"PANC-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)胞培養(yǎng)經(jīng)驗(yàn)分享】啟蒙老師的重要性：一般進(jìn)實(shí)驗(yàn)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(yíng)養(yǎng)液、細(xì)胞瓶的擺放位置、滅菌處理程序、開(kāi)蓋手法、細(xì)胞吹打手法等等。要學(xué)會(huì)他們的正確操作，在第一次的時(shí)候就要重視。像養(yǎng)孩子一樣養(yǎng)細(xì)胞，細(xì)胞有時(shí)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、溫度不夠等異常現(xiàn)象，也好及時(shí)解決這些意外，避免重復(fù)實(shí)驗(yàn)帶來(lái)的更大痛苦。好細(xì)胞要及時(shí)保種：細(xì)胞要分批傳代，這樣即使有一批出了問(wèn)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(méi)。當(dāng)時(shí)可后悔沒(méi)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(guò)程中要細(xì)細(xì)體會(huì)，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

WEHI3B 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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：OS-732細(xì)胞、HepG2/C3A細(xì)胞、Madison細(xì)胞

HPMEC Cells;背景說(shuō)明：肺微血管；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Hela-mock細(xì)胞、GEO細(xì)胞、FAK+/+細(xì)胞

LN-229 Cells;背景說(shuō)明：詳見(jiàn)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：RGCs細(xì)胞、786-0細(xì)胞、hSCC-25細(xì)胞

PANC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：這株人胰腺癌細(xì)胞株源自于胰腺癌導(dǎo)管細(xì)胞，其倍增時(shí)間為５２小時(shí)。染色體研究表明，該細(xì)胞染色體眾數(shù)為６３，包括３個(gè)獨(dú)特標(biāo)記的染色體和１個(gè)小環(huán)狀染色體。該細(xì)胞的生長(zhǎng)可被１unit/ml的左旋天冬酰胺酶抑制；能在軟瓊脂上生長(zhǎng)；能在裸鼠上成瘤。

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線(xiàn)：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(lèi)、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(lèi)、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)

PANC-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

MOLT4 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(mén)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：HME-1細(xì)胞、VeroE6細(xì)胞、Medical University of Graz-Chordoma 1細(xì)胞

BSC-1 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：COV 504細(xì)胞、Tn5B1-4細(xì)胞、RBMVEC細(xì)胞

HNE-3 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SK ES 01細(xì)胞、SK 1細(xì)胞、HOS-MNNG細(xì)胞

LM3 Cells;背景說(shuō)明：詳見(jiàn)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：HCC1500細(xì)胞、UCLA-SO-M14細(xì)胞、H-35細(xì)胞

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線(xiàn)：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)胞復(fù)蘇相關(guān)注意事項(xiàng)：１.取細(xì)胞的過(guò)程中注意帶HAO防凍手套，護(hù)目鏡。此項(xiàng)尤為重要，細(xì)胞凍存管可能漏入，解凍時(shí)凍存管中的氣溫急劇上升，可導(dǎo)致爆炸。２.凍存的問(wèn)題：凍存的配置已是常識(shí)，在這里不作詳述，但二甲基亞砜(DMSO )對(duì)細(xì)胞不是完全無(wú)毒副作用，在常溫下，二甲基亞砜對(duì)細(xì)胞的毒副作較大，因此，必須在１-２min內(nèi)使凍存完全融化。如果復(fù)蘇溫度太慢，會(huì)造成細(xì)胞的損傷，二甲基亞砜(DMSO)ZuiHAO選擇進(jìn)口產(chǎn)品。３.離心前須加入少量培養(yǎng)。細(xì)胞解凍后二甲基亞砜濃度較GAO，注意加入少量培養(yǎng)可稀釋其濃度，以減少對(duì)細(xì)胞的損傷。４.離心問(wèn)題：目前主要有兩種見(jiàn)解。一種是解凍后的細(xì)胞懸直接吹打均勻后分裝到培養(yǎng)瓶中進(jìn)行培養(yǎng)，第二天換。因?yàn)殡x心的目的是兩個(gè)，去除DMSO，去除死細(xì)胞，這個(gè)是標(biāo)準(zhǔn)流程，但對(duì)一般人來(lái)說(shuō)，把握不HAO離心轉(zhuǎn)速和時(shí)間，轉(zhuǎn)的不夠活細(xì)胞沉底的少，細(xì)胞就全被扔掉了，轉(zhuǎn)過(guò)了活細(xì)胞會(huì)受壓過(guò)大，死亡。此外在操作過(guò)程中容易污染，所以不推薦。另一種說(shuō)法為細(xì)胞懸中含有二甲基亞砜(DMSO)，DMSO對(duì)細(xì)胞有一定的毒副作用，所以須將離心后的體前倒凈，且一定倒干凈。我在試驗(yàn)中按照常規(guī)的離心分裝的方法進(jìn)行復(fù)蘇，結(jié)果無(wú)異常。５.細(xì)胞貼壁少的問(wèn)題：教科書(shū)中說(shuō)明凍存細(xì)胞解凍時(shí)１ml細(xì)胞要加１０ml-１５ml培養(yǎng)，而在我的試驗(yàn)中的經(jīng)驗(yàn)總結(jié)為培養(yǎng)基越少細(xì)胞越容易貼附。６.復(fù)蘇細(xì)胞分裝的問(wèn)題：試驗(yàn)中我的經(jīng)驗(yàn)總結(jié)為復(fù)蘇１管細(xì)胞一般可分裝到１-２只培養(yǎng)瓶中，分裝過(guò)多，細(xì)胞濃度過(guò)低，不利于細(xì)胞的貼壁。７.加培養(yǎng)基的量放入問(wèn)題：這個(gè)量的多少的把握主要涉及到的問(wèn)題DMSO的濃度，從如果你加培養(yǎng)基的太少，那么DMSO的濃度就會(huì)比較大，就會(huì)影響細(xì)胞生長(zhǎng)，從以前的資料來(lái)看，DMSO的濃度在小于０.５%的時(shí)候?qū)σ话慵?xì)胞沒(méi)有什么影響，還有一個(gè)說(shuō)法是１%。所以如果你的凍存的濃度是１０%DMSO的話(huà)那么加１０ml以上的培養(yǎng)基就恰HAO稀釋到了無(wú)害濃度。

LWnt3A Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NCI-H2195細(xì)胞、NCI-H2330細(xì)胞、SGC-7901細(xì)胞

LS1034 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：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：NRK-52E細(xì)胞、NCL-H548細(xì)胞、SK-N-F1細(xì)胞

MDA 435 Cells;背景說(shuō)明：乳腺癌;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SP2細(xì)胞、A-375.S2細(xì)胞、T47D細(xì)胞

NB9 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：１０ １：５０每２ - ３周；每周換液２-３次。;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：WM451細(xì)胞、A-9細(xì)胞、MPC11細(xì)胞

C-32 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代，２天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：EST81細(xì)胞、Cloudman M3細(xì)胞、UK Pan-1細(xì)胞

alphaTC1 Clone 6 Cells;背景說(shuō)明：胰島素瘤；a細(xì)胞；C５７BL/６xDBA/２;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：CCRF.CEM細(xì)胞、HBE135-E6E7細(xì)胞、ZR-75-1細(xì)胞

H-747 Cells;背景說(shuō)明：詳見(jiàn)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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：HPC-Y5細(xì)胞、H727細(xì)胞、VMRC-LCD細(xì)胞

373 MG Cells;背景說(shuō)明：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(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：OEC19細(xì)胞、MAVER1細(xì)胞、NCIH295R細(xì)胞

Mac-1 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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：U87細(xì)胞、SNU761細(xì)胞、3396細(xì)胞

NB1RGB Cells;背景說(shuō)明：皮膚；成纖維細(xì)胞；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SK-MEL-2-LUC細(xì)胞、H-1819細(xì)胞、SHIN-3細(xì)胞

D341Med Cells;背景說(shuō)明：詳見(jiàn)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：髓母細(xì)胞樣;相關(guān)產(chǎn)品有：NCI-H2405細(xì)胞、U20S細(xì)胞、MDA-MB-157細(xì)胞

Panc_04_03 Cells;背景說(shuō)明：詳見(jiàn)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：YD38細(xì)胞、J 111細(xì)胞、SNU-739細(xì)胞

FHs74Int Cells;背景說(shuō)明：小腸;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：D341細(xì)胞、KP-N-RT-BM細(xì)胞、CAL85-1細(xì)胞

769P Cells;背景說(shuō)明：該細(xì)胞系１９７５年建系，源自一位６３歲白人女性的初期透明細(xì)胞腺癌組織，細(xì)胞呈圓形且邊界不清，核漿比大，有微絨毛及橋粒。該細(xì)胞可在軟瓊脂上生長(zhǎng)。 ;傳代方法：１：４—１：１２傳代，２—３天換液一次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：AHH1細(xì)胞、AU-565細(xì)胞、H-1770細(xì)胞

My-La 2059 Cells;背景說(shuō)明：皮膚；T淋巴細(xì)胞瘤;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：U-266 AR1細(xì)胞、H345細(xì)胞、MIMVEC細(xì)胞

AAV-293 Cells;背景說(shuō)明：我們推薦使用AAV-２９３細(xì)胞株繁殖腺病毒相關(guān)重組病毒。 AAV-２９３源自普遍使用的 HEK２９３細(xì)胞株，但產(chǎn)生的病毒滴度更高。 HEK２９３細(xì)胞是剪切過(guò)的腺病毒５型DNA轉(zhuǎn)染的人胚腎細(xì)胞。 跟HEK２９３細(xì)胞一樣，AAV-２９３細(xì)胞反式表達(dá)腺病毒E１基因，當(dāng)共轉(zhuǎn)染三個(gè)AAV助質(zhì)粒(一個(gè)含ITR的質(zhì)粒，pAAV-RC, 和E１缺失助質(zhì)粒)時(shí)，可以產(chǎn)生有感染力的腺病毒-相關(guān)病毒顆粒。;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長(zhǎng)滿(mǎn)。;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：P19細(xì)胞、A1847細(xì)胞、HECV細(xì)胞

ECC-12 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：RCC10細(xì)胞、SCL1細(xì)胞、Lec1細(xì)胞

13008 Cells(提供STR鑒定圖譜)

Abcam HeLa CDKN1A KO Cells(提供STR鑒定圖譜)

AG15898 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRE275 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XG125 Cells(提供STR鑒定圖譜)

C0024 Cells(提供STR鑒定圖譜)

CW10005 Cells(提供STR鑒定圖譜)

DA05560 Cells(提供STR鑒定圖譜)

GHOST(3).CCR1 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(mǎn)。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Sp2/mIL-6細(xì)胞、HEK293-A細(xì)胞、EU-4細(xì)胞

PANC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

Mv.1.Lu Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：YAC細(xì)胞、BC-027細(xì)胞、LICCF細(xì)胞

Sol8 Cells;背景說(shuō)明：骨骼?。籆３H;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：RAW2647細(xì)胞、Oregon J-111細(xì)胞、U-118MG細(xì)胞

253J B-V 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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MNNG/HOS Cl #5細(xì)胞、HEC-1A細(xì)胞、H838細(xì)胞

H-2291 Cells;背景說(shuō)明：詳見(jiàn)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：SuDHL 4細(xì)胞、BCaP-37細(xì)胞、HeLa/DDP細(xì)胞

LNCaP-Clone-FGC Cells;背景說(shuō)明：人前列腺癌細(xì)胞LNCaP克隆FGC是從一位５０歲白人男性(血型B+)的左鎖骨淋巴結(jié)針刺活檢中分離，該患者經(jīng)確診為前列腺癌轉(zhuǎn)移。 這株細(xì)胞對(duì)５-α-二睪酮(生長(zhǎng)調(diào)節(jié)子和酸性脂酶產(chǎn)物)有響應(yīng)。這株細(xì)胞并不形成一致的單層，而是形成集落，在傳代時(shí)可以用滴管反復(fù)吹吸打碎。它們僅僅輕輕地吸附在基底上，不形成匯合，很快使培養(yǎng)基變酸。生長(zhǎng)很慢。傳代后４８小時(shí)內(nèi)不應(yīng)擾動(dòng)。當(dāng)培養(yǎng)瓶封包后，多數(shù)細(xì)胞從培養(yǎng)瓶底分離，懸浮在培養(yǎng)基中。收到后，在通常培養(yǎng)單層細(xì)胞的條件下培養(yǎng)２４到４８小時(shí)，以合細(xì)胞再貼壁。;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長(zhǎng)滿(mǎn)。;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：H1954細(xì)胞、3T6 Swiss Albino細(xì)胞、Tj-905細(xì)胞

1H7G10D10F7 Cells(提供STR鑒定圖譜)

HNEpC Cells;背景說(shuō)明：鼻粘膜；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Jurkat-77細(xì)胞、M-NFS-60細(xì)胞、C4-I細(xì)胞

H2085 Cells;背景說(shuō)明：詳見(jiàn)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：Epstein-Barr-1細(xì)胞、MC3T3, E1 subgroup-4 clone細(xì)胞、H1618細(xì)胞

WEHI-3B Cells;背景說(shuō)明：白血?。籅ALB/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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Okayama University Medical School-23細(xì)胞、H1385細(xì)胞、GA-10-Clone-4細(xì)胞

NK-92MI Cells;背景說(shuō)明：NK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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SLMT1細(xì)胞、SUPB-15細(xì)胞、NCI-SNU-407細(xì)胞

SK-MEL24 Cells;背景說(shuō)明：詳見(jiàn)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

NCIH847 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SUPM2細(xì)胞、Pa16C細(xì)胞、H23細(xì)胞

SW-403 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２—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：TF-1a細(xì)胞、HSC5細(xì)胞、Lewis-Lung細(xì)胞

BT-B Cells;背景說(shuō)明：詳見(jiàn)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;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：HET1A細(xì)胞、Eph4 1424細(xì)胞、G-292 clone A141B1細(xì)胞

HAP1 APOBEC3A (-) 2 Cells(提供STR鑒定圖譜)

HAP1 SLC26A2 (-) 2 Cells(提供STR鑒定圖譜)

TE8 Cells;背景說(shuō)明：詳見(jiàn)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(mǎn)。;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：RASMC細(xì)胞、NKM-1細(xì)胞、PLA-801D細(xì)胞

H446 Cells;背景說(shuō)明：該細(xì)胞是１９８２年由CarneyD和GazdarAF等從一位小細(xì)胞肺癌患者的胸腔積液中建立的。細(xì)胞的原始形態(tài)并不具有小細(xì)胞肺癌特征。這個(gè)細(xì)胞株是小細(xì)胞肺癌的生化和形態(tài)學(xué)上的變種，表達(dá)神經(jīng)元特有的烯醇酶和腦型肌酸激酶同工酶；左旋多巴脫羧酶、蠶素、抗利尿激素、催產(chǎn)素或胃泌激素釋放肽未達(dá)到可檢測(cè)水平。與正常細(xì)胞相比，該細(xì)胞c-mycDNA序列擴(kuò)增約２０倍，RNA增加１５倍。最初傳代培養(yǎng)基用含有５%FBS的RPMI１６４０，另外添加１０nM化可的松、０.００５mg/ml胰島素、０.０１mg/ml轉(zhuǎn)鐵;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁/懸浮生長(zhǎng)，混合;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：SUIT 2細(xì)胞、OV-CA 432細(xì)胞、SF 767細(xì)胞

A-375 Cells;背景說(shuō)明：A３７５源自一位５４歲女性，是Giard DJ等人建立的一系列細(xì)胞株中的一株。該細(xì)胞可在免疫抑制小鼠上成瘤，在瓊脂上形成克隆。;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：H647ell細(xì)胞、A.704細(xì)胞、Hs683T細(xì)胞

COR L279 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：LAN-1細(xì)胞、BLO 11細(xì)胞、MDA-157細(xì)胞

T_T_ Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１０^５ cells/６０mm dish;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：BN-CL2細(xì)胞、NCIH82細(xì)胞、LP1細(xì)胞

MDCK-2 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：３傳代，３-４天傳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：Ku812F細(xì)胞、HS578T細(xì)胞、Swiss/3T3細(xì)胞

CHG5 Cells;背景說(shuō)明：少突神經(jīng)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(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：BE2-M17細(xì)胞、OCI-Ly1細(xì)胞、UCLA-SO-M20細(xì)胞

BEL 7404 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：消化３-５分鐘。１：２。３天內(nèi)可長(zhǎng)滿(mǎn)。;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：Colo205細(xì)胞、JiyoyeP-2003細(xì)胞、HIMEC細(xì)胞

IAR 2-28 Cells(提供STR鑒定圖譜)

LG-1 Cells(提供STR鑒定圖譜)

NBCCS-1AW Cells(提供STR鑒定圖譜)

PACS1001i-GM27160 Cells(提供STR鑒定圖譜)

S004925 Cells(提供STR鑒定圖譜)

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

UQi001-A Cells(提供STR鑒定圖譜)

HAP1 STIM1 (-) 4 Cells(提供STR鑒定圖譜)

IOSE 80 Cells;背景說(shuō)明：卵巢；上皮細(xì)胞；SV４０轉(zhuǎn)化；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：H2330細(xì)胞、NALM-6細(xì)胞、FHC細(xì)胞

Fetal Rhesus Kidney-4 Cells;背景說(shuō)明：胚胎；腎；自發(fā)永生；雌性;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：IGR-OV1細(xì)胞、HOS TE85細(xì)胞、LAN-6細(xì)胞

KP4 Cells;背景說(shuō)明：詳見(jiàn)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：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NS653細(xì)胞、F9細(xì)胞、VP229細(xì)胞

FHs 74 Int Cells;背景說(shuō)明：小腸;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：KPL1細(xì)胞、H-510細(xì)胞、HEC-251細(xì)胞

NCI/ADR-RES Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：FM-88細(xì)胞、DC 2.4細(xì)胞、L-cell細(xì)胞

NCI/ADR-RES Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：FM-88細(xì)胞、DC 2.4細(xì)胞、L-cell細(xì)胞

Hs739T Cells;背景說(shuō)明：詳見(jiàn)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：混合型;相關(guān)產(chǎn)品有：OCI-Ly 7細(xì)胞、B-cell with DC Morphology細(xì)胞、H-2171細(xì)胞

MD Anderson-Metastatic Breast-468 Cells;背景說(shuō)明：該細(xì)胞是１９７７年由CailleauR等從一位患有轉(zhuǎn)移性乳腺癌的５１歲黑人女性的胸腔積液中分離得到的。雖然供體組織的G６PD等位基因雜合，但此細(xì)胞株始終表現(xiàn)為G６PDA表型。P５３基因２７３位密碼子存在G→A突變，從而導(dǎo)致Arg→His替代。每個(gè)細(xì)胞上存在１×１０６個(gè)EGF受體。;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：上皮樣;相關(guān)產(chǎn)品有：YH-13細(xì)胞、SLK細(xì)胞、NCIH1869細(xì)胞

MOPC Cells;背景說(shuō)明：少突膠質(zhì)前體 Cells;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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HS-294細(xì)胞、GM3570細(xì)胞、C57 Mouse Tumor 64細(xì)胞

GTL-16 Cells;背景說(shuō)明：胃癌；肝轉(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：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：H35 Reuber細(xì)胞、SNG-M細(xì)胞、Colo205細(xì)胞

NCI-841 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：３—１：５傳代，;生長(zhǎng)特性：混合型生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：AML-2細(xì)胞、Rat1細(xì)胞、LS180細(xì)胞

NCI-H1238 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NCI-H1668細(xì)胞、BAC1.2F5細(xì)胞、SKMEL-31細(xì)胞

HT 1376 Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：PG-4(S+L-)細(xì)胞、Panc-327細(xì)胞、NCIH1993細(xì)胞

SF-767 Cells;背景說(shuō)明：腦瘤；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SNU251細(xì)胞、IOSE-Mar細(xì)胞、CT 26細(xì)胞

LC-1-sq Cells;背景說(shuō)明：詳見(jiàn)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(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：RH35細(xì)胞、P30OHK細(xì)胞、Panc_03_27細(xì)胞

THP1-Dual KI-hSTING-R232 Cells(提供STR鑒定圖譜)

JROECL19 Cells;背景說(shuō)明：詳見(jiàn)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：LC1/Sq細(xì)胞、U118細(xì)胞、BT483細(xì)胞

M-14 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：３傳代;生長(zhǎng)特性：混合生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SW626細(xì)胞、NIH 3T6細(xì)胞、BNL-CL.2細(xì)胞

Hs 578Bst Cells;背景說(shuō)明：乳腺 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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HCC1171細(xì)胞、Tu686細(xì)胞、J82細(xì)胞

GC1-SPG Cells;背景說(shuō)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(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SaOS-2細(xì)胞、SUM149-PT細(xì)胞、H-1048細(xì)胞

NCI-H522 Cells;背景說(shuō)明：詳見(jiàn)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：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：SJCRH30細(xì)胞、RIN-m 14B細(xì)胞、H2170細(xì)胞

B16 Cells;背景說(shuō)明：該細(xì)胞源于C５７BL/６J小鼠黑色素瘤，可以產(chǎn)生黑色素，同基因小鼠體內(nèi)移植可成瘤;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：梭形;相關(guān)產(chǎn)品有：Panc-08.13細(xì)胞、CCD33Co細(xì)胞、Panc-8_13細(xì)胞

PANC-1人胰腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

SCC15 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：８?jìng)鞔?，?３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：H1092細(xì)胞、NCI-H1694細(xì)胞、Colo699細(xì)胞

Hepatoma-22 Cells;背景說(shuō)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(shí)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(cè)，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(shí)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(zhǎng)特性：懸浮;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：NCI.H522細(xì)胞、Colo320細(xì)胞、B-104細(xì)胞

SKNFI Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：４傳代，每周換液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：Acanthosis Nigricans 3rd attempt-CArcinoma細(xì)胞、NCI-H1155細(xì)胞、WBF344細(xì)胞

SNG-M Cells;背景說(shuō)明：詳見(jiàn)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：多邊形;相關(guān)產(chǎn)品有：SKMEL5細(xì)胞、PIEC細(xì)胞、CNE-1細(xì)胞

H2122 Cells;背景說(shuō)明：詳見(jiàn)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：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：HTR-8/SV-neo細(xì)胞、ANA1細(xì)胞、Mel-RM細(xì)胞

Bx-PC3 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(mǎn)。;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：Hs832T細(xì)胞、B95.8細(xì)胞、MX-1細(xì)胞

NCIH2286 Cells;背景說(shuō)明：詳見(jiàn)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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：橢圓形;相關(guān)產(chǎn)品有：CORL105細(xì)胞、SNT8細(xì)胞、Y3M細(xì)胞

NCI-H1563 Cells;背景說(shuō)明：詳見(jiàn)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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：H4-II-EC3細(xì)胞、ANA-1細(xì)胞、KYSE-410細(xì)胞

BayGenomics ES cell line RRB035 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XE323 Cells(提供STR鑒定圖譜)

CT43 Cells(提供STR鑒定圖譜)

mGC5 Cells(提供STR鑒定圖譜)

Sp2/3-3 Cells(提供STR鑒定圖譜)

LRG Cells(提供STR鑒定圖譜)

" "PubMed=1630814

Ruggeri B.A., Zhang S.-Y., Caamano J., DiRado M., Flynn S.D., Klein-Szanto A.J.P.

Human pancreatic carcinomas and cell lines reveal frequent and multiple alterations in the p53 and Rb-1 tumor-suppressor genes.

Oncogene 7:1503-1511(1992)

PubMed=7809022; DOI=10.1097/00006676-199409000-00018

Sumi S., Beauchamp R.D., Townsend C.M. Jr., Pour P.M., Ishizuka J., Thompson J.C.

Lovastatin inhibits pancreatic cancer growth regardless of RAS mutation.

Pancreas 9:657-661(1994)

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=9023415; DOI=10.1006/cimm.1996.1062

Seki N., Hoshino T., Kikuchi M., Hayashi A., Itoh K.

HLA-A locus-restricted and tumor-specific CTLs in tumor-infiltrating lymphocytes of patients with non-small cell lung cancer.

Cell. Immunol. 175:101-110(1997)

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=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=11169957; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1014>3.0.CO;2-U

Wallrapp C., Hahnel S., Boeck W., Soder A., Mincheva A., Lichter P., Leder G., Gansauge F., Sorio C., Scarpa A., Gress T.M.

Loss of the Y chromosome is a frequent chromosomal imbalance in pancreatic cancer and allows differentiation to chronic pancreatitis.

Int. J. Cancer 91:340-344(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=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=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=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=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=15770730; DOI=10.3748/wjg.v11.i10.1521; PMCID=PMC4305696

Ma J.-H., Patrut E., Schmidt J., Knaebel H.-P., Buchler M.W., Marten A.

Synergistic effects of interferon-alpha in combination with chemoradiation on human pancreatic adenocarcinoma.

World J. Gastroenterol. 11:1521-1528(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)

PubMed=18575732; DOI=10.3892/or.20.1.155

Kawaoka T., Oka M., Takashima M., Ueno T., Yamamoto K., Yahara N., Yoshino S., Hazama S.

Adoptive immunotherapy for pancreatic cancer: cytotoxic T lymphocytes stimulated by the MUC1-expressing human pancreatic cancer cell line YPK-1.

Oncol. Rep. 20:155-163(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

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=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=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=21515691; DOI=10.1074/jbc.M111.226795; PMCID=PMC3121343

McCluskey J.T., Hamid M., Guo-Parke H., McClenaghan N.H., Gomis R., Flatt P.R.

Development and functional characterization of insulin-releasing human pancreatic beta cell lines produced by electrofusion.

J. Biol. Chem. 286:21982-21992(2011)

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)

PubMed=23325432; DOI=10.1101/gr.147942.112; PMCID=PMC3589544

Varley K.E., Gertz J., Bowling K.M., Parker S.L., Reddy T.E., Pauli-Behn F., Cross M.K., Williams B.A., Stamatoyannopoulos J.A., Crawford G.E., Absher D.M., Wold B.J., Myers R.M.

Dynamic DNA methylation across diverse human cell lines and tissues.

Genome Res. 23:555-567(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=25394408; DOI=10.3892/or.2014.3599

Wang C.-F., Zhang W.-W., Fu M.-J., Yang A.-Q., Huang H.-H., Xie J.-M.

Establishment of human pancreatic cancer gemcitabine-resistant cell line with ribonucleotide reductase overexpression.

Oncol. Rep. 33:383-390(2015)

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=26884312; DOI=10.1038/srep21648; PMCID=PMC4756684

Gradiz R., Silva H.C., Carvalho L., Botelho M.F., Mota-Pinto A.

MIA PaCa-2 and PANC-1 -- pancreas ductal adenocarcinoma cell lines with neuroendocrine differentiation and somatostatin receptors.

Sci. Rep. 6:21648-21648(2016)

PubMed=27067801; DOI=10.1186/s12885-016-2297-y; PMCID=PMC4828819

Miura K., Kimura K., Amano R., Yamazoe S., Ohira G., Murata A., Nishio K., Hasegawa T., Yashiro M., Nakata B., Ohira M., Hirakawa K.

Establishment and characterization of new cell lines of anaplastic pancreatic cancer, which is a rare malignancy: OCUP-A1 and OCUP-A2.

BMC Cancer 16:268.1-268.13(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=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=30156359; DOI=10.1111/cas.13783; PMCID=PMC6215881

Sato T., Muramatsu T., Tanabe M., Inazawa J.

Identification and characterization of transforming growth factor beta induced in circulating tumor cell subline from pancreatic cancer cell line.

Cancer Sci. 109:3623-3633(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=31037374; DOI=10.1007/s00216-019-01814-1

Lagies S., Schlimpert M., Braun L.M., Kather M., Plagge J., Erbes T., Wittel U.A., Kammerer B.

Unraveling altered RNA metabolism in pancreatic cancer cells by liquid-chromatography coupling to ion mobility mass spectrometry.

Anal. Bioanal. Chem. 411:6319-6328(2019)

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

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

Next-generation characterization of the Cancer Cell Line Encyclopedia.

Nature 569:503-508(2019)"