"Caki-1人腎透明細(xì)胞癌皮膚轉(zhuǎn)移細(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)

當(dāng)T25瓶復(fù)蘇細(xì)胞收到貨時(shí)，請(qǐng)觀察好細(xì)胞狀態(tài)后，將T25細(xì)胞瓶壁進(jìn)行75%酒精消毒，將T25瓶置于37度培養(yǎng)箱放置2-4h，以便穩(wěn)定細(xì)胞狀態(tài)，當(dāng)細(xì)胞密度達(dá)80%-90%，即可進(jìn)行首次傳代培養(yǎng)；干冰運(yùn)輸?shù)募?xì)胞凍存管收到貨后，需立即轉(zhuǎn)入液氮保存或直接進(jìn)行復(fù)蘇(第三天換液并檢查復(fù)蘇細(xì)胞密度，以便進(jìn)行下一步)。 能夠在實(shí)驗(yàn)室條件下進(jìn)行大量培養(yǎng)和繁殖。這種細(xì)胞系在分子生物學(xué)和生物技術(shù)研究中十分常用。

換液周期：每周2-3次

Japanese Tissue Culture-39 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長(zhǎng)滿。;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：HCT-8細(xì)胞、Human Embryo Lung-1細(xì)胞、LLC-PK(1)細(xì)胞

SupT1 Cells;背景說(shuō)明：詳見(jiàn)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)胞樣　;相關(guān)產(chǎn)品有：HB611細(xì)胞、HCC1171細(xì)胞、H4-IIE-C3細(xì)胞

NCI H508 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NB9細(xì)胞、NK-92.05細(xì)胞、J45.01細(xì)胞

Caki-1人腎透明細(xì)胞癌皮膚轉(zhuǎn)移細(xì)胞代次低|培養(yǎng)基|送STR圖譜

背景信息：該細(xì)胞超微結(jié)構(gòu)中包含許多微絨毛、少許微絲、許多小線粒體、發(fā)達(dá)的高爾基休和內(nèi)質(zhì)網(wǎng)、許多脂滴和多層體、次級(jí)溶酶體，沒(méi)有發(fā)現(xiàn)病毒顆粒。

┈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；

絕大部分細(xì)胞消化只要用胰酶潤(rùn)洗一遍即可：吸去胰酶后，殘留的那些無(wú)法計(jì)算體積的附著在細(xì)胞表面的微量胰酶在37℃一般不到2min足夠消化細(xì)胞(絕大部分1min不到)。對(duì)于這些細(xì)胞原則上不要用胰酶孵育細(xì)胞，連續(xù)這樣傳代，對(duì)細(xì)胞傷害很大。簡(jiǎn)單的程序是PBS潤(rùn)洗吸去，胰酶潤(rùn)洗吸去，然后37℃消化。什么算是消化好了呢？不需要把細(xì)胞全部消化成間隔分布很離散的單個(gè)圓形才算消化好了，一般你肉眼觀察貼壁細(xì)胞層，只要能移動(dòng)了，多半呈沙狀移動(dòng)，其實(shí)已經(jīng)是可以了。一般能移動(dòng)了，說(shuō)明細(xì)胞與培養(yǎng)基質(zhì)材料的附著已經(jīng)消失了，細(xì)胞之間的附著也已經(jīng)消失了，細(xì)胞已經(jīng)獨(dú)立分布了(雖然沒(méi)有呈現(xiàn)很廣的離散分布)。這個(gè)時(shí)候應(yīng)該停止消化，不要等到看到鏡下所有細(xì)胞都分離得非常好，間隙很大，才停止。細(xì)胞系在貼壁的過(guò)程中仍然會(huì)聚集，這個(gè)是貼壁培養(yǎng)的細(xì)胞，尤其是腫瘤細(xì)胞的一個(gè)特性，你可以嘗試，準(zhǔn)備100%的單個(gè)細(xì)胞懸液，貼壁后觀察細(xì)胞，仍然是幾個(gè)幾個(gè)細(xì)胞聚集在一起。一些懸浮培養(yǎng)細(xì)胞也是如此，容易聚集，不要過(guò)幾個(gè)小時(shí)就拿出來(lái)吹打成單細(xì)胞懸液。細(xì)胞只要能從基質(zhì)上脫離下來(lái)，即使是成片的(比如Calu-3細(xì)胞)，吹打不超過(guò)20次(一般10次即可)，成小規(guī)模聚集(10個(gè)細(xì)胞左右)是正常的，不要再去延長(zhǎng)消化時(shí)間，等待單細(xì)胞懸液出現(xiàn)。比較難消化的細(xì)胞：潤(rùn)洗方法5min還不能消化，以結(jié)腸癌細(xì)胞為例，比如：HCT15、LS411和KM12細(xì)胞，胰酶消化，一般10 cm培養(yǎng)皿，一次加入300ul-500ul就足夠了。即使這樣難消化的細(xì)胞，一般不超過(guò)5min，即可見(jiàn)細(xì)胞成片移動(dòng)，就應(yīng)該停止消化。一些正常細(xì)胞也會(huì)有難消化的時(shí)候，比如tsDC細(xì)胞，用胰酶孵育，3min左右即可看到成片沙狀移動(dòng)。

產(chǎn)品包裝：復(fù)蘇發(fā)貨：T25培養(yǎng)瓶(一瓶)或凍存發(fā)貨：1ml凍存管(兩支)

來(lái)源說(shuō)明：細(xì)胞主要來(lái)源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫(kù)

Caki-1人腎透明細(xì)胞癌皮膚轉(zhuǎn)移細(xì)胞代次低|培養(yǎng)基|送STR圖譜

物種來(lái)源：人源、鼠源等其它物種來(lái)源

MDCC-MSB-1 Cells;背景說(shuō)明：淋巴瘤;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：C-33-A細(xì)胞、RDES-1細(xì)胞、NCI-H1623細(xì)胞

HUT-125 Cells;背景說(shuō)明：腺鱗狀肺癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HEL-92_1_7細(xì)胞、hTERT-RPE-1細(xì)胞、VeroE6細(xì)胞

Hs 611.T Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代；每周換液２-３次。;生長(zhǎng)特性：混合型;形態(tài)特性：淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：PE/CA-PJ34 (clone C12)細(xì)胞、P3/X63-Ag8細(xì)胞、HPAF/CD18細(xì)胞

IMCD3 Cells;背景說(shuō)明：腎；內(nèi)髓集合管；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：P560細(xì)胞、MKN-1細(xì)胞、NCI-H2052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(méi)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(lái)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(lái)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?chē)?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(lái)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(wú)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(guò)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(wú)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(guò)程中會(huì)死亡脫落，在換的時(shí)候可以清除掉！

Swiss-3T3 Cells;背景說(shuō)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(zhǎng)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(cè)結(jié)果顯示該細(xì)胞鼠痘病毒陰性；在中生長(zhǎng)較好，在某些玻璃表面上可能狀態(tài)不佳；細(xì)胞生長(zhǎng)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(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：H-1688細(xì)胞、Capan2細(xì)胞、HCC1395細(xì)胞

C57 Mouse Tumor 93 Cells;背景說(shuō)明：結(jié)腸癌；C５７BL/ICRF;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Ramos(RA1)細(xì)胞、HeLa-229細(xì)胞、Sf21細(xì)胞

MV 3 Cells;背景說(shuō)明：黑色素瘤；淋巴結(jié)轉(zhuǎn)移；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MDAMB361細(xì)胞、UCLA SO M21細(xì)胞、Stanford University Pediatric T-cell line 1細(xì)胞

PL12 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：16HBE140細(xì)胞、PA-TU-8988S細(xì)胞、HIBEpiC細(xì)胞

Hs729 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代；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：Panc 08.13細(xì)胞、HONE1細(xì)胞、MC3T3-E細(xì)胞

Hu-P-T4 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：COV362細(xì)胞、697細(xì)胞、Menschliche Und Tierische Zellkulture-3細(xì)胞

HuNS1 Cells;背景說(shuō)明：詳見(jiàn)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)胞樣;相關(guān)產(chǎn)品有：HHFK細(xì)胞、MPASMC細(xì)胞、ACHN細(xì)胞

PC9 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：CNE1細(xì)胞、HME-1細(xì)胞、SU-DHL-6細(xì)胞

PG-4(S+L-) Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：F36P細(xì)胞、NCI-H157細(xì)胞、VCaP細(xì)胞

SNU-407 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HCC-44細(xì)胞、SK UT 1細(xì)胞、TE-1細(xì)胞

KRC-Y Cells;背景說(shuō)明：腎透明細(xì)胞癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Human Foreskin Fibroblast細(xì)胞、EAC細(xì)胞、Y3M細(xì)胞

LLC-MK2 Cells;背景說(shuō)明：胚胎；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(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Primary Liver Carcinoma/Poliomyelitis Research Foundation/5細(xì)胞、PC3細(xì)胞、L-M (TK-)細(xì)胞

ADR-RES Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SG231細(xì)胞、B-16細(xì)胞、Hs600T細(xì)胞

CEM-C1 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng)　;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Reuber H35細(xì)胞、AG06814-J細(xì)胞、Hs 729細(xì)胞

Menschliche Und Tierische Zellkulture-1 Cells;背景說(shuō)明：骨髓增生異常綜合征；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NCIH1838細(xì)胞、H157細(xì)胞、SK 1細(xì)胞

PK136 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NFS60細(xì)胞、Vero-76細(xì)胞、Institute for Medical Research-90細(xì)胞

SJSA-1 Cells;背景說(shuō)明：詳見(jiàn)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：PECAPJ34細(xì)胞、HAC-84細(xì)胞、MDA.MB.435細(xì)胞

Abcam A-549 HERC5 KO 2 Cells(提供STR鑒定圖譜)

Abcam THP-1 SRF KO Cells(提供STR鑒定圖譜)

BayGenomics ES cell line CSD355 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRT110 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTC277 Cells(提供STR鑒定圖譜)

CHKS-3 Cells(提供STR鑒定圖譜)

DA02197 Cells(提供STR鑒定圖譜)

DA06154 Cells(提供STR鑒定圖譜)

GM00649 Cells(提供STR鑒定圖譜)

LM1 Cells;背景說(shuō)明：腎癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MDA231-LM2-4175細(xì)胞、TCC Sup細(xì)胞、149PT細(xì)胞

Caki-1人腎透明細(xì)胞癌皮膚轉(zhuǎn)移細(xì)胞代次低|培養(yǎng)基|送STR圖譜

J 111 Cells;背景說(shuō)明：?jiǎn)魏思?xì)胞白血病;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NCI-H2030細(xì)胞、MRMT-1細(xì)胞、L929細(xì)胞

NCI-H920 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HLEC-B3細(xì)胞、Gingival carcinoma Neck Metastasis細(xì)胞、CORL279細(xì)胞

H-211 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：３-４天換液１次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SUM 190細(xì)胞、HT1197細(xì)胞、CEM C7細(xì)胞

VMRCLCD Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：L-5178-Y-R細(xì)胞、PaTu-8988s細(xì)胞、Astrocyte type I clone細(xì)胞

H-661 Cells;背景說(shuō)明：該細(xì)胞１９８２年建系，源自一位患有大細(xì)胞肺癌的男性的胸腔積液。該細(xì)胞角蛋白、波形蛋白陽(yáng)性。;傳代方法：１：３—１：５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：PCI-4M細(xì)胞、MKN7細(xì)胞、HCC1359細(xì)胞

2E5.G10 Cells(提供STR鑒定圖譜)

32D:cl3 Cells;背景說(shuō)明：骨髓淋巴瘤；C３H/HeJ;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Farage OL細(xì)胞、LS174細(xì)胞、HepG2/C3A細(xì)胞

SK-OV-433 Cells;背景說(shuō)明：卵巢癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：KYSE-450細(xì)胞、WIL2S細(xì)胞、DMS 273細(xì)胞

U-87-MG Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MFHL-2細(xì)胞、A375細(xì)胞、T98 G細(xì)胞

HDLM2 Cells;背景說(shuō)明：霍奇金淋巴瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HT-115細(xì)胞、HIC細(xì)胞、Duke University 4475細(xì)胞

SK-MEL2 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代，２-３天換液１次。;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：多邊形的;相關(guān)產(chǎn)品有：COLO824細(xì)胞、NCIH2286細(xì)胞、NBL-2細(xì)胞

MKN45 Cells;背景說(shuō)明：該細(xì)胞系由S Akiyama建立，源于一位３５歲患有印戒細(xì)胞癌的女性的胃淋巴結(jié)。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁+懸浮;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：TE-671細(xì)胞、MCMEC細(xì)胞、SVG(P12)細(xì)胞

Panc 3.27 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：J774細(xì)胞、P3JHR-1細(xì)胞、HS852.T細(xì)胞

HCEC Cells;背景說(shuō)明：角膜；上皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HARAB細(xì)胞、VSC4.1細(xì)胞、B104 [Rat neuroblastoma]細(xì)胞

GM16396 Cells(提供STR鑒定圖譜)

HAP1 HADHA (-) 2 Cells(提供STR鑒定圖譜)

OCIAML4 Cells;背景說(shuō)明：急性髓系白血?。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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NG10815細(xì)胞、A2780/Taxol細(xì)胞、3T3 clone A31細(xì)胞

A-101D Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：４-１：６傳代，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：OCI/AML-3細(xì)胞、FRTL-5 Cl 2細(xì)胞、TE-15細(xì)胞

CHP 100 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：PANC3.27細(xì)胞、RWPE-1細(xì)胞、Hs-611-T細(xì)胞

YH Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：NL-20細(xì)胞、Virginia Mason Research Center-Lung Cancer D細(xì)胞、NCIH596細(xì)胞

SNU119 Cells;背景說(shuō)明：卵巢癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MDA1386細(xì)胞、MUTZ-3細(xì)胞、CL1-0細(xì)胞

SNU739 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：CF-PAC1細(xì)胞、149 PT細(xì)胞、SNU-484細(xì)胞

PaTu-8988s Cells;背景說(shuō)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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：8305-C細(xì)胞、EBC-1/original細(xì)胞、SCC154細(xì)胞

H-157 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng)　;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：U266 B1細(xì)胞、NCI-H1876細(xì)胞、Panc10.05細(xì)胞

Hp-SWN-14F Cells(提供STR鑒定圖譜)

JHC Cells(提供STR鑒定圖譜)

MCRIi031-A-3 Cells(提供STR鑒定圖譜)

ND21845 Cells(提供STR鑒定圖譜)

PR00643 Cells(提供STR鑒定圖譜)

Ubigene A-549 TAB3 KO Cells(提供STR鑒定圖譜)

v6.5 Trerf1-K1 Cells(提供STR鑒定圖譜)

HAP1 SSBP4 (-) 2 Cells(提供STR鑒定圖譜)

JB6 Cl 30 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮樣;相關(guān)產(chǎn)品有：MD Anderson-Metastatic Breast-435細(xì)胞、HEY-A8細(xì)胞、NCIH1184細(xì)胞

H-526 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：每周換液２-３次。;生長(zhǎng)特性：懸浮生長(zhǎng) ;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：HMEC-1細(xì)胞、GM05384細(xì)胞、Mono-Mac-1細(xì)胞

QGP 1 Cells;背景說(shuō)明：胰腺癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：H-35細(xì)胞、LTEPsm細(xì)胞、CATH.a細(xì)胞

SUD-4 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：CHOK1細(xì)胞、H4-II-E-C3細(xì)胞、CHL-IU細(xì)胞

Porcine Kidney-15 Cells;背景說(shuō)明：PK-１５細(xì)胞建系于１９５５（Stice,E）。是PK-１a細(xì)胞的克隆系。該細(xì)胞系可用于多種病毒的增值及特性研究。另外，電鏡觀察發(fā)現(xiàn)，PK-１５細(xì)胞內(nèi)有C-型病毒顆粒存在，是研究C-型病毒的材料。;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：PLA801C細(xì)胞、LS-1034細(xì)胞、8305C_1細(xì)胞

Porcine Kidney-15 Cells;背景說(shuō)明：PK-１５細(xì)胞建系于１９５５（Stice,E）。是PK-１a細(xì)胞的克隆系。該細(xì)胞系可用于多種病毒的增值及特性研究。另外，電鏡觀察發(fā)現(xiàn)，PK-１５細(xì)胞內(nèi)有C-型病毒顆粒存在，是研究C-型病毒的材料。;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：PLA801C細(xì)胞、LS-1034細(xì)胞、8305C_1細(xì)胞

DMS 79 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代；每周換液２-３次。;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：SH-SY5Y Parental細(xì)胞、Cates-1B細(xì)胞、HN6細(xì)胞

HPMC Cells;背景說(shuō)明：腹膜間皮 Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：FF-WT-BJ細(xì)胞、HEL-92_1_7細(xì)胞、RFL6細(xì)胞

HEK 293FT Cells;背景說(shuō)明：該細(xì)胞穩(wěn)定表達(dá)SV４０大T抗原，并且促進(jìn)最適病毒產(chǎn)物的產(chǎn)生。;傳代方法：１：２傳代;生長(zhǎng)特性：懸浮生長(zhǎng);形態(tài)特性：圓形;相關(guān)產(chǎn)品有：CBRH7919細(xì)胞、HBE細(xì)胞、IAR 20細(xì)胞

Hs839T Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代，２-３天換液１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：U-87MG ATCC細(xì)胞、PANC0203細(xì)胞、SK-Hep1細(xì)胞

Porcine Kidney-13 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：４傳代，每周換液２—３次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：H-1048細(xì)胞、P3HRI細(xì)胞、HPAF II細(xì)胞

Pro-Lec1.3C Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：3T3 clone A31細(xì)胞、UACC 812細(xì)胞、NCI-H1770細(xì)胞

BC3H1 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：T9細(xì)胞、OC 316細(xì)胞、NS-20Y細(xì)胞

Mel624 Cells;背景說(shuō)明：黑色素瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：NCIH847細(xì)胞、CAL 148細(xì)胞、SK Mel 24細(xì)胞

Hs 706.T Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２—１：３傳代；每周換液２-３次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：NUGC4細(xì)胞、HCC1438細(xì)胞、HCC-1599細(xì)胞

SK-N-LE Cells(提供STR鑒定圖譜)

MARC-145 Cells;背景說(shuō)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(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：MC-26細(xì)胞、HUVEC細(xì)胞、HOMEC細(xì)胞

HUCCT1 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：４傳代;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：Hs-343-T細(xì)胞、MT-3 [Human leukocytes]細(xì)胞、Bx-PC3細(xì)胞

HSC-1 Cells;背景說(shuō)明：皮膚鱗癌；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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：293 H細(xì)胞、HOP 62細(xì)胞、WI-38細(xì)胞

HHFK Cells;背景說(shuō)明：毛囊；角質(zhì) Cells;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：HEMCSS細(xì)胞、MDA-MB-134細(xì)胞、Michigan Cancer Foundation-10A細(xì)胞

EAhy926 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：Hs.27細(xì)胞、C-33 A細(xì)胞、NCI-322細(xì)胞

HMEC-1 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：LICCF細(xì)胞、5637細(xì)胞、APRE-19細(xì)胞

Caki-1人腎透明細(xì)胞癌皮膚轉(zhuǎn)移細(xì)胞代次低|培養(yǎng)基|送STR圖譜

Hs274T Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代,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：NCI-H1437細(xì)胞、CAOV3細(xì)胞、PC-9/S1細(xì)胞

MCF 7 Cells;背景說(shuō)明：MCF-７細(xì)胞保留了多個(gè)分化了的乳腺上皮的特性，包括：能通過(guò)胞質(zhì)雌激素受體加工雌二醇并能形成圓形復(fù)合物（domes）。該細(xì)胞含有Tx-４癌基因。腫瘤壞死因子α（TNFalpha）可以抑制MCF-７細(xì)胞的生長(zhǎng)?？勾萍に靥幚砑?xì)胞能調(diào)變IGFBP＇S的分泌。;傳代方法：１：２傳代，３-４天長(zhǎng)滿;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：293-GP細(xì)胞、MyLa2059細(xì)胞、NCI-H2444細(xì)胞

KMY1022 Cells;背景說(shuō)明：B淋巴細(xì)胞；EBV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：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：OCILY-19細(xì)胞、CT26.CL25細(xì)胞、HCC0095細(xì)胞

OCI-Ly01 Cells;背景說(shuō)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(zhǎng)特性：懸浮;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：Hs 578Bst細(xì)胞、Walker-Ca.256細(xì)胞、FBHE細(xì)胞

BetaTC6 Cells;背景說(shuō)明：這株細(xì)胞來(lái)源于轉(zhuǎn)基因小鼠中生長(zhǎng)的一個(gè)胰腫瘤(胰島素瘤)。這種小鼠攜帶了大鼠胰島素II基因啟動(dòng)子調(diào)控的SV４０早期基因的假基因結(jié)構(gòu)。細(xì)胞包含豐富的胰島素和小量的胰高血糖素及生長(zhǎng)抑素。響應(yīng)葡萄糖而分泌胰島素;傳代方法：１：２-１：４傳代，每２-３天換液一次;生長(zhǎng)特性：貼壁生長(zhǎng);形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：NIH-OVCAR-3細(xì)胞、SW 579細(xì)胞、HANK細(xì)胞

QGY 7701 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：消化３-５分鐘，１：２,３天內(nèi)可長(zhǎng)滿;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：NCI H23細(xì)胞、H4-IIE-C3細(xì)胞、BPH1細(xì)胞

SP2/0 Ag-14 Cells;背景說(shuō)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(niǎo)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：H87細(xì)胞、HT 115細(xì)胞、BC-020細(xì)胞

Wien133 Cells;背景說(shuō)明：詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長(zhǎng)特性：貼壁或懸浮，詳見(jiàn)產(chǎn)品說(shuō)明書(shū)部分;形態(tài)特性：詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有：IOSE 29細(xì)胞、MB 157細(xì)胞、HMy2.CIR細(xì)胞

BayGenomics ES cell line KST064 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XB742 Cells(提供STR鑒定圖譜)

CMT64/61 Cells(提供STR鑒定圖譜)

MANEX7374N-10C4 Cells(提供STR鑒定圖譜)

S1E4 Cells(提供STR鑒定圖譜)

YS-TM-R-TC Cells(提供STR鑒定圖譜)

" "PubMed=571047

Fogh J.

Cultivation, characterization, and identification of human tumor cells with emphasis on kidney, testis, and bladder tumors.

Natl. Cancer Inst. Monogr. 49:5-9(1978)

PubMed=6244232

Williams R.D.

Human urologic cancer cell lines.

Invest. Urol. 17:359-363(1980)

PubMed=6935474; DOI=10.1093/jnci/66.2.239

Wright W.C., Daniels W.P., Fogh J.

Distinction of seventy-one cultured human tumor cell lines by polymorphic enzyme analysis.

J. Natl. Cancer Inst. 66:239-247(1981)

PubMed=7017212; DOI=10.1093/jnci/66.6.1003

Pollack M.S., Heagney S.D., Livingston P.O., Fogh J.

HLA-A, B, C and DR alloantigen expression on forty-six cultured human tumor cell lines.

J. Natl. Cancer Inst. 66:1003-1012(1981)

PubMed=7459858

Rousset M., Zweibaum A., Fogh J.

Presence of glycogen and growth-related variations in 58 cultured human tumor cell lines of various tissue origins.

Cancer Res. 41:1165-1170(1981)

PubMed=6582512; DOI=10.1073/pnas.81.2.568; PMCID=PMC344720

Mattes M.J., Cordon-Cardo C., Lewis J.L. Jr., Old L.J., Lloyd K.O.

Cell surface antigens of human ovarian and endometrial carcinoma defined by mouse monoclonal antibodies.

Proc. Natl. Acad. Sci. U.S.A. 81:568-572(1984)

PubMed=3518877; DOI=10.3109/07357908609038260

Fogh J.

Human tumor lines for cancer research.

Cancer Invest. 4:157-184(1986)

PubMed=3335022

Alley M.C., Scudiero D.A., Monks A., Hursey M.L., Czerwinski M.J., Fine D.L., Abbott B.J., Mayo J.G., Shoemaker R.H., Boyd M.R.

Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay.

Cancer Res. 48:589-601(1988)

PubMed=2041050; DOI=10.1093/jnci/83.11.757

Monks A., Scudiero D.A., Skehan P., Shoemaker R.H., Paull K.D., Vistica D.T., Hose C.D., Langley J., Cronise P., Vaigro-Wolff A., Gray-Goodrich M., Campbell H., Mayo J.G., Boyd M.R.

Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines.

J. Natl. Cancer Inst. 83:757-766(1991)

PubMed=7591954; DOI=10.1111/j.1349-7006.1995.tb03087.x; PMCID=PMC5920923

Kinoshita H., Yamada H., Ogawa O., Kakehi Y., Osaka M., Nakamura E., Mishina M., Habuchi T., Takahashi R., Sugiyama T., Yoshida O.

Contribution of chromosome 9p21-22 deletion to the progression of human renal cell carcinoma.

Jpn. J. Cancer Res. 86:795-799(1995)

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=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=10723130; DOI=10.1038/sj.onc.1203449

Alimov A., Kost-Alimova M., Liu J., Li C.-D., Bergerheim U.S.R., Imreh S., Klein G., Zabarovsky E.R.

Combined LOH/CGH analysis proves the existence of interstitial 3p deletions in renal cell carcinoma.

Oncogene 19:1392-1399(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=15604581; DOI=10.1159/000081597

Ikemoto S., Sugimura K., Yoshida N., Kuratsukuri K., Wada S., Nakatani T.

Comparative antitumor activity of 5-fluorouracil and 5'-deoxy-5-fluorouridine in combination with interferon-alpha in renal cell carcinoma cell lines.

Urol. Int. 73:348-353(2004)

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=17212712; DOI=10.1111/j.1399-0039.2006.00725.x

Komohara Y., Suekane S., Noguchi M., Matsuoka K., Yamada A., Itoh K.

Expression of APOBEC3G in kidney cells.

Tissue Antigens 69:95-98(2007)

PubMed=17804913; DOI=10.1159/000107804

Glube N., Giessl A., Wolfrum U., Langguth P.

Caki-1 cells represent an in vitro model system for studying the human proximal tubule epithelium.

Nephron Exp. Nephrol. 107:e47-e56(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=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)

PubMed=30260228; DOI=10.1021/acs.jproteome.8b00538

Knott M.E., Manzi M., Zabalegui N., Salazar M.O., Puricelli L.I., Monge M.E.

Metabolic footprinting of a clear cell renal cell carcinoma in vitro model for human kidney cancer detection.

J. Proteome Res. 17:3877-3888(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=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)"