"ACHN人腎細(xì)胞腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

傳代比例：1:2-1:4(首次傳代建議1:2)

生長(zhǎng)特性：貼壁生長(zhǎng)

細(xì)胞系的選擇需要考慮到細(xì)胞系的功能特點(diǎn)、生長(zhǎng)速率、鋪板效率、生長(zhǎng)條件和生長(zhǎng)特征、克隆效率、培養(yǎng)方式等因素，如果您想高產(chǎn)量表達(dá)重組蛋白，您可以選擇可以懸浮生長(zhǎng)的快速生長(zhǎng)細(xì)胞系。細(xì)胞培養(yǎng)的操作步驟主要包括傳代、換液、凍存和復(fù)蘇。這些步驟確保了細(xì)胞能夠在實(shí)驗(yàn)室環(huán)境中長(zhǎng)期存活并繼續(xù)增殖。傳代是將細(xì)胞從一個(gè)容器轉(zhuǎn)移到另一個(gè)容器的過程，以擴(kuò)大細(xì)胞數(shù)量；換液是為了清除代謝廢物并補(bǔ)充新鮮培養(yǎng)基；凍存則是為了長(zhǎng)期保存細(xì)胞，而復(fù)蘇則是重新激活冷凍保存的細(xì)胞使其恢復(fù)正常生長(zhǎng)。

換液周期：每周2-3次

BEL 7405 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(zhǎng)特性：貼壁;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：NCI-H128細(xì)胞、D-341細(xì)胞、IOSE80UBC細(xì)胞

CCD 19Lu Cells;背景說明：肺成纖維細(xì)胞；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：TE 671細(xì)胞、HCC1569細(xì)胞、H2198細(xì)胞

VERO76 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(zhǎng)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：AN3CA細(xì)胞、SCC090細(xì)胞、CAKI.1細(xì)胞

ACHN人腎細(xì)胞腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：該細(xì)胞１９７９年建系，源自一名２２歲患有腎細(xì)胞腺癌的白人男性的胸腔積。干擾素可抑制該細(xì)胞的生長(zhǎng)，該細(xì)胞多用于干擾素及其誘導(dǎo)劑的抗增殖研究。

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線：1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q：3┈1┈8┈0┈8┈0┈7┈3┈2┈4；

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(cè)；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(tái)，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(zhǎng)特性和后續(xù)的實(shí)驗(yàn)需求進(jìn)行傳代，比如我養(yǎng)的Hepa1-6就長(zhǎng)的比較快，不是著急用的話，我就會(huì)按1E6個(gè)細(xì)胞/T75培養(yǎng)瓶進(jìn)行傳代；但如果后兩天要用，就會(huì)適當(dāng)多傳一點(diǎn)；還可通過顯微鏡計(jì)數(shù)后，直接用于細(xì)胞鋪板，繼續(xù)后續(xù)的實(shí)驗(yàn)。

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)

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

ACHN人腎細(xì)胞腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來源：人源、鼠源等其它物種來源

Det 562 Cells;背景說明：器官：咽頭 疾病：癌 取材轉(zhuǎn)移灶：胸水;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：上皮細(xì)胞;相關(guān)產(chǎn)品有：Loucy細(xì)胞、G402細(xì)胞、NCI-H1882細(xì)胞

P3-X63-Ag8.653 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(zhǎng)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：IMR 32細(xì)胞、SMMC 7721細(xì)胞、HCC-15細(xì)胞

H69C 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(zhǎng)特性：懸浮生長(zhǎng)，聚團(tuán);形態(tài)特性：聚團(tuán)懸浮;相關(guān)產(chǎn)品有：H522細(xì)胞、MEF (CF-1)細(xì)胞、Jurkat E6-1細(xì)胞

HKC Cells;背景說明：胚胎；腎小管；上皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SW-982細(xì)胞、PL9細(xì)胞、BL1339細(xì)胞

┈訂┈購(gòu)(技術(shù)服務(wù))┈熱┈線：1┈3┈6┈4┈1┈9┈3┈0┈7┈9┈1【微信同號(hào)】┈Q┈Q：3┈1┈8┈0┈8┈0┈7┈3┈2┈4；

形態(tài)特性：上皮細(xì)胞樣

貼壁消化難題：１，先用PBS 把細(xì)胞洗兩遍，使瓶?jī)?nèi)沒有血清了，減少對(duì)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(shí)，拿著瓶口，運(yùn)用手腕的力量輕輕震蕩瓶?jī)?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(shí)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(shí)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(shì))，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(shí)驗(yàn)，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(huì)死亡脫落，在換的時(shí)候可以清除掉！

Walker/LLC-WRC256 Cells;背景說明：腹水癌;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：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：INS1-E細(xì)胞、CL1-0細(xì)胞、Vero 76 clone E-6細(xì)胞

VMM-5A Cells;背景說明：黑色素瘤；神經(jīng)節(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：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：CC-LP-I細(xì)胞、AtT20細(xì)胞、PL-9細(xì)胞

TE 32.T 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，３-４天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：梭型和大的多核細(xì)胞;相關(guān)產(chǎn)品有：SF 767細(xì)胞、WEHI-3B細(xì)胞、C1498細(xì)胞

Soleus clone 8 Cells;背景說明：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：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Rat Glomerular Endothelial細(xì)胞、HT 1080細(xì)胞、OCI-LY-10細(xì)胞

NCIH1623 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MRC5細(xì)胞、PLA801-95D細(xì)胞、HRA19細(xì)胞

CCD-966SK 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(zhǎng)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：P3X63Ag8653細(xì)胞、H-1836細(xì)胞、PJ34細(xì)胞

BT-474 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(zhǎng)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：T-47-D細(xì)胞、Ly10細(xì)胞、BC-028細(xì)胞

Y1 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(zhǎng)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：CaSki細(xì)胞、28SC細(xì)胞、LS-123細(xì)胞

HS-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(zhǎng)特性：貼壁;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：HEK293-F細(xì)胞、HEK293細(xì)胞、TN5B14細(xì)胞

HVSMC 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(zhǎng)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：OCI-AML5細(xì)胞、1.1B4細(xì)胞、BLO 11細(xì)胞

NCI-H1755 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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：BEAS2B細(xì)胞、Leukemia 1210細(xì)胞、LCLC103H細(xì)胞

16HBEo- 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(zhǎng)特性：貼壁生長(zhǎng)　;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCIH3255細(xì)胞、MH7A細(xì)胞、aNK細(xì)胞

SDBMSC Cells;背景說明：骨髓間充質(zhì)干細(xì)胞；SD;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：hSCC-25細(xì)胞、HSAS4細(xì)胞、VMM39細(xì)胞

NCL-H548 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(zhǎng)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：MOLM13細(xì)胞、HH [Human lymphoma]細(xì)胞、BEAS 2B細(xì)胞

NCI-H2108 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(zhǎng)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：COLO 684細(xì)胞、D6P2T細(xì)胞、University of Arizona Cell Culture-893細(xì)胞

hTERT-RPE1 Cells;背景說明：視網(wǎng)膜色素上皮；hTERT永生；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Hs821T細(xì)胞、STTG1細(xì)胞、DR2R 1610細(xì)胞

COLO357 Cells;背景說明：胰腺癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCI-H810細(xì)胞、WM-239-A細(xì)胞、Anip-973細(xì)胞

Abcam HEK293T NSUN2 KO Cells(提供STR鑒定圖譜)

AG11506 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRA026 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XE085 Cells(提供STR鑒定圖譜)

BY00162 Cells(提供STR鑒定圖譜)

CRIS Cells(提供STR鑒定圖譜)

DA04307 Cells(提供STR鑒定圖譜)

DA04853 Cells(提供STR鑒定圖譜)

ftiPSf-19 Cells(提供STR鑒定圖譜)

MCA 38 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(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：MeSoTheliOma-211H細(xì)胞、NSI/1-Ag4-1細(xì)胞、GC-1spg細(xì)胞

ACHN人腎細(xì)胞腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

OsA-CL Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：５-１：１０傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：TE11細(xì)胞、TE6細(xì)胞、NRK 52E細(xì)胞

CEM-T4 Cells;背景說明：急性T淋巴細(xì)胞白血??；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MDA-MB 468細(xì)胞、OCI-AML-2細(xì)胞、MDCK (NBL-2)細(xì)胞

PIG1 Cells;背景說明：皮膚；黑色素細(xì)胞；HPV１６轉(zhuǎn)化；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：L78細(xì)胞、FTC133細(xì)胞、SKMEL24細(xì)胞

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(zhǎng)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

D10G41 Cells;背景說明：T淋巴細(xì)胞；AKR/J;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SUM-102細(xì)胞、AR4IP細(xì)胞、bEnd3細(xì)胞

12B2E1 Cells(提供STR鑒定圖譜)

ZR-75-30 Cells;背景說明：ZR-７５-３０源自一位４７歲女性黑人更年期侵入性導(dǎo)管癌患者的腹水。 細(xì)胞定性為人，非-HeLa，惡性乳房上皮癌起始。;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：EBC-1/original細(xì)胞、SiHa細(xì)胞、EAC-E2G8細(xì)胞

Hs 822.T 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２-３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：SK-N-MC細(xì)胞、CV 1細(xì)胞、GCT0404細(xì)胞

F442-A Cells;背景說明：脂肪前體細(xì)胞；雄性；Swiss albino;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MOLT-16細(xì)胞、DH 82細(xì)胞、UCLA-SO-M14細(xì)胞

ATN1 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(zhǎng)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：NOR 10細(xì)胞、GM-215細(xì)胞、H-727細(xì)胞

MDCK supertube 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(zhǎng)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：MF2059細(xì)胞、NCIH1693細(xì)胞、NBL-4細(xì)胞

C4-2 Cells;背景說明：前列腺癌；左鎖骨上淋巴結(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：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：BC-024細(xì)胞、NCI-H1693細(xì)胞、MDAMB453細(xì)胞

IOSE29 Cells;背景說明：卵巢；上皮細(xì)胞；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：C32r細(xì)胞、SCC7細(xì)胞、CORL26細(xì)胞

H-1755 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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NCIH2342細(xì)胞、COLO-680N細(xì)胞、OCI-AML-3細(xì)胞

Ha1-1.16 Cells(提供STR鑒定圖譜)

HAP1 RING1 (-) 3 Cells(提供STR鑒定圖譜)

NSC34 Cells;背景說明：神經(jīng)元;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：NTera 2/cl.D1細(xì)胞、H.Ep. #2細(xì)胞、LC1-Sq細(xì)胞

CAL148 Cells;背景說明：乳腺癌；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(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Hs895T細(xì)胞、QG-56細(xì)胞、SKOV-433細(xì)胞

LS-513 Cells;背景說明：詳見相關(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：上皮樣;相關(guān)產(chǎn)品有：NCIH1792細(xì)胞、OCIAML4細(xì)胞、brain-derived Endothelial cells.3細(xì)胞

Hs832T Cells;背景說明：卵巢，惡性囊腫;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：PA I細(xì)胞、SCL I細(xì)胞、mIMCD-3細(xì)胞

GM05384 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(zhǎng)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：RWPE1細(xì)胞、MCF10-A細(xì)胞、SW403細(xì)胞

MMQ Cells;背景說明：垂體瘤;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：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Potorous tridactylus Kidney 2細(xì)胞、PANC0504細(xì)胞、EBTr (NBL-4)細(xì)胞

ZR75-30 Cells;背景說明：ZR-７５-３０源自一位４７歲女性黑人更年期侵入性導(dǎo)管癌患者的腹水。 細(xì)胞定性為人，非-HeLa，惡性乳房上皮癌起始。;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：NCI-H1522細(xì)胞、SCC VII細(xì)胞、HEC1-B細(xì)胞

MC3T3 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(zhǎng)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：P3-NS1/1-Ag4-1細(xì)胞、Panc 02細(xì)胞、COLO 201細(xì)胞

HVRDe008-A-1 Cells(提供STR鑒定圖譜)

LaNCE hiPSC-31 Cells(提供STR鑒定圖譜)

MUSCSDi001-A-2 Cells(提供STR鑒定圖譜)

OS3-HGPRT- Cells(提供STR鑒定圖譜)

RPE1_APC_836 Cells(提供STR鑒定圖譜)

Ubigene A-549 MST1R KO Cells(提供STR鑒定圖譜)

UT-SCC-1B Cells(提供STR鑒定圖譜)

HG02232 Cells(提供STR鑒定圖譜)

HT-1197 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：５-１：１０傳代，２天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：766T細(xì)胞、GA-10 (Clone 4)細(xì)胞、HCT-8/V細(xì)胞

MLOY4 Cells;背景說明：骨；SV４０轉(zhuǎn)化;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：PC615.3細(xì)胞、GM346細(xì)胞、GM00346細(xì)胞

Hs 683 Cells;背景說明：該細(xì)胞源自７６歲白人男性的左顳葉側(cè)膠質(zhì)瘤組織，有微絨毛，無橋粒。 ;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：成纖維細(xì)胞;相關(guān)產(chǎn)品有：RDES細(xì)胞、Hs606細(xì)胞、HuH-6細(xì)胞

MDAMB415 Cells;背景說明：這株細(xì)胞表達(dá)WNT７B癌基因。８１６８０８８].帶瘤患者來自巴拉圭，雖然填報(bào)的是白人，但細(xì)胞表型存在G６PDＡ型，顯示其屬于混血。細(xì)胞株形成平展延伸的上皮細(xì)胞樣，在電鏡下呈現(xiàn)結(jié)節(jié)，伴隨著延伸的微管和微板。不容易用胰酶消化。;傳代方法：消化５-１０分鐘。１：２。４-５天長(zhǎng)滿。;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：293F細(xì)胞、SCL-I細(xì)胞、MDA436細(xì)胞

SRA01/04 Cells;背景說明：晶狀體；上皮細(xì)胞；SV４０轉(zhuǎn)化；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SUM-149PT細(xì)胞、MAEC細(xì)胞、Colo-201細(xì)胞

SRA01/04 Cells;背景說明：晶狀體；上皮細(xì)胞；SV４０轉(zhuǎn)化；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SUM-149PT細(xì)胞、MAEC細(xì)胞、Colo-201細(xì)胞

WM-239 Cells;背景說明：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(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：C8D1A細(xì)胞、Kit 225-K6細(xì)胞、2PK3細(xì)胞

COLO 201 Cells;背景說明：該細(xì)胞源自一位７０歲白人男性，CSAp (CSAp-)和CEA陰性。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮+貼壁;形態(tài)特性：淋巴細(xì)胞;相關(guān)產(chǎn)品有：Madin Darby Canine Kidney細(xì)胞、HuP-T3細(xì)胞、Bovine Turbinate細(xì)胞

Transformed Human Liver Epithelial-2 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；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：OKT3細(xì)胞、MOLM-13細(xì)胞、RAW264細(xì)胞

Kuramochi Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：１０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：OCI-AML-4細(xì)胞、OP9細(xì)胞、SNU-C1細(xì)胞

SRS-82 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(zhǎng)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：BIC-1細(xì)胞、MDA-MB415細(xì)胞、UMNSAH-DF-1細(xì)胞

Sp2/0-Ag14 Cells;背景說明：該細(xì)胞是由綿羊紅細(xì)胞免疫的BALB/c小鼠脾細(xì)胞和P３X６３Ag８骨髓瘤細(xì)胞融合得到的。該細(xì)胞不分泌免疫球蛋白，對(duì)２０μg/ml的８-氮鳥嘌呤有抗性，對(duì)HAT比較敏感；該細(xì)胞可以作為細(xì)胞融合時(shí)的B細(xì)胞組分用于制備雜交瘤；鼠痘病毒陰性。;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：SUDHL5細(xì)胞、OCI-Ly 8細(xì)胞、CEMO-1細(xì)胞

RCC4 Cells;背景說明：腎透明細(xì)胞癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：KM933細(xì)胞、NCI-SNU-423細(xì)胞、HEK 293-F細(xì)胞

FDCP-1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：２-３天換液１次;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：M21細(xì)胞、HCC1599細(xì)胞、GT1-1細(xì)胞

AML12 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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MC-3T3-E1細(xì)胞、PIG3細(xì)胞、Panc-08.13細(xì)胞

TAF11 Cells(提供STR鑒定圖譜)

CPA47 Cells;背景說明：肺血管；內(nèi)皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：C3H10T1/2細(xì)胞、U251-MG細(xì)胞、AR4IP細(xì)胞

CMT-64 Cells;背景說明：肺腺癌；雌性；C５７;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：GP2d細(xì)胞、tdott細(xì)胞、UMNSAH-DF1細(xì)胞

Ontario Cancer Institute-Acute Myeloid Leukemia-3 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(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SNU-869細(xì)胞、SK-Col-1細(xì)胞、D341細(xì)胞

MV4;11 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(zhǎng)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：Transformed Human Liver Epithelial-2細(xì)胞、LICR-HN6細(xì)胞、PA1細(xì)胞

293-EBNA1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：１０傳代；每周２次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：NS-1-Ag4-1細(xì)胞、RAW264.7細(xì)胞、Blotchy fibroblast-11細(xì)胞

PANC0327 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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：3T3 L1細(xì)胞、EU-2細(xì)胞、Granta-519細(xì)胞

ACHN人腎細(xì)胞腺癌細(xì)胞代次低|培養(yǎng)基|送STR圖譜

Hs 729 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：SK Hep1細(xì)胞、YES-2細(xì)胞、JB-6 Cl 30細(xì)胞

A101D Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：６傳代，２-３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：SNU-C2B細(xì)胞、NCI-A549細(xì)胞、B6Tert-1細(xì)胞

EHEB Cells;背景說明：B細(xì)胞白血?。慌?傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：KYSE-270細(xì)胞、SK-N-DZ細(xì)胞、Rh30細(xì)胞

COR-L51 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(zhǎng)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：C26細(xì)胞、MMAc-Serum Free細(xì)胞、RSC96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(zhǎng)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(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：COV-362細(xì)胞、Hs 739.T細(xì)胞、RPMI-1846細(xì)胞

D10G41 Cells;背景說明：T淋巴細(xì)胞；AKR/J;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：SUM-102細(xì)胞、BSC-1細(xì)胞、WM239A細(xì)胞

Line 697 Cells;背景說明：B淋巴細(xì)胞白血??；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：RCC-10細(xì)胞、HeLa/DDP細(xì)胞、Jurkat Clone E6-1細(xì)胞

P31-FUJ Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：５傳代;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：P3HR-1細(xì)胞、HuT-78細(xì)胞、NCI-H460細(xì)胞

BayGenomics ES cell line CSJ090 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line SYA359 Cells(提供STR鑒定圖譜)

CC58 Cells(提供STR鑒定圖譜)

M02/05/01 Cells(提供STR鑒定圖譜)

RD-C6 Cells(提供STR鑒定圖譜)

RT4-D6P2T Cells(提供STR鑒定圖譜)

" "PubMed=10074909; DOI=10.1002/(SICI)1097-0215(19990315)80:6<799::AID-IJC1>3.0.CO;2-U

Dumas F., Gala J.-L., Berteau P., Brasseur F., Eschwege P., Paradis V., Lacour B., Philippe M., Loric S.

Molecular expression of PSMA mRNA and protein in primary renal tumors.

Int. J. Cancer 80:799-803(1999)

PubMed=10700174; DOI=10.1038/73432

Ross D.T., Scherf U., Eisen M.B., Perou C.M., Rees C., Spellman P.T., Iyer V.R., Jeffrey S.S., van de Rijn M., Waltham M.C., Pergamenschikov A., Lee J.C.F., Lashkari D., Shalon D., Myers T.G., Weinstein J.N., Botstein D., Brown P.O.

Systematic variation in gene expression patterns in human cancer cell lines.

Nat. Genet. 24:227-235(2000)

PubMed=10929426; DOI=10.1007/s002400000103

Shintaku I., Kawagoe N., Yutani S., Hoshi S., Orikasa S., Yoshizumi O., Itoh K.

Expression of the SART1 tumor rejection antigen in renal cell carcinoma.

Urol. Res. 28:178-184(2000)

PubMed=11146448; DOI=10.1002/1097-0215(200002)9999:9999<::AID-IJC1034>3.0.CO;2-S

Kondo K.-i., Yao M., Kobayashi K., Ota S., Yoshida M., Kaneko S., Baba M., Sakai N., Kishida T., Kawakami S., Uemura H., Nagashima Y., Nakatani Y., Hosaka M.

PTEN/MMAC1/TEP1 mutations in human primary renal-cell carcinomas and renal carcinoma cell lines.

Int. J. Cancer 91:219-224(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=15748285; DOI=10.1186/1479-5876-3-11; PMCID=PMC555742

Adams S., Robbins F.-M., Chen D., Wagage D., Holbeck S.L., Morse H.C. 3rd, Stroncek D., Marincola F.M.

HLA class I and II genotype of the NCI-60 cell lines.

J. Transl. Med. 3:11.1-11.8(2005)

PubMed=17088437; DOI=10.1158/1535-7163.MCT-06-0433; PMCID=PMC2705832

Ikediobi O.N., Davies H.R., Bignell G.R., Edkins S., Stevens C., O'Meara S., Santarius T., Avis T., Barthorpe S., Brackenbury L., Buck G., Butler A.P., Clements J., Cole J., Dicks E., Forbes S., Gray K., Halliday K., Harrison R., Hills K., Hinton J., Hunter C., Jenkinson A., Jones D., Kosmidou V., Lugg R., Menzies A., Miroo T., Parker A., Perry J., Raine K.M., Richardson D., Shepherd R., Small A., Smith R., Solomon H., Stephens P.J., Teague J.W., Tofts C., Varian J., Webb T., West S., Widaa S., Yates A., Reinhold W.C., Weinstein J.N., Stratton M.R., Futreal P.A., Wooster R.

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

Mol. Cancer Ther. 5:2606-2612(2006)

PubMed=17409424; DOI=10.1158/0008-5472.CAN-06-4571

Furge K.A., Chen J.-D., Koeman J., Swiatek P.J., Dykema K., Lucin K., Kahnoski R., Yang X.-M.J., Teh B.T.

Detection of DNA copy number changes and oncogenic signaling abnormalities from gene expression data reveals MYC activation in high-grade papillary renal cell carcinoma.

Cancer Res. 67:3171-3176(2007)

PubMed=19372543; DOI=10.1158/1535-7163.MCT-08-0921; PMCID=PMC4020356

Lorenzi P.L., Reinhold W.C., Varma S., Hutchinson A.A., Pommier Y., Chanock S.J., Weinstein J.N.

DNA fingerprinting of the NCI-60 cell line panel.

Mol. Cancer Ther. 8:713-724(2009)

PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113

Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.

Signatures of mutation and selection in the cancer genome.

Nature 463:893-898(2010)

PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662

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)

PubMed=22068913; DOI=10.1073/pnas.1111840108; PMCID=PMC3219108

Gillet J.-P., Calcagno A.M., Varma S., Marino M., Green L.J., Vora M.I., Patel C., Orina J.N., Eliseeva T.A., Singal V., Padmanabhan R., Davidson B., Ganapathi R., Sood A.K., Rueda B.R., Ambudkar S.V., Gottesman M.M.

Redefining the relevance of established cancer cell lines to the study of mechanisms of clinical anti-cancer drug resistance.

Proc. Natl. Acad. Sci. U.S.A. 108:18708-18713(2011)

PubMed=22336246; DOI=10.1016/j.bmc.2012.01.017

Kong D.-X., Yamori T.

JFCR39, a panel of 39 human cancer cell lines, and its application in the discovery and development of anticancer drugs.

Bioorg. Med. Chem. 20:1947-1951(2012)

PubMed=22347499; DOI=10.1371/journal.pone.0031628; PMCID=PMC3276511

Ruan X.-Y., Kocher J.-P.A., Pommier Y., Liu H.-F., Reinhold W.C.

Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap trios, and relation to fragile site location.

PLoS ONE 7:E31628-E31628(2012)

PubMed=22384151; DOI=10.1371/journal.pone.0032096; PMCID=PMC3285665

Lee J.-S., Kim Y.K., Kim H.J., Hajar S., Tan Y.L., Kang N.-Y., Ng S.H., Yoon C.N., Chang Y.-T.

Identification of cancer cell-line origins using fluorescence image-based phenomic screening.

PLoS ONE 7:E32096-E32096(2012)

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=22628656; DOI=10.1126/science.1218595; PMCID=PMC3526189

Jain M., Nilsson R., Sharma S., Madhusudhan N., Kitami T., Souza A.L., Kafri R., Kirschner M.W., Clish C.B., Mootha V.K.

Metabolite profiling identifies a key role for glycine in rapid cancer cell proliferation.

Science 336:1040-1044(2012)

PubMed=22949125; DOI=10.1002/ijc.27822

Pawlowski R., Muhl S.M., Sulser T., Krek W., Moch H., Schraml P.

Loss of PBRM1 expression is associated with renal cell carcinoma progression.

Int. J. Cancer 132:E11-E17(2013)

PubMed=23856246; DOI=10.1158/0008-5472.CAN-12-3342; PMCID=PMC4893961

Abaan O.D., Polley E.C., Davis S.R., Zhu Y.-L.J., Bilke S., Walker R.L., Pineda M.A., Gindin Y., Jiang Y., Reinhold W.C., Holbeck S.L., Simon R.M., Doroshow J.H., Pommier Y., Meltzer P.S.

The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology.

Cancer Res. 73:4372-4382(2013)

PubMed=23933261; DOI=10.1016/j.celrep.2013.07.018

Moghaddas Gholami A., Hahne H., Wu Z.-X., Auer F.J., Meng C., Wilhelm M., Kuster B.

Global proteome analysis of the NCI-60 cell line panel.

Cell Rep. 4:609-620(2013)

PubMed=24279929; DOI=10.1186/2049-3002-1-20; PMCID=PMC4178206

Dolfi S.C., Chan L.L.-Y., Qiu J., Tedeschi P.M., Bertino J.R., Hirshfield K.M., Oltvai Z.N., Vazquez A.

The metabolic demands of cancer cells are coupled to their size and protein synthesis rates.

Cancer Metab. 1:20.1-20.13(2013)

PubMed=24477694; DOI=10.1007/s00432-014-1593-7

Tanaka T., Torigoe T., Hirohashi Y., Sato E., Honma I., Kitamura H., Masumori N., Tsukamoto T., Sato N.

Hypoxia-inducible factor (HIF)-independent expression mechanism and novel function of HIF prolyl hydroxylase-3 in renal cell carcinoma.

J. Cancer Res. Clin. Oncol. 140:503-513(2014)

PubMed=24670534; DOI=10.1371/journal.pone.0092047; PMCID=PMC3966786

Varma S., Pommier Y., Sunshine M., Weinstein J.N., Reinhold W.C.

High resolution copy number variation data in the NCI-60 cancer cell lines from whole genome microarrays accessible through CellMiner.

PLoS ONE 9:E92047-E92047(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=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=26972028; DOI=10.1016/j.jprot.2016.03.008

Masuishi Y., Kimura Y., Arakawa N., Hirano H.

Identification of glycosylphosphatidylinositol-anchored proteins and omega-sites using TiO2-based affinity purification followed by hydrogen fluoride treatment.

J. Proteomics 139:77-83(2016)

PubMed=27141528; DOI=10.1016/j.dib.2016.04.001; PMCID=PMC4838930

Masuishi Y., Kimura Y., Arakawa N., Hirano H.

Data for identification of GPI-anchored peptides and omega-sites in cancer cell lines.

Data Brief 7:1302-1305(2016)

PubMed=27377824; DOI=10.1038/sdata.2016.52; PMCID=PMC4932877

Mestdagh P., Lefever S., Volders P.-J., Derveaux S., Hellemans J., Vandesompele J.

Long non-coding RNA expression profiling in the NCI60 cancer cell line panel using high-throughput RT-qPCR.

Sci. Data 3:160052-160052(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=27807467; DOI=10.1186/s13100-016-0078-4; PMCID=PMC5087121

Zampella J.G., Rodic N., Yang W.R., Huang C.R.L., Welch J., Gnanakkan V.P., Cornish T.C., Boeke J.D., Burns K.H.

A map of mobile DNA insertions in the NCI-60 human cancer cell panel.

Mob. DNA 7:20.1-20.11(2016)

PubMed=27993170; DOI=10.1186/s12943-016-0565-8; PMCID=PMC5168717

Brodaczewska K.K., Szczylik C., Fiedorowicz M., Porta C., Czarnecka A.M.

Choosing the right cell line for renal cell cancer research.

Mol. Cancer 15:83.1-83.15(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=28489074; DOI=10.1038/ncomms15165; PMCID=PMC5436135

Sinha R., Winer A.G., Chevinsky M.S., Jakubowski C., Chen Y.-B., Dong Y.-Y., Tickoo S.K., Reuter V.E., Russo P., Coleman J.A., Sander C., Hsieh J.J.-D., Hakimi A.A.

Analysis of renal cancer cell lines from two major resources enables genomics-guided cell line selection.

Nat. Commun. 8:15165.1-15165.10(2017)"