"LoVo人結(jié)腸癌細(xì)胞全年復(fù)蘇|已有STR圖譜

傳代比例：1:2-1:4(首次傳代建議1:2)

生長特性：貼壁生長

【細(xì)胞培養(yǎng)經(jīng)驗(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，如營養(yǎng)液、細(xì)胞瓶的擺放位置、滅菌處理程序、開蓋手法、細(xì)胞吹打手法等等。要學(xué)會他們的正確操作，在第一次的時(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?，F(xiàn)象，也好及時(shí)解決這些意外，避免重復(fù)實(shí)驗(yàn)帶來的更大痛苦。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題，還有一批備用的。像后者一般人可能不容易做到。但這是我血的教訓(xùn)，有一次細(xì)胞污染了，全軍覆沒。當(dāng)時(shí)可后悔沒有保種。細(xì)胞跟人一樣，不同的細(xì)胞，培養(yǎng)特性是不一樣的。培養(yǎng)過程中要細(xì)細(xì)體會，不同細(xì)胞系使用不同的培養(yǎng)基和血清。

換液周期：每周2-3次

LC-2/ad Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：TE-85 clone 5細(xì)胞、SDBMSC細(xì)胞、AG 9細(xì)胞

NCI-SNU-601 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：U87 MG細(xì)胞、NIH3T3-L1細(xì)胞、H2591細(xì)胞

95C Cells;背景說明：肺巨細(xì)胞癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：BT474細(xì)胞、Lu-99A細(xì)胞、UO.31細(xì)胞

背景信息：LoVo建自１９７１年，從診斷為結(jié)腸腺癌的５６歲男性白人的一個(gè)轉(zhuǎn)移到左鎖骨上區(qū)的腫瘤結(jié)節(jié)建系。癌基因Ｃ-myc,K-ras,H-ras,N-ras,Myb,sis和fos的表達(dá)呈陽性。癌基因N-myc的表達(dá)未做檢測。它在裸鼠中能成瘤。與１０７細(xì)胞聯(lián)合皮下接種５只裸鼠２１天后全部成瘤。表達(dá)腫瘤特異的核基質(zhì)蛋白蛋白CC-３和CC-４。

LoVo人結(jié)腸癌細(xì)胞全年復(fù)蘇|已有STR圖譜

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)

ATCC細(xì)胞庫(American Type Culture Colection)，該中心一直致力于細(xì)胞分類、鑒定和保藏工作。ATCC是全球最大的生物資源保藏中心，ATCC通過行業(yè)標(biāo)準(zhǔn)產(chǎn)品、服務(wù)和創(chuàng)新解決方案支持全球?qū)W術(shù)、政府、生物技術(shù)、制藥、食品、農(nóng)業(yè)和工業(yè)領(lǐng)域的科學(xué)進(jìn)步。ATCC提供的服務(wù)和定制解決方案包括細(xì)胞和微生物培養(yǎng)、鑒定、生物衍生物的開發(fā)和生產(chǎn)、性能測試和生物資源保藏服務(wù)。美國國家標(biāo)準(zhǔn)協(xié)會(ANSI)認(rèn)可了ATCC標(biāo)準(zhǔn)開發(fā)組織，并制定了標(biāo)準(zhǔn)協(xié)議，以確保生物材料的可靠性和可重復(fù)性。ATCC的使命是為了獲取、鑒定、保存、開發(fā)、標(biāo)準(zhǔn)化和分發(fā)生物資源和生物信息，以提高和應(yīng)用生物科學(xué)知識。

PSN1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：６傳代，２-３天換液１次。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：SVEC4-10細(xì)胞、TOV21G細(xì)胞、DiFi細(xì)胞

NCI-747 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：４傳代，每周換液２次;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：Ramos-2G6-4C10細(xì)胞、CHG5細(xì)胞、FRO81-2細(xì)胞

C3H/10T1/2 clone 8 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：TE 32細(xì)胞、PIG1細(xì)胞、RPMI-8402細(xì)胞

9D4.9.1 Cells(提供STR鑒定圖譜)

來源說明：細(xì)胞主要來源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫

物種來源：人源、鼠源等其它物種來源

LoVo人結(jié)腸癌細(xì)胞全年復(fù)蘇|已有STR圖譜

形態(tài)特性：上皮細(xì)胞樣

細(xì)胞株(系)的使用，為醫(yī)學(xué)研究和測試工作帶來了大的方便。但細(xì)胞的傳代是有限制的，長期連續(xù)傳代的細(xì)胞，不僅消耗大量的人力和物力，而且細(xì)胞的生長與形態(tài)等會有一定退變或轉(zhuǎn)化，因而細(xì)胞失去原有的遺傳性，有時(shí)還會由于細(xì)胞污染而造成傳代中斷，種子丟失。因此，在實(shí)際工作中常需凍存一定數(shù)量的細(xì)胞，以備替換使用。細(xì)胞冷凍與復(fù)蘇是細(xì)胞培養(yǎng) 室的常規(guī)工作和通用技術(shù)。目前，細(xì)胞凍存Zui常用的技術(shù)是冷凍保存法，主要采用加適量保護(hù)劑的緩慢冷凍法凍存細(xì)胞。細(xì)胞在不加任何保護(hù)劑的情況下直接冷凍，細(xì)胞內(nèi)外的水分會很快形成冰晶，從而引起一系列不良反應(yīng)。如細(xì)胞脫水使局部電解質(zhì)濃度增GAO，pH值改變，部分蛋白質(zhì)由于上述原因而變性，引起細(xì)胞內(nèi)部空間結(jié)構(gòu)紊亂，溶酶體膜由此遭到損傷而釋放出溶酶體酶，使細(xì)胞內(nèi)結(jié)構(gòu)成分造成破壞，線粒體腫脹，功能丟失，并造成能量代謝障礙。胞膜上的類脂蛋白復(fù)合體也易破壞引起細(xì)胞膜通透性的改變，使細(xì)胞內(nèi)容物丟失。如果細(xì)胞內(nèi)冰晶形成較多，隨冷凍溫度的降低，冰晶體積膨脹造成細(xì)胞核DNA空間構(gòu)型發(fā)生不可逆的損傷，而致細(xì)胞死亡。因此，細(xì)胞冷凍技術(shù)的關(guān)鍵是盡可能地減少細(xì)胞內(nèi)水分，減少細(xì)胞內(nèi)冰晶的形成。采用甘油或二甲基亞砜作保護(hù)劑，這兩種物質(zhì)分子量小，溶解度大，易穿透細(xì)胞，可以使冰點(diǎn)下降，提GAO細(xì)胞膜對水的通透性，且對細(xì)胞無明顯毒性。慢速冷凍方法又可使細(xì)胞內(nèi)的水分滲出細(xì)胞外，減少胞內(nèi)形成冰結(jié)晶的機(jī)會，從而減少冰晶對細(xì)胞的損傷。

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

H-28 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代，每周換液２-３次;生長特性：貼壁生長;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCIH2126細(xì)胞、NCI-H2228細(xì)胞、UACC-812細(xì)胞

BAR-T Cells;背景說明：食管；HGNC-TERT轉(zhuǎn)化；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HEK-293F細(xì)胞、H22-H8D8細(xì)胞、CWR-22rv1細(xì)胞

ChaGo-K-1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：８傳代；每周換液２次。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：Michigan Cancer Foundation-7細(xì)胞、LS123細(xì)胞、CAKI1細(xì)胞

MAVER Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：５傳代；２-３天換液１次。;生長特性：懸浮生長;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：HuH 6細(xì)胞、FL-83B細(xì)胞、P3.NS-1/1.Ag4.1細(xì)胞

H-1385 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：WIL2 Secreting細(xì)胞、H125細(xì)胞、Bat lung細(xì)胞

MARC 145 Cells;背景說明：胚腎；自發(fā)永生;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：CoCL2細(xì)胞、CP70細(xì)胞、T-T細(xì)胞

H-23 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３傳代；３-４天１次。;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：L 363細(xì)胞、SK-N-BE(2C)細(xì)胞、NCI-H187細(xì)胞

F56 [Human neoplasm] Cells;背景說明：F５６是一株人的腺癌細(xì)胞系，可用于腺癌發(fā)生機(jī)制的研究，也可用于抗癌藥物的篩選。;傳代方法：１：２傳代;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：CL-11細(xì)胞、PANC-02-03細(xì)胞、TE-85 clone 5細(xì)胞

Hep 3B Cells;背景說明：肝癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Factor Dependent Continuous-Paterson 1細(xì)胞、SNGM細(xì)胞、HEK 293 c18細(xì)胞

NG10815 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：P30-OHK細(xì)胞、B78細(xì)胞、IOSE-80細(xì)胞

Panc-3_27 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：WiDr細(xì)胞、SUIT 2細(xì)胞、PC3M-2B4細(xì)胞

ChaGo K-1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：８傳代；每周換液２次。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：UCH1細(xì)胞、HIT clone T15細(xì)胞、KYSE 510細(xì)胞

NCI-H2073 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代 ;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：Gerner 7666細(xì)胞、HS-68細(xì)胞、B35細(xì)胞

Pt-K2 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MDA 231-LM2-4175細(xì)胞、HFT-8810細(xì)胞、HKF細(xì)胞

GT38 Cells;背景說明：胃癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：TOG細(xì)胞、CoCL3細(xì)胞、Mv 1 Lu細(xì)胞

NB19-RIKEN Cells;背景說明：神經(jīng)母細(xì)胞瘤；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MODE-K細(xì)胞、NCI-H2342細(xì)胞、IPEC-J2細(xì)胞

Abcam HCT 116 KRT19 KO Cells(提供STR鑒定圖譜)

AG07613 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSJ151 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line TEA009 Cells(提供STR鑒定圖譜)

BJTTHi003-A Cells(提供STR鑒定圖譜)

CL1DNEO Cells(提供STR鑒定圖譜)

DA03396 Cells(提供STR鑒定圖譜)

eCG 50.5 Cells(提供STR鑒定圖譜)

GM05209 Cells(提供STR鑒定圖譜)

H-920 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：JVM3細(xì)胞、SNU475細(xì)胞、NCIH2052細(xì)胞

NCI747 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：４傳代，每周換液２次;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：N87細(xì)胞、KYSE0520細(xì)胞、NCI-H735細(xì)胞

V-79-4 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HBZY 1細(xì)胞、C3H/10T1/2 clone 8細(xì)胞、A204細(xì)胞

High-5 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCIH446細(xì)胞、CL-40細(xì)胞、HCC-1359細(xì)胞

OCI-LY-1 Cells;背景說明：彌漫大B淋巴瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Hs 445細(xì)胞、L6細(xì)胞、SMMC7721細(xì)胞

H3255 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長特性：貼壁生長　;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：RCC-4細(xì)胞、KP4細(xì)胞、KU-812F細(xì)胞

NCI-H2106 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２次。;生長特性：懸浮生長;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Institute for Medical Research-32細(xì)胞、SK-OV-433細(xì)胞、VMM-5A細(xì)胞

VeroC1008 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Bronchial Epithelium transformed with Ad12-SV40 2B細(xì)胞、CEMO-1細(xì)胞、EST81細(xì)胞

LoVo人結(jié)腸癌細(xì)胞全年復(fù)蘇|已有STR圖譜

Rat 2 Cells;背景說明：成纖維細(xì)胞；自發(fā)永生；Fischer ３４４;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：AR4IP細(xì)胞、TEV-1細(xì)胞、253J B-V細(xì)胞

AC29 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HEC-1-B細(xì)胞、H8細(xì)胞、GM3190細(xì)胞

K-1735 Cells;背景說明：黑色素瘤； C３H/HeN;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：786.O細(xì)胞、Calu 6細(xì)胞、HSAS3細(xì)胞

BAEC Cells;背景說明：主動脈；內(nèi)皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：C28/I2細(xì)胞、H295細(xì)胞、LK2細(xì)胞

BEAS-2B Cells;背景說明：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抗原染色陽性。;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長滿;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：PA-1細(xì)胞、143TK-細(xì)胞、HCC0078細(xì)胞

BEAS-2B Cells;背景說明：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抗原染色陽性。;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長滿;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：PA-1細(xì)胞、143TK-細(xì)胞、HCC0078細(xì)胞

HDQ-P1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HCT.116細(xì)胞、A-673細(xì)胞、HIEC細(xì)胞

HAP1 ABCC1 (-) 3 Cells(提供STR鑒定圖譜)

HAP1 SCML2 (-) 2 Cells(提供STR鑒定圖譜)

CTV1 Cells;背景說明：急性T淋巴細(xì)胞白血?。荒行?傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Intestinal Epithelioid Cell line No. 6細(xì)胞、NEC細(xì)胞、PANC.1細(xì)胞

MHCC97H Cells;背景說明：來源于中山醫(yī)院，用人肝癌細(xì)胞株MHCC９７-H接種裸鼠，進(jìn)行３次肺轉(zhuǎn)移篩選，取肺轉(zhuǎn)移瘤建成皮下接種后高度自發(fā)性肺轉(zhuǎn)移的肝癌細(xì)胞系;傳代方法：１：２傳代;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：Melanoma 14細(xì)胞、M-O7e細(xì)胞、H2030細(xì)胞

HL-60 Cells;背景說明：該細(xì)胞由CollinsSJ從一位患有急性早幼粒細(xì)胞性白血病的３６歲白人女性的外周血中分離建立；可自發(fā)分化，或在鹽、次黃嘌呤、佛波醇肉豆蔻酸(PMA,TPA)、DMSO(１%to１.５%)、D和視黃酸的刺激下發(fā)生分化；PMA刺激后可分泌TNF-α。該細(xì)胞具有吞噬活性和趨化反應(yīng)，癌基因myc陽性，表達(dá)補(bǔ)體受體和FcR。;傳代方法：維持細(xì)胞濃度在１×１０５-１×１０６/ml,每２-３天換液１次。;生長特性：懸浮生長;形態(tài)特性：髓母細(xì)胞樣;相關(guān)產(chǎn)品有：Panc-813細(xì)胞、CX-1細(xì)胞、KNS62細(xì)胞

3T3 Cells;背景說明：３T３細(xì)胞株是１９６２年Todaro G和Green H從分離的瑞士小鼠胚胎中建立的；該細(xì)胞的生長受接觸性抑制，匯合狀態(tài)的單層細(xì)胞密度為４００００個(gè)細(xì)胞/平方厘米；檢測結(jié)果顯示該細(xì)胞鼠痘病毒陰性；在中生長較好，在某些玻璃表面上可能狀態(tài)不佳；細(xì)胞生長飽和時(shí)其密度可以達(dá)到約５００００ cells/cm２。;傳代方法：１：３傳代；３-４天１次。;生長特性：貼壁生長;形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：Me-Wo細(xì)胞、WERIRb1細(xì)胞、Line 207細(xì)胞

NB9 Cells;背景說明：詳見相關(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。;生長特性：貼壁生長;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

NPA'87 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Lewis-Lung細(xì)胞、HBZY1細(xì)胞、87 MG細(xì)胞

TFK1 Cells;背景說明：膽管癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：ID8細(xì)胞、H520細(xì)胞、HCC1143細(xì)胞

MFM-223 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SKLU-1細(xì)胞、KM12-SM細(xì)胞、P3X63Ag8-6-5-3細(xì)胞

HyCyte H4-II KO-rInsrr Cells(提供STR鑒定圖譜)

LC-06-JCK Cells(提供STR鑒定圖譜)

MZ-MEL-18 Cells(提供STR鑒定圖譜)

OUN-1 Cells(提供STR鑒定圖譜)

RPMI-8432 Cells(提供STR鑒定圖譜)

Ubigene HEK293 PPA2 KO Cells(提供STR鑒定圖譜)

WG3733 Cells(提供STR鑒定圖譜)

HARA [Human B-cell IHW] Cells(提供STR鑒定圖譜)

GLC82 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCTC 929細(xì)胞、Panc5.04細(xì)胞、TE-8細(xì)胞

Rat Fetal Lung-6 Cells;背景說明：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。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：JB6 [Mouse]細(xì)胞、HUV-EC-C細(xì)胞、SK-MEL-2細(xì)胞

MM1S Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代，２-３天換液１次。;生長特性：混合生長;形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：L-1210細(xì)胞、FAT細(xì)胞、B5537SKIN細(xì)胞

293H Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SMC-1細(xì)胞、HEK (AD293)細(xì)胞、MSB-1細(xì)胞

CEM-CCRF (CAMR) Cells;背景說明：G.E. Foley 等人建立了類淋巴母細(xì)胞細(xì)胞株CCRF-CEM。 細(xì)胞是１９６４年１１月從一位四歲白人女性急性淋巴細(xì)胞白血病患者的外周血白血球衣中得到。此細(xì)胞系從香港收集而來。;傳代方法：１：２傳代。３天內(nèi)可長滿。;生長特性：懸浮生長;形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：H-358細(xì)胞、SKM-1細(xì)胞、Epstein-Barr-3細(xì)胞

CEM-CCRF (CAMR) Cells;背景說明：G.E. Foley 等人建立了類淋巴母細(xì)胞細(xì)胞株CCRF-CEM。 細(xì)胞是１９６４年１１月從一位四歲白人女性急性淋巴細(xì)胞白血病患者的外周血白血球衣中得到。此細(xì)胞系從香港收集而來。;傳代方法：１：２傳代。３天內(nèi)可長滿。;生長特性：懸浮生長;形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：H-358細(xì)胞、SKM-1細(xì)胞、Epstein-Barr-3細(xì)胞

JKT-1 Cells;背景說明：精原瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HEYA8細(xì)胞、NCI-SNU-449細(xì)胞、HCC0366細(xì)胞

RGCs Cells;背景說明：視網(wǎng)膜；神經(jīng)節(jié) Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SK-MES-1細(xì)胞、C81-61細(xì)胞、3T6 Swiss Albino細(xì)胞

Eph4 1424 Cells;背景說明：乳腺癌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HDMEC細(xì)胞、RBMVEC細(xì)胞、LC-2-Ad細(xì)胞

RBSMC Cells;背景說明：腦動脈；平滑肌;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：LNCaP-C4-2細(xì)胞、MDA MB231細(xì)胞、HFT 8810細(xì)胞

CFSC-8B Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：L-6 myoblast細(xì)胞、HCAEC細(xì)胞、M20 [Human melanoma]細(xì)胞

CHL-1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：６—１：１０傳代;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：NCI-128細(xì)胞、HEK/EBNA細(xì)胞、MGH-U1細(xì)胞

RMS13 Cells;背景說明：肺泡橫紋肌肉瘤；骨髓轉(zhuǎn)移;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：WM115-mel細(xì)胞、P3 NS1 Ag4細(xì)胞、SP2細(xì)胞

CHO Cells;背景說明：１９５７年，PuckTT從成年中國倉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;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：MT-2細(xì)胞、EVSAT細(xì)胞、HECCL-1細(xì)胞

Swiss 3T3 Cells;背景說明：３T３細(xì)胞株是１９６２年Todaro G和Green H從分離的瑞士小鼠胚胎中建立的；該細(xì)胞的生長受接觸性抑制，匯合狀態(tài)的單層細(xì)胞密度為４００００個(gè)細(xì)胞/平方厘米；檢測結(jié)果顯示該細(xì)胞鼠痘病毒陰性；在中生長較好，在某些玻璃表面上可能狀態(tài)不佳；細(xì)胞生長飽和時(shí)其密度可以達(dá)到約５００００ cells/cm２。;傳代方法：１：３傳代；３-４天１次。;生長特性：貼壁生長;形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：JROECL 19細(xì)胞、624細(xì)胞、HNE2細(xì)胞

TCC-SUPrGEMCI20 Cells(提供STR鑒定圖譜)

OCI-Ly 18 Cells;背景說明：彌漫大B細(xì)胞淋巴瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：8305C細(xì)胞、F81細(xì)胞、P-3J細(xì)胞

GM637A Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HO-8910 PM細(xì)胞、686LN-M4e細(xì)胞、Hs 746.T細(xì)胞

MCF 7B Cells;背景說明：浸潤性導(dǎo)管癌；胸腔積液轉(zhuǎn)移；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：J-111細(xì)胞、CCD 1112SK細(xì)胞、Hep 2細(xì)胞

T_T_ Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１０^５ cells/６０mm dish;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：BN-CL2細(xì)胞、NCIH82細(xì)胞、LP1細(xì)胞

WIL2S Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：TGW細(xì)胞、HOC細(xì)胞、SF-539細(xì)胞

U373-MG Cells;背景說明：膠質(zhì)瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Human Melanoma Cell Bowes細(xì)胞、HCC1954細(xì)胞、Me-Wo細(xì)胞

RKO_AS45 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCL-H548細(xì)胞、X63-Ag8.653細(xì)胞、Saos2細(xì)胞

CHL1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：６—１：１０傳代;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：MBMEC細(xì)胞、NCI-H220細(xì)胞、MDA157細(xì)胞

LoVo人結(jié)腸癌細(xì)胞全年復(fù)蘇|已有STR圖譜

HFLS Cells;背景說明：滑膜；成纖維 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MPC11細(xì)胞、HCC-9204細(xì)胞、HEM細(xì)胞

SK-RC-39 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：PE/CA-PJ34細(xì)胞、Huh 7.5.1細(xì)胞、GM03571細(xì)胞

SF17 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HCC2157細(xì)胞、IPLB-SF-21-AE細(xì)胞、Mouse Forestomach Carcinoma細(xì)胞

GC-2spd(ts) Cells;背景說明：精母細(xì)胞；SV４０轉(zhuǎn)化；BALB/c;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Lilly Laboratories Cell-Monkey Kidney 2細(xì)胞、JM1細(xì)胞、BNL-HCC細(xì)胞

SK-NSH Cells;背景說明：SK-N-SH細(xì)胞系由J.L.Bieder建系，它與SK-N-MC所不同的是倍增時(shí)間較長且多巴胺-β-羥基酶水平較高。 SK-N-SH在細(xì)胞介導(dǎo)的細(xì)胞毒性試驗(yàn)中用作靶細(xì)胞系。;傳代方法：１：２傳代;生長特性：懸浮生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：BHK 21細(xì)胞、EFM-192C細(xì)胞、NCI-SNU-475細(xì)胞

SUM 102 Cells;背景說明：乳腺癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SK BR 03細(xì)胞、H157細(xì)胞、SK Mel 24細(xì)胞

BayGenomics ES cell line CSH170 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRU529 Cells(提供STR鑒定圖譜)

BCL1 clone CW13.20-3B3 Cells(提供STR鑒定圖譜)

KKF Cells(提供STR鑒定圖譜)

PCRP-ZNF485-1G1 Cells(提供STR鑒定圖譜)

NOBEC-1 Cells(提供STR鑒定圖譜)

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Browning M.J., Krausa P., Rowan A.J., Bicknell D.C., Bodmer J.G., Bodmer W.F.

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Cottu P.-H., Muzeau F., Estreicher A., Flejou J.-F., Iggo R.D., Thomas G., Hamelin R.

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Screening the p53 status of human cell lines using a yeast functional assay.

Mol. Carcinog. 19:243-253(1997)

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Ilyas M., Tomlinson I.P.M., Rowan A.J., Pignatelli M., Bodmer W.F.

Beta-catenin mutations in cell lines established from human colorectal cancers.

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Sparks A.B., Morin P.J., Vogelstein B., Kinzler K.W.

Mutational analysis of the APC/beta-catenin/Tcf pathway in colorectal cancer.

Cancer Res. 58:1130-1134(1998)

PubMed=9715273; DOI=10.1038/sj.onc.1201986

Eshleman J.R., Casey G., Kochera M.E., Sedwick W.D., Swinler S.E., Veigl M.L., Willson J.K.V., Schwartz S., Markowitz S.D.

Chromosome number and structure both are markedly stable in RER colorectal cancers and are not destabilized by mutation of p53.

Oncogene 17:719-725(1998)

PubMed=10674020; DOI=10.1016/S0959-8049(99)00206-3

Ku J.-L., Yoon K.-A., Kim D.-Y., Park J.-G.

Mutations in hMSH6 alone are not sufficient to cause the microsatellite instability in colorectal cancer cell lines.

Eur. J. Cancer 35:1724-1729(1999)

PubMed=10612807; DOI=10.1002/(SICI)1098-2264(200002)27:2<183::aid-gcc10>3.0.CO;2-P; PMCID=PMC4721570

Ghadimi B.M., Sackett D.L., Difilippantonio M.J., Schrock E., Neumann T., Jauho A., Auer G., Ried T.

Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations.

Genes Chromosomes Cancer 27:183-190(2000)

PubMed=10737795; DOI=10.1073/pnas.97.7.3352; PMCID=PMC16243

Rowan A.J., Lamlum H., Ilyas M., Wheeler J.M.D., Straub J., Papadopoulou A., Bicknell D.C., Bodmer W.F., Tomlinson I.P.M.

APC mutations in sporadic colorectal tumors: a mutational 'hotspot' and interdependence of the 'two hits'.

Proc. Natl. Acad. Sci. U.S.A. 97:3352-3357(2000)

PubMed=11226274; DOI=10.1073/pnas.041603298; PMCID=PMC30173

Abdel-Rahman W.M., Katsura K., Rens W., Gorman P.A., Sheer D., Bicknell D.C., Bodmer W.F., Arends M.J., Wyllie A.H., Edwards P.A.W.

Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement.

Proc. Natl. Acad. Sci. U.S.A. 98:2538-2543(2001)

PubMed=11314036; DOI=10.1038/sj.onc.1204211

Forgacs E., Wren J.D., Kamibayashi C., Kondo M., Xu X.L., Markowitz S.D., Tomlinson G.E., Muller C.Y., Gazdar A.F., Garner H.R., Minna J.D.

Searching for microsatellite mutations in coding regions in lung, breast, ovarian and colorectal cancers.

Oncogene 20:1005-1009(2001)

PubMed=11414198; DOI=10.1007/s004320000207

Lahm H., Andre S., Hoeflich A., Fischer J.R., Sordat B., Kaltner H., Wolf E., Gabius H.-J.

Comprehensive galectin fingerprinting in a panel of 61 human tumor cell lines by RT-PCR and its implications for diagnostic and therapeutic procedures.

J. Cancer Res. Clin. Oncol. 127:375-386(2001)

PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459

Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.

Short tandem repeat profiling provides an international reference standard for human cell lines.

Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)

PubMed=11526487; DOI=10.1038/sj.onc.1204611

Gayet J., Zhou X.-P., Duval A., Rolland S., Hoang J.-M., Cottu P.-H., Hamelin R.

Extensive characterization of genetic alterations in a series of human colorectal cancer cell lines.

Oncogene 20:5025-5032(2001)

PubMed=11668190; DOI=10.1177/002215540104901105

Quentmeier H., Osborn M., Reinhardt J., Zaborski M., Drexler H.G.

Immunocytochemical analysis of cell lines derived from solid tumors.

J. Histochem. Cytochem. 49:1369-1378(2001)

PubMed=12068308; DOI=10.1038/nature00766

Davies H.R., Bignell G.R., Cox C., Stephens P.J., Edkins S., Clegg S., Teague J.W., Woffendin H., Garnett M.J., Bottomley W., Davis N., Dicks E., Ewing R., Floyd Y., Gray K., Hall S., Hawes R., Hughes J., Kosmidou V., Menzies A., Mould C., Parker A., Stevens C., Watt S., Hooper S., Wilson R., Jayatilake H., Gusterson B.A., Cooper C.S., Shipley J.M., Hargrave D., Pritchard-Jones K., Maitland N.J., Chenevix-Trench G., Riggins G.J., Bigner D.D., Palmieri G., Cossu A., Flanagan A.M., Nicholson A., Ho J.W.C., Leung S.Y., Yuen S.T., Weber B.L., Seigler H.F., Darrow T.L., Paterson H.F., Marais R., Marshall C.J., Wooster R., Stratton M.R., Futreal P.A.

Mutations of the BRAF gene in human cancer.

Nature 417:949-954(2002)

PubMed=12584437; DOI=10.1159/000068544

Melcher R., Koehler S., Steinlein C., Schmid M., Mueller C.R., Luehrs H., Menzel T., Scheppach W., Moerk H., Scheurlen M., Koehrle J., Al-Taie O.

Spectral karyotype analysis of colon cancer cell lines of the tumor suppressor and mutator pathway.

Cytogenet. Genome Res. 98:22-28(2002)

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Hempen P.M., Zhang L., Bansal R.K., Iacobuzio-Donahue C.A., Murphy K.M., Maitra A., Vogelstein B., Whitehead R.H., Markowitz S.D., Willson J.K.V., Yeo C.J., Hruban R.H., Kern S.E.

Evidence of selection for clones having genetic inactivation of the activin A type II receptor (ACVR2) gene in gastrointestinal cancers.

Cancer Res. 63:994-999(2003)

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Seitz S., Wassmuth P., Plaschke J., Schackert H.K., Karsten U., Santibanez-Koref M.F., Schlag P.M., Scherneck S.

Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines.

Genes Chromosomes Cancer 37:29-35(2003)

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Melcher R., Maisch S., Koehler S., Bauer M., Steinlein C., Schmid M., Kudlich T., Schauber J., Luehrs H., Menzel T., Scheppach W.

SKY and genetic fingerprinting reveal a cross-contamination of the putative normal colon epithelial cell line NCOL-1.

Cancer Genet. Cytogenet. 158:84-87(2005)

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Mashima T., Oh-hara T., Sato S., Mochizuki M., Sugimoto Y., Yamazaki K., Hamada J.-i., Tada M., Moriuchi T., Ishikawa Y., Kato Y., Tomoda H., Yamori T., Tsuruo T.

p53-defective tumors with a functional apoptosome-mediated pathway: a new therapeutic target.

J. Natl. Cancer Inst. 97:765-777(2005)

PubMed=16418264; DOI=10.1073/pnas.0510146103; PMCID=PMC1327731

Liu Y., Bodmer W.F.

Analysis of p53 mutations and their expression in 56 colorectal cancer cell lines.

Proc. Natl. Acad. Sci. U.S.A. 103:976-981(2006)

PubMed=16854228; DOI=10.1186/1476-4598-5-29; PMCID=PMC1550420

Bandres Elizalde E.M., Cubedo E., Agirre X., Malumbres R., Zarate R., Ramirez N., Abajo A., Navarro A., Moreno I., Monzo M., Garcia-Foncillas J.

Identification by real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues.

Mol. Cancer 5:29.1-29.10(2006)

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Emaduddin M., Bicknell D.C., Bodmer W.F., Feller S.M.

Cell growth, global phosphotyrosine elevation, and c-Met phosphorylation through Src family kinases in colorectal cancer cells.

Proc. Natl. Acad. Sci. U.S.A. 105:2358-2362(2008)

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Knutsen T., Padilla-Nash H.M., Wangsa D., Barenboim-Stapleton L., Camps J., McNeil N.E., Difilippantonio M.J., Ried T.

Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines.

Genes Chromosomes Cancer 49:204-223(2010)

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Karger A., Bettin B., Lenk M., Mettenleiter T.C.

Rapid characterisation of cell cultures by matrix-assisted laser desorption/ionisation mass spectrometric typing.

J. Virol. Methods 164:116-121(2010)

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=20570890; DOI=10.1158/0008-5472.CAN-10-0192; PMCID=PMC2943514

Janakiraman M., Vakiani E., Zeng Z.-S., Pratilas C.A., Taylor B.S., Chitale D., Halilovic E., Wilson M., Huberman K., Ricarte Filho J.C.M., Persaud Y., Levine D.A., Fagin J.A., Jhanwar S.C., Mariadason J.M., Lash A., Ladanyi M., Saltz L.B., Heguy A., Paty P.B., Solit D.B.

Genomic and biological characterization of exon 4 KRAS mutations in human cancer.

Cancer Res. 70:5901-5911(2010)

PubMed=20606684; DOI=10.1038/sj.bjc.6605780; PMCID=PMC2920028

Bracht K., Nicholls A.M., Liu Y., Bodmer W.F.

5-fluorouracil response in a large panel of colorectal cancer cell lines is associated with mismatch repair deficiency.

Br. J. Cancer 103:340-346(2010)

PubMed=20831567; DOI=10.1111/j.1582-4934.2010.01170.x; PMCID=PMC3918049

Ma Y.-L., Zhang P., Wang F., Moyer M.P., Yang J.-J., Liu Z.-H., Peng J.-Y., Chen H.-Q., Zhou Y.-K., Liu W.-J., Qin H.-L.

Human embryonic stem cells and metastatic colorectal cancer cells shared the common endogenous human microRNA-26b.

J. Cell. Mol. Med. 15:1941-1954(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=24042735; DOI=10.1038/oncsis.2013.35; PMCID=PMC3816225

Ahmed D., Eide P.W., Eilertsen I.A., Danielsen S.A., Eknaes M., Hektoen M., Lind G.E., Lothe R.A.

Epigenetic and genetic features of 24 colon cancer cell lines.

Oncogenesis 2:e71.1-e71.8(2013)

PubMed=24755471; DOI=10.1158/0008-5472.CAN-14-0013

Mouradov D., Sloggett C., Jorissen R.N., Love C.G., Li S., Burgess A.W., Arango D., Strausberg R.L., Buchanan D., Wormald S., O'Connor L., Wilding J.L., Bicknell D.C., Tomlinson I.P.M., Bodmer W.F., Mariadason J.M., Sieber O.M.

Colorectal cancer cell lines are representative models of the main molecular subtypes of primary cancer.

Cancer Res. 74:3238-3247(2014)

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