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BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書,BT-549
  • BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書,BT-549

BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

價(jià)格 詢價(jià)
包裝 1000000細(xì)胞數(shù) 2000000細(xì)胞數(shù)
最小起訂量 1000000細(xì)胞數(shù)
發(fā)貨地 上海
更新日期 2025-02-23
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書英文名稱:BT-549
品牌: ATCC\RCB等產(chǎn)地: 國(guó)外
保存條件: 常溫培養(yǎng)或液氮凍存純度規(guī)格: BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書
產(chǎn)品類別: 化學(xué)試劑
種屬: 詳見產(chǎn)品資料組織: 詳見產(chǎn)品資料
細(xì)胞系: 詳見產(chǎn)品資料細(xì)胞形態(tài): 詳見產(chǎn)品資料
生長(zhǎng)狀態(tài): 詳見產(chǎn)品資料靶點(diǎn): 詳見產(chǎn)品資料
應(yīng)用: 詳見產(chǎn)品資料
2025-02-23 BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書 BT-549 1000000細(xì)胞數(shù)/RMB;2000000細(xì)胞數(shù)/RMB ATCC\RCB等 國(guó)外 常溫培養(yǎng)或液氮凍存 BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書 化學(xué)試劑

"BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

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)

細(xì)胞培養(yǎng)無菌操作步驟和注意事項(xiàng):1.打開無菌工作臺(tái)及凈化室的紫外燈,消毒半小時(shí)以上。2.進(jìn)入凈化室前先關(guān)閉紫外燈,打開超凈臺(tái)風(fēng)機(jī),等待30min以上,以排盡臭氧。3.穿HAO隔離衣,戴HAO口罩,帽子。4.風(fēng)淋2分鐘。5.0.1%水泡手,擦干。6.點(diǎn)燃酒精燈;超凈臺(tái)內(nèi)應(yīng)避免放入過多的物品;使用的吸管,滴管,試管,培養(yǎng)瓶等均事先滅菌。7.打開各類瓶蓋前先過火,以固定灰塵;打開的瓶口、試管口過火焰,鑷子使用前應(yīng)經(jīng)火焰燒灼。8.水平式風(fēng)機(jī)的超凈臺(tái),應(yīng)使瓶口斜置,應(yīng)盡量避免瓶口敞開直立。9.同一根吸管或滴管不應(yīng)連續(xù)用于幾個(gè)不同的細(xì)胞系;吸取培養(yǎng)基的吸管應(yīng)離開培養(yǎng)瓶或試管口0.5cm,避免伸入培養(yǎng)瓶口或試管口;以防止細(xì)胞系的互相混雜污染。10.漏在培養(yǎng)瓶上或臺(tái)上的體,立即用酒精棉球擦凈。11.操作完畢后恢復(fù)工作臺(tái)面。

換液周期:每周2-3次

QGP1 Cells;背景說明:胰腺癌;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)品說明書;相關(guān)產(chǎn)品有:NCI-H220細(xì)胞、MT-2J細(xì)胞、LS-180細(xì)胞

HRA-19 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCI-H441細(xì)胞、aTC1-6細(xì)胞、HL 60細(xì)胞

KASUMI1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:原粒細(xì)胞;相關(guān)產(chǎn)品有:9L細(xì)胞、Tca-8113細(xì)胞、NCI-H295R細(xì)胞

BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

背景信息:該細(xì)胞1978年由W.G.Coutinho和E.Y.Lasfargues建系,源自一位72歲患有乳腺導(dǎo)管癌的白人女性,來源組織包括乳頭及浸潤(rùn)導(dǎo)管。該細(xì)胞形態(tài)包括上皮樣細(xì)胞及多核巨細(xì)胞,可分泌一種粘性物質(zhì)。

【細(xì)胞培養(yǎng)經(jīng)驗(yàn)分享】啟蒙老師的重要性:一般進(jìn)實(shí)驗(yàn)室都有師兄師姐帶著做,他們就是你做細(xì)胞的啟蒙老師。他們的操作手法、細(xì)節(jié)、理論講解就成了你操作的準(zhǔn)則,如營(yíng)養(yǎng)液、細(xì)胞瓶的擺放位置、滅菌處理程序、開蓋手法、細(xì)胞吹打手法等等。要學(xué)會(huì)他們的正確操作,在第一次的時(shí)候就要重視。像養(yǎng)孩子一樣養(yǎng)細(xì)胞,細(xì)胞有時(shí)真的很脆弱,最好每天都去看看它,以防止出現(xiàn)培養(yǎng)箱缺水、缺二氧化碳、停電、溫度不夠等異?,F(xiàn)象,也好及時(shí)解決這些意外,避免重復(fù)實(shí)驗(yàn)帶來的更大痛苦。好細(xì)胞要及時(shí)保種:細(xì)胞要分批傳代,這樣即使有一批出了問題,還有一批備用的。像后者一般人可能不容易做到。但這是我血的教訓(xùn),有一次細(xì)胞污染了,全軍覆沒。當(dāng)時(shí)可后悔沒有保種。細(xì)胞跟人一樣,不同的細(xì)胞,培養(yǎng)特性是不一樣的。培養(yǎng)過程中要細(xì)細(xì)體會(huì),不同細(xì)胞系使用不同的培養(yǎng)基和血清。

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)

來源說明:細(xì)胞主要來源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫

IR 983F Cells;背景說明:骨髓瘤;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:半貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MDA-MB-231 #4175細(xì)胞、Detroit-562細(xì)胞、HCT GEO細(xì)胞

SKNO-1 Cells;背景說明: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)品說明書;相關(guān)產(chǎn)品有:HEC-151細(xì)胞、IEC-18細(xì)胞、C32 [Human melanoma]細(xì)胞

HTh74 Cells;背景說明:未分化甲狀腺癌;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)品說明書;相關(guān)產(chǎn)品有:NCI-H1568細(xì)胞、KG1A細(xì)胞、KY-50細(xì)胞

JeKo 1 Cells;背景說明:一位套細(xì)胞淋巴瘤患者的巨細(xì)胞變種顯示白血病轉(zhuǎn)變,從其外周血單核細(xì)胞出發(fā)建立了MCL細(xì)胞株JeKo-1。 JeKo-1細(xì)胞EB病毒陰性,并表達(dá)一種B細(xì)胞表型的IgM。 細(xì)胞過表達(dá)cyclin D1, Bcl-2, c-Myc 及 Rb 蛋白。 Bcl-1/J(H)基因重排得到了PCR證實(shí)。 JeKo-1細(xì)胞在SCID小鼠中高成瘤。 [PubMed: 9753063];傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿。;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:HPAF-2細(xì)胞、TE-8細(xì)胞、hOMF細(xì)胞

BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

物種來源:人源、鼠源等其它物種來源

形態(tài)特性:上皮細(xì)胞樣

【懸浮型細(xì)胞的傳代操作】1)吸出細(xì)胞培養(yǎng),放入離心管中,離心1000rpm 5分鐘;2)吸掉上清,加入適量之新鮮培養(yǎng)基,混和均勻后,依稀釋比例轉(zhuǎn)移至新的培養(yǎng)瓶中,以正常培養(yǎng)條件培養(yǎng)?!咀⒁馐马?xiàng)】1)嚴(yán)格的無菌操作;2)適度消化:消化的時(shí)間受消化的種類、配制時(shí)間、加入培養(yǎng)瓶中的量等諸多因素的影響,消化過程中應(yīng)該注意培養(yǎng)細(xì)胞形態(tài)的變化,一旦胞質(zhì)回縮,連接變松散,或有成片浮起的跡象就要立即終止消化。附:EDA(0.02%四乙二鈉)消化配方:EDA 0.20g,NaCl 8.00g,KCl 0.20g,KH2PO4 0.02g,葡萄糖 2.00g,0.5%紅4ml,加入蒸餾水定容至1000ml。10磅20minGAO壓滅菌,使用時(shí)調(diào)節(jié)PH值到7.4。注意EDA不能被血清中和,使用后培養(yǎng)瓶要徹底清洗,否則再培養(yǎng)時(shí)細(xì)胞容易脫壁。

HEK 293FT Cells;背景說明:該細(xì)胞穩(wěn)定表達(dá)SV40大T抗原,并且促進(jìn)最適病毒產(chǎn)物的產(chǎn)生。;傳代方法:1:2傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:圓形;相關(guān)產(chǎn)品有:CBRH7919細(xì)胞、HBE細(xì)胞、IAR 20細(xì)胞

BS-C-1 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:U87-MG細(xì)胞、RCC-4細(xì)胞、H-1693細(xì)胞

RCC 7860 Cells;背景說明: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:COLO-205細(xì)胞、WEHI231細(xì)胞、CAKI 2細(xì)胞

OsA-CL Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:5-1:10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:TE11細(xì)胞、TE6細(xì)胞、NRK 52E細(xì)胞

K299 Cells;背景說明: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)品說明書;相關(guān)產(chǎn)品有:CL34細(xì)胞、H-2347細(xì)胞、NK-92細(xì)胞

ARH 77 Cells;背景說明: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:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞樣 ;相關(guān)產(chǎn)品有:UMUC-14細(xì)胞、MDA-453細(xì)胞、HET1A細(xì)胞

NTERA-2 cl.D1 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:GM02219細(xì)胞、HMC3細(xì)胞、B16/F1細(xì)胞

H-2081 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:隨細(xì)胞的密度而增加;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:聚團(tuán)懸浮;相關(guān)產(chǎn)品有:PK 15細(xì)胞、NuTu-19細(xì)胞、HCC-1569細(xì)胞

SKO3 Cells;背景說明:SK-OV-3由G.Trempe和L.J.Old在1973年從卵巢腫瘤病人的腹水分離得到。 此細(xì)胞對(duì)腫瘤壞死因子和幾種細(xì)胞毒性藥物包括白喉毒素、順鉑和阿霉素均耐受。 在裸鼠中致瘤,且形成與卵巢原位癌一致的中度分化的腺癌。;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:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:143 B細(xì)胞、NCIH460細(xì)胞、CV-1 in Origin Simian-7細(xì)胞

H2073 Cells;背景說明: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:253J B-V細(xì)胞、CSQT-2細(xì)胞、McA-RH8994細(xì)胞

P3X63 AG 8.653 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:C33細(xì)胞、P-2003細(xì)胞、PANC-10-05細(xì)胞

Duke University 145 Cells;背景說明:DU 145 是從一位有3年淋巴細(xì)胞白血病史的前列腺癌患者的腦部轉(zhuǎn)移灶中建立的。該細(xì)胞系未檢測(cè)到激素敏感性,酸性酶陽性,單個(gè)的細(xì)胞可在軟瓊脂中形成集落。對(duì)此細(xì)胞和原始腫瘤的亞顯微結(jié)構(gòu)分析可見微絨毛、微絲、細(xì)胞橋粒、線粒體、發(fā)達(dá)的高爾基體和異質(zhì)溶酶體。該細(xì)胞不表達(dá)前列腺抗原。;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:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:M619細(xì)胞、D-283 Med細(xì)胞、Japanese Tissue Culture-39細(xì)胞

WSU-DLCL-2 Cells;背景說明: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)品說明書;相關(guān)產(chǎn)品有:UWB1.289+BRCA1細(xì)胞、MuM-2C細(xì)胞、H.Ep.-2細(xì)胞

SUM102PT Cells;背景說明:乳腺癌;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)品說明書;相關(guān)產(chǎn)品有:H-920細(xì)胞、TE 354.T細(xì)胞、Chang liver細(xì)胞

4T1 Cells;背景說明:4T1是從410.4瘤株中未經(jīng)誘變篩得的6-鳥嘌噙抗性細(xì)胞株。當(dāng)注射到BALB/c小鼠中時(shí),4T1自發(fā)產(chǎn)生高轉(zhuǎn)移腫瘤,可轉(zhuǎn)移到肺,肝,淋巴結(jié)和大腦,同時(shí)在注射部位形成始發(fā)灶。誘導(dǎo)轉(zhuǎn)移時(shí)不需要摘除始發(fā)灶。4T1細(xì)胞在BALB/c小鼠中的生長(zhǎng)與轉(zhuǎn)移特性與人體中的乳腺癌十分相近。這種腫瘤是人VI期乳腺癌的動(dòng)物模型。4T1-誘導(dǎo)的腫瘤在手術(shù)后及未手術(shù)情況下轉(zhuǎn)移的動(dòng)力學(xué)相近,可以用作手術(shù)后及未手術(shù)模型。跟其他腫瘤模型相比,由于4T1的抗6-鳥嘌噙特性,微小的轉(zhuǎn)移細(xì)胞團(tuán)(少到僅僅1個(gè))也可以在許多遠(yuǎn)端器官中檢測(cè)到。沒必要數(shù)淋巴結(jié)或稱重器官。;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:BSC40細(xì)胞、T173細(xì)胞、SK_HEP1細(xì)胞

DV90 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SRA01/04 (HLE)細(xì)胞、RenCa細(xì)胞、373 MG細(xì)胞

BC-025 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Ramos G6.C10細(xì)胞、Human Microglia Clone 3細(xì)胞、NCI-H748細(xì)胞

BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

A-PTC Cells(提供STR鑒定圖譜)

Abcam MCF-7 PGF KO Cells(提供STR鑒定圖譜)

B'SYS CHO Nav1.5 Duo Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRO504 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YHC043 Cells(提供STR鑒定圖譜)

CE-1 Cells(提供STR鑒定圖譜)

DA01205 Cells(提供STR鑒定圖譜)

EURACi004-A Cells(提供STR鑒定圖譜)

GM07321 Cells(提供STR鑒定圖譜)

Karpas-299 Cells;背景說明: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)品說明書;相關(guān)產(chǎn)品有:HCM細(xì)胞、SHIN-3細(xì)胞、Rat Lung Epithelial-6-T-antigen Negative細(xì)胞

SUM-52 Cells;背景說明:乳腺癌;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)品說明書;相關(guān)產(chǎn)品有:AG 9細(xì)胞、B16/F0細(xì)胞、HCC 2185細(xì)胞

Tb 1 Lu (NBL-12) Cells;背景說明:肺;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)品說明書;相關(guān)產(chǎn)品有:VMM-5A細(xì)胞、SU-DHL-2細(xì)胞、RASMCs細(xì)胞

HFL 1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;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:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:MIA Paca2細(xì)胞、Panc 04.03細(xì)胞、HCC-1937細(xì)胞

SF 539 Cells;背景說明:膠質(zhì)瘤;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)品說明書;相關(guān)產(chǎn)品有:SNU739細(xì)胞、HTR-8/SV-neo細(xì)胞、NH6細(xì)胞

KU 812 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:骨髓母細(xì)胞;相關(guān)產(chǎn)品有:A9 (Hamprecht)細(xì)胞、SK-MEL-28細(xì)胞、SKUT-1細(xì)胞

AR58A314.1 Cells(提供STR鑒定圖譜)

FU-MMT-1 Cells;背景說明:子宮肉瘤;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)品說明書;相關(guān)產(chǎn)品有:KG-1a細(xì)胞、H-522細(xì)胞、SK-Mel 2細(xì)胞

IOSE 80 Cells;背景說明:卵巢;上皮細(xì)胞;SV40轉(zhuǎn)化;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)品說明書;相關(guān)產(chǎn)品有:H2330細(xì)胞、NALM-6細(xì)胞、FHC細(xì)胞

C28/I2 Cells;背景說明:軟骨;SV40轉(zhuǎn)化;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)品說明書;相關(guān)產(chǎn)品有:CHO/dhFr-細(xì)胞、Hos TE-85細(xì)胞、526 mel細(xì)胞

PANC0403 Cells;背景說明: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:上皮樣;相關(guān)產(chǎn)品有:L-540細(xì)胞、RGE細(xì)胞、A704細(xì)胞

HEC-1A Cells;背景說明:這株細(xì)胞及其亞株HEC-1-B是H.Kuramoto及其同事1968年從一位IA期子宮內(nèi)膜癌患者身上分離得到的。PAF可以誘導(dǎo)其c-fos的表達(dá)。;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:Oka-C1細(xì)胞、SK Col 1細(xì)胞、OEC33細(xì)胞

HT55 Cells;背景說明: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:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:SUM 159PT細(xì)胞、UM-UC-14細(xì)胞、ML-2細(xì)胞

H2330 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MeT-5A細(xì)胞、OEC19細(xì)胞、hTERTHME1細(xì)胞

G519 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCI H747細(xì)胞、OVCAR-432細(xì)胞、GTL 16細(xì)胞

GM09911 Cells(提供STR鑒定圖譜)

HAP1 BPTF (-) 2 Cells(提供STR鑒定圖譜)

SL1 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Cates-1B細(xì)胞、NCI-H2347細(xì)胞、TFK1細(xì)胞

Human Embryonic Kidney 293 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:My-La 2059細(xì)胞、NKL細(xì)胞、NKL細(xì)胞

LN299 Cells;背景說明:膠質(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)品說明書;相關(guān)產(chǎn)品有:Rat1細(xì)胞、ROS 17/28細(xì)胞、EB-1細(xì)胞

CCD-1095Sk Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SCC 9細(xì)胞、hFOB 1.19細(xì)胞、HCO細(xì)胞

hEM15A Cells;背景說明:子宮內(nèi)膜間質(zhì)細(xì)胞;永生化;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)品說明書;相關(guān)產(chǎn)品有:NCI-H2591細(xì)胞、U-251_MG細(xì)胞、M-14細(xì)胞

TE 32.T Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:4傳代,3-4天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:梭型和大的多核細(xì)胞;相關(guān)產(chǎn)品有:SF 767細(xì)胞、WEHI-3B細(xì)胞、C1498細(xì)胞

LNCaP subline C4-2 Cells;背景說明:前列腺癌;左鎖骨上淋巴結(jié)轉(zhuǎn)移;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)品說明書;相關(guān)產(chǎn)品有:Swiss3T3細(xì)胞、SK_HEP1細(xì)胞、CHO/dhFr-細(xì)胞

SUPB15 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿。;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:SN12C-PM6細(xì)胞、HRPEpiC細(xì)胞、A 2058細(xì)胞

HG03368 Cells(提供STR鑒定圖譜)

ICRmt-1 Cells(提供STR鑒定圖譜)

LNCaP-CS10 Cells(提供STR鑒定圖譜)

NCI-H3030 Cells(提供STR鑒定圖譜)

PathHunter DLD1 MTNR1A Total GPCR Internalization Cells(提供STR鑒定圖譜)

Ubigene HEK293 S1PR3 KO Cells(提供STR鑒定圖譜)

WIBRe001-A-35 Cells(提供STR鑒定圖譜)

HG01527 Cells(提供STR鑒定圖譜)

HuTu-80 Cells;背景說明: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:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:Alpha Mouse Liver 12細(xì)胞、3T3-L1 ad細(xì)胞、Vero from pool #76細(xì)胞

Colo699 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:H-2330細(xì)胞、H-661細(xì)胞、HCT116/L細(xì)胞

M109 Cells;背景說明:肺癌;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)品說明書;相關(guān)產(chǎn)品有:JAR細(xì)胞、RGC5細(xì)胞、Hs895.T細(xì)胞

P3/NSI/1-AG4-1 Cells;背景說明:這是P3X63Ag8(ATCCTIB-9)的一個(gè)不分泌克隆。Kappa鏈合成了但不分泌。能抗0.1mM8-氮雜鳥嘌呤但不能在HAT培養(yǎng)基中生長(zhǎng)。據(jù)報(bào)道它是由于缺失了3-酮類固醇還原酶活性的膽固醇營(yíng)養(yǎng)缺陷型。檢測(cè)表明肢骨發(fā)育畸形病毒(鼠痘)陰性。;傳代方法:1:2傳代,3天內(nèi)可長(zhǎng)滿。;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:SW 1088細(xì)胞、Alexander細(xì)胞、CAL-148細(xì)胞

RM1 Cells;背景說明:前列腺癌;C57BL/6;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)品說明書;相關(guān)產(chǎn)品有:NCIH208細(xì)胞、RAMSCs細(xì)胞、CFPAC-1細(xì)胞

OVCA433 Cells;背景說明:卵巢癌;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)品說明書;相關(guān)產(chǎn)品有:EC-9706細(xì)胞、JCA-1細(xì)胞、NCI-H2029細(xì)胞

8305-C Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:6傳代;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:CDC/EU.HMEC-1細(xì)胞、TGHAVSMC細(xì)胞、MCF12F細(xì)胞

Rca-B Cells;背景說明:鱗癌;SD大鼠;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)品說明書;相關(guān)產(chǎn)品有:GT39細(xì)胞、MDA-MB 231細(xì)胞、NCI-H1792細(xì)胞

CRFK Cells;背景說明:腎;自發(fā)永生;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)品說明書;相關(guān)產(chǎn)品有:TCC-PAN2細(xì)胞、JVM3細(xì)胞、NCI.H522細(xì)胞

TMK-1 Cells;背景說明:胃癌;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)品說明書;相關(guān)產(chǎn)品有:MGHU3細(xì)胞、SF 295細(xì)胞、BOWES細(xì)胞

OVCAR 5 Cells;背景說明:卵巢癌;腹水轉(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)品說明書;相關(guān)產(chǎn)品有:Nb-2細(xì)胞、MTC-TT細(xì)胞、SW527細(xì)胞

OVCAR3 Cells;背景說明:該細(xì)胞1982年由T.C. Hamilton等建系,源自一位60卵巢腺癌的腹水,是卵巢癌抗藥性研究的模型。;傳代方法:1:2—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:BLO-11細(xì)胞、SNB.19細(xì)胞、NCI-H711細(xì)胞

Hs822T Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:4傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:BL6細(xì)胞、HR-1細(xì)胞、HLE細(xì)胞

HKBML Cells;背景說明:腦;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)品說明書;相關(guān)產(chǎn)品有:HL-1細(xì)胞、8226細(xì)胞、SW 962細(xì)胞

CaSki Cells;背景說明:這株細(xì)胞是從小腸腸系膜轉(zhuǎn)移灶的細(xì)胞中建立的。 據(jù)報(bào)道,它含有完整的HPV-16(每個(gè)細(xì)胞大約600個(gè)拷貝)和HPV-18相關(guān)序列。;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:HSF2細(xì)胞、EL 4細(xì)胞、KMS26細(xì)胞

SaOS-1 Cells(提供STR鑒定圖譜)

Hs729 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2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:Panc 08.13細(xì)胞、HONE1細(xì)胞、MC3T3-E細(xì)胞

SK-Mel 1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:維持細(xì)胞濃度在1×105-2×105,每周補(bǔ)液2-3次。;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:球形的;相關(guān)產(chǎn)品有:Hs 683細(xì)胞、KYSE 140細(xì)胞、Murine Leydig Tumor Cell line-1細(xì)胞

HCC-9724 Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:LN299細(xì)胞、L-6 myoblast細(xì)胞、697細(xì)胞

JVM3 Cells;背景說明:慢性髓白血??;女性;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)品說明書;相關(guān)產(chǎn)品有:NCI-SNU-761細(xì)胞、MDA-MB-231細(xì)胞、SH-SY5Y細(xì)胞

GM-215 Cells;背景說明:肺;自發(fā)永生;雄性;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)品說明書;相關(guān)產(chǎn)品有:H2286細(xì)胞、KP-N-YN細(xì)胞、MonoMac 6細(xì)胞

HCMEC(BL12-H) Cells;背景說明:結(jié)腸微血管;內(nèi)皮 Cells;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)品說明書;相關(guān)產(chǎn)品有:OVCAR10細(xì)胞、NCI-H1404細(xì)胞、AMO-1細(xì)胞

B16 F1 Cells;背景說明: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:JROECL33細(xì)胞、H-1703細(xì)胞、LC-MS細(xì)胞

U266B1 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代,2-3天傳一代;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:OV433細(xì)胞、EO771細(xì)胞、OV1063細(xì)胞

S3-HeLa Cells;背景說明:該細(xì)胞是1955年由PuckTT,MarcusPI和CieciuraSJ建系的,含HPV-18序列;角蛋白陽性;可用于與染色體突變、細(xì)胞營(yíng)養(yǎng)、集落形成相關(guān)的哺乳動(dòng)物細(xì)胞的克隆分析。;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:Hi-five細(xì)胞、RPTEC/TERT 1細(xì)胞、HNTEC細(xì)胞

LA 4 Cells;背景說明:肺癌;A/He;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)品說明書;相關(guān)產(chǎn)品有:T/G HA-VSMC細(xì)胞、CHO細(xì)胞、H-1781細(xì)胞

SUM 102 Cells;背景說明:乳腺癌;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)品說明書;相關(guān)產(chǎn)品有:Swiss-3T3細(xì)胞、H647ell細(xì)胞、RPMI8226細(xì)胞

PANC-08-13 Cells;背景說明: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:上皮樣;相關(guān)產(chǎn)品有:SUM102細(xì)胞、CCD19Lu細(xì)胞、LL/2 (LLC1)細(xì)胞

OCI-AML-3 Cells;背景說明:急性髓系白血??;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)品說明書;相關(guān)產(chǎn)品有:Hs 606.T細(xì)胞、H4細(xì)胞、KYSE 70細(xì)胞

MRAEC Cells;背景說明: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)品說明書部分;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Rat Basophilic Leukemia-1細(xì)胞、H-35細(xì)胞、COV-362細(xì)胞

BT-549人乳腺管癌復(fù)蘇細(xì)胞保種中心|帶STR證書

BayGenomics ES cell line RRD163 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XF065 Cells(提供STR鑒定圖譜)

DBA A.Sp Cells(提供STR鑒定圖譜)

MLB13MYC clone 17 Cells(提供STR鑒定圖譜)

T3-3H1 Cells(提供STR鑒定圖譜)

LUEi005-B Cells(提供STR鑒定圖譜)

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BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants.

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Wasielewski M., Elstrodt F., Klijn J.G.M., Berns E.M.J.J., Schutte M.

Thirteen new p53 gene mutants identified among 41 human breast cancer cell lines.

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PubMed=17088437; DOI=10.1158/1535-7163.MCT-06-0433; PMCID=PMC2705832

Ikediobi O.N., Davies H.R., Bignell G.R., Edkins S., Stevens C., O'Meara S., Santarius T., Avis T., Barthorpe S., Brackenbury L., Buck G., Butler A.P., Clements J., Cole J., Dicks E., Forbes S., Gray K., Halliday K., Harrison R., Hills K., Hinton J., Hunter C., Jenkinson A., Jones D., Kosmidou V., Lugg R., Menzies A., Miroo T., Parker A., Perry J., Raine K.M., Richardson D., Shepherd R., Small A., Smith R., Solomon H., Stephens P.J., Teague J.W., Tofts C., Varian J., Webb T., West S., Widaa S., Yates A., Reinhold W.C., Weinstein J.N., Stratton M.R., Futreal P.A., Wooster R.

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

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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.

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The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.

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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.

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Jain M., Nilsson R., Sharma S., Madhusudhan N., Kitami T., Souza A.L., Kafri R., Kirschner M.W., Clish C.B., Mootha V.K.

Metabolite profiling identifies a key role for glycine in rapid cancer cell proliferation.

Science 336:1040-1044(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=23856246; DOI=10.1158/0008-5472.CAN-12-3342; PMCID=PMC4893961

Abaan O.D., Polley E.C., Davis S.R., Zhu Y.-L.J., Bilke S., Walker R.L., Pineda M.A., Gindin Y., Jiang Y., Reinhold W.C., Holbeck S.L., Simon R.M., Doroshow J.H., Pommier Y., Meltzer P.S.

The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology.

Cancer Res. 73:4372-4382(2013)


PubMed=23933261; DOI=10.1016/j.celrep.2013.07.018

Moghaddas Gholami A., Hahne H., Wu Z.-X., Auer F.J., Meng C., Wilhelm M., Kuster B.

Global proteome analysis of the NCI-60 cell line panel.

Cell Rep. 4:609-620(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=24279929; DOI=10.1186/2049-3002-1-20; PMCID=PMC4178206

Dolfi S.C., Chan L.L.-Y., Qiu J., Tedeschi P.M., Bertino J.R., Hirshfield K.M., Oltvai Z.N., Vazquez A.

The metabolic demands of cancer cells are coupled to their size and protein synthesis rates.

Cancer Metab. 1:20.1-20.13(2013)


PubMed=24670534; DOI=10.1371/journal.pone.0092047; PMCID=PMC3966786

Varma S., Pommier Y., Sunshine M., Weinstein J.N., Reinhold W.C.

High resolution copy number variation data in the NCI-60 cancer cell lines from whole genome microarrays accessible through CellMiner.

PLoS ONE 9:E92047-E92047(2014)


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)


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=25892236; DOI=10.1016/j.celrep.2015.03.050; PMCID=PMC4425736

Lawrence R.T., Perez E.M., Hernandez D., Miller C.P., Haas K.M., Irie H.Y., Lee S.-I., Blau C.A., Villen J.

The proteomic landscape of triple-negative breast cancer.

Cell Rep. 11:630-644(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=27377824; DOI=10.1038/sdata.2016.52; PMCID=PMC4932877

Mestdagh P., Lefever S., Volders P.-J., Derveaux S., Hellemans J., Vandesompele J.

Long non-coding RNA expression profiling in the NCI60 cancer cell line panel using high-throughput RT-qPCR.

Sci. Data 3:160052-160052(2016)


PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469

Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.

A landscape of pharmacogenomic interactions in cancer.

Cell 166:740-754(2016)


PubMed=27807467; DOI=10.1186/s13100-016-0078-4; PMCID=PMC5087121

Zampella J.G., Rodic N., Yang W.R., Huang C.R.L., Welch J., Gnanakkan V.P., Cornish T.C., Boeke J.D., Burns K.H.

A map of mobile DNA insertions in the NCI-60 human cancer cell panel.

Mob. DNA 7:20.1-20.11(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.

Cancer Cell 31:225-239(2017)


PubMed=28287265; DOI=10.1021/acs.jproteome.6b00470; PMCID=PMC5557415

Yen T.-Y., Bowen S., Yen R., Piryatinska A., Macher B.A., Timpe L.C.

Glycoproteins in claudin-low breast cancer cell lines have a unique expression profile.

J. Proteome Res. 16:1391-1400(2017)


PubMed=28889351; DOI=10.1007/s10549-017-4496-x

Saunus J.M., Smart C.E., Kutasovic J.R., Johnston R.L., Kalita-de Croft P., Miranda M., Rozali E.N., Vargas A.C., Reid L.E., Lorsy E., Cocciardi S., Seidens T., McCart Reed A.E., Dalley A.J., Wockner L.F., Johnson J., Sarkar D., Askarian-Amiri M.E., Simpson P.T., Khanna K.K., Chenevix-Trench G., Al-Ejeh F., Lakhani S.R.

Multidimensional phenotyping of breast cancer cell lines to guide preclinical research.

Breast Cancer Res. Treat. 167:289-301(2018)


PubMed=30613774; DOI=10.1126/sciadv.aau7314; PMCID=PMC6314821

Vande Voorde J., Ackermann T., Pfetzer N., Sumpton D., Mackay G., Kalna G., Nixon C., Blyth K., Gottlieb E., Tardito S.

Improving the metabolic fidelity of cancer models with a physiological cell culture medium.

Sci. Adv. 5:eaau7314.1-eaau7314.14(2019)


PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675

Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.

An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

Cancer Res. 79:1263-1273(2019)"


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