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U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜,U251 cells
  • U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜,U251 cells
  • U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜,U251 cells
  • U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜,U251 cells

U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜

價格 詢價
包裝 1000000Cells/瓶 2000000Cells/瓶
最小起訂量 1000000Cells/瓶
發(fā)貨地 上海
文件下載 檢測報告COA
更新日期 2025-02-09
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜英文名稱:U251 cells
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: U251人膠質(zhì)瘤細(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: 詳見細(xì)胞說明書
應(yīng)用: 詳見細(xì)胞說明書貨號: 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: 人源或其它動物來源等
保質(zhì)期: 可長期保存(液氮低溫凍存)
2025-02-09 U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜 U251 cells 1000000Cells/瓶/1RMB;2000000Cells/瓶/1RMB 1 ATCC、DSMZ等 美國、歐洲、德國等 低溫避光 U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜 ATCC細(xì)胞庫

"U251人膠質(zhì)瘤細(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)胞培養(yǎng)經(jīng)驗分享】啟蒙老師的重要性:一般進(jìn)實驗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)會他們的正確操作,在第一次的時候就要重視。像養(yǎng)孩子一樣養(yǎng)細(xì)胞,細(xì)胞有時真的很脆弱,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,也好及時解決這些意外,避免重復(fù)實驗帶來的更大痛苦。好細(xì)胞要及時保種: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,不同細(xì)胞系使用不同的培養(yǎng)基和血清。

換液周期:每周2-3次

L-M (TK-) 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:Sp2/0細(xì)胞、SKGT2細(xì)胞、SKG IIIa細(xì)胞

GM03570E 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:SU-DHL-2細(xì)胞、WM-239A細(xì)胞、Lu-165細(xì)胞

H1563 Cells;背景說明: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次。;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:GM00346細(xì)胞、T98細(xì)胞、MT2細(xì)胞

U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息:最初是從一名患有惡性膠質(zhì)瘤的患者的腦組織中分離并培養(yǎng)的。是一種人膠質(zhì)瘤細(xì)胞系,表達(dá)多種膠質(zhì)瘤標(biāo)志蛋白,如膠質(zhì)纖維酸性蛋白(GFAP)、巢蛋白(Nestin)、神經(jīng)細(xì)胞黏附分子(NCAM)和SALL4。

┈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】┈Q┈Q:3┈1┈8┈0┈8┈0┈7┈3┈2┈4;

貼壁細(xì)胞(adherent cells):該類細(xì)胞的生長必須有可以貼附的支持物表面,細(xì)胞依靠自身分泌的或培養(yǎng)基中提供的貼附因子才能在該表面上生長,繁殖;當(dāng)細(xì)胞在該表面生長后,一般形成兩種形態(tài),即成纖維樣細(xì)胞性或上皮樣細(xì)胞;其生長過程分為游離期、貼壁期、潛伏期、對數(shù)期、平臺期和衰退期。懸浮細(xì)胞(suspension cell):不貼附于生長物,細(xì)胞呈圓形,呈單個細(xì)胞或者細(xì)小細(xì)胞團(tuán),懸浮細(xì)胞生長空間大,傳代方便,能夠大量增殖。

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

U251人膠質(zhì)瘤細(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

IPLB-SF 21 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:HITT15細(xì)胞、RIN Cl-5F細(xì)胞、CLL-CII細(xì)胞

MEG01 Cells;背景說明:MEG-01細(xì)胞株源自一位CML患者成巨核細(xì)胞轉(zhuǎn)換期的骨髓細(xì)胞。細(xì)胞質(zhì)因子VIII和表面球蛋白IIb/IIIa,-Schiff(PAS)反應(yīng),α醋酸酯酶和酸性酶陽性。髓過氧化物酶,α酯酶,化醋酸AS-D酯酶和堿性酶陰性。用單克隆抗體BA-1(抗B細(xì)胞,粒性白細(xì)胞),HPL-3(抗球蛋白IIb/IIIa)和20.3(抗單核細(xì)胞,血小板)染色成陽性。其他淋巴和骨髓類抗體成陰性。;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)胞樣;相關(guān)產(chǎn)品有:OVCAR4細(xì)胞、Hs706T細(xì)胞、Murine Long bone Osteocyte-Y4細(xì)胞

Large Cell Lung Cancer-103H 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:WPMY-1細(xì)胞、A2780CP細(xì)胞、NCI-SNU-423細(xì)胞

McARH7777 Cells;背景說明:肝癌;雌性;Buffalo;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:NCIADR.RES細(xì)胞、MRCV細(xì)胞、MASMC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】┈Q┈Q:3┈1┈8┈0┈8┈0┈7┈3┈2┈4;

形態(tài)特性:成纖維細(xì)胞樣

正確的細(xì)胞復(fù)蘇需知事項:細(xì)胞凍存HAO了,接下來要注意什么問題呢?沒錯,就是記得到時間了,拿出來復(fù)蘇。那么,細(xì)胞復(fù)蘇的過程中又有哪些該注意的事項呢?細(xì)胞活力和形態(tài)檢查的作用何在?活力檢查——千萬不要使用不健康的細(xì)胞,可能有污染(真菌、支原體等),如果發(fā)現(xiàn)有污染毫不猶豫的丟棄!形態(tài)檢查——檢查細(xì)胞的固有形態(tài)和生長行為。凍存細(xì)胞:補充新的培養(yǎng)——在您開始凍存細(xì)胞的前一天補充新的培養(yǎng)。在細(xì)胞長至70%單層時收獲細(xì)胞,計數(shù)活細(xì)胞數(shù),用凍存調(diào)整細(xì)胞密度~5 x106  s/ml (根據(jù)不同的細(xì)胞類型調(diào)整);凍存——用凍存洗細(xì)胞并用凍存重懸細(xì)胞,有不同類型的凍存,根據(jù)細(xì)胞類型選擇Zui合適的凍存(常用的凍存成分有):5-10% DMSO——注意確保DMSO不含有其他的毒性物質(zhì);5-15%甘油;如果細(xì)胞在無血清培養(yǎng)基內(nèi)生長,應(yīng)在50%條件培養(yǎng)基內(nèi)(細(xì)胞在無血清培養(yǎng)基內(nèi)生長24小時)內(nèi)凍存和復(fù)蘇。在凍存管上標(biāo)記HAO細(xì)胞類型,日期,凍存人等信息,并保證每凍存管不超過1.5ml。放入罐之前記錄凍存管的數(shù)量和位置。以Zui快的速度轉(zhuǎn)移凍存管知罐內(nèi),因此,此步驟ZuiHAO使用干冰,或者把凍存管浸入裝有的小盒內(nèi)。此外還要注意,在凍存管上沒有足夠的空間記錄細(xì)胞的詳細(xì)信息,做HAO記錄是非常非常重要的!還有一個Zui重要的,一定要在異地的罐內(nèi)保存同樣的一份細(xì)胞,以免其中的一個罐出現(xiàn)問題!細(xì)胞正確的復(fù)蘇方式和正確的凍存方式同樣重要,熟記以下要點:當(dāng)從罐內(nèi)取出細(xì)胞時,有可能會出現(xiàn)凍存管破裂的情況,使用保護(hù)面罩和防護(hù)服十分必要;其實,細(xì)胞復(fù)蘇只是一個簡單的實驗,不過這其中卻不可避免有一些需要注意的細(xì)節(jié),不然,也不一定會盡如人意。例如說,人身健康方面:一定要記得做HAO防凍工作,戴上護(hù)目鏡;盡量降低DMSO對細(xì)胞的損傷等等。

Chang Cells 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:Z138細(xì)胞、G-361細(xì)胞、KYSE450細(xì)胞

BC-028 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:FHC細(xì)胞、H446細(xì)胞、IAR20細(xì)胞

NCIH196 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:6傳代;每周換液2-3次。;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:YES 2細(xì)胞、AZ521細(xì)胞、ZR75-1細(xì)胞

HIT T15 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:SuDHL 8細(xì)胞、DH82細(xì)胞、TCMK-1細(xì)胞

SKNFI Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4傳代,每周換液2次;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:Acanthosis Nigricans 3rd attempt-CArcinoma細(xì)胞、NCI-H1155細(xì)胞、WBF344細(xì)胞

CC-LP-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:HCC-2279細(xì)胞、TE-11細(xì)胞、HEC1B細(xì)胞

P3-NS1/1-Ag4-1 Cells;背景說明:這是P3X63Ag8(ATCCTIB-9)的一個不分泌克隆。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:NHLF細(xì)胞、NCI-H524細(xì)胞、Caco 2細(xì)胞

KU1919 Cells;背景說明:膀胱癌;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:MC9細(xì)胞、NMC-G1細(xì)胞、Panc 04.03細(xì)胞

BEND Cells;背景說明:子宮內(nèi)膜;上皮細(xì)胞;雌性;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:SJ-Rh 30細(xì)胞、HBMEC細(xì)胞、MOLP-2細(xì)胞

T2 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,每周換液2—3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-38細(xì)胞、Mel-624細(xì)胞、Hs-695-T細(xì)胞

DLD1 Cells;背景說明:DLD-1是1977-1979年間D.L.Dexter和同事分離的兩株結(jié)直腸腺癌細(xì)胞株中的一株。在ATCC和其它地方進(jìn)行的DNAfingerprinting和染色體組型分析表明這株細(xì)胞與HCT-15(CCL-225)相似,說明這兩者是來自同一個人的不同克隆。他們的遺傳起源可通過DNAfingerprinting證實,但染色體組型分析顯示它們?nèi)狈θ旧w標(biāo)記一致改變或數(shù)目上一致改變。細(xì)胞的CSAp陰性(CSAp-)。DLD-1細(xì)胞的p53抗原表達(dá)呈陽性(p53抗原產(chǎn)生了一個C->;傳代方法:消化5分鐘。1:2。4-5天長滿。;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:AgC11x3A細(xì)胞、Roswell Park Memorial Institute 1846細(xì)胞、Mahlavu細(xì)胞

UMNSAH-DF1 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:成纖維母細(xì)胞樣;相關(guān)產(chǎn)品有:PC10細(xì)胞、BE(2)-M17細(xì)胞、CAL-12T細(xì)胞

GAK Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:8.4 x 10^4 cells / sq.cm.;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:RSC-364細(xì)胞、C-28I2細(xì)胞、SVEC4-10細(xì)胞

GCT0404 Cells;背景說明:骨巨細(xì)胞瘤;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:HS766T細(xì)胞、Roswell Park Memorial Institute 1788細(xì)胞、SL1細(xì)胞

UCH1 Cells;背景說明:骶骨脊索瘤;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:HBZY1細(xì)胞、H-650細(xì)胞、P3J HR1-K細(xì)胞

Tu686 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:UCLA-RO 81細(xì)胞、SUM102細(xì)胞、RPMI8402細(xì)胞

C127 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:M 1細(xì)胞、PTK 1細(xì)胞、TE6細(xì)胞

18b Cells(提供STR鑒定圖譜)

Abcam HeLa LIF KO Cells(提供STR鑒定圖譜)

AG23105 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRF552 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XG757 Cells(提供STR鑒定圖譜)

C0814 Cells(提供STR鑒定圖譜)

CW60418 Cells(提供STR鑒定圖譜)

DA05667 Cells(提供STR鑒定圖譜)

GL15 Cells(提供STR鑒定圖譜)

J-774A.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:CEM-CCRF細(xì)胞、OCI-Ly 19細(xì)胞、PC12(高分化)細(xì)胞

U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜

WEHI 3 Cells;背景說明:白血??;BALB/c;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:NCI-H292細(xì)胞、Hs27F細(xì)胞、Clone 15 HL-60細(xì)胞

HAEC Cells;背景說明:主動脈;內(nèi)皮 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:Baby Hamster Kidney 21細(xì)胞、A-72細(xì)胞、DU4475細(xì)胞

RPTEC/TERT 1 Cells;背景說明:腎;近端小管上皮;HGNC-TERT轉(zhuǎn)化;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:RFL6細(xì)胞、NCIH1568細(xì)胞、Psi2 DAP細(xì)胞

BE(2)-C Cells;背景說明:神經(jīng)母細(xì)胞瘤;骨髓轉(zhuǎn)移;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:NCI-H209細(xì)胞、MESSA/Dx5細(xì)胞、COLO679細(xì)胞

NCI-H1437 Cells;背景說明: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次。;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:H2141細(xì)胞、MV 3細(xì)胞、KBM-7/Hap8細(xì)胞

211F3 Cells(提供STR鑒定圖譜)

SKM1 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:QBC-939細(xì)胞、KBM-5細(xì)胞、NCIH647細(xì)胞

PC 61-5-3 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:GM637細(xì)胞、NIH-3T3細(xì)胞、BNL.CL2細(xì)胞

KMST-6 Cells;背景說明:胚成纖維細(xì)胞;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:DF-1細(xì)胞、TK+/- (clone 3.7.2C)細(xì)胞、NCIH441細(xì)胞

NCI-H711 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:P3/X63/Ag8細(xì)胞、BEL-7405細(xì)胞、EoL-1-cell細(xì)胞

H4IIE 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:H-1975細(xì)胞、M109細(xì)胞、C4I細(xì)胞

SW1088 Cells;背景說明:星形膠質(zhì)瘤;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:P3X63NS1細(xì)胞、SUDHL-2細(xì)胞、SW-1573細(xì)胞

HPAF2 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:EB-2細(xì)胞、NCI-H1373細(xì)胞、NCIH358細(xì)胞

HBL1 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:U2-OS細(xì)胞、VSMC細(xì)胞、D324細(xì)胞

h1RPE7 Cells(提供STR鑒定圖譜)

HAP1 PUSL1 (-) 2 Cells(提供STR鑒定圖譜)

32D clone3 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:A9細(xì)胞、4T1-A細(xì)胞、PANC-02-03細(xì)胞

HCT116 Cells;背景說明:結(jié)腸腺癌;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:Rat podocyte細(xì)胞、MKN 45細(xì)胞、SK-N-BE(2)C細(xì)胞

MMVECs Cells;背景說明:心肌微血管;內(nèi)皮 Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MFE 280細(xì)胞、MOLT16細(xì)胞、JIMT1細(xì)胞

Hx147 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:343 MG細(xì)胞、BJAB細(xì)胞、COLO 394細(xì)胞

MOLT3 Cells;背景說明:急性T淋巴細(xì)胞白血?。荒行?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:NCI-H660細(xì)胞、P3 (Jiyoye)細(xì)胞、293 c18細(xì)胞

KASUMI6 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每周2-3次。;生長特性:懸浮生長;形態(tài)特性:成髓細(xì)胞;相關(guān)產(chǎn)品有:NCIH1435細(xì)胞、OCI/AML-3細(xì)胞、RMG1細(xì)胞

C-4-I Cells;背景說明:宮頸鱗癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Capan2細(xì)胞、beta-TC6細(xì)胞、Jijoye細(xì)胞

DBTRG-05MG Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:6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;相關(guān)產(chǎn)品有:EBTr細(xì)胞、HB611細(xì)胞、NCI-SNU-216細(xì)胞

HuH7-SLC22A9-KO-c5 Cells(提供STR鑒定圖譜)

L1210/TZR Cells(提供STR鑒定圖譜)

MSY00350IN Cells(提供STR鑒定圖譜)

OKT4 Cells(提供STR鑒定圖譜)

Royan C29 Cells(提供STR鑒定圖譜)

UAB-iPSC-PKD2-cKO NP/null #1 Cells(提供STR鑒定圖譜)

UMGi140-A Cells(提供STR鑒定圖譜)

HG02061 Cells(提供STR鑒定圖譜)

Mel RM Cells;背景說明:黑色素瘤;神經(jīng)節(jié)轉(zhuǎn)移;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長特性:貼壁;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MFC細(xì)胞、HEK-293-F細(xì)胞、H2135細(xì)胞

RPMI6666 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:CCRF/CEM-C7細(xì)胞、MPP89細(xì)胞、DH 82細(xì)胞

H22 Cells;背景說明:1952年,前蘇聯(lián)醫(yī)學(xué)科學(xué)院腫瘤研究所以C3HA小鼠誘發(fā)的H22肝癌實體瘤的瘤細(xì)胞懸液,昆明種小鼠皮下移植后,轉(zhuǎn)腹水瘤。經(jīng)檢測,該瘤株在Km小鼠、615小鼠、C57BL/6小鼠、BALB/C小鼠體內(nèi)可以形成實體瘤和腹水瘤。;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:KYSE 70細(xì)胞、Y3Ag1.2.3細(xì)胞、Glioma 261細(xì)胞

H-1755 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:NCIH2342細(xì)胞、COLO-680N細(xì)胞、OCI-AML-3細(xì)胞

HLF-a 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:TW01細(xì)胞、MDAMB330細(xì)胞、COLO.205細(xì)胞

HLF-a 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:TW01細(xì)胞、MDAMB330細(xì)胞、COLO.205細(xì)胞

SBC-3 Cells;背景說明:小細(xì)胞肺癌;骨髓轉(zhuǎn)移;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:HCC4006細(xì)胞、NCIH716細(xì)胞、RM-1細(xì)胞

GC1-SPG Cells;背景說明:精原細(xì)胞;SV40轉(zhuǎn)化;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:SaOS-2細(xì)胞、SUM149-PT細(xì)胞、H-1048細(xì)胞

CT26WT Cells;背景說明:CT26細(xì)胞是被N-亞硝基-N-甲基脲烷(NNMU)誘導(dǎo)得到的未分化的小鼠結(jié)腸癌細(xì)胞,該細(xì)胞的一個克隆形成的細(xì)胞系被命名為CT26.WT。CT26.WT被逆轉(zhuǎn)錄病毒載體LXSN穩(wěn)定轉(zhuǎn)化形成了一個致死性的亞克隆CT26.CL25,這一病毒載體含有l(wèi)acZ基因、編碼腫瘤相關(guān)抗原(TAA)和beta半乳糖苷酶。CT26.WT和CT26.CL25細(xì)胞在小鼠中生長速度和致死率都很相似,不同的是CT26.CL25細(xì)胞可以表達(dá)腫瘤相關(guān)抗原和beta半乳糖苷酶,因此這兩株細(xì)胞可以聯(lián)合用于免疫治療和宿主免疫反應(yīng)的研究。 ;傳代方法:1:4-1:10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:RAW-264.7細(xì)胞、hRMECs細(xì)胞、P3JHR-1細(xì)胞

SKG IIIa 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:HS578T細(xì)胞、NIH:OVCAR-3細(xì)胞、WEHI 3細(xì)胞

HITT15 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:CNE-1細(xì)胞、Lu-65細(xì)胞、HR-1細(xì)胞

HLEC 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:50.B1細(xì)胞、HEK293A細(xì)胞、KE-39細(xì)胞

CCRF-CEM/S Cells;背景說明:G.E. Foley 等人建立了類淋巴母細(xì)胞細(xì)胞株CCRF-CEM。 細(xì)胞是1964年11月從一位四歲白人女性急性淋巴細(xì)胞白血病患者的外周血白血球衣中得到。此細(xì)胞系從香港收集而來。;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)胞樣;相關(guān)產(chǎn)品有:Panc05.04細(xì)胞、PANC0403細(xì)胞、MLOY4細(xì)胞

NCIH2196 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;每周換液2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:HCT/Taxo1細(xì)胞、CAOV4細(xì)胞、RKO_AS45細(xì)胞

231-luc 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:BTT739細(xì)胞、HCC-2185細(xì)胞、RPE1-hTERT細(xì)胞

t-HUE4 Cells(提供STR鑒定圖譜)

Mink Lung 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:NCI-H1915細(xì)胞、HCC-44細(xì)胞、LNCaP clone FGC細(xì)胞

NCIH196 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:4-1:6傳代;每周換液2-3次。;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:YES 2細(xì)胞、AZ521細(xì)胞、ZR75-1細(xì)胞

MZCRC1 Cells;背景說明:甲狀腺髓樣癌;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:PNT-1A細(xì)胞、YD15細(xì)胞、HLF-a細(xì)胞

H-1522 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:KNS-42細(xì)胞、CAL-78細(xì)胞、Hs 766.T細(xì)胞

U-251 MG Cells;背景說明: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。;生長特性:貼壁;形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:AML-EOL-1細(xì)胞、AMO1細(xì)胞、PC615.3細(xì)胞

B35 Cells;背景說明:神經(jīng)母細(xì)胞瘤;BDIX;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:HT-3細(xì)胞、NCI-H1688細(xì)胞、MeT-5A細(xì)胞

U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送STR圖譜

OCI-Ly18 Cells;背景說明:彌漫大B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。;生長特性:懸浮;形態(tài)特性:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:HCC9724細(xì)胞、C-643細(xì)胞、LoVo細(xì)胞

NCIH1694 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:3-4天換液1次。;生長特性:懸浮生長;形態(tài)特性:聚團(tuán)懸浮;相關(guān)產(chǎn)品有:GC1-SPG細(xì)胞、S3-HeLa細(xì)胞、Hs 636 T細(xì)胞

SO-RB50 Cells;背景說明:視網(wǎng)膜母細(xì)胞瘤;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:U118-MG細(xì)胞、NP69SV40T細(xì)胞、H-660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,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,同時在注射部位形成始發(fā)灶。誘導(dǎo)轉(zhuǎn)移時不需要摘除始發(fā)灶。4T1細(xì)胞在BALB/c小鼠中的生長與轉(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)也可以在許多遠(yuǎn)端器官中檢測到。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)可長滿;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:BSC40細(xì)胞、8402細(xì)胞、Giant Cell Tumor細(xì)胞

GM01232E Cells;背景說明:1971年1月,該細(xì)胞由ReidTW及其同事從病人右眼切除的腫瘤進(jìn)行原代培養(yǎng)建立而成,此病人有很強的視網(wǎng)膜母細(xì)胞瘤的母系家族遺傳性。該細(xì)胞的超微結(jié)構(gòu),如核膜內(nèi)折、三層膜結(jié)構(gòu)、大的被膜小泡、環(huán)孔板、微管、中心粒、基粒等都與原始腫瘤相似。;傳代方法:1:2傳代;生長特性:懸浮生長;形態(tài)特性:圓形,成簇生長;相關(guān)產(chǎn)品有:P3.times.63 Ag8.653細(xì)胞、FL-83B細(xì)胞、NCTC-929細(xì)胞

A431 Cells;背景說明:該細(xì)胞源自一位患有皮膚鱗狀細(xì)胞癌的85歲女性,是GiardDJ等人建立的一系列細(xì)胞株中的一株。該細(xì)胞在免疫抑制小鼠體內(nèi)可成瘤,在瓊脂上培養(yǎng)可形成克??;是一個超三倍體人細(xì)胞株。;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:HS688AT細(xì)胞、HEC-1-A細(xì)胞、DH 82細(xì)胞

RAW-264.7 Cells;背景說明:單核巨噬細(xì)胞白血??;雄性;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:MHHCALL2細(xì)胞、SF-763細(xì)胞、MFM223細(xì)胞

P3-X63-Ag8 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:DHL4細(xì)胞、H661細(xì)胞、SKRC-20細(xì)胞

BayGenomics ES cell line RRR472 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTA004 Cells(提供STR鑒定圖譜)

HyCyte B16-F10-Luc Cells(提供STR鑒定圖譜)

PCRP-JAZF1-1C2 Cells(提供STR鑒定圖譜)

GFP2 Cells(提供STR鑒定圖譜)

HPSI0115i-iuad_3 Cells(提供STR鑒定圖譜)

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Saigusa K., Hashimoto N., Tsuda H., Yokoi S., Maruno M., Yoshimine T., Aoyagi M., Ohno K., Imoto I., Inazawa J.

Overexpressed Skp2 within 5p amplification detected by array-based comparative genomic hybridization is associated with poor prognosis of glioblastomas.

Cancer Sci. 96:676-683(2005)


PubMed=16391870; DOI=10.3892/or.15.2.463

Castigli E., Sciaccaluga M., Schiavoni G., Brozzi F., Fabiani R., Gorello P., Gianfranceschi G.L.

GL15 and U251 glioblastoma-derived human cell lines are peculiarly susceptible to induction of mitotic death by very low concentrations of okadaic acid.

Oncol. Rep. 15:463-470(2006)


PubMed=16697959; DOI=10.1016/j.ccr.2006.03.030

Lee J., Kotliarova S., Kotliarov Y., Li A.-G., Su Q., Donin N.M., Pastorino S., Purow B.W., Christopher N., Zhang W., Park J.K., Fine H.A.

Tumor stem cells derived from glioblastomas cultured in bFGF and EGF more closely mirror the phenotype and genotype of primary tumors than do serum-cultured cell lines.

Cancer Cell 9:391-403(2006)


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.

Mol. Cancer Ther. 5:2606-2612(2006)


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Rieger J., Frank B., Weller M., Wick W.

Mechanisms of resistance of human glioma cells to Apo2 ligand/TNF-related apoptosis-inducing ligand.

Cell. Physiol. Biochem. 20:23-34(2007)


PubMed=19372543; DOI=10.1158/1535-7163.MCT-08-0921; PMCID=PMC4020356

Lorenzi P.L., Reinhold W.C., Varma S., Hutchinson A.A., Pommier Y., Chanock S.J., Weinstein J.N.

DNA fingerprinting of the NCI-60 cell line panel.

Mol. Cancer Ther. 8:713-724(2009)


PubMed=19435942; DOI=10.1215/15228517-2009-025; PMCID=PMC2743214

Ichimura K., Pearson D.M., Kocialkowski S., Backlund L.M., Chan R., Jones D.T.W., Collins V.P.

IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas.

Neuro-oncol. 11:341-347(2009)


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=20593219; DOI=10.1007/s11060-010-0283-9

Blough M.D., Beauchamp D.C., Westgate M.R., Kelly J.J.P., Cairncross J.G.

Effect of aberrant p53 function on temozolomide sensitivity of glioma cell lines and brain tumor initiating cells from glioblastoma.

J. Neurooncol. 102:1-7(2011)


PubMed=22068913; DOI=10.1073/pnas.1111840108; PMCID=PMC3219108

Gillet J.-P., Calcagno A.M., Varma S., Marino M., Green L.J., Vora M.I., Patel C., Orina J.N., Eliseeva T.A., Singal V., Padmanabhan R., Davidson B., Ganapathi R., Sood A.K., Rueda B.R., Ambudkar S.V., Gottesman M.M.

Redefining the relevance of established cancer cell lines to the study of mechanisms of clinical anti-cancer drug resistance.

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


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)


PubMed=22347499; DOI=10.1371/journal.pone.0031628; PMCID=PMC3276511

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=22570425; DOI=10.1093/neuonc/nos072; PMCID=PMC3367844

Bady P., Diserens A.-C., Castella V., Kalt S., Heinimann K., Hamou M.-F., Delorenzi M., Hegi M.E.

DNA fingerprinting of glioma cell lines and considerations on similarity measurements.

Neuro-oncol. 14:701-711(2012)


PubMed=22628656; DOI=10.1126/science.1218595; PMCID=PMC3526189

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=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=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=24810477; DOI=10.1002/cam4.219; PMCID=PMC4303149

Torsvik A., Stieber D., Enger P.O., Golebiewska A., Molven A., Svendsen A., Westermark B., Niclou S.P., Olsen T.K., Chekenya Enger M., Bjerkvig R.

U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells.

Cancer Med. 3:812-824(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=25894527; DOI=10.1371/journal.pone.0121314; PMCID=PMC4404347

Bausch-Fluck D., Hofmann A., Bock T., Frei A.P., Cerciello F., Jacobs A., Moest H., Omasits U., Gundry R.L., Yoon C., Schiess R., Schmidt A., Mirkowska P., Hartlova A.S., Van Eyk J.E., Bourquin J.-P., Aebersold R., Boheler K.R., Zandstra P.W., Wollscheid B.

A mass spectrometric-derived cell surface protein atlas.

PLoS ONE 10:E0121314-E0121314(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=27582061; DOI=10.1126/scitranslmed.aaf6853

Allen M., Bjerke M., Edlund H., Nelander S., Westermark B.

Origin of the U87MG glioma cell line: good news and bad news.

Sci. Transl. Med. 8:354re3.1-354re3.4(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=29716531; DOI=10.1186/s12885-018-4394-6; PMCID=PMC5930953

Hegge B., Sjottem E., Mikkola I.

Generation of a PAX6 knockout glioblastoma cell line with changes in cell cycle distribution and sensitivity to oxidative stress.

BMC Cancer 18:496.1-496.19(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=30971826; DOI=10.1038/s41586-019-1103-9

Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Nature 568:511-516(2019)"


關(guān)鍵字: U251人膠質(zhì)瘤細(xì)胞代次低|培養(yǎng)基|送S;復(fù)蘇細(xì)胞系;細(xì)胞STR鑒定報告;細(xì)胞STR鑒定圖譜;ATCC|DSMZ細(xì)胞庫;

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