"LoVo人結腸癌細胞全年復蘇|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
【細胞培養(yǎng)經(jīng)驗分享】啟蒙老師的重要性:一般進實驗室都有師兄師姐帶著做,他們就是你做細胞的啟蒙老師。他們的操作手法、細節(jié)、理論講解就成了你操作的準則,如營養(yǎng)液、細胞瓶的擺放位置、滅菌處理程序、開蓋手法、細胞吹打手法等等。要學會他們的正確操作,在第一次的時候就要重視。像養(yǎng)孩子一樣養(yǎng)細胞,細胞有時真的很脆弱,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,也好及時解決這些意外,避免重復實驗帶來的更大痛苦。好細胞要及時保種:細胞要分批傳代,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,有一次細胞污染了,全軍覆沒。當時可后悔沒有保種。細胞跟人一樣,不同的細胞,培養(yǎng)特性是不一樣的。培養(yǎng)過程中要細細體會,不同細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:詳見相關文獻介紹;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;相關產(chǎn)品有:TE-85 clone 5細胞、SDBMSC細胞、AG 9細胞
NCI-SNU-601 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:U87 MG細胞、NIH3T3-L1細胞、H2591細胞
95C Cells;背景說明:肺巨細胞癌;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;相關產(chǎn)品有:BT474細胞、Lu-99A細胞、UO.31細胞
背景信息:LoVo建自1971年,從診斷為結腸腺癌的56歲男性白人的一個轉移到左鎖骨上區(qū)的腫瘤結節(jié)建系。癌基因C-myc,K-ras,H-ras,N-ras,Myb,sis和fos的表達呈陽性。癌基因N-myc的表達未做檢測。它在裸鼠中能成瘤。與107細胞聯(lián)合皮下接種5只裸鼠21天后全部成瘤。表達腫瘤特異的核基質蛋白蛋白CC-3和CC-4。
LoVo人結腸癌細胞全年復蘇|已有STR圖譜
產(chǎn)品包裝:復蘇發(fā)貨:T25培養(yǎng)瓶(一瓶)或凍存發(fā)貨:1ml凍存管(兩支)
ATCC細胞庫(American Type Culture Colection),該中心一直致力于細胞分類、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)標準產(chǎn)品、服務和創(chuàng)新解決方案支持全球學術、政府、生物技術、制藥、食品、農(nóng)業(yè)和工業(yè)領域的科學進步。ATCC提供的服務和定制解決方案包括細胞和微生物培養(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。美國國家標準協(xié)會(ANSI)認可了ATCC標準開發(fā)組織,并制定了標準協(xié)議,以確保生物材料的可靠性和可重復性。ATCC的使命是為了獲取、鑒定、保存、開發(fā)、標準化和分發(fā)生物資源和生物信息,以提高和應用生物科學知識。
PSN1 Cells;背景說明:詳見相關文獻介紹;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:上皮細胞;相關產(chǎn)品有:SVEC4-10細胞、TOV21G細胞、DiFi細胞
NCI-747 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:Ramos-2G6-4C10細胞、CHG5細胞、FRO81-2細胞
C3H/10T1/2 clone 8 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:TE 32細胞、PIG1細胞、RPMI-8402細胞
9D4.9.1 Cells(提供STR鑒定圖譜)
來源說明:細胞主要來源ATCC、ECACC、DSMZ、RIKEN等細胞庫
物種來源:人源、鼠源等其它物種來源
LoVo人結腸癌細胞全年復蘇|已有STR圖譜
形態(tài)特性:上皮細胞樣
細胞株(系)的使用,為醫(yī)學研究和測試工作帶來了大的方便。但細胞的傳代是有限制的,長期連續(xù)傳代的細胞,不僅消耗大量的人力和物力,而且細胞的生長與形態(tài)等會有一定退變或轉化,因而細胞失去原有的遺傳性,有時還會由于細胞污染而造成傳代中斷,種子丟失。因此,在實際工作中常需凍存一定數(shù)量的細胞,以備替換使用。細胞冷凍與復蘇是細胞培養(yǎng) 室的常規(guī)工作和通用技術。目前,細胞凍存Zui常用的技術是冷凍保存法,主要采用加適量保護劑的緩慢冷凍法凍存細胞。細胞在不加任何保護劑的情況下直接冷凍,細胞內外的水分會很快形成冰晶,從而引起一系列不良反應。如細胞脫水使局部電解質濃度增GAO,pH值改變,部分蛋白質由于上述原因而變性,引起細胞內部空間結構紊亂,溶酶體膜由此遭到損傷而釋放出溶酶體酶,使細胞內結構成分造成破壞,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合體也易破壞引起細胞膜通透性的改變,使細胞內容物丟失。如果細胞內冰晶形成較多,隨冷凍溫度的降低,冰晶體積膨脹造成細胞核DNA空間構型發(fā)生不可逆的損傷,而致細胞死亡。因此,細胞冷凍技術的關鍵是盡可能地減少細胞內水分,減少細胞內冰晶的形成。采用甘油或二甲基亞砜作保護劑,這兩種物質分子量小,溶解度大,易穿透細胞,可以使冰點下降,提GAO細胞膜對水的通透性,且對細胞無明顯毒性。慢速冷凍方法又可使細胞內的水分滲出細胞外,減少胞內形成冰結晶的機會,從而減少冰晶對細胞的損傷。
HT-55 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:BT-474細胞、NS1/1-Ag4.1細胞、HLEB-3細胞
H-28 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:NCIH2126細胞、NCI-H2228細胞、UACC-812細胞
BAR-T Cells;背景說明:食管;HGNC-TERT轉化;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;相關產(chǎn)品有:HEK-293F細胞、H22-H8D8細胞、CWR-22rv1細胞
ChaGo-K-1 Cells;背景說明:詳見相關文獻介紹;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:上皮細胞;相關產(chǎn)品有:Michigan Cancer Foundation-7細胞、LS123細胞、CAKI1細胞
MAVER Cells;背景說明:詳見相關文獻介紹;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:淋巴母細胞;相關產(chǎn)品有:HuH 6細胞、FL-83B細胞、P3.NS-1/1.Ag4.1細胞
H-1385 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:WIL2 Secreting細胞、H125細胞、Bat lung細胞
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;相關產(chǎn)品有:CoCL2細胞、CP70細胞、T-T細胞
H-23 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:L 363細胞、SK-N-BE(2C)細胞、NCI-H187細胞
F56 [Human neoplasm] Cells;背景說明:F56是一株人的腺癌細胞系,可用于腺癌發(fā)生機制的研究,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:上皮細胞樣;相關產(chǎn)品有:CL-11細胞、PANC-02-03細胞、TE-85 clone 5細胞
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;相關產(chǎn)品有:Factor Dependent Continuous-Paterson 1細胞、SNGM細胞、HEK 293 c18細胞
NG10815 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:P30-OHK細胞、B78細胞、IOSE-80細胞
Panc-3_27 Cells;背景說明:詳見相關文獻介紹;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關產(chǎn)品有:WiDr細胞、SUIT 2細胞、PC3M-2B4細胞
ChaGo K-1 Cells;背景說明:詳見相關文獻介紹;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:上皮細胞;相關產(chǎn)品有:UCH1細胞、HIT clone T15細胞、KYSE 510細胞
NCI-H2073 Cells;背景說明:詳見相關文獻介紹;傳代方法:1:3-1:6傳代 ;生長特性:貼壁生長;形態(tài)特性:上皮細胞;相關產(chǎn)品有:Gerner 7666細胞、HS-68細胞、B35細胞
Pt-K2 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:MDA 231-LM2-4175細胞、HFT-8810細胞、HKF細胞
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;相關產(chǎn)品有:TOG細胞、CoCL3細胞、Mv 1 Lu細胞
NB19-RIKEN Cells;背景說明:神經(jīng)母細胞瘤;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;相關產(chǎn)品有:MODE-K細胞、NCI-H2342細胞、IPEC-J2細胞
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:詳見相關文獻介紹;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;相關產(chǎn)品有:JVM3細胞、SNU475細胞、NCIH2052細胞
NCI747 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:N87細胞、KYSE0520細胞、NCI-H735細胞
V-79-4 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:HBZY 1細胞、C3H/10T1/2 clone 8細胞、A204細胞
High-5 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:NCIH446細胞、CL-40細胞、HCC-1359細胞
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;相關產(chǎn)品有:Hs 445細胞、L6細胞、SMMC7721細胞
H3255 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:RCC-4細胞、KP4細胞、KU-812F細胞
NCI-H2106 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:Institute for Medical Research-32細胞、SK-OV-433細胞、VMM-5A細胞
VeroC1008 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:Bronchial Epithelium transformed with Ad12-SV40 2B細胞、CEMO-1細胞、EST81細胞
LoVo人結腸癌細胞全年復蘇|已有STR圖譜
Rat 2 Cells;背景說明:成纖維細胞;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;相關產(chǎn)品有:AR4IP細胞、TEV-1細胞、253J B-V細胞
AC29 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:HEC-1-B細胞、H8細胞、GM3190細胞
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;相關產(chǎn)品有:786.O細胞、Calu 6細胞、HSAS3細胞
BAEC Cells;背景說明:主動脈;內皮 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;相關產(chǎn)品有:C28/I2細胞、H295細胞、LK2細胞
BEAS-2B Cells;背景說明:從一位非癌個體的正常人支氣管上皮病理切片分離出上皮細胞。這些細胞用腺病毒12-SV40病毒雜交病毒感染并克隆。DEAS-2B細胞保留了對血清反應進行鱗關分化的能力,并有用于篩選誘導或影響分化及致癌的化學或生物制劑。細胞角蛋白及SV40抗原染色陽性。;傳代方法:消化3-5分鐘。1:2。3天內可長滿;生長特性:貼壁生長;形態(tài)特性:上皮細胞樣;相關產(chǎn)品有:PA-1細胞、143TK-細胞、HCC0078細胞
BEAS-2B Cells;背景說明:從一位非癌個體的正常人支氣管上皮病理切片分離出上皮細胞。這些細胞用腺病毒12-SV40病毒雜交病毒感染并克隆。DEAS-2B細胞保留了對血清反應進行鱗關分化的能力,并有用于篩選誘導或影響分化及致癌的化學或生物制劑。細胞角蛋白及SV40抗原染色陽性。;傳代方法:消化3-5分鐘。1:2。3天內可長滿;生長特性:貼壁生長;形態(tài)特性:上皮細胞樣;相關產(chǎn)品有:PA-1細胞、143TK-細胞、HCC0078細胞
HDQ-P1 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:HCT.116細胞、A-673細胞、HIEC細胞
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淋巴細胞白血病;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;相關產(chǎn)品有:Intestinal Epithelioid Cell line No. 6細胞、NEC細胞、PANC.1細胞
MHCC97H Cells;背景說明:來源于中山醫(yī)院,用人肝癌細胞株MHCC97-H接種裸鼠,進行3次肺轉移篩選,取肺轉移瘤建成皮下接種后高度自發(fā)性肺轉移的肝癌細胞系;傳代方法:1:2傳代;生長特性:貼壁生長;形態(tài)特性:上皮樣;相關產(chǎn)品有:Melanoma 14細胞、M-O7e細胞、H2030細胞
HL-60 Cells;背景說明:該細胞由CollinsSJ從一位患有急性早幼粒細胞性白血病的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。該細胞具有吞噬活性和趨化反應,癌基因myc陽性,表達補體受體和FcR。;傳代方法:維持細胞濃度在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:髓母細胞樣;相關產(chǎn)品有:Panc-813細胞、CX-1細胞、KNS62細胞
3T3 Cells;背景說明:3T3細胞株是1962年Todaro G和Green H從分離的瑞士小鼠胚胎中建立的;該細胞的生長受接觸性抑制,匯合狀態(tài)的單層細胞密度為40000個細胞/平方厘米;檢測結果顯示該細胞鼠痘病毒陰性;在中生長較好,在某些玻璃表面上可能狀態(tài)不佳;細胞生長飽和時其密度可以達到約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:成纖維細胞樣;相關產(chǎn)品有:Me-Wo細胞、WERIRb1細胞、Line 207細胞
NB9 Cells;背景說明:詳見相關文獻介紹;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)細胞;相關產(chǎn)品有:WM451細胞、A-9細胞、MPC11細胞
NPA'87 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:Lewis-Lung細胞、HBZY1細胞、87 MG細胞
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;相關產(chǎn)品有:ID8細胞、H520細胞、HCC1143細胞
MFM-223 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:SKLU-1細胞、KM12-SM細胞、P3X63Ag8-6-5-3細胞
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:詳見相關文獻介紹;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;相關產(chǎn)品有:NCTC 929細胞、Panc5.04細胞、TE-8細胞
Rat Fetal Lung-6 Cells;背景說明:胚肺;成纖維細胞;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;相關產(chǎn)品有:JB6 [Mouse]細胞、HUV-EC-C細胞、SK-MEL-2細胞
MM1S Cells;背景說明:詳見相關文獻介紹;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:淋巴母細胞樣;相關產(chǎn)品有:L-1210細胞、FAT細胞、B5537SKIN細胞
293H Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:SMC-1細胞、HEK (AD293)細胞、MSB-1細胞
CEM-CCRF (CAMR) Cells;背景說明:G.E. Foley 等人建立了類淋巴母細胞細胞株CCRF-CEM。 細胞是1964年11月從一位四歲白人女性急性淋巴細胞白血病患者的外周血白血球衣中得到。此細胞系從香港收集而來。;傳代方法:1:2傳代。3天內可長滿。;生長特性:懸浮生長;形態(tài)特性:淋巴母細胞樣;相關產(chǎn)品有:H-358細胞、SKM-1細胞、Epstein-Barr-3細胞
CEM-CCRF (CAMR) Cells;背景說明:G.E. Foley 等人建立了類淋巴母細胞細胞株CCRF-CEM。 細胞是1964年11月從一位四歲白人女性急性淋巴細胞白血病患者的外周血白血球衣中得到。此細胞系從香港收集而來。;傳代方法:1:2傳代。3天內可長滿。;生長特性:懸浮生長;形態(tài)特性:淋巴母細胞樣;相關產(chǎn)品有:H-358細胞、SKM-1細胞、Epstein-Barr-3細胞
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;相關產(chǎn)品有:HEYA8細胞、NCI-SNU-449細胞、HCC0366細胞
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;相關產(chǎn)品有:SK-MES-1細胞、C81-61細胞、3T6 Swiss Albino細胞
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;相關產(chǎn)品有:HDMEC細胞、RBMVEC細胞、LC-2-Ad細胞
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;相關產(chǎn)品有:LNCaP-C4-2細胞、MDA MB231細胞、HFT 8810細胞
CFSC-8B Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:L-6 myoblast細胞、HCAEC細胞、M20 [Human melanoma]細胞
CHL-1 Cells;背景說明:詳見相關文獻介紹;傳代方法:1:6—1:10傳代;生長特性:貼壁生長;形態(tài)特性:上皮細胞;相關產(chǎn)品有:NCI-128細胞、HEK/EBNA細胞、MGH-U1細胞
RMS13 Cells;背景說明:肺泡橫紋肌肉瘤;骨髓轉移;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;相關產(chǎn)品有:WM115-mel細胞、P3 NS1 Ag4細胞、SP2細胞
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細胞;廣泛用于生物制品的表達。;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;相關產(chǎn)品有:MT-2細胞、EVSAT細胞、HECCL-1細胞
Swiss 3T3 Cells;背景說明:3T3細胞株是1962年Todaro G和Green H從分離的瑞士小鼠胚胎中建立的;該細胞的生長受接觸性抑制,匯合狀態(tài)的單層細胞密度為40000個細胞/平方厘米;檢測結果顯示該細胞鼠痘病毒陰性;在中生長較好,在某些玻璃表面上可能狀態(tài)不佳;細胞生長飽和時其密度可以達到約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:成纖維細胞樣;相關產(chǎn)品有:JROECL 19細胞、624細胞、HNE2細胞
TCC-SUPrGEMCI20 Cells(提供STR鑒定圖譜)
OCI-Ly 18 Cells;背景說明:彌漫大B細胞淋巴瘤;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;相關產(chǎn)品有:8305C細胞、F81細胞、P-3J細胞
GM637A Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:HO-8910 PM細胞、686LN-M4e細胞、Hs 746.T細胞
MCF 7B Cells;背景說明:浸潤性導管癌;胸腔積液轉移;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;相關產(chǎn)品有:J-111細胞、CCD 1112SK細胞、Hep 2細胞
T_T_ Cells;背景說明:詳見相關文獻介紹;傳代方法:10^5 cells/60mm dish;生長特性:貼壁生長;形態(tài)特性:上皮細胞樣;相關產(chǎn)品有:BN-CL2細胞、NCIH82細胞、LP1細胞
WIL2S Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:TGW細胞、HOC細胞、SF-539細胞
U373-MG Cells;背景說明:膠質瘤;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;相關產(chǎn)品有:Human Melanoma Cell Bowes細胞、HCC1954細胞、Me-Wo細胞
RKO_AS45 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:NCL-H548細胞、X63-Ag8.653細胞、Saos2細胞
CHL1 Cells;背景說明:詳見相關文獻介紹;傳代方法:1:6—1:10傳代;生長特性:貼壁生長;形態(tài)特性:上皮細胞;相關產(chǎn)品有:MBMEC細胞、NCI-H220細胞、MDA157細胞
LoVo人結腸癌細胞全年復蘇|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;相關產(chǎn)品有:MPC11細胞、HCC-9204細胞、HEM細胞
SK-RC-39 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:PE/CA-PJ34細胞、Huh 7.5.1細胞、GM03571細胞
SF17 Cells;背景說明:詳見相關文獻介紹;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;相關產(chǎn)品有:HCC2157細胞、IPLB-SF-21-AE細胞、Mouse Forestomach Carcinoma細胞
GC-2spd(ts) Cells;背景說明:精母細胞;SV40轉化;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;相關產(chǎn)品有:Lilly Laboratories Cell-Monkey Kidney 2細胞、JM1細胞、BNL-HCC細胞
SK-NSH Cells;背景說明:SK-N-SH細胞系由J.L.Bieder建系,它與SK-N-MC所不同的是倍增時間較長且多巴胺-β-羥基酶水平較高。 SK-N-SH在細胞介導的細胞毒性試驗中用作靶細胞系。;傳代方法:1:2傳代;生長特性:懸浮生長;形態(tài)特性:上皮細胞樣;相關產(chǎn)品有:BHK 21細胞、EFM-192C細胞、NCI-SNU-475細胞
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;相關產(chǎn)品有:SK BR 03細胞、H157細胞、SK Mel 24細胞
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)
" "PubMed=8464898; DOI=10.1073/pnas.90.7.2842; PMCID=PMC46192
Browning M.J., Krausa P., Rowan A.J., Bicknell D.C., Bodmer J.G., Bodmer W.F.
Tissue typing the HLA-A locus from genomic DNA by sequence-specific PCR: comparison of HLA genotype and surface expression on colorectal tumor cell lines.
Proc. Natl. Acad. Sci. U.S.A. 90:2842-2845(1993)
PubMed=8197130; DOI=10.1073/pnas.91.11.4751; PMCID=PMC43866
Bicknell D.C., Rowan A.J., Bodmer W.F.
Beta 2-microglobulin gene mutations: a study of established colorectal cell lines and fresh tumors.
Proc. Natl. Acad. Sci. U.S.A. 91:4751-4755(1994)
PubMed=7651727
Kastrinakis W.V., Ramchurren N., Rieger K.M., Hess D.T., Loda M., Steele G., Summerhayes I.C.
Increased incidence of p53 mutations is associated with hepatic metastasis in colorectal neoplastic progression.
Oncogene 11:647-652(1995)
PubMed=9000147
Cottu P.-H., Muzeau F., Estreicher A., Flejou J.-F., Iggo R.D., Thomas G., Hamelin R.
Inverse correlation between RER+ status and p53 mutation in colorectal cancer cell lines.
Oncogene 13:2727-2730(1996)
PubMed=9000572
Hoang J.-M., Cottu P.-H., Thuille B., Salmon R.J., Thomas G., Hamelin R.
BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines.
Cancer Res. 57:300-303(1997)
PubMed=9290701; DOI=10.1002/(SICI)1098-2744(199708)19:4<243::aid-mc5>3.0.CO;2-D
Jia L.-Q., Osada M., Ishioka C., Gamo M., Ikawa S., Suzuki T., Shimodaira H., Niitani T., Kudo T., Akiyama M., Kimura N., Matsuo M., Mizusawa H., Tanaka N., Koyama H., Namba M., Kanamaru R., Kuroki T.
Screening the p53 status of human cell lines using a yeast functional assay.
Mol. Carcinog. 19:243-253(1997)
PubMed=9294210; DOI=10.1073/pnas.94.19.10330; PMCID=PMC23362
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.
Proc. Natl. Acad. Sci. U.S.A. 94:10330-10334(1997)
PubMed=9515795
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)
PubMed=12615714
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)
PubMed=12661003; DOI=10.1002/gcc.10196
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)
PubMed=15771911; DOI=10.1016/j.cancergencyto.2004.08.023
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)
PubMed=15900046; DOI=10.1093/jnci/dji133
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)
PubMed=18258742; DOI=10.1073/pnas.0712176105; PMCID=PMC2268141
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)
PubMed=19927377; DOI=10.1002/gcc.20730; PMCID=PMC2818350
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)
PubMed=19941903; DOI=10.1016/j.jviromet.2009.11.022
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)
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=25926053; DOI=10.1038/ncomms8002
Medico E., Russo M., Picco G., Cancelliere C., Valtorta E., Corti G., Buscarino M., Isella C., Lamba S., Martinoglio B., Veronese S., Siena S., Sartore-Bianchi A., Beccuti M., Mottolese M., Linnebacher M., Cordero F., Di Nicolantonio F., Bardelli A.
The molecular landscape of colorectal cancer cell lines unveils clinically actionable kinase targets.
Nat. Commun. 6:7002.1-7002.10(2015)
PubMed=25944804; DOI=10.1158/1078-0432.CCR-14-2457
Bazzocco S., Dopeso H., Carton-Garcia F., Macaya I., Andretta E., Chionh F., Rodrigues P., Garrido M., Alazzouzi H., Nieto R., Sanchez A., Schwartz S. Jr., Bilic J., Mariadason J.M., Arango D.
Highly expressed genes in rapidly proliferating tumor cells as new targets for colorectal cancer treatment.
Clin. Cancer Res. 21:3695-3704(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=26537799; DOI=10.1074/mcp.M115.051235; PMCID=PMC4762531
Holst S., Deuss A.J.M., van Pelt G.W., van Vliet S.J., Garcia-Vallejo J.J., Koeleman C.A.M., Deelder A.M., Mesker W.E., Tollenaar R.A.E.M., Rombouts Y., Wuhrer M.
N-glycosylation profiling of colorectal cancer cell lines reveals association of fucosylation with differentiation and caudal type homebox 1 (CDX1)/villin mRNA expression.
Mol. Cell. Proteomics 15:124-140(2016)
PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X.-M., Egan R.K., Liu Q.-S., Miroo T., Mitropoulos X., Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)
PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
Li J., Zhao W., Akbani R., Liu W.-B., Ju Z.-L., Ling S.-Y., Vellano C.P., Roebuck P., Yu Q.-H., Eterovic A.K., Byers L.A., Davies M.A., Deng W.-L., Gopal Y.N.V., Chen G., von Euw E.M., Slamon D.J., Conklin D., Heymach J.V., Gazdar A.F., Minna J.D., Myers J.N., Lu Y.-L., Mills G.B., Liang H.
Characterization of human cancer cell lines by reverse-phase protein arrays.
Cancer Cell 31:225-239(2017)
PubMed=28683746; DOI=10.1186/s12943-017-0691-y; PMCID=PMC5498998
Berg K.C.G., Eide P.W., Eilertsen I.A., Johannessen B., Bruun J., Danielsen S.A., Bjornslett M., Meza-Zepeda L.A., Eknaes M., Lind G.E., Myklebost O., Skotheim R.I., Sveen A., Lothe R.A.
Multi-omics of 34 colorectal cancer cell lines -- a resource for biomedical studies.
Mol. Cancer 16:116.1-116.16(2017)
PubMed=28854368; DOI=10.1016/j.celrep.2017.08.010; PMCID=PMC5583477
Roumeliotis T.I., Williams S.P., Goncalves E., Alsinet C., Del Castillo Velasco-Herrera M., Aben N., Ghavidel F.Z., Michaut M., Schubert M., Price S., Wright J.C., Yu L., Yang M., Dienstmann R., Guinney J.H., Beltrao P., Brazma A., Pardo M., Stegle O., Adams D.J., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Choudhary J.S.
Genomic determinants of protein abundance variation in colorectal cancer cells.
Cell Rep. 20:2201-2214(2017)
PubMed=29101300; DOI=10.15252/msb.20177701; PMCID=PMC5731344
Frejno M., Zenezini Chiozzi R., Wilhelm M., Koch H., Zheng R.-S., Klaeger S., Ruprecht B., Meng C., Kramer K., Jarzab A., Heinzlmeir S., Johnstone E., Domingo E., Kerr D.J., Jesinghaus M., Slotta-Huspenina J., Weichert W., Knapp S., Feller S.M., Kuster B.
Pharmacoproteomic characterisation of human colon and rectal cancer.
Mol. Syst. Biol. 13:951-951(2017)
PubMed=29444439; DOI=10.1016/j.celrep.2018.01.051; PMCID=PMC6343826
Yuan T.L., Amzallag A., Bagni R., Yi M., Afghani S., Burgan W., Fer N., Strathern L.A., Powell K., Smith B., Waters A.M., Drubin D.A., Thomson T., Liao R., Greninger P., Stein G.T., Murchie E., Cortez E., Egan R.K., Procter L., Bess M., Cheng K.T., Lee C.-S., Lee L.C., Fellmann C., Stephens R., Luo J., Lowe S.W., Benes C.H., McCormick F.
Differential effector engagement by oncogenic KRAS.
Cell Rep. 22:1889-1902(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=30971826; DOI=10.1038/s41586-019-1103-9
Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.
Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.
Nature 568:511-516(2019)
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)"
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