., Mero P., Misquitta C., Normand J., Haider M., Ketela T., Wrana J.L., Rottapel R., Neel B.G., Moffat J.

Essential gene profiles in breast, pancreatic, and ovarian cancer cells.

Cancer Discov. 2:172-189(2012)

PubMed=23151021; DOI=10.1186/1471-2164-13-619; PMCID=PMC3546428

Grigoriadis A., Mackay A., Noel E., Wu P.-J., Natrajan R., Frankum J., Reis-Filho J.S., Tutt A.

Molecular characterisation of cell line models for triple-negative breast cancers.

BMC Genomics 13:619.1-619.14(2012)

PubMed=23601657; DOI=10.1186/bcr3415; PMCID=PMC3672661

Riaz M., van Jaarsveld M.T.M., Hollestelle A., Prager-van der Smissen W.J.C., Heine A.A.J., Boersma A.W.M., Liu J.-J., Helmijr J.C.A., Ozturk B., Smid M., Wiemer E.A.C., Foekens J.A., Martens J.W.M.

miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs.

Breast Cancer Res. 15:R33.1-R33.17(2013)

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=24094812; DOI=10.1016/j.ccr.2013.08.020; PMCID=PMC3931310

Timmerman L.A., Holton T., Yuneva M., Louie R.J., Padro M., Daemen A., Hu M., Chan D.A., Ethier S.P., van 't Veer L.J., Polyak K., McCormick F., Gray J.W.

Glutamine sensitivity analysis identifies the xCT antiporter as a common triple-negative breast tumor therapeutic target.

Cancer Cell 24:450-465(2013)

PubMed=24162158; DOI=10.1007/s10549-013-2743-3; PMCID=PMC3832776

Prat A., Karginova O., Parker J.S., Fan C., He X.-P., Bixby L.M., Harrell J.C., Roman E., Adamo B., Troester M.A., Perou C.M.

Characterization of cell lines derived from breast cancers and normal mammary tissues for the study of the intrinsic molecular subtypes.

Breast Cancer Res. Treat. 142:237-255(2013)

PubMed=24176112; DOI=10.1186/gb-2013-14-10-r110; PMCID=PMC3937590

Daemen A., Griffith O.L., Heiser L.M., Wang N.J., Enache O.M., Sanborn Z., Pepin F., Durinck S., Korkola J.E., Griffith M., Hur J.S., Huh N., Chung J., Cope L., Fackler M.J., Umbricht C.B., Sukumar S., Seth P., Sume V.P., Jakkula L.R., Lu Y.-L., Mills G.B., Cho R.J., Collisson E.A., van 't Veer L.J., Spellman P.T., Gray J.W.

Modeling precision treatment of breast cancer.

Genome Biol. 14:R110.1-R110.14(2013)

PubMed=25960936; DOI=10.4161/21624011.2014.954893; PMCID=PMC4355981

Boegel S., Lower M., Bukur T., Sahin U., Castle J.C.

A catalog of HLA type, HLA expression, and neo-epitope candidates in human cancer cell lines.

OncoImmunology 3:e954893.1-e954893.12(2014)

PubMed=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652

Cowley G.S., Weir B.A., Vazquez F., Tamayo P., Scott J.A., Rusin S., East-Seletsky A., Ali L.D., Gerath W.F.J., Pantel S.E., Lizotte P.H., Jiang G.-Z., Hsiao J., Tsherniak A., Dwinell E., Aoyama S., Okamoto M., Harrington W., Gelfand E.T., Green T.M., Tomko M.J., Gopal S., Wong T.C., Li H.-B., Howell S., Stransky N., Liefeld T., Jang D., Bistline J., Meyers B.H., Armstrong S.A., Anderson K.C., Stegmaier K., Reich M., Pellman D., Boehm J.S., Mesirov J.P., Golub T.R., Root D.E., Hahn W.C.

Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies.

Sci. Data 1:140035-140035(2014)

PubMed=25485619; DOI=10.1038/nbt.3080

Klijn C., Durinck S., Stawiski E.W., Haverty P.M., Jiang Z.-S., Liu H.-B., Degenhardt J., Mayba O., Gnad F., Liu J.-F., Pau G., Reeder J., Cao Y., Mukhyala K., Selvaraj S.K., Yu M.-M., Zynda G.J., Brauer M.J., Wu T.D., Gentleman R.C., Manning G., Yauch R.L., Bourgon R., Stokoe D., Modrusan Z., Neve R.M., de Sauvage F.J., Settleman J., Seshagiri S., Zhang Z.-M.

A comprehensive transcriptional portrait of human cancer cell lines.

Nat. Biotechnol. 33:306-312(2015)

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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=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076

Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.

Characterization of human cancer cell lines by reverse-phase protein arrays.

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