"BxPC-3人原位胰腺腺癌細(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

YD38 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：AG06814-J細(xì)胞、OVCAR-8/ADR細(xì)胞、143B細(xì)胞

RCC4 Cells;背景說(shuō)明：腎透明細(xì)胞癌；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：KM933細(xì)胞、NCI-SNU-423細(xì)胞、HEK 293-F細(xì)胞

SU86_86 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：HFL-I細(xì)胞、Melan-a細(xì)胞、L-Wnt3A細(xì)胞

BxPC-3人原位胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：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(ACHTB-７９)。

┈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)

BxPC-3人原位胰腺腺癌細(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

HEL92.1.7 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：MLMEC細(xì)胞、MDA157細(xì)胞、GM05372細(xì)胞

143 B Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：５傳代；每周換液２-３次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：混合型;相關(guān)產(chǎn)品有：NCI-SNU-407細(xì)胞、ARO-81細(xì)胞、SKM-1細(xì)胞

RS411 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：NT2-D1細(xì)胞、LAN-5細(xì)胞、HEK293-FT細(xì)胞

IPLB-SF 21AE 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：SKO3細(xì)胞、Intestinal Porcine Epithelial Cell line-J2細(xì)胞、HCC-2108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)胞傳代培養(yǎng)實(shí)驗(yàn)：體外培養(yǎng)的原代細(xì)胞或細(xì)胞株要在體外持續(xù)地培養(yǎng)就必須傳代，以便獲得穩(wěn)定的細(xì)胞株或得到大量的同種細(xì)胞，并維持細(xì)胞種的延續(xù)。培養(yǎng)的細(xì)胞形成單層匯合以后，由于密度過(guò)大生存空間不足而引起營(yíng)養(yǎng)枯竭，將培養(yǎng)的細(xì)胞分散，從容器中取出，以１:２或１:３以上的比率轉(zhuǎn)移到另外的容器中進(jìn)行培養(yǎng)，即為傳代培養(yǎng)；細(xì)胞“一代”指從細(xì)胞接種到分離再培養(yǎng)的一段期間，與細(xì)胞世代或倍增不同。在一代中，細(xì)胞培增３～６次。細(xì)胞傳代后，一般經(jīng)過(guò)三個(gè)階段：游離期、指數(shù)增生期和停止期。常用細(xì)胞分裂指數(shù)表示細(xì)胞增殖的旺盛程度，即細(xì)胞群的分裂相數(shù)/１００個(gè)細(xì)胞。一般細(xì)胞分裂指數(shù)介于０.２％～０.５％，腫瘤細(xì)胞可達(dá)３～５％；細(xì)胞接種２～３天分裂增殖旺盛，是活力ZuiHAO時(shí)期，稱指數(shù)增生期(對(duì)數(shù)生長(zhǎng)期)，適宜進(jìn)行各種試驗(yàn)。實(shí)驗(yàn)步驟：１.將長(zhǎng)成的培養(yǎng)細(xì)胞從二氧化碳培養(yǎng)箱中取出，在超凈工作臺(tái)中倒掉瓶?jī)?nèi)的培養(yǎng)，加入少許消化。(以面蓋住細(xì)胞為宜)，靜置５～１０分鐘。２.在倒置鏡下觀察被消化的細(xì)胞，如果細(xì)胞變圓，相互之間不再連接成片，這時(shí)應(yīng)立即在超凈臺(tái)中將消化倒掉，加入３～５ml新鮮培養(yǎng)，吹打，制成細(xì)胞懸。３.將細(xì)胞懸吸出２ml左右，加到另一個(gè)培養(yǎng)瓶中并向每個(gè)瓶中分別加３ml左右培養(yǎng)，蓋HAO瓶塞，送回二氧化碳培養(yǎng)箱中，繼續(xù)進(jìn)行培養(yǎng)。一般情況，傳代后的細(xì)胞在２小時(shí)左右就能附著在培養(yǎng)瓶壁上，２～４天就可在瓶?jī)?nèi)形成單層，需要再次進(jìn)行傳代。

Panc-02 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-UC3細(xì)胞、LC-2 ad細(xì)胞、MARC-145細(xì)胞

L132 Cells;背景說(shuō)明：胚肺；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：SW 579細(xì)胞、UCLA SO M14細(xì)胞、SK-LMS-1細(xì)胞

Roswell Park Memorial Institute 8402 Cells;背景說(shuō)明：急性T淋巴細(xì)胞白血??；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：Centre Antoine Lacassagne-39細(xì)胞、NCI-H378細(xì)胞、CAL-33細(xì)胞

SKGIIIA Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：２x１０^４ cells/ml;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：Strain L-929細(xì)胞、MDAMB415細(xì)胞、H1672細(xì)胞

MS 751 Cells;背景說(shuō)明：這株細(xì)胞是J. Sykes于１９７４年建立的（參考ATCC HTB-３３）。有報(bào)告稱MS７５１細(xì)胞含有人乳頭狀瘤病毒１８ (HPV-１８)序列。[２２９９５] [２３１８０]后來(lái)發(fā)現(xiàn)MS７５１細(xì)胞包含HPV-４５基因組的一部分，而其中E６/E７區(qū)域表達(dá)呈poly(A)+RNA的形式。[４９７２１];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：OVCA5細(xì)胞、BALB 3T3 clone A31細(xì)胞、NCI-H520細(xì)胞

Fao 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：上皮細(xì)胞;相關(guān)產(chǎn)品有：RPMI #8226細(xì)胞、Keio University-19-19細(xì)胞、BEL 7402細(xì)胞

E6-1 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：FRhK-4細(xì)胞、293 c18細(xì)胞、143 B細(xì)胞

HDLM-2 Cells;背景說(shuō)明：霍奇金淋巴瘤；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：MHCC-97細(xì)胞、D407細(xì)胞、H2106細(xì)胞

LC1 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：PAa細(xì)胞、EA. hy 926細(xì)胞、AN3 CA細(xì)胞

MCF-12A Cells;背景說(shuō)明：非致瘤性乳腺上皮細(xì)胞；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：LSC-1細(xì)胞、SKHEP-1細(xì)胞、EB-2細(xì)胞

L-M[TK-] 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：FRTL 5細(xì)胞、H2286細(xì)胞、C57 Mouse Tumor 93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

786O Cells;背景說(shuō)明：該細(xì)胞源自一位原發(fā)性腎透明細(xì)胞癌患者。該細(xì)胞有微絨毛和橋粒，能在軟瓊脂上生長(zhǎng)。此細(xì)胞生成一種PTH（甲狀旁腺素）樣的多肽，與乳癌和肺癌中生成的肽相似，其N端序列與PTH相似，具有PTH樣活性，分子量為６０００D。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：OCI-Ly 1細(xì)胞、NCI/ADR-RES細(xì)胞、NCI-H441-4細(xì)胞

ARIP 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：AR4-2J細(xì)胞、H1666細(xì)胞、CFSC-2G細(xì)胞

WM 451-Lu 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：HCC2185細(xì)胞、H-716細(xì)胞、MKN 45細(xì)胞

293 H 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：RGC5細(xì)胞、NCI-H2291細(xì)胞、H-125細(xì)胞

A2780CP70 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：P3 NS1 Ag4/1細(xì)胞、THLE2細(xì)胞、B16 melanoma細(xì)胞

Abcam A-549 ISM1 KO 1 Cells(提供STR鑒定圖譜)

Abcam U-87MG GABRA1 KO Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSG038 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRT394 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC444 Cells(提供STR鑒定圖譜)

CHO CT52 Cells(提供STR鑒定圖譜)

DA02320 Cells(提供STR鑒定圖譜)

DA05090 Cells(提供STR鑒定圖譜)

GAK14 Cells(提供STR鑒定圖譜)

TGBC11T 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：Co 205細(xì)胞、CLONE M3細(xì)胞、CMT167細(xì)胞

BxPC-3人原位胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

MDA1386 Cells;背景說(shuō)明：舌鱗癌；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：BT-549細(xì)胞、CEM/C1細(xì)胞、MN-60細(xì)胞

NCI-H2081 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：隨細(xì)胞的密度而增加;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：聚團(tuán)懸浮;相關(guān)產(chǎn)品有：NCI-H102細(xì)胞、Mouse podocyte細(xì)胞、Evsa-T細(xì)胞

NCIH1648 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;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：NRK-49F細(xì)胞、Hs343T細(xì)胞、NS-1細(xì)胞

Human Lung Microvascular Endothelial Cell line-5a Cells;背景說(shuō)明：肺微血管；內(nèi)皮細(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(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：HS940細(xì)胞、S.B.細(xì)胞、Ca761細(xì)胞

LS-411N 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２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：N-87細(xì)胞、H1648細(xì)胞、MESSA細(xì)胞

168FAR Cells(提供STR鑒定圖譜)

NCIH295R Cells;背景說(shuō)明：腎上腺皮質(zhì)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：TI-73細(xì)胞、NCIH1755細(xì)胞、NCI-H2591細(xì)胞

RAW 264.7 Cells;背景說(shuō)明：?jiǎn)魏司奘杉?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(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：NCI-H2172細(xì)胞、MFM-223細(xì)胞、SK-GT-4細(xì)胞

H-1876 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：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：DHL-6細(xì)胞、SNU-182細(xì)胞、AML-193細(xì)胞

ECV 304 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：SK-MEL24細(xì)胞、NCI-H596細(xì)胞、THLE-2細(xì)胞

H-740 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：UACC 812細(xì)胞、H-1436細(xì)胞、HNE-2細(xì)胞

HUSMC Cells;背景說(shuō)明：子宮；平滑肌細(xì)胞；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：H-847細(xì)胞、Hep G2細(xì)胞、COLO 320F細(xì)胞

HIEC Cells;背景說(shuō)明：腸；上皮 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：Hs 600.T細(xì)胞、DoHH-2細(xì)胞、CCRF.CEM細(xì)胞

343MG 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：Fox/NY細(xì)胞、ECC-12細(xì)胞、BCP-1細(xì)胞

GM18365 Cells(提供STR鑒定圖譜)

HAP1 IFI44L (-) Cells(提供STR鑒定圖譜)

RH35 Cells;背景說(shuō)明：在糖皮質(zhì)激素、胰島素或cAMP衍生物的誘導(dǎo)下可以產(chǎn)生酪酸基轉(zhuǎn)移酶；可被逆轉(zhuǎn)錄病毒感染；可產(chǎn)生白蛋白、轉(zhuǎn)鐵蛋白、凝血酶原；在AxC大鼠中可以成瘤。;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：Hs606T細(xì)胞、SK-N-BE(2)C細(xì)胞、HCE-T細(xì)胞

639V Cells;背景說(shuō)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(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：Hs695T細(xì)胞、OPM2細(xì)胞、SUDHL-4細(xì)胞

Ramos.G6.C10 Cells;背景說(shuō)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(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：MC-3T3細(xì)胞、ONS-76細(xì)胞、HUC細(xì)胞

P3JHR-1 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：SV40-MES13細(xì)胞、NCI-H920細(xì)胞、SKNBE細(xì)胞

KP-2 Cells;背景說(shuō)明：胰腺癌；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：NBL-S細(xì)胞、Colo-206F細(xì)胞、NCI-SNU-16細(xì)胞

HS-294 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：混合星狀和多邊形;相關(guān)產(chǎn)品有：KPL-4細(xì)胞、RIN-m5F細(xì)胞、Huh 7.5細(xì)胞

A2008 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：OsACL細(xì)胞、AU-Mel細(xì)胞、H-35 Reuber細(xì)胞

H7721 Cells;背景說(shuō)明：用Northernblot方法，未能檢測(cè)到細(xì)胞中１.３kbLFIRE-１/HFREP-１mRNA的表達(dá)。;傳代方法：１：３傳代，２-３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：OCI-Ly 18細(xì)胞、NCIH2073細(xì)胞、PY8119細(xì)胞

HPS0248 Cells(提供STR鑒定圖譜)

JHU234i Cells(提供STR鑒定圖譜)

MDA-MB-231/Luc Cells(提供STR鑒定圖譜)

ND36883 Cells(提供STR鑒定圖譜)

PrecisION hKv4.3/KCHiP1-CHO Cells(提供STR鑒定圖譜)

Ubigene A-549 CACNG6 KO Cells(提供STR鑒定圖譜)

UOK102 Cells(提供STR鑒定圖譜)

Hep-G2-THRA MUT p.I116N;A225T;M388I Cells(提供STR鑒定圖譜)

COLO680N 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：CCC-HSF-1細(xì)胞、SNU182細(xì)胞、LS411N細(xì)胞

B/C3T3 Cells;背景說(shuō)明：胚胎；成纖維；自發(fā)永生；雄性；BALB/c;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說(shuō)明書;相關(guān)產(chǎn)品有：NCI-H1672細(xì)胞、HMC細(xì)胞、HNE3細(xì)胞

WERI-Rb 1 Cells;背景說(shuō)明：WERI-Rb-I細(xì)胞株是１９７４年R.M. McFall 和 T.W. Sery建立的兩株人眼癌細(xì)胞系中的一株。 細(xì)胞能在Difco Bacto-Agar中存活但不形成克隆。 掃描電鏡顯示在表面囊泡，板狀偽足和微絨毛在數(shù)量上和頻率上的改變。 細(xì)胞分化研究，腫瘤治療的動(dòng)物模型和生化評(píng)價(jià)都涉及這株細(xì)胞。;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：圓形細(xì)胞聚集成葡萄狀;相關(guān)產(chǎn)品有：C4-2細(xì)胞、RK13細(xì)胞、Y3-Ag1,2,3細(xì)胞

AN3-CA Cells;背景說(shuō)明：AN３CA細(xì)胞建系于１９６４年。它衍生于子宮內(nèi)膜癌患者淋巴結(jié)轉(zhuǎn)移組織，具有癌細(xì)胞的基本特性，能在體外長(zhǎng)期傳代培養(yǎng)，接種實(shí)驗(yàn)動(dòng)物產(chǎn)生明顯腫瘤。但細(xì)胞的生物學(xué)特性及超微結(jié)構(gòu)尚未深入研究，僅發(fā)現(xiàn)該細(xì)胞系促黑激素合成為陰性。細(xì)胞常用于人子宮內(nèi)膜癌細(xì)胞生物學(xué)及其相關(guān)特性研究。;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：UCLA-SO-M20細(xì)胞、GM16136細(xì)胞、SNK-1細(xì)胞

SK-MEL-31 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，２-３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：CHO cell clone K1細(xì)胞、Centre Antoine Lacassagne-39細(xì)胞、PC 61.5.3細(xì)胞

SK-MEL-31 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，２-３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：CHO cell clone K1細(xì)胞、Centre Antoine Lacassagne-39細(xì)胞、PC 61.5.3細(xì)胞

GM-215 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：H2286細(xì)胞、KP-N-YN細(xì)胞、MonoMac 6細(xì)胞

Calf Pulmonary Artery Endothelial Cells;背景說(shuō)明：肺血管；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：GTL16細(xì)胞、T47-D細(xì)胞、MDA-468細(xì)胞

HELF 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：BAR-T細(xì)胞、MBT-2細(xì)胞、CAL-120細(xì)胞

GM637A 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：HO-8910 PM細(xì)胞、686LN-M4e細(xì)胞、Hs 746.T細(xì)胞

SK-MEL24 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：星形的;相關(guān)產(chǎn)品有：IGROV 1細(xì)胞、EFM192B細(xì)胞、COLO-1細(xì)胞

SK-MEL-1 Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：維持細(xì)胞濃度在１×１０５-２×１０５,每周補(bǔ)液２-３次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：球形的;相關(guān)產(chǎn)品有：BV173細(xì)胞、ACC-M細(xì)胞、MDA-436細(xì)胞

HUT-226 Cells;背景說(shuō)明：１９８０年分離建立。;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：RCC23細(xì)胞、COLO-699細(xì)胞、OVCAR10細(xì)胞

MUS-M1 Cells;背景說(shuō)明：小腸；平滑肌;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：KE-37細(xì)胞、PCI-4M細(xì)胞、BNCL2細(xì)胞

BT Cells;背景說(shuō)明：鼻甲；自發(fā)永生；Holstein;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-Ly 19細(xì)胞、SHP-77細(xì)胞、SCC25細(xì)胞

SL1 Cells(提供STR鑒定圖譜)

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

HT144mel 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：成纖維細(xì)胞;相關(guān)產(chǎn)品有：MDAMB435細(xì)胞、HPAF細(xì)胞、CHL1細(xì)胞

Human Epidermoid carcinoma #2 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：HCC1569細(xì)胞、NBL-4細(xì)胞、NS20Y細(xì)胞

NCI-H508 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：293-H細(xì)胞、NCI660細(xì)胞、JVM3細(xì)胞

NCIH64 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：Colo-201細(xì)胞、HL-1細(xì)胞、HOP62細(xì)胞

HR-8348 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：MV(4;11)細(xì)胞、NCI-H441細(xì)胞、PLC/PRF5細(xì)胞

BxPC-3人原位胰腺腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

EFM-192C 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：C-33A細(xì)胞、MDAPC2B細(xì)胞、293-H細(xì)胞

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

PC-9/GR 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：PC 61-5-3細(xì)胞、NCI-H2172細(xì)胞、MDA MB 134VI細(xì)胞

GalK1 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：CaEs17細(xì)胞、OVCAR 432細(xì)胞、CEMC7細(xì)胞

K 562 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：Walker/LLC-WRC 256細(xì)胞、Lewis lung carcinoma line 1細(xì)胞、SNU16細(xì)胞

SG231 Cells;背景說(shuō)明：肝內(nèi)膽管癌；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：K7M2細(xì)胞、BCP1細(xì)胞、HuH7細(xì)胞

MX-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：QBC-939細(xì)胞、LS-411N細(xì)胞、L-6 myoblast細(xì)胞

Mo 59J Cells;背景說(shuō)明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：６-１：８?jìng)鞔幻恐軗Q液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：Hs852細(xì)胞、NCI-SNU-668細(xì)胞、MRC 5細(xì)胞

BayGenomics ES cell line CSG413 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRU317 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC771 Cells(提供STR鑒定圖譜)

Keck MirKO ES cell line Mir124a-3 Cells(提供STR鑒定圖譜)

PCRP-ZNF202-1C2 Cells(提供STR鑒定圖譜)

mTX3 Cells(提供STR鑒定圖譜)

" "PubMed=8426738

Kalthoff H., Schmiegel W.H., Roeder C., Kasche D., Schmidt A., Lauer G., Thiele H.-G., Honold G., Pantel K., Riethmuller G., Scherer E., Maurer J., Maacke H., Deppert W.

p53 and K-RAS alterations in pancreatic epithelial cell lesions.

Oncogene 8:289-298(1993)

PubMed=7961102; DOI=10.1111/j.1349-7006.1994.tb02898.x; PMCID=PMC5919355

Suwa H., Yoshimura T., Yamaguchi N., Kanehira K., Manabe T., Imamura M., Hiai H., Fukumoto M.

K-ras and p53 alterations in genomic DNA and transcripts of human pancreatic adenocarcinoma cell lines.

Jpn. J. Cancer Res. 85:1005-1014(1994)

PubMed=8026879; DOI=10.1002/ijc.2910580207

Berrozpe G., Schaeffer J., Peinado M.A., Real F.X., Perucho M.

Comparative analysis of mutations in the p53 and K-ras genes in pancreatic cancer.

Int. J. Cancer 58:185-191(1994)

PubMed=8194712; DOI=10.1016/0016-5085(94)90422-7

Simon B., Weinel R., Hohne M., Watz J., Schmidt J., Kortner G., Arnold R.

Frequent alterations of the tumor suppressor genes p53 and DCC in human pancreatic carcinoma.

Gastroenterology 106:1645-1651(1994)

PubMed=8286197; DOI=10.1038/bjc.1994.24; PMCID=PMC1968784

Lohr J.-M., Trautmann B., Gottler M., Peters S., Zauner I., Maillet B., Kloppel G.

Human ductal adenocarcinomas of the pancreas express extracellular matrix proteins.

Br. J. Cancer 69:144-151(1994)

PubMed=21607521; DOI=10.3892/or.1.6.1223

Iguchi H., Morita R., Yasuda D., Takayanagi R., Ikeda Y., Takada Y., Shimazoe T., Nawata H., Kono A.

Alterations of the p53 tumor-suppressor gene and ki-ras oncogene in human pancreatic cancer-derived cell-lines with different metastatic potential.

Oncol. Rep. 1:1223-1227(1994)

PubMed=9788440; DOI=10.1038/sj.onc.1202118

Villanueva A., Garcia C., Paules Blazquez A.B., Vicente M., Megias M., Reyes G., de Villalonga P., Agell N., Lluis F., Bachs O., Capella G.

Disruption of the antiproliferative TGF-beta signaling pathways in human pancreatic cancer cells.

Oncogene 17:1969-1978(1998)

PubMed=10027410; DOI=10.1016/S0002-9440(10)65298-4; PMCID=PMC1850008

Ghadimi B.M., Schrock E., Walker R.L., Wangsa D., Jauho A., Meltzer P.S., Ried T.

Specific chromosomal aberrations and amplification of the AIB1 nuclear receptor coactivator gene in pancreatic carcinomas.

Am. J. Pathol. 154:525-536(1999)

PubMed=10408907; DOI=10.1016/S0304-3835(98)00380-2

Bartsch D.K., Barth P., Bastian D., Ramaswamy A., Gerdes B., Chaloupka B., Deiss Y., Simon B., Schudy A.

Higher frequency of DPC4/Smad4 alterations in pancreatic cancer cell lines than in primary pancreatic adenocarcinomas.

Cancer Lett. 139:43-49(1999)

PubMed=11115575; DOI=10.3892/or.8.1.89

Sun C.-L., Yamato T., Furukawa T., Ohnishi Y., Kijima H., Horii A.

Characterization of the mutations of the K-ras, p53, p16, and SMAD4 genes in 15 human pancreatic cancer cell lines.

Oncol. Rep. 8:89-92(2001)

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=12692724; DOI=10.1007/s00428-003-0784-4

Sipos B., Moser S., Kalthoff H., Torok V., Lohr J.-M., Kloppel G.

A comprehensive characterization of pancreatic ductal carcinoma cell lines: towards the establishment of an in vitro research platform.

Virchows Arch. 442:444-452(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=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=18298655; DOI=10.1111/j.1582-4934.2008.00289.x; PMCID=PMC3828895

Pilarsky C., Ammerpohl O., Sipos B., Dahl E., Hartmann A., Wellmann A., Braunschweig T., Lohr J.-M., Jesenofsky R., Friess H., Wente M.N., Kristiansen G., Jahnke B., Denz A., Ruckert F., Schackert H.K., Kloppel G., Kalthoff H., Saeger H.-D., Grutzmann R.

Activation of Wnt signalling in stroma from pancreatic cancer identified by gene expression profiling.

J. Cell. Mol. Med. 12:2823-2835(2008)

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)

CLPUB00416

Oberlin L.

Treatment of pancreatic carcinoma cell lines in vitro and vivo with a monoclonal antibody against the transferrin receptor.

Thesis VMD (2009); Justus-Liebig-Universitat Giessen; Giessen; Germany

PubMed=20037478; DOI=10.4161/cbt.8.21.9685; PMCID=PMC2824894

Kent O.A., Mullendore M.E., Wentzel E.A., Lopez-Romero P., Tan A.-C., Alvarez H., West K.M., Ochs M.F., Hidalgo M., Arking D.E., Maitra A., Mendell J.T.

A resource for analysis of microRNA expression and function in pancreatic ductal adenocarcinoma cells.

Cancer Biol. Ther. 8:2013-2024(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=27073551; DOI=10.3892/ol.2016.4289; PMCID=PMC4812595

Fujiwara M., Kanayama K., Hirokawa Y.S., Shiraishi T.

ASF-4-1 fibroblast-rich culture increases chemoresistance and mTOR expression of pancreatic cancer BxPC-3 cells at the invasive front in vitro, and promotes tumor growth and invasion in vivo.

Oncol. Lett. 11:2773-2779(2016)

PubMed=27229158; DOI=10.1038/cgt.2016.23; PMCID=PMC5007605

Schreiber R., Mezencev R., Matyunina L.V., McDonald J.F.

Evidence for the role of microRNA 374b in acquired cisplatin resistance in pancreatic cancer cells.

Cancer Gene Ther. 23:241-245(2016)

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=27910856; DOI=10.1038/cgt.2016.71; PMCID=PMC5159445

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