"CFPAC-1人胰腺癌細(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)胞系的選擇需要考慮到細(xì)胞系的功能特點(diǎn)、生長(zhǎng)速率、鋪板效率、生長(zhǎng)條件和生長(zhǎng)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(zhǎng)的快速生長(zhǎng)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(zhǎng)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(zhǎng)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(zhǎng)。

換液周期：每周2-3次

SK-ChA-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：CHL細(xì)胞、PC-3細(xì)胞、TOV-112D細(xì)胞

IMR32 Cells;背景說(shuō)明：該細(xì)胞是１９６７年４月由NicholsWW,LeeJ和DwightS建立，來(lái)源于一名１３月齡白人男嬰腹部腫塊，臨床診斷為神經(jīng)母細(xì)胞瘤，伴有極少部位的類器官樣分化。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：存在兩種細(xì)胞類型，小的神經(jīng)母細(xì)胞樣細(xì)胞和大的透明成纖維樣細(xì)胞;相關(guān)產(chǎn)品有：Tu686細(xì)胞、TE8細(xì)胞、266 Bl細(xì)胞

H719 Cells;背景說(shuō)明：小細(xì)胞肺癌；骨髓轉(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：半貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：CAL-78細(xì)胞、MV411細(xì)胞、HuT 78細(xì)胞

CFPAC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：是一種人胰腺導(dǎo)管腺癌(Pancreatic Ductal Adenocarcinoma, PDAC)細(xì)胞系，建自26歲白人男性囊性纖維變性(CF)的肝轉(zhuǎn)移灶，該患者合并有囊腫性纖維化。CFPAC-1細(xì)胞表達(dá)囊性纖維變性跨膜調(diào)節(jié)因子(CFTR)，CFPAC-1細(xì)胞形態(tài)為上皮細(xì)胞樣且頂端微絨毛極化。CFPAC-1細(xì)胞表達(dá)胰腺管細(xì)胞特征性的細(xì)胞角蛋白和癌胚抗原。

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

貼壁細(xì)胞(adherent cells)：該類細(xì)胞的生長(zhǎng)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(zhǎng)，繁殖；當(dāng)細(xì)胞在該表面生長(zhǎng)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(zhǎng)過程分為游離期、貼壁期、潛伏期、對(duì)數(shù)期、平臺(tái)期和衰退期。懸浮細(xì)胞(suspension cell)：不貼附于生長(zhǎng)物，細(xì)胞呈圓形，呈單個(gè)細(xì)胞或者細(xì)小細(xì)胞團(tuán)，懸浮細(xì)胞生長(zhǎng)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(lái)源說(shuō)明：細(xì)胞主要來(lái)源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫(kù)

CFPAC-1人胰腺癌細(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

LN229 Cells;背景說(shuō)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(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：Hs 870.T細(xì)胞、H647ell細(xì)胞、Swiss3T3細(xì)胞

H-1568 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；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：HKC細(xì)胞、Me Wo細(xì)胞、NP69SV40T細(xì)胞

NuTu-19 Cells;背景說(shuō)明：卵巢癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SUP-B15細(xì)胞、WI 38細(xì)胞、Tb 1-Lu細(xì)胞

IB-RS-2 Cells;背景說(shuō)明：腎；自發(fā)永生;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：CNE細(xì)胞、RIMEC細(xì)胞、MDA-MB-435-S細(xì)胞

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

形態(tài)特性：上皮細(xì)胞樣

細(xì)胞凍存復(fù)蘇材料與方法步驟：常用的細(xì)胞冷凍貯存器為貯存器，規(guī)格有３５L和５０L兩種。使用時(shí)要注意以下幾點(diǎn)：(１)一般兩周需充一次，至少一個(gè)月充一次。溫度達(dá)-１９６℃，使用時(shí)注意勿讓濺到皮膚上，以免引起凍傷。(２)容器為雙層結(jié)構(gòu)，中間為真空層，瓶口有雙層焊接處，應(yīng)防止焊接部裂開。(３)在裝入時(shí)，要注意緩慢小心，并用厚紙卷筒或制漏斗作引導(dǎo)，使直達(dá)瓶底，如有專用灌注裝置則更HAO。若為初次使用，加時(shí)更要緩慢，以免溫度驟降而使容器損壞。細(xì)胞凍存時(shí)常備的材料有：０.２５%胰蛋白酶，含１０%～２０%的血清培養(yǎng)，DMSO(分析純)或無(wú)色新鮮甘油(１２１°C蒸氣GAO壓消毒)，２mL安瓿(或?qū)Ｓ眉?xì)胞凍存管)、吸管、離心管、噴燈、紗布袋(或凍存管架)等。主要操作步驟為：(１)選擇處于對(duì)數(shù)生長(zhǎng)期的細(xì)胞，在凍存前一天ZuiHAO換。將多個(gè)培養(yǎng)瓶中的細(xì)胞培養(yǎng) 去掉，用０.２５%胰蛋白酶消化。適時(shí)去掉胰蛋白酶，加入少量新培養(yǎng)。用吸管吸取培養(yǎng)反復(fù)吹打瓶壁上的細(xì)胞，使其成為均勻分散的細(xì)胞懸。懸浮生產(chǎn)細(xì)胞則不要消化處理。然后將細(xì)胞收集于離心管中離心(１０００r/min，１０分鐘)。(２)去上清，加入含２０%小牛血清的完全培養(yǎng)基，于４℃預(yù)冷１５分鐘后，逐滴加入已無(wú)菌的DMSO或甘油，用吸管輕輕吹打使細(xì)胞均勻，細(xì)胞濃度為３×１０６～１×１０７/mL之間。(３)將上述細(xì)胞分裝于安瓿或?qū)Ｓ美鋬鏊芰瞎苤?，安瓿裝１～１.５mL在火焰噴燈上封口，封口處要完全封閉，圓滑無(wú)勾。冷凍管要將蓋子蓋緊，并標(biāo)記HAO細(xì)胞名稱和凍存日期，同時(shí)作HAO登記(日期、細(xì)胞種類及代次、凍存支數(shù))。(４)將裝HAO細(xì)胞的安瓿或凍存管裝入沙布袋內(nèi);置于容器頸口處存放過夜，次日轉(zhuǎn)入中。采用控制降溫速度的方法也可采用下列步驟：先將安瓿置入４℃冰箱中２～３小時(shí)，再移至冰箱冷凍室內(nèi)３～４小時(shí)，再吊入容器頸氣態(tài)部分存放２小時(shí)，Zui后沉入中。細(xì)胞凍存在中可以長(zhǎng)期保存，但為妥善起見，凍存半年后，ZuiHAO取出一只安瓿細(xì)胞復(fù)蘇培養(yǎng)，觀察生長(zhǎng)情況，然后再繼續(xù)凍存。

H1355 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：NBL-3細(xì)胞、SN-12C細(xì)胞、NCI-H250細(xì)胞

CCK-81 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：H6c7細(xì)胞、MA-c細(xì)胞、Mouse Colon 38細(xì)胞

293-EBNA1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：１０傳代；每周２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：NS-1-Ag4-1細(xì)胞、RAW264.7細(xì)胞、Blotchy fibroblast-11細(xì)胞

CHO-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：OPM-2細(xì)胞、NTera2 cl.D1細(xì)胞、KMB17細(xì)胞

HOK Cells;背景說(shuō)明：口腔角質(zhì) Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：T98 G細(xì)胞、HSC-2細(xì)胞、SW962細(xì)胞

H-64 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：IOSE-80細(xì)胞、RDES細(xì)胞、HPASMC細(xì)胞

MIMVEC Cells;背景說(shuō)明：腸粘膜微血管；內(nèi)皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：A2780細(xì)胞、CCLP1細(xì)胞、SW-780細(xì)胞

SVOG Cells;背景說(shuō)明：卵巢；顆粒 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Panc-1-P細(xì)胞、HCC94細(xì)胞、B10BR細(xì)胞

WM 115 Cells;背景說(shuō)明：黑色素瘤；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：FU-OV-1細(xì)胞、N-2a細(xì)胞、BT325細(xì)胞

N-2a Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代；２-３天換液１次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SUDHL16細(xì)胞、B16-BL6細(xì)胞、NCI.H226細(xì)胞

C-6 Cells;背景說(shuō)明：膠質(zhì)細(xì)胞株C６是由Benda等用N-nitrosomethylurea誘導(dǎo)的大鼠膠質(zhì)瘤克隆，并經(jīng)過一系列的體外培養(yǎng)和動(dòng)物傳代交替后建成的。 當(dāng)細(xì)胞從低密度生長(zhǎng)到滿瓶時(shí)，S-１００產(chǎn)量增加１０倍。;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：MRC9細(xì)胞、JIMT細(xì)胞、GM-637細(xì)胞

Human fetal lung fibroblast 1 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：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：OCI AML3細(xì)胞、LC-1 sq細(xì)胞、WM239細(xì)胞

BALL1 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：Wien 133細(xì)胞、HEH2細(xì)胞、UCLA-SO-M21細(xì)胞

TSU-Pr1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：H1568細(xì)胞、COLO-829細(xì)胞、R.K.13細(xì)胞

HEK 293-EBNA Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：１０傳代；每周２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：HIT clone T15細(xì)胞、NCIH211細(xì)胞、SUM-52-PE細(xì)胞

MCF 10A Cells;背景說(shuō)明：乳腺；上皮細(xì)胞；自發(fā)永生；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：OCI-Ly01細(xì)胞、HBdSMC細(xì)胞、University of Michigan-Renal Carcinoma-2細(xì)胞

SNU-119 Cells;背景說(shuō)明：卵巢癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：HL7702細(xì)胞、IBRS2細(xì)胞、PaCa2細(xì)胞

Abcam HEK293 TUBB2B KO Cells(提供STR鑒定圖譜)

AG0880 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line KST264 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XB865 Cells(提供STR鑒定圖譜)

BRC-37 Cells(提供STR鑒定圖譜)

COLO 16 Cells(提供STR鑒定圖譜)

DA03856 Cells(提供STR鑒定圖譜)

DA05034 Cells(提供STR鑒定圖譜)

G4-2 Cells(提供STR鑒定圖譜)

FUOV1 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：COLO320 DM細(xì)胞、MonoMac 6細(xì)胞、MNNGHOS細(xì)胞

CFPAC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

Sf21 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：U-251_MG細(xì)胞、NHRF細(xì)胞、HT-3細(xì)胞

HO1-N1 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：SU-DHL-8細(xì)胞、Dakiki細(xì)胞、YH-13細(xì)胞

OV-1063 Cells;背景說(shuō)明：卵巢上皮細(xì)胞癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：C127細(xì)胞、SKMES1細(xì)胞、HCT-15細(xì)胞

NPC-039 Cells;背景說(shuō)明：鼻咽癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：MCF 7B細(xì)胞、PE/CA-PJ-34細(xì)胞、Sp2/O-Ag14細(xì)胞

OCI/AML2 Cells;背景說(shuō)明：急性髓系白血?。荒行?傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：BrCL18細(xì)胞、CORL26細(xì)胞、MDA415細(xì)胞

15C12 Cells(提供STR鑒定圖譜)

C8D1A Cells;背景說(shuō)明：該永生化細(xì)胞系源自出生８天小鼠小腦組織，由B Pessac, D Trisler建立。該細(xì)胞具有小神經(jīng)膠質(zhì)細(xì)胞特征。該細(xì)胞為GFAP陽(yáng)性細(xì)胞，除此之外，沒有檢測(cè)到其它神經(jīng)膠質(zhì)神經(jīng)元或小神經(jīng)膠質(zhì)細(xì)胞的分子標(biāo)記。;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：NCIH1930細(xì)胞、HELA-GFP細(xì)胞、Dunn LM8細(xì)胞

hTERT RPE1 Cells;背景說(shuō)明：視網(wǎng)膜色素上皮；hTERT永生；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：RPMI-8226細(xì)胞、MHCC97-H細(xì)胞、H-2108細(xì)胞

HPAF-2 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：L Wnt-3A細(xì)胞、NCI-H2107細(xì)胞、HMC3細(xì)胞

HEL 92.1.7 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周２-３次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：成淋巴細(xì)胞;相關(guān)產(chǎn)品有：MA104細(xì)胞、MSTO-211 H細(xì)胞、T-24細(xì)胞

G402 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：６傳代，每周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：MOLP2細(xì)胞、TE353.SK細(xì)胞、PANC403細(xì)胞

SK-Col-1 Cells;背景說(shuō)明：該細(xì)胞來(lái)源于結(jié)直腸病人的轉(zhuǎn)移性腹水。;傳代方法：１：２-１：３傳代，每周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：H-1838細(xì)胞、NIE-115細(xì)胞、TYK-nu細(xì)胞

OC-3-VGH 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：SUDHL-6細(xì)胞、PJ34細(xì)胞、SUD-4細(xì)胞

PANC 813 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：HCT GEO細(xì)胞、MESSADX5細(xì)胞、PM6細(xì)胞

GM23382 Cells(提供STR鑒定圖譜)

HAP1 MTCH1 (-) 3 Cells(提供STR鑒定圖譜)

NCI-H187 Cells;背景說(shuō)明：經(jīng)典小細(xì)胞肺癌；胸腔積液轉(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：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：RCK8細(xì)胞、Y 1細(xì)胞、HEK-293H細(xì)胞

Doubling time: ~50 hours (ATCC). 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：OV1/P細(xì)胞、HFL細(xì)胞、RBSMC細(xì)胞

NCI-H1781 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：253JBV細(xì)胞、NHEK細(xì)胞、ESC-410細(xì)胞

H-250 Cells;背景說(shuō)明：小細(xì)胞肺癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：半貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：H520細(xì)胞、Functional Liver Cell-7細(xì)胞、OUMS-27細(xì)胞

NCTC clone 929 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：MDAMB157細(xì)胞、SU-DHL-1細(xì)胞、CCD19Lu細(xì)胞

LUDLU-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：HOP62細(xì)胞、SY5Y細(xì)胞、NCIH1734細(xì)胞

MAC1 Cells;背景說(shuō)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(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：MuM-2B細(xì)胞、HCC-1428細(xì)胞、SACC-LM細(xì)胞

NCI-H2066 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２-３次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：聚團(tuán)懸浮;相關(guān)產(chǎn)品有：Panc_08_13細(xì)胞、Hs606T細(xì)胞、3T3細(xì)胞

HQ00870 Cells(提供STR鑒定圖譜)

KE-6 Cells(提供STR鑒定圖譜)

MHHi006-A Cells(提供STR鑒定圖譜)

NLGIP-5876 Cells(提供STR鑒定圖譜)

RBL182T Cells(提供STR鑒定圖譜)

Ubigene HeLa SLC12A4 KO Cells(提供STR鑒定圖譜)

XP42RO-hTERT Cells(提供STR鑒定圖譜)

HCT116-SLC25A38-KO-c11 Cells(提供STR鑒定圖譜)

B16-F10 Cells;背景說(shuō)明：B１６-F１０是B１６-F０的亞系。;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：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Sp2/mIL-6細(xì)胞、HEK293-A細(xì)胞、EU-4細(xì)胞

HTR-8 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：NCI-H2330細(xì)胞、MDA-157細(xì)胞、V 79細(xì)胞

MES-13 Cells;背景說(shuō)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(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：OSK-1細(xì)胞、CTLL(2)細(xì)胞、Calu3細(xì)胞

IEC-18 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：McA-RH7777細(xì)胞、CTV1細(xì)胞、Kit 225細(xì)胞

Chang liver 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：COS-7細(xì)胞、IB-RS2細(xì)胞、L-6TG細(xì)胞

Chang liver 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：COS-7細(xì)胞、IB-RS2細(xì)胞、L-6TG細(xì)胞

Bronchial Epithelium transformed with Ad12-SV40 2B Cells;背景說(shuō)明：從一位非癌個(gè)體的正常人支氣管上皮病理切片分離出上皮細(xì)胞。這些細(xì)胞用腺病毒１２-SV４０病毒雜交病毒感染并克隆。DEAS-２B細(xì)胞保留了對(duì)血清反應(yīng)進(jìn)行鱗關(guān)分化的能力，并有用于篩選誘導(dǎo)或影響分化及致癌的化學(xué)或生物制劑。細(xì)胞角蛋白及SV４０抗原染色陽(yáng)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);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：QBC(939)細(xì)胞、JB 6細(xì)胞、HIT T15細(xì)胞

PBMC Cells;背景說(shuō)明：外周血單核 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：kms 11細(xì)胞、LLC-MK-2細(xì)胞、526-mel細(xì)胞

SW-579 Cells;背景說(shuō)明：在裸鼠中成瘤(產(chǎn)生三級(jí)惡性紡錘狀巨細(xì)胞瘤)。 ;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：OCI/AML3細(xì)胞、M-G63細(xì)胞、MAVER細(xì)胞

MDA330 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：Pt K2細(xì)胞、PG [Human lung carcinoma]細(xì)胞、ROS-17/2.8細(xì)胞

CHO-ori Cells;背景說(shuō)明：１９５７年，PuckTT從成年中國(guó)倉(cāng)鼠卵巢的活檢組織建立了CHO細(xì)胞；廣泛用于生物制品的表達(dá)。;傳代方法：１：３傳代，３-４天換液一次;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：FL 62891細(xì)胞、X63-Ag 8.6.5.3細(xì)胞、HCASMC細(xì)胞

CL1.0 Cells;背景說(shuō)明：肺癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：COR-L 105細(xì)胞、M14-MEL細(xì)胞、MMAc-Serum Free細(xì)胞

U138 Cells;背景說(shuō)明：星形細(xì)胞瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：EJ-1細(xì)胞、SW-1353細(xì)胞、EC-9706細(xì)胞

C3H-10T1/2 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見產(chǎn)品說(shuō)明書部分;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：MUTZ-3細(xì)胞、ATN1細(xì)胞、Hs 281.T細(xì)胞

AG06814-J Cells;背景說(shuō)明：LeonardHayflick建系；有限傳代細(xì)胞系；壽命為５０±１０代（倍增時(shí)間２４h）；來(lái)自妊娠３個(gè)月的正常胚胎肺組織。該細(xì)胞系是第一個(gè)用于人制備的人二倍體細(xì)胞；培養(yǎng)基中添加TNFα可以加快細(xì)胞生長(zhǎng)。;傳代方法：１：２-１：４傳代；２-３天換液１次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：BAC1.2F5細(xì)胞、Pt K2細(xì)胞、LWnt-3A細(xì)胞

STAN272i-726C4 Cells(提供STR鑒定圖譜)

NCI-H2030 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：TK+/- (clone 3.7.2C)細(xì)胞、H-2591細(xì)胞、BIU-87/Adr細(xì)胞

H1975 Cells;背景說(shuō)明：這株細(xì)胞于１９８８年七月建株。組織提供者是一位非吸煙人士。;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：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：GM0637細(xì)胞、Spodoptera frugiperda clone 9細(xì)胞、Human Epidermoid carcinoma #2細(xì)胞

HuT 78 Cells;背景說(shuō)明：皮膚；T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：LS 174T細(xì)胞、SKMEL3細(xì)胞、ST細(xì)胞

RFL 6 Cells;背景說(shuō)明：胚肺；成纖維細(xì)胞；SD大鼠;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：BT 325細(xì)胞、HEC1-A細(xì)胞、SUM52細(xì)胞

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：ROS-17/2.8細(xì)胞、H146細(xì)胞、SKNFI細(xì)胞

IHH Cells;背景說(shuō)明：肝;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：HS5細(xì)胞、Jurkat-E6細(xì)胞、LPC-H12細(xì)胞

CFPAC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

FRTL-5 Cells;背景說(shuō)明：甲狀腺；自發(fā)永生；Fischer;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-675-T細(xì)胞、P3X63Ag8.653細(xì)胞、SO-RB50細(xì)胞

H-292 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：８?jìng)鞔?；?３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：WEHI164細(xì)胞、PC3M細(xì)胞、NCI-H-128細(xì)胞

P3J.HR1K Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每２-３天換液;生長(zhǎng)特性：懸浮生長(zhǎng) ;形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：H-510A細(xì)胞、B16BL6細(xì)胞、SUSM1細(xì)胞

LU165 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：WIL2-S細(xì)胞、HCCC-9810細(xì)胞、TI-73細(xì)胞

Ej138 Cells;背景說(shuō)明：膀胱癌；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：Hi5細(xì)胞、H-87細(xì)胞、NK10a細(xì)胞

IFRS1 Cells;背景說(shuō)明：雪旺 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：SNU-423細(xì)胞、MDA 231-LM2-4175細(xì)胞、OVCAR 4細(xì)胞

U-343-MG 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：PANC-10-05細(xì)胞、AR4-2J細(xì)胞、A-704細(xì)胞

253J-BV Cells;背景說(shuō)明：膀胱癌；淋巴結(jié)轉(zhuǎn)移；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：RC-K8細(xì)胞、GTL 16細(xì)胞、MIA PaCa-2細(xì)胞

BayGenomics ES cell line RRR242 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YHD217 Cells(提供STR鑒定圖譜)

HT26 Cells(提供STR鑒定圖譜)

PCRP-HHEX-1D3 Cells(提供STR鑒定圖譜)

ERC-18M Cells(提供STR鑒定圖譜)

HPS2733 Cells(提供STR鑒定圖譜)

" "PubMed=11169959; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1049>3.0.CO;2-C

Sirivatanauksorn V., Sirivatanauksorn Y., Gorman P.A., Davidson J.M., Sheer D., Moore P.S., Scarpa A., Edwards P.A.W., Lemoine N.R.

Non-random chromosomal rearrangements in pancreatic cancer cell lines identified by spectral karyotyping.

Int. J. Cancer 91:350-358(2001)

PubMed=11787853; DOI=10.1007/s004280100474

Moore P.S., Sipos B., Orlandini S., Sorio C., Real F.X., Lemoine N.R., Gress T.M., Bassi C., Kloppel G., Kalthoff H., Ungefroren H., Lohr J.-M., Scarpa A.

Genetic profile of 22 pancreatic carcinoma cell lines. Analysis of K-ras, p53, p16 and DPC4/Smad4.

Virchows Arch. 439:798-802(2001)

PubMed=12800145; DOI=10.1002/gcc.10218

Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.

Genes Chromosomes Cancer 37:333-345(2003)

PubMed=14695172

Iacobuzio-Donahue C.A., Ashfaq R., Maitra A., Adsay N.V., Shen-Ong G.L.-C., Berg K., Hollingsworth M.A., Cameron J.L., Yeo C.J., Kern S.E., Goggins M.G., Hruban R.H.

Highly expressed genes in pancreatic ductal adenocarcinomas: a comprehensive characterization and comparison of the transcription profiles obtained from three major technologies.

Cancer Res. 63:8614-8622(2003)

PubMed=15126341; DOI=10.1158/0008-5472.CAN-03-3159

Heidenblad M., Schoenmakers E.F.P.M., Jonson T., Gorunova L., Veltman J.A., van Kessel A.G., Hoglund M.

Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.

Cancer Res. 64:3052-3059(2004)

PubMed=15367885; DOI=10.1097/00006676-200410000-00004

Loukopoulos P., Kanetaka K., Takamura M., Shibata T., Sakamoto M., Hirohashi S.

Orthotopic transplantation models of pancreatic adenocarcinoma derived from cell lines and primary tumors and displaying varying metastatic activity.

Pancreas 29:193-203(2004)

PubMed=15463957; DOI=10.1016/j.jcf.2004.05.040

Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.

Established cell lines used in cystic fibrosis research.

J. Cyst. Fibros. 3:191-196(2004)

PubMed=15688027; DOI=10.1038/sj.onc.1208383

Heidenblad M., Lindgren D., Veltman J.A., Jonson T., Mahlamaki E.H., Gorunova L., van Kessel A.G., Schoenmakers E.F.P.M., Hoglund M.

Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.

Oncogene 24:1794-1801(2005)

PubMed=16912165; DOI=10.1158/0008-5472.CAN-06-0721

Calhoun E.S., Hucl T., Gallmeier E., West K.M., Arking D.E., Maitra A., Iacobuzio-Donahue C.A., Chakravarti A., Hruban R.H., Kern S.E.

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.

Cancer Res. 66:7920-7928(2006)

PubMed=18380791; DOI=10.1111/j.1349-7006.2008.00779.x; PMCID=PMC11158928

Suzuki A., Shibata T., Shimada Y., Murakami Y., Horii A., Shiratori K., Hirohashi S., Inazawa J., Imoto I.

Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.

Cancer Sci. 99:986-994(2008)

DOI=10.4172/jpb.1000057

Yamada M., Fujii K., Koyama K., Hirohashi S., Kondo T.

The proteomic profile of pancreatic cancer cell lines corresponding to carcinogenesis and metastasis.

J. Proteomics Bioinformatics 2:1-18(2009)

PubMed=19077451; DOI=10.1159/000178871

Harada T., Chelala C., Crnogorac-Jurcevic T., Lemoine N.R.

Genome-wide analysis of pancreatic cancer using microarray-based techniques.

Pancreatology 9:13-24(2009)

PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113

Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

Signatures of mutation and selection in the cancer genome.

Nature 463:893-898(2010)

PubMed=20418756; DOI=10.1097/MPA.0b013e3181c15963; PMCID=PMC2860631

Deer E.L., Gonzalez-Hernandez J., Coursen J.D., Shea J.E., Ngatia J.G., Scaife C.L., Firpo M.A., Mulvihill S.J.

Phenotype and genotype of pancreatic cancer cell lines.

Pancreas 39:425-435(2010)

PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027

Barretina J.G., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehar J., Kryukov G.V., Sonkin D., Reddy A., Liu M., Murray L., Berger M.F., Monahan J.E., Morais P., Meltzer J., Korejwa A., Jane-Valbuena J., Mapa F.A., Thibault J., Bric-Furlong E., Raman P., Shipway A., Engels I.H., Cheng J., Yu G.-Y.K., Yu J.-J., Aspesi P. Jr., de Silva M., Jagtap K., Jones M.D., Wang L., Hatton C., Palescandolo E., Gupta S., Mahan S., Sougnez C., Onofrio R.C., Liefeld T., MacConaill L.E., Winckler W., Reich M., Li N.-X., Mesirov J.P., Gabriel S.B., Getz G., Ardlie K., Chan V., Myer V.E., Weber B.L., Porter J., Warmuth M., Finan P., Harris J.L., Meyerson M.L., Golub T.R., Morrissey M.P., Sellers W.R., Schlegel R., Garraway L.A.

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

Nature 483:603-607(2012)

PubMed=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396

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

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

Cancer Discov. 2:172-189(2012)

DOI=10.4172/2324-9293.1000104

Wagenhauser M.U., Ruckert F., Niedergethmann M., Grutzmann R., Saeger H.-D.

Distribution of characteristic mutations in native ductal adenocarcinoma of the pancreas and pancreatic cancer cell lines.

Cell Biol. Res. Ther. 2:1000104.1-1000104.5(2013)

PubMed=25167228; DOI=10.1038/bjc.2014.475; PMCID=PMC4453732

Hamidi H., Lu M., Chau K., Anderson L., Fejzo M.S., Ginther C., Linnartz R., Zubel A., Slamon D.J., Finn R.S.

KRAS mutational subtype and copy number predict in vitro response of human pancreatic cancer cell lines to MEK inhibition.

Br. J. Cancer 111:1788-1801(2014)

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

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

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

Sci. Data 1:140035-140035(2014)

PubMed=25485619; DOI=10.1038/nbt.3080

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

A comprehensive transcriptional portrait of human cancer cell lines.

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

PubMed=25877200; DOI=10.1038/nature14397

Yu M., Selvaraj S.K., Liang-Chu M.M.Y., Aghajani S., Busse M., Yuan J., Lee G., Peale F.V., Klijn C., Bourgon R., Kaminker J.S., Neve R.M.

A resource for cell line authentication, annotation and quality control.

Nature 520:307-311(2015)

PubMed=26216984; DOI=10.1073/pnas.1501605112; PMCID=PMC4538616

Daemen A., Peterson D., Sahu N., McCord R., Du X.-N., Liu B., Kowanetz K., Hong R., Moffat J., Gao M., Boudreau A., Mroue R., Corson L., O'Brien T., Qing J., Sampath D., Merchant M., Yauch R.L., Manning G., Settleman J., Hatzivassiliou G., Evangelista M.

Metabolite profiling stratifies pancreatic ductal adenocarcinomas into subtypes with distinct sensitivities to metabolic inhibitors.

Proc. Natl. Acad. Sci. U.S.A. 112:E4410-E4417(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=27259358; DOI=10.1074/mcp.M116.058313; PMCID=PMC4974343

Humphrey E.S., Su S.-P., Nagrial A.M., Hochgrafe F., Pajic M., Lehrbach G.M., Parton R.G., Yap A.S., Horvath L.G., Chang D.K., Biankin A.V., Wu J.-M., Daly R.J.

Resolution of novel pancreatic ductal adenocarcinoma subtypes by global phosphotyrosine profiling.

Mol. Cell. Proteomics 15:2671-2685(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=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=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)"