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Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Hs 578T
  • Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Hs 578T
  • Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Hs 578T
  • Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜,Hs 578T

Hs 578T人乳腺癌細(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 2025-02-10
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜英文名稱:Hs 578T
品牌: ATCC、DSMZ等產(chǎn)地: 美國(guó)、歐洲、德國(guó)等
保存條件: 低溫避光純度規(guī)格: Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜
產(chǎn)品類別: ATCC細(xì)胞庫(kù)
種屬: 詳見細(xì)胞說(shuō)明書組織: 詳見細(xì)胞說(shuō)明書
細(xì)胞系: 詳見細(xì)胞說(shuō)明書細(xì)胞形態(tài): 詳見細(xì)胞說(shuō)明書
生長(zhǎng)狀態(tài): 詳見細(xì)胞說(shuō)明書靶點(diǎn): 詳見細(xì)胞說(shuō)明書
應(yīng)用: 詳見細(xì)胞說(shuō)明書貨號(hào): 詳見細(xì)胞說(shuō)明書
規(guī)格: 1*10^6cells/T25(1瓶)或1ml凍存管(2支)是否進(jìn)口: 來(lái)源ATCC、DSMZ、ECACC等細(xì)胞庫(kù)
組織來(lái)源: 詳見細(xì)胞說(shuō)明書是否是腫瘤細(xì)胞: 詳見細(xì)胞說(shuō)明書
器官來(lái)源: 詳見細(xì)胞說(shuō)明書品系: 詳見細(xì)胞說(shuō)明書
免疫類型: 詳見細(xì)胞說(shuō)明書物種來(lái)源: 人源或其它動(dòng)物來(lái)源等
保質(zhì)期: 可長(zhǎng)期保存(液氮低溫凍存)
2025-02-10 Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 Hs 578T 1000000Cells/瓶/1RMB;2000000Cells/瓶/1RMB 1 ATCC、DSMZ等 美國(guó)、歐洲、德國(guó)等 低溫避光 Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜 ATCC細(xì)胞庫(kù)

"Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

傳代比例:1:2-1:4(首次傳代建議1:2)

生長(zhǎng)特性:貼壁生長(zhǎng)

細(xì)胞系的應(yīng)用:1)免疫組化研究2)RNA干擾研究3)藥物作用研究4)慢病毒轉(zhuǎn)染研究等其它應(yīng)用。細(xì)胞系通常用于實(shí)驗(yàn)研究,如增殖、遷移、侵襲等。細(xì)胞系在多個(gè)領(lǐng)域的研究中被廣泛應(yīng)用,包括基礎(chǔ)醫(yī)學(xué)、臨床試驗(yàn)、藥物篩選和分子生物學(xué)研究。這些研究不僅在中國(guó),也在日本、美國(guó)和歐洲等多個(gè)國(guó)家和地區(qū)進(jìn)行。

換液周期:每周2-3次

HCC-1806 Cells;背景說(shuō)明:該細(xì)胞源自一位患有乳腺髓樣癌的44歲黑人女性,表達(dá)WNT7B癌基因,細(xì)胞與細(xì)胞邊界處有細(xì)胞橋粒、微絨毛、張力細(xì)絲。;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:D324 Med細(xì)胞、RBL 2H3細(xì)胞、HCS2/8細(xì)胞

RWPE1 Cells;背景說(shuō)明:腫瘤抑制基因: p53 + [PubMed: 9214605] pRB + [PubMed: 9214605] 一位正常男性前列腺組織切片的周圍區(qū)域的上皮細(xì)胞用單拷貝的人乳頭瘤病毒的18(HPV-18)進(jìn)行轉(zhuǎn)化,建立了RWPE-1 (ATCC CRL-11609) 細(xì)胞株 [PubMed: 9214605]. 在三維Matrigel培養(yǎng)時(shí),在雄激素作用下,RWPE-1細(xì)胞形成腺胞并向培養(yǎng)基中分泌PSA。[PubMed: 11170142]. 當(dāng)與Matrigel或基質(zhì)細(xì)胞混合注射雄性裸鼠時(shí),RWPE-1細(xì)胞也能形成腺胞[PubMed: 11304724] 并產(chǎn)生PSA。 來(lái)源于RWPE-1的細(xì)胞再用Kirstin鼠類腫瘤病毒轉(zhuǎn)染Ki-ras基因,建立了能成瘤的RWPE-2細(xì)胞株(ATCC CRL-11610) [PubMed: 9214605] 和 RWPE2-W99 (ATCC CRL-2853) 細(xì)胞株。 另外,用N--N-(MNU)處理RWPE-1,建立了一系列模擬前列腺癌進(jìn)程中不同時(shí)期的成瘤細(xì)胞株。 它們是 WPE1-NA22 (ATCC CRL-2849), WPE1-NB14 (ATCC CRL-2850, WPE1-NB11 (ATCC CRL-2851) 和 WPE1-NB26 (ATCC CRL-2852) 細(xì)胞株。 據(jù)提供者報(bào)道,RWPE-1 細(xì)胞株(ATCC CRL-11609)經(jīng)過(guò)檢測(cè),乙肝、丙肝、人免疫缺陷病毒都呈陰性。;傳代方法:1:3傳代,2-3天傳一代。;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:Walker-256細(xì)胞、mIMCD3細(xì)胞、P3-X63-Ag8.653細(xì)胞

MV-4-11 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:OCILY-3細(xì)胞、SPC-A1細(xì)胞、UACC-893細(xì)胞

Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息:是一種來(lái)源于人的乳腺癌細(xì)胞系,最初從一名51歲女性患者的乳腺癌組織中分離得到。它與正常成纖維細(xì)胞樣細(xì)胞株Hs 578Bst起源于同一位患者。Hs 578T細(xì)胞最初是多角形的,但在傳代過(guò)程中選擇并克隆了星形的細(xì)胞形態(tài)。電鏡下觀察發(fā)現(xiàn),Hs 578T細(xì)胞內(nèi)酪蛋白顆粒聚集、橋粒緊密連接、脂質(zhì)體和光滑內(nèi)質(zhì)網(wǎng)小泡。Hs 578T細(xì)胞與Hs 578Bst細(xì)胞一樣,未檢測(cè)到雌激素受體和內(nèi)生病毒。

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

DSMZ菌株保藏中心成立于1969年,是德國(guó)的國(guó)家菌種保藏中心。該中心一直致力于細(xì)菌、真菌、質(zhì)粒、抗菌素、人體和動(dòng)物細(xì)胞、植物病毒等的分類、鑒定和保藏工作。DSMZ菌種保藏中心是歐洲規(guī)模最大的生物資源中心,保藏有動(dòng)物細(xì)胞500多株。Riken BRC成立于1920年,是英國(guó)的國(guó)家菌種保藏中心。該中心一直致力于細(xì)菌、真菌、植物病毒等的分類、鑒定和保藏工作。日本Riken BRC(Riken生物資源保藏中心)是全球三大典型培養(yǎng)物收集中心之一。Riken保藏中心提供了很多細(xì)胞系。在世界范圍內(nèi),這些細(xì)胞系,都在醫(yī)學(xué)、科學(xué)和獸醫(yī)中具有重要意義。Riken生物資源中心支持了各種學(xué)術(shù)、健康、食品和獸醫(yī)機(jī)構(gòu)的研究工作,并在世界各地不同組織的微生物實(shí)驗(yàn)室和研究機(jī)構(gòu)中使用。

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

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

Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來(lái)源:人源、鼠源等其它物種來(lái)源

SKNBE-1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SKOV-433細(xì)胞、BC3H-1細(xì)胞、JS1細(xì)胞

TN5B14 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MV4;11細(xì)胞、SKES-1細(xì)胞、F56 [Human neoplasm]細(xì)胞

SK-N-BE(2C) Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MOLP8細(xì)胞、INS1E細(xì)胞、LM2-4175細(xì)胞

Oka-C1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H-719細(xì)胞、NCI-H322細(xì)胞、HHFK細(xì)胞

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

形態(tài)特性:上皮細(xì)胞樣

貼壁細(xì)胞的消化方法介紹:1、胰酶。這是用得Zui多的。一般濃度在0.25-0.5%。作用時(shí)間根據(jù)細(xì)胞種類、作用溫度等因素而變化很大,從幾分鐘到幾十分鐘不等。0.25%的胰酶作用于單層貼壁的細(xì)胞,在37度條件下,一般消化1-5分鐘就足夠了。終止是用血清。主要作用于細(xì)胞間。配制時(shí)不能用含、鎂的平衡,否則影響活性。保存于-20度。2、膠原酶。這種方法比較少,一般是用原代培養(yǎng)時(shí),從組織消化下細(xì)胞。這種方法作用溫和,對(duì)細(xì)胞損傷較小,但是,價(jià)格也較貴。中止同樣是用血清。3、EDA。用得也是非常多。一般濃度在0.02%左右。作用于細(xì)胞與間質(zhì),對(duì)細(xì)胞間也有一定作用。注意,它能顯著影響pH值,而且在弱堿性條件下才易溶。因此,配制時(shí)應(yīng)調(diào)節(jié)HAO堿度。它不能被終和。因此,消化下來(lái)的細(xì)胞要洗一遍。4、商品化的無(wú)酶消化。個(gè)人的使用經(jīng)常覺(jué)得對(duì)細(xì)胞的損傷比較大,但是分離成單細(xì)胞懸的能力確實(shí)比較強(qiáng)。5、物理法。直接吹打或用細(xì)胞刮子將細(xì)胞刮下來(lái)。6、冷凍法。此方法僅能用于細(xì)胞傳代時(shí)。無(wú)法使組織上的細(xì)胞脫落下來(lái)。本方法的原理,我想是因細(xì)胞冷凍后收縮,從而從培養(yǎng)瓶上脫落下來(lái)。YOU點(diǎn)是:對(duì)細(xì)胞損傷小,不需要中止或洗細(xì)胞,方便,不需要另外配制消化。別適用那些貼壁不是別緊,又別嬌氣的細(xì)胞。不足是細(xì)胞常成小片脫落。此種方法曾用于因用其它方法傳代導(dǎo)致大量細(xì)胞死亡操作的間充質(zhì)干細(xì)胞、DC細(xì)胞的培養(yǎng),效果非常滿意。具體過(guò)程是:1、用較多的4度的PBS 洗滌一遍細(xì)胞(以6孔板為例,加1.5ml/孔),2、再加0.5毫升4度的PBS,靜置操作臺(tái)上,很快細(xì)胞就小片脫落,3、輕輕吹打,細(xì)胞即完全脫落,4、按一定比例傳代。

HPAF-II Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Reh細(xì)胞、DMS114細(xì)胞、A375-SM細(xì)胞

A704 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3—1:4傳代,每周換液2-3次;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:VP229細(xì)胞、HFLS細(xì)胞、Hs606細(xì)胞

MDA-MB-231-GFP Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:EJ細(xì)胞、LuCL4細(xì)胞、BTI-Tn-5B1-4細(xì)胞

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

RKO-AS-45-1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SGC996細(xì)胞、SuDHL 5細(xì)胞、Vero 76 clone E6細(xì)胞

CCD 966SK Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MS 751細(xì)胞、DHL8細(xì)胞、TGBC11TKB細(xì)胞

KE37 Cells;背景說(shuō)明:急性T淋巴細(xì)胞白血??;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(shuō)明書;相關(guān)產(chǎn)品有:H2107細(xì)胞、J111細(xì)胞、M14細(xì)胞

HCCC9810 Cells;背景說(shuō)明:HCCC-9810細(xì)胞株源自一位女性肝膽管細(xì)胞癌患者。 HCCC-9810細(xì)胞呈上皮細(xì)胞樣,染色體模式數(shù)為71,但染色體數(shù)目可以在22-117的范圍內(nèi)變動(dòng)。倍增時(shí)間為20.4小時(shí)。 AFP,CEA和CA19-9的分泌水平低,在裸鼠中的成瘤率為20%。;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:Hs 840.T細(xì)胞、MEL細(xì)胞、Human Lung Microvascular Endothelial Cell line-5a細(xì)胞

NCIH1781 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Jijoye細(xì)胞、NRK52E細(xì)胞、Sarcoma OSteogenic-2細(xì)胞

TE 354.T Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng) ;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:NFHIOSE-80細(xì)胞、EB-1細(xì)胞、RPMI 7951細(xì)胞

TE14 Cells;背景說(shuō)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:上皮樣;相關(guān)產(chǎn)品有:C3H/10T1/2 clone 8細(xì)胞、OVCAR10細(xì)胞、7404細(xì)胞

hTERT-HME-1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:293-EBNA細(xì)胞、HGF-1細(xì)胞、KOPN-8細(xì)胞

Ly18 Cells;背景說(shuō)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(zhǎng)特性:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:NCIH28細(xì)胞、TC-1 [Mouse lung]細(xì)胞、P3.times.63 Ag8.653細(xì)胞

MMAc-SF Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:HEB細(xì)胞、Kit-225-K6細(xì)胞、MB157細(xì)胞

Roswell Park Memorial Institute 7666 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:G-Olig2細(xì)胞、Centre Antoine Lacassagne-85-1細(xì)胞、Wistar Institute-38細(xì)胞

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

KP-4 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:ES-2細(xì)胞、IR983F細(xì)胞、P-19細(xì)胞

Abcam A-549 MAP3K11 KO 1 Cells(提供STR鑒定圖譜)

Abcam U-87MG VCAN KO Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSG203 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRU009 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC588 Cells(提供STR鑒定圖譜)

CHO SSF3/pMOZ uPA clone 1 Cells(提供STR鑒定圖譜)

DA02411 Cells(提供STR鑒定圖譜)

E195 Cells(提供STR鑒定圖譜)

GM04545 Cells(提供STR鑒定圖譜)

746T Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MNNG-HOS (Cl#5)細(xì)胞、PC3M-2B4細(xì)胞、VM-CUB1細(xì)胞

Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

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

RT-BM-1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成神經(jīng)細(xì)胞;相關(guān)產(chǎn)品有:HUC-1細(xì)胞、HCC1806細(xì)胞、GM 2132細(xì)胞

149 PT Cells;背景說(shuō)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(shuō)明書;相關(guān)產(chǎn)品有:Hs 578T細(xì)胞、H-9細(xì)胞、SNU878細(xì)胞

CMT-93 Cells;背景說(shuō)明:結(jié)腸癌;C57BL/ICRF;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Bac1 2F5細(xì)胞、D341MD細(xì)胞、H1105細(xì)胞

TGBC-11-TKB Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:RPMI7951細(xì)胞、J82 COT細(xì)胞、LC-1 sq細(xì)胞

7E3-N Cells(提供STR鑒定圖譜)

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

SUDHL-2 Cells;背景說(shuō)明:彌漫性大細(xì)胞淋巴瘤;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:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:LP-1細(xì)胞、SK-N-BE-2細(xì)胞、8226細(xì)胞

801-D Cells;背景說(shuō)明:這是一株高轉(zhuǎn)移肺癌。;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:IPEC1細(xì)胞、Panc02細(xì)胞、PANC0813細(xì)胞

NCI-H1993 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2—1:6傳代;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:PTK 1細(xì)胞、HuH-6細(xì)胞、P3/NS1/Ag4-1細(xì)胞

LTEP-s Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:IEC6細(xì)胞、CCRF-CEM/S細(xì)胞、TR 146細(xì)胞

OVCAR-3 Cells;背景說(shuō)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:TE10細(xì)胞、SW1417細(xì)胞、LN-382細(xì)胞

Hep II Cells;背景說(shuō)明:最初認(rèn)為這個(gè)細(xì)胞源自喉上皮癌,但隨后通過(guò)同功酶分析、HeLa標(biāo)記染色體和DNA指紋分析發(fā)現(xiàn),起源細(xì)胞已被HeLa污染。 角蛋白免疫過(guò)氧化物酶染色陽(yáng)性。;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:NCIH1581細(xì)胞、Anglne細(xì)胞、MHCCLM3細(xì)胞

TOV-112D Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代,3-4天換液1次。;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:ECGI10細(xì)胞、HEK293-H細(xì)胞、Hs68細(xì)胞

GM17576 Cells(提供STR鑒定圖譜)

HAP1 HPS1 (-) 3 Cells(提供STR鑒定圖譜)

C4-I Cells;背景說(shuō)明:宮頸鱗癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:BpRc1細(xì)胞、D-341 Med細(xì)胞、Hs 888.Lu細(xì)胞

Caco-2 Cells;背景說(shuō)明:細(xì)胞株分離自一個(gè)原發(fā)性結(jié)腸癌。當(dāng)細(xì)胞長(zhǎng)滿時(shí),表現(xiàn)出典型的腸細(xì)胞分化的特征。Caco-2細(xì)胞表達(dá)維生素A酸結(jié)合蛋白I和視黃醇結(jié)合蛋白II,角蛋白陽(yáng)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:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:M-1 myeloid leukemia細(xì)胞、HLF細(xì)胞、J774細(xì)胞

PLA 802 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:MCF-7ADR細(xì)胞、Fukuoka University-Malignant mixed Mullerian Tumor-1細(xì)胞、MGH-UI細(xì)胞

3D4/21 Cells;背景說(shuō)明:肺泡巨噬細(xì)胞;SV40轉(zhuǎn)化;Landrace;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:32D CL3細(xì)胞、MNNG/HOS Cl #5細(xì)胞、TFH細(xì)胞

CORL23 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:DoTc2細(xì)胞、Madin Darby Bovine Kidney細(xì)胞、RF/6A細(xì)胞

3 LL Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:UM-UC14細(xì)胞、NCI-H1954細(xì)胞、GM03671細(xì)胞

H1238 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Dysplastic Oral Keratinocyte細(xì)胞、PC-3M-IE8細(xì)胞、A549-Taxol細(xì)胞

624-mel Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:HSC-5 [Human skin squamous cell carcinoma]細(xì)胞、aNK細(xì)胞、NUGC-2細(xì)胞

HPS0135 Cells(提供STR鑒定圖譜)

JHU149i Cells(提供STR鑒定圖譜)

MDA 435TR Cells(提供STR鑒定圖譜)

ND32823 Cells(提供STR鑒定圖譜)

PR01168 Cells(提供STR鑒定圖譜)

TYR1-hiPSC7 Cells(提供STR鑒定圖譜)

UM-SCC-92 EGFR KO Cells(提供STR鑒定圖譜)

HES [Human contaminated endometrial epithelial] Cells(提供STR鑒定圖譜)

TFH Cells;背景說(shuō)明:輔助性T Cells;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:RAW 264.7細(xì)胞、NU-GC-2細(xì)胞、OCILY-10細(xì)胞

V79-1 Cells;背景說(shuō)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(shuō)明書;相關(guān)產(chǎn)品有:MM96L細(xì)胞、Capan1細(xì)胞、HEY-A8細(xì)胞

WILL2 Cells;背景說(shuō)明:彌漫大B淋巴瘤;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H-128細(xì)胞、CORL279細(xì)胞、OVCAR-4細(xì)胞

HCC-1187 Cells;背景說(shuō)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:混合生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:High 5細(xì)胞、Wistar Institute-38細(xì)胞、OCI-Ly8細(xì)胞

COLO-394 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H810細(xì)胞、T2 (174 x CEM.T2)細(xì)胞、NBL-12細(xì)胞

COLO-394 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H810細(xì)胞、T2 (174 x CEM.T2)細(xì)胞、NBL-12細(xì)胞

MKN7 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:Panc 1細(xì)胞、HS-445細(xì)胞、WM266mel細(xì)胞

JB6 Cl 30-7b Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:T-ALL-1細(xì)胞、Jurkat-77細(xì)胞、NCI-H2030細(xì)胞

HS-940-T Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代,2-3天換液1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:Hs940-T細(xì)胞、WILL-2細(xì)胞、HSF2細(xì)胞

BE(2)M-17 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:P3X63 AG8-653細(xì)胞、GM00637B細(xì)胞、50.B1細(xì)胞

COLO-829 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:6傳代,2-3天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成纖維細(xì)胞;相關(guān)產(chǎn)品有:A-10細(xì)胞、SW48細(xì)胞、CA 46細(xì)胞

Colon26 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:ABE-8.1/2細(xì)胞、TE 85.T細(xì)胞、BCECs細(xì)胞

WEHI 3B Cells;背景說(shuō)明:白血??;BALB/c;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Tca-8113細(xì)胞、4T1.2細(xì)胞、Nb2-11細(xì)胞

PF-382 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:HuT-102細(xì)胞、Hs888 Lu細(xì)胞、SNU-398細(xì)胞

H22-H8D8 Cells;背景說(shuō)明:肝癌;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(shuō)明書;相關(guān)產(chǎn)品有:CHL1細(xì)胞、NCI-H69C細(xì)胞、HS-294-T細(xì)胞

Skin.2.6A2.1A8 Cells(提供STR鑒定圖譜)

NOR 10 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:Capan1細(xì)胞、CTX TNA2細(xì)胞、Hut292細(xì)胞

MZ-CRC-1 Cells;背景說(shuō)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(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:H2030細(xì)胞、KM933細(xì)胞、SUM 102細(xì)胞

Biopsy xenograft of Pancreatic Carcinoma line-3 Cells;背景說(shuō)明:這個(gè)細(xì)胞株不表達(dá)囊腫性纖維化跨膜電導(dǎo)調(diào)節(jié)子(CFTR)。CFTR陽(yáng)性的細(xì)胞株是Capan-1(ATCCHTB-79)。;傳代方法:消化5-10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:FU-97細(xì)胞、OCM-1細(xì)胞、WM-451Lu細(xì)胞

MOLT 4 Cells;背景說(shuō)明:MOLT-4與MOLT-3來(lái)源于一名19歲的男性急性淋巴細(xì)胞性白血病的復(fù)發(fā)患者,該患者前期接受過(guò)多種藥物聯(lián)合化療。MOLT-4細(xì)胞系為T淋巴細(xì)胞起源,p53基因的第248位密碼子有一個(gè)G→A突變,不表達(dá)p53,不表達(dá)免疫球蛋白或EB病毒;可產(chǎn)生高水平的末端脫氧核糖轉(zhuǎn)移酶;表達(dá)CD1(49%),CD2(35%),CD3A(26%)B(33%)C(34%),CD4(55%),CD5(72%),CD6(22%),CD7(77%)。;傳代方法:1:2傳代;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞樣;圓形;相關(guān)產(chǎn)品有:NCI-H676B細(xì)胞、NBLAN5T細(xì)胞、TMK-1細(xì)胞

LP1 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SW480細(xì)胞、HCC 94細(xì)胞、AML12細(xì)胞

HT-55 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:BT-474細(xì)胞、NS1/1-Ag4.1細(xì)胞、HLEB-3細(xì)胞

Hs 578T人乳腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

SKNEP-1 Cells;背景說(shuō)明:超微結(jié)構(gòu)有少許微絨毛,連接復(fù)合物,形態(tài)完整的高爾基體,內(nèi)質(zhì)網(wǎng)多為光滑型,脂滴,沒(méi)有病毒棵粒。;傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿。;生長(zhǎng)特性:半貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:HuLEC-5a細(xì)胞、KM-12細(xì)胞、786-O細(xì)胞

L23/P Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:ETCC007細(xì)胞、Mink細(xì)胞、Primary Liver Carcinoma/Poliomyelitis Research Foundation/5細(xì)胞

MHHCALL2 Cells;背景說(shuō)明:急性B淋巴細(xì)胞白血?。慌?傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:SK-MEL-24細(xì)胞、Mouse Forestomach Carcinoma細(xì)胞、WM35細(xì)胞

SNUC2A Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:每周兩次換液;生長(zhǎng)特性:松散附著、多單元的聚合;形態(tài)特性:上皮細(xì)胞樣;相關(guān)產(chǎn)品有:A 549細(xì)胞、OsACL細(xì)胞、Panc-1-P細(xì)胞

HeLa229 Cells;背景說(shuō)明:宮頸癌;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:RT-BM-1細(xì)胞、SCC4細(xì)胞、KM.12細(xì)胞

PC-3 Cells;背景說(shuō)明:PC-3源于一位62歲白人男性IV級(jí)前列腺腺癌患者的骨轉(zhuǎn)移灶;有低水平的酸性酶活性和5-α-睪酮還原酶活性。;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),在軟瓊脂中成簇生長(zhǎng),并可懸浮生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:Lec1細(xì)胞、H-1703細(xì)胞、SW-620細(xì)胞

KYSE-70 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁或懸浮,詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性:詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有:JTC-28細(xì)胞、LTEP-s細(xì)胞、Colo741細(xì)胞

BaF3 Cells;背景說(shuō)明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代;3-4天1次。;生長(zhǎng)特性:懸浮生長(zhǎng);形態(tài)特性:圓形;相關(guān)產(chǎn)品有:A2780-CP細(xì)胞、HD-LM-2細(xì)胞、H-1666細(xì)胞

BayGenomics ES cell line CSG095 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRT486 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC479 Cells(提供STR鑒定圖譜)

JM8A3 Cells(提供STR鑒定圖譜)

PCRP-YY1-1B2 Cells(提供STR鑒定圖譜)

M14-23 Cells(提供STR鑒定圖譜)

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Neoplasia 6:187-194(2004)


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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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Sjoblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., Farrell C., Meeh P., Markowitz S.D., Willis J.E., Dawson D., Willson J.K.V., Gazdar A.F., Hartigan J., Wu L., Liu C.-S., Parmigiani G., Park B.H., Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W., Velculescu V.E.

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

BMC Cancer 10:15.1-15.10(2010)


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

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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.

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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.

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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=24009699; DOI=10.1371/journal.pone.0072704; PMCID=PMC3751845

Liu X., Nie H., Zhang Y.-B., Yao Y.-F., Maitikabili A., Qu Y.-P., Shi S.-L., Chen C.-Y., Li Y.

Cell surface-specific N-glycan profiling in breast cancer.

PLoS ONE 8:E72704-E72704(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=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

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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.

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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.

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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.

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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.

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PubMed=29671673; DOI=10.1080/24701394.2018.1461852

Hedberg A., Knutsen E., Lovhaugen A.S., Jorgensen T.E., Perander M., Johansen S.D.

Cancer-specific SNPs originate from low-level heteroplasmic variants in human mitochondrial genomes of a matched cell line pair.

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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.

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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)"


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