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SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,SK-OV-3
  • SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,SK-OV-3
  • SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,SK-OV-3
  • SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,SK-OV-3

SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

價(jià)格 詢價(jià)
包裝 1000000Cells/瓶 2000000Cells/瓶
最小起訂量 1000000Cells/瓶
發(fā)貨地 上海
文件下載 檢測(cè)報(bào)告COA
更新日期 2025-07-11
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜英文名稱:SK-OV-3
品牌: ATCC、DSMZ等產(chǎn)地: 美國、歐洲、德國等
保存條件: 低溫避光純度規(guī)格: SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜
產(chǎn)品類別: ATCC細(xì)胞庫
種屬: 詳見細(xì)胞說明書組織: 詳見細(xì)胞說明書
細(xì)胞系: 詳見細(xì)胞說明書細(xì)胞形態(tài): 詳見細(xì)胞說明書
生長狀態(tài): 詳見細(xì)胞說明書靶點(diǎn): 詳見細(xì)胞說明書
應(yīng)用: 詳見細(xì)胞說明書貨號(hào): 詳見細(xì)胞說明書
規(guī)格: 1*10^6cells/T25(1瓶)或1ml凍存管(2支)是否進(jìn)口: 來源ATCC、DSMZ、ECACC等細(xì)胞庫
組織來源: 詳見細(xì)胞說明書是否是腫瘤細(xì)胞: 詳見細(xì)胞說明書
器官來源: 詳見細(xì)胞說明書品系: 詳見細(xì)胞說明書
免疫類型: 詳見細(xì)胞說明書物種來源: 人源或其它動(dòng)物來源等
保質(zhì)期: 可長期保存(液氮低溫凍存)
2025-07-11 SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 SK-OV-3 1000000Cells/瓶/1RMB;2000000Cells/瓶/1RMB 1 ATCC、DSMZ等 美國、歐洲、德國等 低溫避光 SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 ATCC細(xì)胞庫

"SK-OV-3人卵巢癌細(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)

生長特性:貼壁生長

細(xì)胞系的選擇需要考慮到細(xì)胞系的功能特點(diǎn)、生長速率、鋪板效率、生長條件和生長特征、克隆效率、培養(yǎng)方式等因素,如果您想高產(chǎn)量表達(dá)重組蛋白,您可以選擇可以懸浮生長的快速生長細(xì)胞系。細(xì)胞培養(yǎng)的操作步驟主要包括傳代、換液、凍存和復(fù)蘇。這些步驟確保了細(xì)胞能夠在實(shí)驗(yàn)室環(huán)境中長期存活并繼續(xù)增殖。傳代是將細(xì)胞從一個(gè)容器轉(zhuǎn)移到另一個(gè)容器的過程,以擴(kuò)大細(xì)胞數(shù)量;換液是為了清除代謝廢物并補(bǔ)充新鮮培養(yǎng)基;凍存則是為了長期保存細(xì)胞,而復(fù)蘇則是重新激活冷凍保存的細(xì)胞使其恢復(fù)正常生長。

換液周期:每周2-3次

Ca9-22 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。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:C643細(xì)胞、MV-4-11細(xì)胞、NCIH128細(xì)胞

Vero 76 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:SK-N-BE(1)細(xì)胞、HM細(xì)胞、PG-4 S+L-細(xì)胞

NCIH358 Cells;背景說明:1981年從一位開始化療之前的患者的腫瘤組織中分離建株。超微結(jié)構(gòu)研究表明細(xì)胞質(zhì)中有Clara細(xì)胞的特征結(jié)構(gòu)細(xì)胞表達(dá)主要的肺表面結(jié)合蛋白SP-A的蛋白和RNA。不表達(dá)SP-B和SP-C。他們?cè)谲洯傊械目寺⌒纬尚蕿椋?83%。;傳代方法:消化3-5分鐘。1:2。3天內(nèi)可長滿。;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:NOMO-1細(xì)胞、Giant Cell Tumor細(xì)胞、COS-1細(xì)胞

SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息: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。

┈訂┈購(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;

公司細(xì)胞系主要引進(jìn)ATCC、DSMZ、JCRB、KCLB、RIKEN、ECACC等細(xì)胞庫,細(xì)胞系體外培養(yǎng),它們會(huì)成長為單層細(xì)胞,附著或緊貼在培養(yǎng)瓶上,或懸浮在體外的溶液中,細(xì)胞系復(fù)蘇周期短,公司細(xì)胞系狀態(tài)良好,飽滿,有光澤等優(yōu)點(diǎn)。EDTA的作用:許多人不用胰酶,只用EDTA,或者用胰酶/EDTA聯(lián)合作用。這里要明白,胰酶切割細(xì)胞外基質(zhì)的一些負(fù)責(zé)粘連和附著的蛋白,而EDTA通過螯合Ca離子,作用于整聯(lián)蛋白的活性,所以EDTA的作用更加溫和。有的人在胰酶里添加一些EDTA,或者對(duì)付特別難消化的細(xì)胞,添加多一些EDTA,就是這個(gè)道理。一般不要試圖延長消化時(shí)間(如果10min還消化不下來的話),而應(yīng)該想其它辦法。

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

SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來源:人源、鼠源等其它物種來源

HuP-T4 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:LAN-6細(xì)胞、OCI/AML-2細(xì)胞、EL4細(xì)胞

H1650_CO Cells;背景說明:該細(xì)胞是從一名27歲白人男性(10年煙齡)支氣管肺泡癌患者的胸腔積液中分離得到的。;傳代方法:1:4-1:6傳代;2-3天換液1次。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:SNGM細(xì)胞、SW948細(xì)胞、H295R細(xì)胞

FOX-NY 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:A-875細(xì)胞、C8161細(xì)胞、MLO-Y4細(xì)胞

L 1210 Cells;背景說明: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;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:BHP10-3細(xì)胞、NCI-SNU-5細(xì)胞、NCI-H2073細(xì)胞

┈訂┈購(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

貼壁消化難題:1,先用PBS 把細(xì)胞洗兩遍,使瓶內(nèi)沒有血清了,減少對(duì)胰酶的中和,然后用新配的0.25%的胰酶加入3ml左右,放在37度,然后可以在細(xì)胞有些消化下來時(shí),拿著瓶口,運(yùn)用手腕的力量輕輕震蕩瓶內(nèi)體,這樣細(xì)胞很快就下來了,還不需要吹打,分散也均勻;2,成團(tuán)、絮狀:消化里加入eda可以減少細(xì)胞成團(tuán)的現(xiàn)象,血清可以終止胰酶的作用,如果是進(jìn)口血清的話也能終止eda的作用。用胰酶消化后胰酶可以倒掉,也可以不倒,直接加血清終止,如果消化中加入了eda的話,就要將消化倒干凈,如果細(xì)胞貼壁要求不是很嚴(yán)格的話,一般不需要進(jìn)行離心。鼻咽癌細(xì)胞的貼壁能力很強(qiáng),用0.5%胰酶(含0.1%EDA)一般要消化12~15min。用PBS洗滌時(shí)要洗凈殘余的培養(yǎng)基,加入胰酶后在培養(yǎng)箱中消化(避免細(xì)胞室溫下受損以及在此溫度時(shí)胰酶活性Zui強(qiáng))至細(xì)胞收縮變圓(可顯微鏡下觀察)且有少許細(xì)胞脫落(有流下來的趨勢(shì)),隨后立即棄去胰酶(如果脫落的細(xì)胞很多且需要大量細(xì)胞實(shí)驗(yàn),則不能棄去胰酶),加入培養(yǎng)基仔細(xì)吹打(不能用無血清培養(yǎng)基或者PBS替代,否則細(xì)胞聚集成團(tuán)塊或絮狀)。一般我都離心一次棄去上清(去除殘留的胰酶及漂浮的死細(xì)胞或細(xì)胞碎片);消化過度:馬上用培養(yǎng)基中和,用吸管吹打細(xì)胞,收集全部的細(xì)胞到以無菌的離心管中800RPM 3分鐘。棄上清,用全培重懸,換新的培養(yǎng)瓶繼續(xù)培養(yǎng),狀態(tài)不HAO的細(xì)胞在培養(yǎng)的過程中會(huì)死亡脫落,在換的時(shí)候可以清除掉!

HOS/MNNG Cells;背景說明:骨肉瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:H-2347細(xì)胞、Centre Antoine Lacassagne-51細(xì)胞、JROECL19細(xì)胞

CAL 51 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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Bac 1.2F5細(xì)胞、Hs27細(xì)胞、L540細(xì)胞

JKT-1 Cells;背景說明:精原瘤;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HEYA8細(xì)胞、NCI-SNU-449細(xì)胞、HCC0366細(xì)胞

P31/Fujioka Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:5傳代;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:B958細(xì)胞、SK BR 03細(xì)胞、D562細(xì)胞

OV1063 Cells;背景說明: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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KYSE-30細(xì)胞、Colon38細(xì)胞、KMS-18細(xì)胞

Human Pancreatic Duct Epithelial Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長 ;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:293H細(xì)胞、MDA415細(xì)胞、HPAC細(xì)胞

H1688 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:T/G HA VSMC細(xì)胞、KLM1細(xì)胞、HEL-299細(xì)胞

CCC-HEL-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:SF763細(xì)胞、MDA.MB.231細(xì)胞、WM-266-mel細(xì)胞

Nb-2 Cells;背景說明:惡性淋巴瘤;雄性;Nb;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:C666-1細(xì)胞、SK MEL 5細(xì)胞、CL40細(xì)胞

RWPE2 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。;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:Stanford University-Diffuse Histiocytic Lymphoma-8細(xì)胞、DMS 153細(xì)胞、SCLC21H細(xì)胞

HNE3 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:GM04678細(xì)胞、KYSE-410細(xì)胞、LM-TK-細(xì)胞

RAW264.7 Cells;背景說明:單核巨噬細(xì)胞白血?。恍坌?;BALB/c;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SK MEL 5細(xì)胞、U-266細(xì)胞、Panc02-H0細(xì)胞

Mouse Bladder Tumor line-2 Cells;背景說明:膀胱移行細(xì)胞癌;C3H/He;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NPA87-1細(xì)胞、Porcine Kidney-15細(xì)胞、IPLB-SF-21細(xì)胞

MAC1 Cells;背景說明:皮膚T淋巴瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MuM-2B細(xì)胞、HCC-1428細(xì)胞、SACC-LM細(xì)胞

REC 1 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,2-3天換液1次;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:HCC-4006細(xì)胞、U266B1細(xì)胞、HOS (TE85, Clone F5)細(xì)胞

P3-X63Ag8 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:HCC 2185細(xì)胞、Reuber H35細(xì)胞、H460細(xì)胞

SW 1990 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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MLE12細(xì)胞、NB19細(xì)胞、R2C細(xì)胞

Abcam A-549 LIMK1 KO Cells(提供STR鑒定圖譜)

Abcam U-87MG SDHB KO Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSG163 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRT603 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC538 Cells(提供STR鑒定圖譜)

CHO Pro-3 MtxRI-6-3 Cells(提供STR鑒定圖譜)

DA02389 Cells(提供STR鑒定圖譜)

DD1322 Cells(提供STR鑒定圖譜)

GM01893 Cells(提供STR鑒定圖譜)

OACP4C 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:B-cell Acute Lymphoblastic Leukemia-1細(xì)胞、EOC 20細(xì)胞、NB-4細(xì)胞

SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

RAMOS2G64C10 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2×105/ml-1×106/ml;根據(jù)細(xì)胞濃度每2-3天補(bǔ)液1次。;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:McCoy細(xì)胞、MADB106細(xì)胞、U-87MG細(xì)胞

H-1882 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:IPECJ2細(xì)胞、K7M2細(xì)胞、MIA PaCa-2細(xì)胞

SKG-3a Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:2x10^4 cells/ml;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:TALL1細(xì)胞、NIT-1細(xì)胞、Hs 604.T細(xì)胞

NCIH1963 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每周換液2次。;生長特性:懸浮生長;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:C1498細(xì)胞、NR-8383細(xì)胞、ES2細(xì)胞

HEK-293-H 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:LK-2細(xì)胞、Reh細(xì)胞、SHG 44細(xì)胞

3H8-G8 Cells(提供STR鑒定圖譜)

Mac-1 Cells;背景說明:皮膚T淋巴瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:U87細(xì)胞、SNU761細(xì)胞、3396細(xì)胞

NCIH1581 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每周換液2次。;生長特性:混合型;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:H-125細(xì)胞、EB-2細(xì)胞、Soleus clone 8細(xì)胞

HCC1500 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3-5天換液;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:OEC33細(xì)胞、HTR-8/SV neo細(xì)胞、H1417細(xì)胞

AC16 [Human hybrid] Cells;背景說明:心肌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SU86.86細(xì)胞、L2細(xì)胞、L23/P細(xì)胞

C33 Cells;背景說明:C-33A細(xì)胞株是N. Auersperg從宮頸癌切片中建立的一系列細(xì)胞株(參見ATCC CRL-1594和ATCC CRL-1595)中的一株。 細(xì)胞一開始就表現(xiàn)出亞二倍體核型及上皮細(xì)胞形態(tài)。 連續(xù)傳代可以觀察到核型不穩(wěn)定。 存在成視網(wǎng)膜細(xì)胞瘤蛋白(pRB),但大小不正常。 P53表達(dá)上調(diào),且有一個(gè)273位密碼子的點(diǎn)突變導(dǎo)致Arg -> Cys的替換。 人乳頭瘤病毒DNA及RNA陰性。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:2B4細(xì)胞、B16-F10--RED細(xì)胞、MNNG-HOS (TE 85, clone F-5)細(xì)胞

LM8 Cells;背景說明:Dunn's骨肉瘤;雌性;C3H;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:ECV 304細(xì)胞、PK-13細(xì)胞、Centre Antoine Lacassagne-62細(xì)胞

Hs 888.T 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;生長特性:貼壁生長;形態(tài)特性:成纖維細(xì)胞和上皮細(xì)胞的混合樣;相關(guān)產(chǎn)品有:SPDC-CCL141細(xì)胞、LC-MS細(xì)胞、TCC-PAN2細(xì)胞

NCC-IT Cells;背景說明: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;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:NCI-H2198細(xì)胞、MGHU1細(xì)胞、SUP-T1細(xì)胞

GM28475 Cells(提供STR鑒定圖譜)

HAP1 PDIK1L (-) 3 Cells(提供STR鑒定圖譜)

SKMel-28 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:8?jìng)鞔?3天換液1次。;生長特性:貼壁生長;形態(tài)特性:星形的;相關(guān)產(chǎn)品有:Line 207細(xì)胞、Hs 888.Lu細(xì)胞、A-498細(xì)胞

GM05372 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:J 774A.1細(xì)胞、HF-91細(xì)胞、FaDu細(xì)胞

32D.3 Cells;背景說明:骨髓淋巴瘤;C3H/HeJ;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:TKB-1細(xì)胞、Hs 636.T細(xì)胞、Capan1細(xì)胞

H1404 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:He-La細(xì)胞、Hs-343-T細(xì)胞、PT-67細(xì)胞

Cloudman S91 melanoma clone M-3 Cells;背景說明:黑色素瘤;雄性;DBA;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:451Lu細(xì)胞、BNL CL.2細(xì)胞、HBL-1 [Human diffuse large B-cell lymphoma]細(xì)胞

Tu177 Cells;背景說明:喉鱗癌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:CMT64細(xì)胞、Mhh-Call 2細(xì)胞、HPDE細(xì)胞

COS1 Cells;背景說明:該細(xì)胞源自CV-1細(xì)胞株,經(jīng)轉(zhuǎn)染編碼野生型T抗原、起始點(diǎn)缺陷突變的SV40得到;細(xì)胞中整合有SV40基因組完整早期區(qū)段的單個(gè)拷貝。該細(xì)胞表達(dá)T抗原,適用于需要SV40T抗原表達(dá)的載體的轉(zhuǎn)染;保留SV40溶細(xì)胞性生長的特性;支持40℃時(shí)溫度敏感性A209病毒的復(fù)制;支持早期區(qū)段缺失的SV40純體的復(fù)制。因含有SV40的DNA序列,該細(xì)胞需要在2級(jí)生物安全柜中操作。;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:Pa14C細(xì)胞、H-1373細(xì)胞、YT細(xì)胞

HCM Cells;背景說明:心肌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HEK-AD293細(xì)胞、AG 9細(xì)胞、WIL2-S細(xì)胞

HS839 Cells(提供STR鑒定圖譜)

KOLF2.1J PRKN R42P SNV/SNV Cells(提供STR鑒定圖譜)

MOCL7 Cells(提供STR鑒定圖譜)

NWR 5765 iPSC-c506 Cells(提供STR鑒定圖譜)

RG-285 Cells(提供STR鑒定圖譜)

UABCATe007-A Cells(提供STR鑒定圖譜)

UMGi158-A-1.1 Cells(提供STR鑒定圖譜)

HAP1 SLIT2 (-) 1 Cells(提供STR鑒定圖譜)

OCI Ly3 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。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Tokyo Medical and Dental university 8細(xì)胞、MDAMB436細(xì)胞、CESS細(xì)胞

FHL 124 Cells;背景說明:晶狀體上皮;自發(fā)永生;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:38C13細(xì)胞、L-M[TK-]細(xì)胞、FRO 81-2細(xì)胞

Rat Basophilic Leukemia-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:Sp2/O-Ag14細(xì)胞、PG-LH7細(xì)胞、CAL-27細(xì)胞

NPA 87 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:L-6TG細(xì)胞、32Dcl3細(xì)胞、Swiss 3T3細(xì)胞

P3X63Ag8-6-5-3 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:SUM102PT細(xì)胞、RINm5F細(xì)胞、RT112細(xì)胞

P3X63Ag8-6-5-3 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:SUM102PT細(xì)胞、RINm5F細(xì)胞、RT112細(xì)胞

NS-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。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)可長滿。;生長特性:懸浮生長;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:H661細(xì)胞、Tb1Lu細(xì)胞、OUMS27細(xì)胞

Mel624 Cells;背景說明:黑色素瘤;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCIH847細(xì)胞、CAL 148細(xì)胞、SK Mel 24細(xì)胞

HIT Cells;背景說明:胰島β細(xì)胞;SV40轉(zhuǎn)化;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SUM-52細(xì)胞、PLA801C細(xì)胞、MEL-526細(xì)胞

Huh7.5 Cells;背景說明:肝癌;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Hs819.T細(xì)胞、L-WRN細(xì)胞、Mono Mac6細(xì)胞

P815 Cells;背景說明:肥大細(xì)胞瘤;雄性;DBA/2;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:SKMEL2細(xì)胞、NPA'87細(xì)胞、hFOB 1.19細(xì)胞

Pa18C Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:HS-766T細(xì)胞、BSC40細(xì)胞、NCI-441細(xì)胞

U266BL 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;生長特性:懸浮生長 ;形態(tài)特性:淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有:HP615細(xì)胞、RMG1細(xì)胞、NOZ細(xì)胞

Normal Rat, August 3, 1983 Cells;背景說明:NR8383(正常大鼠,1983年8月3日)來源于肺灌洗時(shí)的正常大鼠肺泡巨噬細(xì)胞。細(xì)胞在gerbil肺細(xì)胞連續(xù)培養(yǎng)液存在下培養(yǎng)了大約8-9個(gè)月。隨后,不再需要外源生長因子。通過有限稀釋法從單個(gè)細(xì)胞克隆并亞克隆NR8383細(xì)胞,并三次用軟瓊脂亞克隆。細(xì)胞表現(xiàn)出巨噬細(xì)胞的特性,吞噬酵母多糖和銅綠,非特異性脂酶活性,F(xiàn)c受體,氧化降解;分泌IL-1,TNFbeta和IL-6,可重復(fù)地響應(yīng)外源生長因子。NR8383細(xì)胞響應(yīng)博萊霉素,分泌TGFbeta前體。在博萊霉素刺激下,TGFbe;傳代方法:1:2傳代;生長特性:半貼壁生長;形態(tài)特性:巨噬細(xì)胞;相關(guān)產(chǎn)品有:HL-60 clone15細(xì)胞、Rat 1細(xì)胞、HOK細(xì)胞

GEO Cells;背景說明:結(jié)腸癌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NCI-H1373細(xì)胞、BSC-40細(xì)胞、OCI-LY-7細(xì)胞

STPLF-fE Cells(提供STR鑒定圖譜)

Kobe university Oral Squamous Cell culture-2 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:2.2 x 10^4 cells/ml ;生長特性:貼壁生長;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

H-2052 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;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:SUM149-PT細(xì)胞、SCL II細(xì)胞、Hs 863.T細(xì)胞

SV40-MES13 Cells;背景說明:腎小球系膜;SV40轉(zhuǎn)化;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KRC Y細(xì)胞、G519細(xì)胞、149 PT細(xì)胞

SK-MEL3 Cells;背景說明: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。;生長特性:貼壁生長;形態(tài)特性:成纖維細(xì)胞;相關(guān)產(chǎn)品有:D283MED細(xì)胞、MDA-MB231細(xì)胞、PaTu 8988s細(xì)胞

OCI-Ly7 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。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:NRK 49F細(xì)胞、HFT 8810細(xì)胞、PC-2 [Human pancreatic carcinoma]細(xì)胞

BC-020 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:C-8161細(xì)胞、Vero E6細(xì)胞、B-16細(xì)胞

SK-OV-3人卵巢癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

2780CP 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。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:KOPN8細(xì)胞、TFH細(xì)胞、CHP-100細(xì)胞

MASMC Cells;背景說明:氣道平滑肌;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MDA-MB-468-RED細(xì)胞、K562/ADR細(xì)胞、RPMI8226細(xì)胞

COLO320 DM Cells;背景說明:該細(xì)胞可產(chǎn)生5-羥色胺、去甲、、ACTH和甲狀旁腺素。角蛋白、波形蛋白弱陽性。培養(yǎng)條件: RPMI 1640  10%FBS;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:懸浮+貼壁;形態(tài)特性:淋巴細(xì)胞;相關(guān)產(chǎn)品有:RCC 7860細(xì)胞、A431/P細(xì)胞、MDA-1386細(xì)胞

SKG-3a Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:2x10^4 cells/ml;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:TALL1細(xì)胞、SKCO-1細(xì)胞、Hs746T細(xì)胞

SKNBE Cells;背景說明:1972年11月從一們多次化療及放療的擴(kuò)散性神經(jīng)母細(xì)胞瘤患兒骨髓穿刺物中建立了SK-N-BE(2)神經(jīng)母細(xì)胞瘤細(xì)胞株。 該細(xì)胞顯示中等水平的多巴胺-β-羥基酶活性。 有報(bào)道稱SK-N-BE(2)細(xì)胞的飽和濃度超過1x106細(xì)胞/平方厘米。細(xì)胞形態(tài)多樣,有的有長突觸,有的呈上皮細(xì)胞樣。 細(xì)胞會(huì)聚集,形成團(tuán)塊并浮起;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:PZ-HPV-7細(xì)胞、NCIH2073細(xì)胞、MGH-UI細(xì)胞

DHL-4 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。;生長特性:懸浮;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:NTHY-ORI3.1細(xì)胞、Mink Lung細(xì)胞、MOLM13細(xì)胞

Human Embryonic Skin Cells;背景說明:皮膚;成纖維 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:PC10細(xì)胞、Fetal Bovine Heart Endothelial細(xì)胞、NCIH345細(xì)胞

NRK-52E Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:NOR 10細(xì)胞、Vero E-6細(xì)胞、COLO320DM細(xì)胞

BayGenomics ES cell line KST302 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XC104 Cells(提供STR鑒定圖譜)

CPTC-APEX1-2 Cells(提供STR鑒定圖譜)

MANNUT12-4B12 Cells(提供STR鑒定圖譜)

S5E5 Cells(提供STR鑒定圖譜)

HOKUG Cells(提供STR鑒定圖譜)

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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.

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Proc. Natl. Acad. Sci. U.S.A. 108:18708-18713(2011)


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Therapeutic reactivation of mutant p53 protein by quinazoline derivatives.

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PubMed=22328975; DOI=10.1158/2159-8290.CD-11-0170; PMCID=PMC3274821

Hanrahan A.J., Schultz N., Westfal M.L., Sakr R.A., Giri D.D., Scarperi S., Janakiraman M., Olvera N., Stevens E.V., She Q.-B., Aghajanian C., King T.A., de Stanchina E., Spriggs D.R., Heguy A., Taylor B.S., Sander C., Rosen N., Levine D.A., Solit D.B.

Genomic complexity and AKT dependence in serous ovarian cancer.

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PubMed=22336246; DOI=10.1016/j.bmc.2012.01.017

Kong D.-X., Yamori T.

JFCR39, a panel of 39 human cancer cell lines, and its application in the discovery and development of anticancer drugs.

Bioorg. Med. Chem. 20:1947-1951(2012)


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Ruan X.-Y., Kocher J.-P.A., Pommier Y., Liu H.-F., Reinhold W.C.

Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap trios, and relation to fragile site location.

PLoS ONE 7:E31628-E31628(2012)


PubMed=22384151; DOI=10.1371/journal.pone.0032096; PMCID=PMC3285665

Lee J.-S., Kim Y.K., Kim H.J., Hajar S., Tan Y.L., Kang N.-Y., Ng S.H., Yoon C.N., Chang Y.-T.

Identification of cancer cell-line origins using fluorescence image-based phenomic screening.

PLoS ONE 7:E32096-E32096(2012)


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.

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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)


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Rahman M., Nakayama K., Rahman M.T., Nakayama N., Ishikawa M., Katagiri A., Iida K., Nakayama S., Otsuki Y., Shih I.-M., Miyazaki K.

Clinicopathologic and biological analysis of PIK3CA mutation in ovarian clear cell carcinoma.

Hum. Pathol. 43:2197-2206(2012)


PubMed=22710073; DOI=10.1016/j.ygyno.2012.06.017; PMCID=PMC3432677

Korch C.T., Spillman M.A., Jackson T.A., Jacobsen B.M., Murphy S.K., Lessey B.A., Jordan V.C., Bradford A.P.

DNA profiling analysis of endometrial and ovarian cell lines reveals misidentification, redundancy and contamination.

Gynecol. Oncol. 127:241-248(2012)


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Stordal B., Timms K., Farrelly A., Gallagher D., Busschots S., Renaud M., Thery J., Williams D., Potter J., Tran T., Korpanty G., Cremona M., Carey M.S., Li J., Li Y., Aslan O., O'Leary J.J., Mills G.B., Hennessy B.T.

BRCA1/2 mutation analysis in 41 ovarian cell lines reveals only one functionally deleterious BRCA1 mutation.

Mol. Oncol. 7:567-579(2013)


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Domcke S., Sinha R., Levine D.A., Sander C., Schultz N.

Evaluating cell lines as tumour models by comparison of genomic profiles.

Nat. Commun. 4:2126.1-2126.10(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=24023729; DOI=10.1371/journal.pone.0072162; PMCID=PMC3762837

Anglesio M.S., Wiegand K.C., Melnyk N., Chow C., Salamanca C.M., Prentice L.M., Senz J., Yang W., Spillman M.A., Cochrane D.R., Shumansky K., Shah S.P., Kalloger S.E., Huntsman D.G.

Type-specific cell line models for type-specific ovarian cancer research.

PLoS ONE 8:E72162-E72162(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=24434149; DOI=10.1016/j.bbrc.2013.12.070

Sinha A., Ignatchenko V., Ignatchenko A., Mejia-Guerrero S., Kislinger T.

In-depth proteomic analyses of ovarian cancer cell line exosomes reveals differential enrichment of functional categories compared to the NCI 60 proteome.

Biochem. Biophys. Res. Commun. 445:694-701(2014)


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=25230021; DOI=10.1371/journal.pone.0103988; PMCID=PMC4167545

Beaufort C.M., Helmijr J.C.A., Piskorz A.M., Hoogstraat M., Ruigrok-Ritstier K., Besselink N., Murtaza M., van IJcken W.F.J., Heine A.A.J., Smid M., Koudijs M.J., Brenton J.D., Berns E.M.J.J., Helleman J.

Ovarian cancer cell line panel (OCCP): clinical importance of in vitro morphological subtypes.

PLoS ONE 9:E103988-E103988(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=25846456; DOI=10.3892/ijo.2015.2951

Takenaka M., Saito M., Iwakawa R., Yanaihara N., Saito M., Kato M., Ichikawa H., Shibata T., Yokota J., Okamoto A., Kohno T.

Profiling of actionable gene alterations in ovarian cancer by targeted deep sequencing.

Int. J. Oncol. 46:2389-2398(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=26169745; DOI=10.1186/s12967-015-0576-z; PMCID=PMC4499939

Halama A., Guerrouahen B.S., Pasquier J., Diboun I., Karoly E.D., Suhre K., Rafii A.

Metabolic signatures differentiate ovarian from colon cancer cell lines.

J. Transl. Med. 13:223.1-223.12(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=26668597; DOI=10.3892/etm.2015.2836; PMCID=PMC4665172

Ruan Z.-Y., Liu J.-H., Kuang Y.-P.

Isolation and characterization of side population cells from the human ovarian cancer cell line SK-OV-3.

Exp. Ther. Med. 10:2071-2078(2015)


PubMed=26925792; DOI=10.4149/315_150930N510

Saczko J., Pilat J., Choromanska A., Rembialkowska N., Bar J.K., Deszcz I., Zalewski J., Kulbacka J.

The effectiveness of chemotherapy and electrochemotherapy on ovarian cell lines in vitro.

Neoplasma 63:450-455(2016)


PubMed=27235858; DOI=10.1016/j.ygyno.2016.05.028; PMCID=PMC4961516

Hernandez L., Kim M.K., Lyle L.T., Bunch K.P., House C.D., Ning F., Noonan A.M., Annunziata C.M.

Characterization of ovarian cancer cell lines as in vivo models for preclinical studies.

Gynecol. Oncol. 142:332-340(2016)


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=28273451; DOI=10.1016/j.celrep.2017.02.028

Medrano M., Communal L., Brown K.R., Iwanicki M., Normand J., Paterson J., Sircoulomb F., Krzyzanowski P.M., Novak M., Doodnauth S.A., Suarez Saiz F.J., Cullis J., Al-awar R., Neel B.G., McPherson J., Drapkin R.I., Ailles L., Mes-Masson A.-M., Rottapel R.

Interrogation of functional cell-surface markers identifies CD151 dependency in high-grade serous ovarian cancer.

Cell Rep. 18:2343-2358(2017)


PubMed=30485824; DOI=10.1016/j.celrep.2018.10.096; PMCID=PMC6481945

Papp E., Hallberg D., Konecny G.E., Bruhm D.C., Adleff V., Noe M., Kagiampakis I., Palsgrove D., Conklin D., Kinose Y., White J.R., Press M.F., Drapkin R.I., Easwaran H., Baylin S.B., Slamon D.J., Velculescu V.E., Scharpf R.B.

Integrated genomic, epigenomic, and expression analyses of ovarian cancer cell lines.

Cell Rep. 25:2617-2633(2018)


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

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

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

Cancer Res. 79:1263-1273(2019)


PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103

Ghandi M., Huang F.W., Jane-Valbuena J., Kryukov G.V., Lo C.C., McDonald E.R. 3rd, Barretina J.G., Gelfand E.T., Bielski C.M., Li H.-X., Hu K., Andreev-Drakhlin A.Y., Kim J., Hess J.M., Haas B.J., Aguet F., Weir B.A., Rothberg M.V., Paolella B.R., Lawrence M.S., Akbani R., Lu Y.-L., Tiv H.L., Gokhale P.C., de Weck A., Mansour A.A., Oh C., Shih J., Hadi K., Rosen Y., Bistline J., Venkatesan K., Reddy A., Sonkin D., Liu M., Lehar J., Korn J.M., Porter D.A., Jones M.D., Golji J., Caponigro G., Taylor J.E., Dunning C.M., Creech A.L., Warren A.C., McFarland J.M., Zamanighomi M., Kauffmann A., Stransky N., Imielinski M., Maruvka Y.E., Cherniack A.D., Tsherniak A., Vazquez F., Jaffe J.D., Lane A.A., Weinstock D.M., Johannessen C.M., Morrissey M.P., Stegmeier F., Schlegel R., Hahn W.C., Getz G., Mills G.B., Boehm J.S., Golub T.R., Garraway L.A., Sellers W.R.

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Nature 569:503-508(2019)"


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