"Hep G2人肝癌細(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

公司細(xì)胞系培養(yǎng)穩(wěn)定、耐活、復(fù)蘇好，提供人源、鼠源、兔源、豬源等不同組織如肺、氣管、支氣管、甲狀腺、胰腺、垂體、腎上腺、扁桃體、胸腺、腎、膀胱、輸尿管、前列腺、心臟、血管等細(xì)胞系。全程提供細(xì)胞系組織來源、生長特性、細(xì)胞形態(tài)、背景資料、培養(yǎng)條件、凍存條件、參考文獻(xiàn)、運輸方式等產(chǎn)品信息及技術(shù)服務(wù)。

換液周期：每周2-3次

Lewis-Lung 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：NCIH187細(xì)胞、CCRF細(xì)胞、HCC-1954細(xì)胞

MDAMB231 Cells;背景說明：MDA-MB-２３１來自患有轉(zhuǎn)移乳腺腺癌的５１歲女病人的胸水。在裸鼠和ALS處理的BALB/c小鼠中，它能形成低分化腺癌（III級）。;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：上皮樣;相關(guān)產(chǎn)品有：MUTZ-1細(xì)胞、PANC-08-13細(xì)胞、H128細(xì)胞

MHHCALL2 Cells;背景說明：急性B淋巴細(xì)胞白血??；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SK-MEL-24細(xì)胞、Mouse Forestomach Carcinoma細(xì)胞、WM35細(xì)胞

背景信息：是一種人肝癌細(xì)胞系，是來自15歲男性白人的組織，該患者患有高度分化的肝細(xì)胞癌；Hep G2細(xì)胞形態(tài)為上皮細(xì)胞樣，模式染色體數(shù)為55；Hep G2細(xì)胞在免疫抑制小鼠中不致瘤。

Hep G2人肝癌細(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)

貼壁細(xì)胞的傳代培養(yǎng)，詳細(xì)步驟如下：首先倒掉培養(yǎng)基，在這一步驟可以收集一些細(xì)胞上清做支原體檢測；加入胰蛋白酶，一般T25是加2mL，蓋好瓶蓋，搖晃T25培養(yǎng)瓶，使胰蛋白酶均勻覆蓋在細(xì)胞表面，放入培養(yǎng)箱2-3min，期間可在顯微鏡下觀察，看到大部分細(xì)胞變圓，即可放入超凈臺，加入2倍的完全培養(yǎng)基，這里就是加4mL培養(yǎng)基，終止消化；將含有胰蛋白酶，細(xì)胞和培養(yǎng)基一起轉(zhuǎn)移到離心管中，1000rpm/3min離心，去掉上清；新鮮的完全培養(yǎng)基重懸，根據(jù)細(xì)胞的生長特性和后續(xù)的實驗需求進(jìn)行傳代，比如我養(yǎng)的Hepa1-6就長的比較快，不是著急用的話，我就會按1E6個細(xì)胞/T75培養(yǎng)瓶進(jìn)行傳代；但如果后兩天要用，就會適當(dāng)多傳一點；還可通過顯微鏡計數(shù)后，直接用于細(xì)胞鋪板，繼續(xù)后續(xù)的實驗。

Ocular Choroidal Melanoma-1 Cells;背景說明：葡萄膜黑色素瘤；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：XuanWei Lung Cancer-05細(xì)胞、A375-SM細(xì)胞、CHP 212細(xì)胞

A3 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：SF-763細(xì)胞、X63-Ag8-653細(xì)胞、NPA87細(xì)胞

NS-1 Cells;背景說明：這是P３X６３Ag８(ATCCTIB-９)的一個不分泌克隆。Kappa鏈合成了但不分泌。能抗０.１mM８-氮雜鳥嘌呤但不能在HAT培養(yǎng)基中生長。據(jù)報道它是由于缺失了３-酮類固醇還原酶活性的膽固醇營養(yǎng)缺陷型。檢測表明肢骨發(fā)育畸形病毒(鼠痘)陰性。;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;相關(guān)產(chǎn)品有：MADB 106細(xì)胞、MLOY4細(xì)胞、KYSE-140細(xì)胞

2G7 [Mouse hybridoma against rat Hmgb1] 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

Hep G2人肝癌細(xì)胞全年復(fù)蘇|已有STR圖譜

形態(tài)特性：上皮細(xì)胞樣

貼壁消化難題：１，先用PBS 把細(xì)胞洗兩遍，使瓶內(nèi)沒有血清了，減少對胰酶的中和，然后用新配的０.２５%的胰酶加入３ml左右，放在３７度，然后可以在細(xì)胞有些消化下來時，拿著瓶口，運用手腕的力量輕輕震蕩瓶內(nèi)體，這樣細(xì)胞很快就下來了，還不需要吹打，分散也均勻；２，成團(tuán)、絮狀：消化里加入eda可以減少細(xì)胞成團(tuán)的現(xiàn)象，血清可以終止胰酶的作用，如果是進(jìn)口血清的話也能終止eda的作用。用胰酶消化后胰酶可以倒掉，也可以不倒，直接加血清終止，如果消化中加入了eda的話，就要將消化倒干凈，如果細(xì)胞貼壁要求不是很嚴(yán)格的話，一般不需要進(jìn)行離心。鼻咽癌細(xì)胞的貼壁能力很強(qiáng)，用０.５%胰酶(含０.１%EDA)一般要消化１２~１５min。用PBS洗滌時要洗凈殘余的培養(yǎng)基，加入胰酶后在培養(yǎng)箱中消化(避免細(xì)胞室溫下受損以及在此溫度時胰酶活性Zui強(qiáng))至細(xì)胞收縮變圓(可顯微鏡下觀察)且有少許細(xì)胞脫落(有流下來的趨勢)，隨后立即棄去胰酶(如果脫落的細(xì)胞很多且需要大量細(xì)胞實驗，則不能棄去胰酶)，加入培養(yǎng)基仔細(xì)吹打(不能用無血清培養(yǎng)基或者PBS替代，否則細(xì)胞聚集成團(tuán)塊或絮狀)。一般我都離心一次棄去上清(去除殘留的胰酶及漂浮的死細(xì)胞或細(xì)胞碎片)；消化過度：馬上用培養(yǎng)基中和，用吸管吹打細(xì)胞，收集全部的細(xì)胞到以無菌的離心管中８００RPM ３分鐘。棄上清，用全培重懸，換新的培養(yǎng)瓶繼續(xù)培養(yǎng)，狀態(tài)不HAO的細(xì)胞在培養(yǎng)的過程中會死亡脫落，在換的時候可以清除掉！

NRK Cells;背景說明：腎；自發(fā)永生；Osborne-Mendel;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：DC2.4細(xì)胞、Sp2/O-Ag14細(xì)胞、NCTC-3960細(xì)胞

EoL-1 cell Cells;背景說明：急性髓系白血??；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：Hs746-T細(xì)胞、NGP細(xì)胞、143BTK-細(xì)胞

B16-BL6 Cells;背景說明：黑色素瘤；雄性；C５７BL/６;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：C6661細(xì)胞、COLO 357細(xì)胞、HLEC-B3細(xì)胞

MALME 3M 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天換液１次。;生長特性：混合生長;形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：A204細(xì)胞、HaCaT細(xì)胞、MDCK II細(xì)胞

MDA-MB-468-RED 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：GM346細(xì)胞、Medical Research Council cell strain-5細(xì)胞、Me Wo細(xì)胞

HUASMC Cells;背景說明：臍動脈平滑肌;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：HC11細(xì)胞、SKLU01細(xì)胞、hTERT-HME1細(xì)胞

NSI/1-Ag4-1 Cells;背景說明：這是P３X６３Ag８(ATCCTIB-９)的一個不分泌克隆。Kappa鏈合成了但不分泌。能抗０.１mM８-氮雜鳥嘌呤但不能在HAT培養(yǎng)基中生長。據(jù)報道它是由于缺失了３-酮類固醇還原酶活性的膽固醇營養(yǎng)缺陷型。檢測表明肢骨發(fā)育畸形病毒(鼠痘)陰性。;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;相關(guān)產(chǎn)品有：NCI-H2066細(xì)胞、Nthy-ori 3.1細(xì)胞、alpha TC1 clone 6細(xì)胞

ZR75_1 Cells;背景說明：該細(xì)胞產(chǎn)生高水平的黏液素MUC-１ mRNA，低水平的MUC-２ mRNA，但不表達(dá)MUC-３基因；表達(dá)雌激素受體。;傳代方法：１：４-１：６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：AML193細(xì)胞、CCC-ESF-1細(xì)胞、RPMI 2650細(xì)胞

SW 839 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：EL 4細(xì)胞、TT細(xì)胞、FU-97細(xì)胞

SUDHL-8 Cells;背景說明：彌漫大B淋巴瘤；腹腔積液轉(zhuǎn)移；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SK-MEL-1細(xì)胞、OCI-Ly18細(xì)胞、LS123細(xì)胞

CEM/0 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：NCI-H1734細(xì)胞、GM01232E細(xì)胞、NTera-2D1細(xì)胞

SCC15 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，２-３天換液１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：H1092細(xì)胞、NCI-H1694細(xì)胞、Colo699細(xì)胞

BIU87 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：H2591細(xì)胞、NCI-H358細(xì)胞、HSAEC1-KT細(xì)胞

U-251 MG Cells;背景說明：U-２５１ MG分離至一位患者的膠質(zhì)母細(xì)胞瘤組織。;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：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：AML-EOL-1細(xì)胞、AMO1細(xì)胞、PC615.3細(xì)胞

HO-8910PM Cells;背景說明：高轉(zhuǎn)移卵巢癌 Cells;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：上皮樣;相關(guān)產(chǎn)品有：3T6細(xì)胞、TYKnu細(xì)胞、T98G細(xì)胞

BL1339 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：３-４天換液１次。;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：L363細(xì)胞、OVISE細(xì)胞、H-358細(xì)胞

RenCa 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：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：NIE 115細(xì)胞、SVOG細(xì)胞、MT-2細(xì)胞

35841 Cells(提供STR鑒定圖譜)

Abcam HeLa UBE3B KO 1 Cells(提供STR鑒定圖譜)

AIDHC-NMC2 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRJ220 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XK172 Cells(提供STR鑒定圖譜)

C40210 Cells(提供STR鑒定圖譜)

DA00280 Cells(提供STR鑒定圖譜)

DA06234 Cells(提供STR鑒定圖譜)

GM00800 Cells(提供STR鑒定圖譜)

H-1355 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：CCC-HIE-2細(xì)胞、BERH-2細(xì)胞、UCLA NPA871細(xì)胞

IPEC-1 Cells;背景說明：小腸；上皮細(xì)胞；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：P3 (Jiyoye)細(xì)胞、CCRF/CEM/0細(xì)胞、SKNO1細(xì)胞

H82 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：５傳代，每周換液２-３次;生長特性：懸浮生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：FRTL-5細(xì)胞、H596細(xì)胞、OCM-1細(xì)胞

NCI-H220 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-1A細(xì)胞、WM 239細(xì)胞、MUTZ1細(xì)胞

BTI-Tn5B14 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：Hs 281.T細(xì)胞、CNE2細(xì)胞、LNCaP-ATCC細(xì)胞

Tca8113 Cells;背景說明：舌鱗癌；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：Hs 695T細(xì)胞、SUDHL-5細(xì)胞、Tu-212細(xì)胞

BV173 Cells;背景說明：慢性粒細(xì)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(guān)產(chǎn)品有：RGC-5細(xì)胞、RBL.2H3細(xì)胞、HS-445細(xì)胞

Hs 746.T 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：SK_N_BE2C細(xì)胞、U87 MG細(xì)胞、Pt K2 (NBL-5)細(xì)胞

Hep G2人肝癌細(xì)胞全年復(fù)蘇|已有STR圖譜

NCI-H1417 Cells;背景說明：小細(xì)胞肺癌；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：KTCTL-140細(xì)胞、SNU-620細(xì)胞、HuT78細(xì)胞

SNU638 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：NIH:OVCAR3細(xì)胞、SP2-0-Ag14細(xì)胞、AD293細(xì)胞

HR8348 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：DHL10細(xì)胞、LS174T細(xì)胞、DMS153細(xì)胞

U-87 MG 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：LAC細(xì)胞、L-6TG細(xì)胞、ST 486細(xì)胞

OVCAR432 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：LU-65M細(xì)胞、Malme-3M細(xì)胞、H-2030細(xì)胞

KYSE 50 Cells;背景說明：食管鱗癌；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：HeLa S3細(xì)胞、HM1900細(xì)胞、Huh7.5.1細(xì)胞

RS4;11 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周２-３次;生長特性：懸浮生長;形態(tài)特性：成淋巴細(xì)胞;相關(guān)產(chǎn)品有：KYSE 150 KYSE150 Kyse150 KY150

細(xì)胞、Colo741細(xì)胞、D10G41細(xì)胞

GM21952 Cells(提供STR鑒定圖譜)

HAP1 MAVS (-) 2 Cells(提供STR鑒定圖譜)

NCI-H446 Cells;背景說明：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;生長特性：貼壁/懸浮生長，混合;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：WM 451-Lu細(xì)胞、TALL1細(xì)胞、H-226細(xì)胞

SaOS Cells;背景說明：該細(xì)胞是FoghJ和TrempeG分離和鑒定的眾多人類腫瘤細(xì)胞系中的一種；該細(xì)胞來自一位１１歲的白人女性的骨肉瘤組織?；颊呓?jīng)過放療以及甲喋呤、阿霉素、長春新堿、環(huán)磷酰胺和aramycin-C等多種藥物治療。該細(xì)胞在免疫抑制小鼠中不致瘤，細(xì)胞表達(dá)表皮生長因子EGF受體、轉(zhuǎn)化生長因子β（１型和２型）受體。;傳代方法：１：２-１：４傳代；每周１-２次。;生長特性：貼壁生長;形態(tài)特性：上皮樣；多角形;相關(guān)產(chǎn)品有：EA.Hy926細(xì)胞、RPMI #8226細(xì)胞、CWR22R-V1細(xì)胞

MLA144 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：HCA7細(xì)胞、LA-4 [Mouse lung adenoma]細(xì)胞、Scott and White No. 13細(xì)胞

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

AN3 CA Cells;背景說明：AN３CA細(xì)胞建系于１９６４年。它衍生于子宮內(nèi)膜癌患者淋巴結(jié)轉(zhuǎn)移組織，具有癌細(xì)胞的基本特性，能在體外長期傳代培養(yǎng)，接種實驗動物產(chǎn)生明顯腫瘤。但細(xì)胞的生物學(xué)特性及超微結(jié)構(gòu)尚未深入研究，僅發(fā)現(xiàn)該細(xì)胞系促黑激素合成為陰性。細(xì)胞常用于人子宮內(nèi)膜癌細(xì)胞生物學(xué)及其相關(guān)特性研究。;傳代方法：１：２傳代;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：BV-2細(xì)胞、Ishikawa細(xì)胞、COLO 679細(xì)胞

HCC-9724 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：LN299細(xì)胞、L-6 myoblast細(xì)胞、697細(xì)胞

SCC9 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：NCI-H2135細(xì)胞、CCD-841-CoTr細(xì)胞、NIH:OVCAR-10細(xì)胞

NCI-H220 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-1A細(xì)胞、WM 239細(xì)胞、MUTZ1細(xì)胞

HPSI0616i-mifg_2 Cells(提供STR鑒定圖譜)

KB-C2.5 Cells(提供STR鑒定圖譜)

MES19 Cells(提供STR鑒定圖譜)

NI-1.9 Cells(提供STR鑒定圖譜)

Raji-hPD-L1 Cells(提供STR鑒定圖譜)

Ubigene A-549 FKBP5 KO Cells(提供STR鑒定圖譜)

UP4-33 Cells(提供STR鑒定圖譜)

HCT116-MFSD9-KO-c12 Cells(提供STR鑒定圖譜)

3T6 Swiss Albino Cells;背景說明：胚胎；成纖維；自發(fā)永生；雄性；Swiss albino;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：D283-MED細(xì)胞、NCI H23細(xì)胞、TI-73細(xì)胞

PLA 802 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：MCF-7ADR細(xì)胞、Fukuoka University-Malignant mixed Mullerian Tumor-1細(xì)胞、MGH-UI細(xì)胞

MPC-5 Cells;背景說明：腎足細(xì)胞；SV４０轉(zhuǎn)化;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCI-SNU-886細(xì)胞、NCIH1703細(xì)胞、MOLM-14細(xì)胞

JROECL19 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：LC1/Sq細(xì)胞、U118細(xì)胞、BT483細(xì)胞

Mc Ardle 7777 Cells;背景說明：肝癌；雌性；Buffalo;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：PLC-PRF-5細(xì)胞、MBMEC細(xì)胞、SUDHL-6細(xì)胞

Mc Ardle 7777 Cells;背景說明：肝癌；雌性；Buffalo;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：PLC-PRF-5細(xì)胞、MBMEC細(xì)胞、SUDHL-6細(xì)胞

NR8383 Cells;背景說明：NR８３８３(正常大鼠，１９８３年８月３日)來源于肺灌洗時的正常大鼠肺泡巨噬細(xì)胞。細(xì)胞在gerbil肺細(xì)胞連續(xù)培養(yǎng)液存在下培養(yǎng)了大約８-９個月。隨后，不再需要外源生長因子。通過有限稀釋法從單個細(xì)胞克隆并亞克隆NR８３８３細(xì)胞，并三次用軟瓊脂亞克隆。細(xì)胞表現(xiàn)出巨噬細(xì)胞的特性，吞噬酵母多糖和銅綠，非特異性脂酶活性，F(xiàn)c受體，氧化降解；分泌IL-１,TNFbeta和IL-６，可重復(fù)地響應(yīng)外源生長因子。NR８３８３細(xì)胞響應(yīng)博萊霉素，分泌TGFbeta前體。在博萊霉素刺激下，TGFbe;傳代方法：１：２傳代;生長特性：半貼壁生長;形態(tài)特性：巨噬細(xì)胞;相關(guān)產(chǎn)品有：HAPI細(xì)胞、WM 451-Lu細(xì)胞、HEK293細(xì)胞

MHH-CALL2 Cells;背景說明：急性B淋巴細(xì)胞白血??；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：D-283MED細(xì)胞、W133細(xì)胞、BE(2)-C細(xì)胞

LK2 Cells;背景說明：肺鱗癌；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：H3396細(xì)胞、PaTu 8988 S細(xì)胞、PC-3M 2B4細(xì)胞

Fetal Rhesus Kidney-4 Cells;背景說明：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。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：IGR-OV1細(xì)胞、HOS TE85細(xì)胞、LAN-6細(xì)胞

Mc Coy Cells;背景說明：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：FHs74 Int細(xì)胞、526細(xì)胞、KASUMI1細(xì)胞

MB 157 Cells;背景說明：該細(xì)胞源自一位患有乳腺髓樣癌的４４歲黑人女性，表達(dá)WNT７B癌基因，細(xì)胞與細(xì)胞邊界處有細(xì)胞橋粒、微絨毛、張力細(xì)絲。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁生長;形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：UPCI:SCC090細(xì)胞、Z-138細(xì)胞、Hepatoma 22細(xì)胞

T-47D 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：149 PT細(xì)胞、HT115細(xì)胞、BCaP-37細(xì)胞

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

RAW264 Cells;背景說明：單核巨噬細(xì)胞白血??；雄性；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：TYK-nu細(xì)胞、CD18細(xì)胞、HIEC6細(xì)胞

ST91/MHT34 Cells(提供STR鑒定圖譜)

TKB-1 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：Human Embryo Lung-1細(xì)胞、AMC-HN-8細(xì)胞、KYSE270細(xì)胞

GM00346B Cells;背景說明：皮下結(jié)締組織；自發(fā)永生；雄性；C３H/An;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：ReNcell CX細(xì)胞、RCC10 RGB細(xì)胞、TR-146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

SK-N-FI Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：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：Tb 1 Lu細(xì)胞、P3/X63/Ag8細(xì)胞、MCF 10A細(xì)胞

RPMI 1846 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：AMC-HN8細(xì)胞、CMT64細(xì)胞、TE85細(xì)胞

HaCaT Cells;背景說明：該細(xì)胞源自一位６２歲患有黑色素瘤男性的病灶外圍正常皮膚，角蛋白、角化細(xì)胞交聯(lián)外膜蛋白、中間絲相關(guān)蛋白陽性。;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：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：HO-1-N-1細(xì)胞、Be Wo細(xì)胞、MGSMC細(xì)胞

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

H510A Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：８傳代；每周換液２次。;生長特性：混合生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：DHL-5細(xì)胞、PLB 985細(xì)胞、COLO-741細(xì)胞

Hep G2人肝癌細(xì)胞全年復(fù)蘇|已有STR圖譜

NCI-322 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：H-2171細(xì)胞、H226細(xì)胞、NCI-H460細(xì)胞

Wien133 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：CHL-CL-11細(xì)胞、Hs 683.T細(xì)胞、L-M(TK-)細(xì)胞

CFSC-2G 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：H2405細(xì)胞、CAL12T細(xì)胞、TE-7細(xì)胞

NCIH1781 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：Jijoye細(xì)胞、beta-TC6細(xì)胞、bEnd.3[BEND3]細(xì)胞

HIEC Cells;背景說明：腸；上皮 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：HSC（Human Schwann）細(xì)胞、SKML-28細(xì)胞、HEK-A細(xì)胞

Hi5 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：HEK293-A細(xì)胞、HEK 293細(xì)胞、RT-BM-1細(xì)胞

BayGenomics ES cell line RRR214 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YHD181 Cells(提供STR鑒定圖譜)

HT16 Cells(提供STR鑒定圖譜)

PCRP-HES1-1A10 Cells(提供STR鑒定圖譜)

ENU-T-1 Cells(提供STR鑒定圖譜)

HPS2559 Cells(提供STR鑒定圖譜)

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Mihara K., Miyazaki M., Kondo T., Fushimi K., Tsuji T., Inoue Y., Fukaya K.-i., Ishioka C., Namba M.

Yeast functional assay of the p53 gene status in human cell lines maintained in our laboratory.

Acta Med. Okayama 51:261-265(1997)

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Wong N., Lai P.B.-S., Pang E., Leung T.W.-T., Lau J.W.-Y., Johnson P.J.

A comprehensive karyotypic study on human hepatocellular carcinoma by spectral karyotyping.

Hepatology 32:1060-1068(2000)

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=11981770; DOI=10.1053/jhep.2002.32668

Clemens D.L., Forman A., Jerrells T.R., Sorrell M.F., Tuma D.J.

Relationship between acetaldehyde levels and cell survival in ethanol-metabolizing hepatoma cells.

Hepatology 35:1196-1204(2002)

PubMed=12029633; DOI=10.1053/jhep.2002.33683

Yasui K., Arii S., Zhao C., Imoto I., Ueda M., Nagai H., Emi M., Inazawa J.

TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas.

Hepatology 35:1476-1484(2002)

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)

DOI=10.1385/CP:1:3-4:313

Pang R.T.-K., Poon T.C.-W., Wong N., Lai P.B.-S., Wong N.L.-Y., Chan C.M.-L., Yu J.W.S., Chan A.T.-C., Sung J.J.-Y.

Comparison of protein expression patterns between hepatocellular carcinoma cell lines and a hepatoblastoma cell line.

Clin. Proteomics 1:313-331(2004)

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Zhai B.-J., Wu F., Shao Z.-Y., Hu K., Zhao C.-L., Wang Z.-B.

Establishment of human hepatocellular carcinoma multidrug-resistance cell line (HepG2/Adm) and study apoptosis induced by low-frequency pulse ultrasound exposure.

Zhonghua Gan Zang Bing Za Zhi 12:95-98(2004)

PubMed=15767549; DOI=10.1158/1535-7163.MCT-04-0234

Nakatsu N., Yoshida Y., Yamazaki K., Nakamura T., Dan S., Fukui Y., Yamori T.

Chemosensitivity profile of cancer cell lines and identification of genes determining chemosensitivity by an integrated bioinformatical approach using cDNA arrays.

Mol. Cancer Ther. 4:399-412(2005)

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Donohue T.M., Osna N.A., Clemens D.L.

Recombinant Hep G2 cells that express alcohol dehydrogenase and cytochrome P450 2E1 as a model of ethanol-elicited cytotoxicity.

Int. J. Biochem. Cell Biol. 38:92-101(2006)

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Sun D.-X., Nassal M.

Stable HepG2- and Huh7-based human hepatoma cell lines for efficient regulated expression of infectious hepatitis B virus.

J. Hepatol. 45:636-645(2006)

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Azari S., Ahmadi N., Jeddi-Tehrani M., Shokri F.

Profiling and authentication of human cell lines using short tandem repeat (STR) loci: report from the National Cell Bank of Iran.

Biologicals 35:195-202(2007)

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Clinically relevant radioresistant cells efficiently repair DNA double-strand breaks induced by X-rays.

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Lopez-Terrada D.H., Cheung S.-W., Finegold M.J., Knowles B.B.

Hep G2 is a hepatoblastoma-derived cell line.

Hum. Pathol. 40:1512-1515(2009)

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Srisomsap C., Sawangareetrakul P., Subhasitanont P., Chokchaichamnankit D., Chiablaem K., Bhudhisawasdi V., Wongkham S., Svasti J.

Proteomic studies of cholangiocarcinoma and hepatocellular carcinoma cell secretomes.

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Rothenberg S.M., Mohapatra G., Rivera M.N., Winokur D., Greninger P., Nitta M., Sadow P.M., Sooriyakumar G., Brannigan B.W., Ulman M.J., Perera R.M., Wang R., Tam A., Ma X.-J., Erlander M., Sgroi D.C., Rocco J.W., Lingen M.W., Cohen E.E.W., Louis D.N., Settleman J., Haber D.A.

A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers.

Cancer Res. 70:2158-2164(2010)

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A comparison of whole genome gene expression profiles of HepaRG cells and HepG2 cells to primary human hepatocytes and human liver tissues.

Drug Metab. Dispos. 38:988-994(2010)

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Di Masi A., Viganotti M., Antoccia A., Magrelli A., Salvatore M., Azzalin G., Tosto F., Lorenzetti S., Maranghi F., Mantovani A., Macino G., Tanzarella C., Taruscio D.

Characterization of HuH6, Hep3B, HepG2 and HLE liver cancer cell lines by WNT/beta-catenin pathway, microRNA expression and protein expression profile.

Cell. Mol. Biol. 56:OL1299-OL1317(2010)

PubMed=21269460; DOI=10.1186/1752-0509-5-17; PMCID=PMC3039570

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Initial characterization of the human central proteome.

BMC Syst. Biol. 5:17.1-17.13(2011)

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Geiger T., Wehner A., Schaab C., Cox J., Mann M.

Comparative proteomic analysis of eleven common cell lines reveals ubiquitous but varying expression of most proteins.

Mol. Cell. Proteomics 11:M111.014050-M111.014050(2012)

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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)

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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)

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Wang K., Lim H.Y., Shi S., Lee J., Deng S.-B., Xie T., Zhu Z., Wang Y.-L., Pocalyko D., Yang W.J., Rejto P.A., Mao M., Park C.-K., Xu J.-C.

Genomic landscape of copy number aberrations enables the identification of oncogenic drivers in hepatocellular carcinoma.

Hepatology 58:706-717(2013)

PubMed=23887712; DOI=10.1038/ncomms3218; PMCID=PMC3731665

Nault J.-C., Mallet M., Pilati C., Calderaro J., Bioulac-Sage P., Laurent C., Laurent A., Cherqui D., Balabaud C., Zucman-Rossi J.

High frequency of telomerase reverse-transcriptase promoter somatic mutations in hepatocellular carcinoma and preneoplastic lesions.

Nat. Commun. 4:2218.1-2218.7(2013)

PubMed=24116068; DOI=10.1371/journal.pone.0075692; PMCID=PMC3792989

Weiskirchen R., Weimer J., Meurer S.K., Kron A., Seipel B., Vater I., Arnold N., Siebert R., Xu L.-M., Friedman S.L., Bergmann C.

Genetic characteristics of the human hepatic stellate cell line LX-2.

PLoS ONE 8:E75692-E75692(2013)

PubMed=24618588; DOI=10.1371/journal.pone.0091433; PMCID=PMC3950186

Chernobrovkin A.L., Zubarev R.A.

Detection of viral proteins in human cells lines by xeno-proteomics: elimination of the last valid excuse for not testing every cellular proteome dataset for viral proteins.

PLoS ONE 9:E91433-E91433(2014)

PubMed=25960936; DOI=10.4161/21624011.2014.954893; PMCID=PMC4355981

Boegel S., Lower M., Bukur T., Sahin U., Castle J.C.

A catalog of HLA type, HLA expression, and neo-epitope candidates in human cancer cell lines.

OncoImmunology 3:e954893.1-e954893.12(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=25574106; DOI=10.3748/wjg.v21.i1.311; PMCID=PMC4284350

Cevik D., Yildiz G., Ozturk M.

Common telomerase reverse transcriptase promoter mutations in hepatocellular carcinomas from different geographical locations.

World J. Gastroenterol. 21:311-317(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=26160117; DOI=10.1093/toxsci/kfv136; PMCID=PMC4583060

Sison-Young R.L.C., Mitsa D., Jenkins R.E., Mottram D., Alexandre E., Richert L., Aerts H., Weaver R.J., Jones R.P., Johann E., Hewitt P.G., Ingelman-Sundberg M., Goldring C.E.P., Kitteringham N.R., Park B.K.

Comparative proteomic characterization of 4 human liver-derived single cell culture models reveals significant variation in the capacity for drug disposition, bioactivation, and detoxication.

Toxicol. Sci. 147:412-424(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=26825538; DOI=10.1016/j.jprot.2016.01.016

Wisniewski J.R., Vildhede A., Noren A., Artursson P.

In-depth quantitative analysis and comparison of the human hepatocyte and hepatoma cell line HepG2 proteomes.

J. Proteomics 136:234-247(2016)

PubMed=27027780; DOI=10.1007/s10565-016-9316-2

Wu Y., Geng X.-C., Wang J.-F., Miao Y.-F., Lu Y.-L., Li B.

The HepaRG cell line, a superior in vitro model to L-02, HepG2 and hiHeps cell lines for assessing drug-induced liver injury.

Cell Biol. Toxicol. 32:37-59(2016)

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