"Hs 578T人乳腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

傳代比例：1:2-1:4(首次傳代建議1:2)

生長特性：貼壁生長

貼壁細(xì)胞的消化方法介紹：１、胰酶。這是用得Zui多的。一般濃度在０.２５-０.５%。作用時間根據(jù)細(xì)胞種類、作用溫度等因素而變化很大，從幾分鐘到幾十分鐘不等。０.２５%的胰酶作用于單層貼壁的細(xì)胞，在３７度條件下，一般消化１-５分鐘就足夠了。終止是用血清。主要作用于細(xì)胞間。配制時不能用含、鎂的平衡，否則影響活性。保存于-２０度。２、膠原酶。這種方法比較少，一般是用原代培養(yǎng)時，從組織消化下細(xì)胞。這種方法作用溫和，對細(xì)胞損傷較小，但是，價格也較貴。中止同樣是用血清。３、EDA。用得也是非常多。一般濃度在０.０２%左右。作用于細(xì)胞與間質(zhì)，對細(xì)胞間也有一定作用。注意，它能顯著影響pH值，而且在弱堿性條件下才易溶。因此，配制時應(yīng)調(diào)節(jié)HAO堿度。它不能被終和。因此，消化下來的細(xì)胞要洗一遍。４、商品化的無酶消化。個人的使用經(jīng)常覺得對細(xì)胞的損傷比較大，但是分離成單細(xì)胞懸的能力確實(shí)比較強(qiáng)。５、物理法。直接吹打或用細(xì)胞刮子將細(xì)胞刮下來。６、冷凍法。此方法僅能用于細(xì)胞傳代時。無法使組織上的細(xì)胞脫落下來。本方法的原理，我想是因細(xì)胞冷凍后收縮，從而從培養(yǎng)瓶上脫落下來。YOU點(diǎn)是：對細(xì)胞損傷小，不需要中止或洗細(xì)胞，方便，不需要另外配制消化。別適用那些貼壁不是別緊，又別嬌氣的細(xì)胞。不足是細(xì)胞常成小片脫落。此種方法曾用于因用其它方法傳代導(dǎo)致大量細(xì)胞死亡操作的間充質(zhì)干細(xì)胞、DC細(xì)胞的培養(yǎng)，效果非常滿意。具體過程是：１、用較多的４度的PBS 洗滌一遍細(xì)胞(以６孔板為例，加１.５ml/孔)，２、再加０.５毫升４度的PBS，靜置操作臺上，很快細(xì)胞就小片脫落，３、輕輕吹打，細(xì)胞即完全脫落，４、按一定比例傳代。

換液周期：每周2-3次

BEL-7404 Cells;背景說明：用Northernblot方法，未能檢測到細(xì)胞中１.３kbLFIRE-１/HFREP-１mRNA的表達(dá)。;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長滿。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：CO115細(xì)胞、RPMI.8226細(xì)胞、High5細(xì)胞

PC-9S1 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：TK 10細(xì)胞、MDA-MB436細(xì)胞、RMG-I細(xì)胞

SCLC-21H Cells;背景說明：小細(xì)胞肺癌；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：SPCA-1細(xì)胞、NCIH2107細(xì)胞、231-luc細(xì)胞

Hs 578T人乳腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

背景信息：是一種來源于人的乳腺癌細(xì)胞系，最初從一名51歲女性患者的乳腺癌組織中分離得到。它與正常成纖維細(xì)胞樣細(xì)胞株Hs 578Bst起源于同一位患者。Hs 578T細(xì)胞最初是多角形的，但在傳代過程中選擇并克隆了星形的細(xì)胞形態(tài)。電鏡下觀察發(fā)現(xiàn)，Hs 578T細(xì)胞內(nèi)酪蛋白顆粒聚集、橋粒緊密連接、脂質(zhì)體和光滑內(nèi)質(zhì)網(wǎng)小泡。Hs 578T細(xì)胞與Hs 578Bst細(xì)胞一樣，未檢測到雌激素受體和內(nèi)生病毒。

細(xì)胞系的應(yīng)用：1)免疫組化研究2)RNA干擾研究3)藥物作用研究4)慢病毒轉(zhuǎn)染研究等其它應(yīng)用。細(xì)胞系通常用于實(shí)驗(yàn)研究，如增殖、遷移、侵襲等。細(xì)胞系在多個領(lǐng)域的研究中被廣泛應(yīng)用，包括基礎(chǔ)醫(yī)學(xué)、臨床試驗(yàn)、藥物篩選和分子生物學(xué)研究。這些研究不僅在中國，也在日本、美國和歐洲等多個國家和地區(qū)進(jìn)行。

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

BC3H-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：769P細(xì)胞、ETCC007細(xì)胞、GEO細(xì)胞

HCC0366 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：MCF/Adr細(xì)胞、RN-c細(xì)胞、NTC200細(xì)胞

HNEpC Cells;背景說明：鼻粘膜；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：Jurkat-77細(xì)胞、M-NFS-60細(xì)胞、C4-I細(xì)胞

OVCAR433 Cells;背景說明：卵巢癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：BEL/FU細(xì)胞、HBZY-1細(xì)胞、Lilly Laboratories Cell-Monkey Kidney 2細(xì)胞

Hs 578T人乳腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

物種來源：人源、鼠源等其它物種來源

形態(tài)特性：上皮細(xì)胞樣

實(shí)驗(yàn)室細(xì)胞培養(yǎng)基知識簡介：干粉培養(yǎng)基：以前大部分實(shí)驗(yàn)室都是用干粉培養(yǎng)基，但配制過程就較為繁瑣，要溶解、調(diào)pH值，過濾，過程中可能會產(chǎn)生一些濃度誤差，而且有些實(shí)驗(yàn)室的水質(zhì)并不理想，所以培養(yǎng)的效果會有差異。如果使用體培養(yǎng)基，這種人為的誤差會減少，因?yàn)楫吘故谴笈抗I(yè)化生產(chǎn)的，批間差會很小。大家是不是感覺體培養(yǎng)基會貴很多，以前是這樣，但現(xiàn)在大家都認(rèn)同了；無血清培養(yǎng)基(Serum-Free Media)，通常以SFM表示，顧名思義，就是在細(xì)胞培養(yǎng)中不需要添加血清，但是在某些應(yīng)用中可能要添加生長因子或細(xì)胞因子。無血清培養(yǎng)基中添加了血清的主要成分：粘附因子、生長因子、必需的營養(yǎng)物質(zhì)和激素等，能減少上述血清帶來的不利因素，使細(xì)胞培養(yǎng)的條件更穩(wěn)定。但它也不是完美的，從有血清培養(yǎng)過渡到無血清培養(yǎng)的條件并不像想象中那么直截了當(dāng)。處于發(fā)育的不同分化階段的細(xì)胞(例如干細(xì)胞與定向前體細(xì)胞相比)需要不同的配方，對生長因子和細(xì)胞因子的選擇尤為重要。而且在去除血清的同時，也去除了一些血清蛋白具有的保護(hù)、解毒作用，因此對試劑、水的純度和儀器清潔度的要求更GAO。另外，它的價格也比普通的培養(yǎng)基貴很多。

U373 MG Cells;背景說明：膠質(zhì)瘤；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：D-341細(xì)胞、NUGC-4細(xì)胞、H-1395細(xì)胞

H-1563 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：NCI-H2023細(xì)胞、MIN6細(xì)胞、NCIH1568細(xì)胞

TE12 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：UMNSAH/DF#1細(xì)胞、Rat podocyte細(xì)胞、OCI-Ly 1細(xì)胞

K1735 Cells;背景說明：黑色素瘤； C３H/HeN;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：C3H 10T1/2細(xì)胞、Hs 742.T細(xì)胞、LI7細(xì)胞

HSC-5 [Human skin squamous cell carcinoma] Cells;背景說明：皮膚鱗癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Y3M細(xì)胞、HPAF2細(xì)胞、MLM細(xì)胞

Caki-1 Cells;背景說明：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、次級溶酶體，沒有發(fā)現(xiàn)病毒顆粒。;傳代方法：１：２-１：４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：NPA-87細(xì)胞、NCIH929細(xì)胞、GM-3573細(xì)胞

Kit 225-K6 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：3T3-F442A細(xì)胞、PIEC細(xì)胞、SK-MEL-3細(xì)胞

NCI-H2228 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２-３次。;生長特性：貼壁生長;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：HEM細(xì)胞、CaES-17細(xì)胞、Jiyoye(P-2003)細(xì)胞

H-1623 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：HOP-92細(xì)胞、Caki-2細(xì)胞、MFM-223細(xì)胞

K7M2 wt Cells;背景說明：骨肉瘤；肺轉(zhuǎn)移；雌性；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：Caov-4細(xì)胞、J-774A.1細(xì)胞、Jeko1細(xì)胞

H283 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。;生長特性：懸浮細(xì)胞的多細(xì)胞聚集體，和一些貼壁 Cells;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：U266 Bl細(xì)胞、beta TC6細(xì)胞、Gerner 7666細(xì)胞

HBZY 1 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：HOS-MNNG細(xì)胞、HEK-293F細(xì)胞、REC1細(xì)胞

H1954 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：Eca109細(xì)胞、HEK-293-FT細(xì)胞、EAC細(xì)胞

HS578T Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：MDA-468細(xì)胞、EAhy 926細(xì)胞、LA-N-6(OAN)細(xì)胞

SW-780 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：U-251 MG細(xì)胞、Kasumi 1細(xì)胞、ID8細(xì)胞

Panc 5.04 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：WBF344細(xì)胞、CA-OV-3細(xì)胞、MESSA Dx5細(xì)胞

A-673 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：消化３-５分鐘。１：２。３天內(nèi)可長滿。;生長特性：貼壁生長;形態(tài)特性：成纖維細(xì)胞;相關(guān)產(chǎn)品有：NCI-H2085細(xì)胞、Biopsy xenograft of Pancreatic Carcinoma line-3細(xì)胞、KG-1a細(xì)胞

Hs 578T人乳腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

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

AG09896 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line NPX305 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line XC510 Cells(提供STR鑒定圖譜)

BT-474 Tam1 Cells(提供STR鑒定圖譜)

COS-7-InVitrus Cells(提供STR鑒定圖譜)

DA04038 Cells(提供STR鑒定圖譜)

DUR 10R Cells(提供STR鑒定圖譜)

GM04290 Cells(提供STR鑒定圖譜)

MC-26 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：HCC-1428細(xì)胞、C3A細(xì)胞、Hs 683細(xì)胞

NCI-H2052 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：６傳代;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：KYSE 180細(xì)胞、H22細(xì)胞、16HBE140細(xì)胞

H1963 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：SK Col 1細(xì)胞、GA-10 clone 4細(xì)胞、MCF-7/ADR細(xì)胞

SK-OV-3 Cells;背景說明：SK-OV-３由G.Trempe和L.J.Old在１９７３年從卵巢腫瘤病人的腹水分離得到。 此細(xì)胞對腫瘤壞死因子和幾種細(xì)胞毒性藥物包括白喉毒素、順鉑和阿霉素均耐受。 在裸鼠中致瘤，且形成與卵巢原位癌一致的中度分化的腺癌。;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：WM-239-A細(xì)胞、TCMK1細(xì)胞、NCIH2405細(xì)胞

NOZC-1 Cells;背景說明：患者有癌性腹膜炎。細(xì)胞為中等分化的管狀膽囊癌。會分泌AFP和CEA。倍增時間４８小時，板植率１４-１９%。細(xì)胞可在裸鼠中成瘤，形態(tài)與原發(fā)腫瘤相似。;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：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：F442A細(xì)胞、MFE-280細(xì)胞、Hs 636.T細(xì)胞

RASMC Cells;背景說明：主動脈；平滑肌 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：OCI-Ly8細(xì)胞、TPC-1細(xì)胞、WSU-DLCL-2細(xì)胞

776.1 Cells(提供STR鑒定圖譜)

MiaPaCa-2 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：TW-039細(xì)胞、FET細(xì)胞、Potorous tridactylus Kidney 1細(xì)胞

H2.35 Cells;背景說明：肝；SV４０轉(zhuǎn)化；雌性；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：LNT-229細(xì)胞、CCD1112Sk細(xì)胞、Karpas 299細(xì)胞

OCI-LY-8 Cells;背景說明：彌漫大B淋巴瘤;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：SKO007細(xì)胞、NCI-H2591細(xì)胞、HOP-62細(xì)胞

MAVER-1 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３-１：５傳代；２-３天換液１次。;生長特性：懸浮生長;形態(tài)特性：淋巴母細(xì)胞;相關(guān)產(chǎn)品有：AML-193細(xì)胞、NCI-H2170細(xì)胞、SNU-520細(xì)胞

HT-1376 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：SUSM1細(xì)胞、NCI-H716細(xì)胞、KBM7細(xì)胞

H-520 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：QGP-1細(xì)胞、UPCI-SCC090細(xì)胞、CPAE細(xì)胞

MRASMC 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：Tohoku Hospital Pediatrics-1細(xì)胞、EC9706細(xì)胞、CCD-18Co細(xì)胞

NCI-H102 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：３傳代,２-３天傳一代;生長特性：懸浮生長 ;形態(tài)特性：圓形；淋巴母細(xì)胞樣;相關(guān)產(chǎn)品有：KHYG1細(xì)胞、B/C3T3細(xì)胞、WIL2 S細(xì)胞

H9 AAVS1-TRE3G-NGN2 RETREG3-/- RETREG2-/- RETREG1-/- TEX264-/- Keima-REEP5 Cells(提供STR鑒定圖譜)

HAP1 REPS1 (-) 2 Cells(提供STR鑒定圖譜)

HEL-92 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：Hs 737.T細(xì)胞、NCIH1184細(xì)胞、PT-K75細(xì)胞

C3H/10T1/2-clone8 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：MSF細(xì)胞、SW-962細(xì)胞、NSC-34細(xì)胞

BNL-CL.2 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：NW-MEL-38細(xì)胞、HSF細(xì)胞、P31-FUJ細(xì)胞

CATH.a Cells;背景說明：神經(jīng)；SV４０轉(zhuǎn)化；C５７BL/６ x DBA/２;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：ECC 12細(xì)胞、NCIADRRES細(xì)胞、SUP-M2細(xì)胞

Hs 27 Cells;背景說明：包皮；成纖維細(xì)胞；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：TE-13細(xì)胞、A101D細(xì)胞、HEP-3B2細(xì)胞

SUM 190PT Cells;背景說明：乳腺癌；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：LS174T細(xì)胞、HeLaS3細(xì)胞、NE-1細(xì)胞

Capan-2 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代，２-３天換液１次。;生長特性：貼壁生長;形態(tài)特性：多邊形;相關(guān)產(chǎn)品有：H-1341細(xì)胞、NOR 10細(xì)胞、NG10815細(xì)胞

PL-45 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：KPNRTBM1細(xì)胞、SAOS 2細(xì)胞、DHL-4細(xì)胞

HuT-12 Cells(提供STR鑒定圖譜)

LA8 Cells(提供STR鑒定圖譜)

MuM-2C Cells(提供STR鑒定圖譜)

ORMES-6 Cells(提供STR鑒定圖譜)

RP1-hiPSC11 Cells(提供STR鑒定圖譜)

Ubigene HEK293 CCDC150 KO Cells(提供STR鑒定圖譜)

WEHI-231 Cells(提供STR鑒定圖譜)

HG01172 Cells(提供STR鑒定圖譜)

D283 Med 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。;生長特性：懸浮細(xì)胞的多細(xì)胞聚集體，和一些貼壁 Cells;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：253JB-V細(xì)胞、L 428細(xì)胞、BC3H1細(xì)胞

H-1155 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。;生長特性：懸浮生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：143BTK-細(xì)胞、LN 229細(xì)胞、hADSCs細(xì)胞

SUDHL5 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：T98-G細(xì)胞、NEC-8細(xì)胞、KP 4細(xì)胞

Tb 1-Lu Cells;背景說明：肺;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：BNL-HCC細(xì)胞、NCIH1688細(xì)胞、GM07404D細(xì)胞

KE-39 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Hs706T細(xì)胞、SUP-B1細(xì)胞、T47D:A細(xì)胞

KE-39 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁或懸浮，詳見產(chǎn)品說明書部分;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Hs706T細(xì)胞、SUP-B1細(xì)胞、T47D:A細(xì)胞

SKGT4 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：BEND細(xì)胞、HCC15細(xì)胞、CCRF SB細(xì)胞

NOR10 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：NCI-SNU-387細(xì)胞、SL-29細(xì)胞、UM-UC14細(xì)胞

NCI-H1299 Cells;背景說明：這株細(xì)胞來源于一個淋巴結(jié)轉(zhuǎn)移?；颊呓邮芰顺跗诜暖?。細(xì)胞均一性的部分缺失p５３蛋白，并缺少p５３蛋白表達(dá)。細(xì)胞可以合成０.１pmol/毫克蛋白的NMB蛋白，而不合成促胃液釋放肽(GRP)。;傳代方法：１：２傳代；３天傳代一次。;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：COR-L23細(xì)胞、Madison 109細(xì)胞、C643細(xì)胞

NG 108-15 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：GM03569B細(xì)胞、MDA-MB-436細(xì)胞、A431細(xì)胞

Kato-III Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２傳代。３天內(nèi)可長滿。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：Ramos 1細(xì)胞、Mel-RM細(xì)胞、ME180細(xì)胞

Kit 225 K6 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：H-1385細(xì)胞、251 MG細(xì)胞、VMM5細(xì)胞

MDAPCa2b Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：１：２-１：４傳代，２-３天換液１次。;生長特性：貼壁生長;形態(tài)特性：上皮細(xì)胞;相關(guān)產(chǎn)品有：TE3細(xì)胞、JM1細(xì)胞、Lieming Xu-2細(xì)胞

GA-10-Clone-4 Cells;背景說明：詳見相關(guān)文獻(xiàn)介紹;傳代方法：每２-３天換液;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：MGH-U3細(xì)胞、NCIH2135細(xì)胞、SKLMS-1細(xì)胞

WM 2664 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：TE-9細(xì)胞、SK-MEL24細(xì)胞、MV411細(xì)胞

T78-1 Cells(提供STR鑒定圖譜)

LMTK- 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：ECV細(xì)胞、MUM2B細(xì)胞、MOLM-13細(xì)胞

RKOAS451 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：T2(174 x CEM.T2)細(xì)胞、H-2141細(xì)胞、H-820細(xì)胞

HuO9 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：SW1990細(xì)胞、MDA-436細(xì)胞、BT.549細(xì)胞

PT-K75 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：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：KBM5細(xì)胞、NCIH548細(xì)胞、HMVEC細(xì)胞

University of Michigan-Urothelial Carcinoma-14 Cells;背景說明：腎癌；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：Fortner's melanotic melanoma #3細(xì)胞、3T3-442A細(xì)胞、HCCC9810細(xì)胞

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

H-719 Cells;背景說明：小細(xì)胞肺癌；骨髓轉(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：半貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：Caki2細(xì)胞、H1155細(xì)胞、HuT 102細(xì)胞

DU-4475 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;生長特性：懸浮，多細(xì)胞聚集;形態(tài)特性：上皮細(xì)胞樣;相關(guān)產(chǎn)品有：HCC1359細(xì)胞、CCD 841 CoTr細(xì)胞、HSKMC細(xì)胞

HB 611 Cells;背景說明：肝母細(xì)胞癌；男性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：RPMI #1846細(xì)胞、CAL12T細(xì)胞、H2405細(xì)胞

MB39 Cells;背景說明：腦瘤;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：Mc Ardle 7777細(xì)胞、3AA細(xì)胞、COR-L51細(xì)胞

SHG44 Cells;背景說明：SHG-４４細(xì)胞株源自一例２-３級前沿淋巴結(jié)星細(xì)胞瘤。染色體組型顯示８９.２%的超三倍體。在Wistar大鼠和裸鼠中接種都能成功。細(xì)胞含有神經(jīng)系統(tǒng)特有的S-１００蛋白和星細(xì)胞特有的GFA蛋白;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：成纖維細(xì)胞樣;相關(guān)產(chǎn)品有：HEK293S細(xì)胞、CFSC-2G細(xì)胞、Douglas Foster-1細(xì)胞

AMO1 Cells;背景說明：漿細(xì)胞骨髓瘤；女性;傳代方法：１：２-１：３傳代；每周換液２-３次。;生長特性：半貼壁;形態(tài)特性：詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有：RKO-AS-45-1細(xì)胞、PANC 327細(xì)胞、RPMI no. 8226細(xì)胞

alpha TC1-6 Cells;背景說明：胰島素瘤；a細(xì)胞；C５７BL/６xDBA/２;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：SKGT2細(xì)胞、GTL-16細(xì)胞、SNU-C1細(xì)胞

MGH-U3 (RN) 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：SW 48細(xì)胞、NCI-H1793細(xì)胞、SkChA1細(xì)胞

Hs 578T人乳腺癌復(fù)蘇細(xì)胞保種中心|帶STR證書

BayGenomics ES cell line RRP138 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YHC200 Cells(提供STR鑒定圖譜)

Hep-56.1C Cells(提供STR鑒定圖譜)

PCRP-CSTF2-1A11 Cells(提供STR鑒定圖譜)

c-SST-2 clone 6 Cells(提供STR鑒定圖譜)

HPS0584 Cells(提供STR鑒定圖譜)

" "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=1961733; DOI=10.1073/pnas.88.23.10657; PMCID=PMC52989

Runnebaum I.B., Nagarajan M., Bowman M., Soto D., Sukumar S.

Mutations in p53 as potential molecular markers for human breast cancer.

Proc. Natl. Acad. Sci. U.S.A. 88:10657-10661(1991)

PubMed=7902062

de la Torre M., Hao X.-Y., Larsson R., Nygren P., Tsuruo T., Mannervik B., Bergh J.

Characterization of four doxorubicin adapted human breast cancer cell lines with respect to chemotherapeutic drug sensitivity, drug resistance associated membrane proteins and glutathione transferases.

Anticancer Res. 13:1425-1430(1993)

DOI=10.1016/B978-0-12-333530-2.50009-5

Leibovitz A.

Cell lines from human breast.

(In book chapter) Atlas of human tumor cell lines; Hay R.J., Park J.-G., Gazdar A.F. (eds.); pp.161-184; Academic Press; New York; USA (1994)

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=10969801

Forozan F., Mahlamaki E.H., Monni O., Chen Y.-D., Veldman R., Jiang Y., Gooden G.C., Ethier S.P., Kallioniemi A.H., Kallioniemi O.-P.

Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data.

Cancer Res. 60:4519-4525(2000)

PubMed=15153330; DOI=10.1593/neo.3292; PMCID=PMC1502105

Watts G.S., Oshiro M.M., Junk D.J., Wozniak R.J., Watterson S.J., Domann F.E., Futscher B.W.

The acetyltransferase p300/CBP-associated factor is a p53 target gene in breast tumor cells.

Neoplasia 6:187-194(2004)

PubMed=15677628; DOI=10.1093/carcin/bgi032

Gorringe K.L., Chin S.-F., Pharoah P.D.P., Staines J.M., Oliveira C., Edwards P.A.W., Caldas C.

Evidence that both genetic instability and selection contribute to the accumulation of chromosome alterations in cancer.

Carcinogenesis 26:923-930(2005)

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=16142302; DOI=10.3892/ijo.27.4.881

de Longueville F., Lacroix M., Barbuto A.-M., Bertholet V., Gallo D., Larsimont D., Marcq L., Zammatteo N., Boffe S., Leclercq G., Remacle J.

Molecular characterization of breast cancer cell lines by a low-density microarray.

Int. J. Oncol. 27:881-892(2005)

PubMed=16397213; DOI=10.1158/0008-5472.CAN-05-2853

Elstrodt F., Hollestelle A., Nagel J.H.A., Gorin M., Wasielewski M., van den Ouweland A.M.W., Merajver S.D., Ethier S.P., Schutte M.

BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants.

Cancer Res. 66:41-45(2006)

PubMed=16541312; DOI=10.1007/s10549-006-9186-z

Wasielewski M., Elstrodt F., Klijn J.G.M., Berns E.M.J.J., Schutte M.

Thirteen new p53 gene mutants identified among 41 human breast cancer cell lines.

Breast Cancer Res. Treat. 99:97-101(2006)

PubMed=16959974; DOI=10.1126/science.1133427

Sjoblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., Farrell C., Meeh P., Markowitz S.D., Willis J.E., Dawson D., Willson J.K.V., Gazdar A.F., Hartigan J., Wu L., Liu C.-S., Parmigiani G., Park B.H., Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W., Velculescu V.E.

The consensus coding sequences of human breast and colorectal cancers.

Science 314:268-274(2006)

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=17157791; DOI=10.1016/j.ccr.2006.10.008; PMCID=PMC2730521

Neve R.M., Chin K., Fridlyand J., Yeh J., Baehner F.L., Fevr T., Clark L., Bayani N., Coppe J.-P., Tong F., Speed T., Spellman P.T., DeVries S., Lapuk A., Wang N.J., Kuo W.-L., Stilwell J.L., Pinkel D., Albertson D.G., Waldman F.M., McCormick F., Dickson R.B., Johnson M.D., Lippman M.E., Ethier S.P., Gazdar A.F., Gray J.W.

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes.

Cancer Cell 10:515-527(2006)

PubMed=17932254; DOI=10.1126/science.1145720

Wood L.D., Parsons D.W., Jones S., Lin J., Sjoblom T., Leary R.J., Shen D., Boca S.M., Barber T.D., Ptak J., Silliman N., Szabo S., Dezso Z., Ustyanksky V., Nikolskaya T., Nikolsky Y., Karchin R., Wilson P.A., Kaminker J.S., Zhang Z.-M., Croshaw R., Willis J.E., Dawson D., Shipitsin M., Willson J.K.V., Sukumar S., Polyak K., Park B.H., Pethiyagoda C.L., Pant P.V.K., Ballinger D.G., Sparks A.B., Hartigan J., Smith D.R., Suh E., Papadopoulos N., Buckhaults P., Markowitz S.D., Parmigiani G., Kinzler K.W., Velculescu V.E., Vogelstein B.

The genomic landscapes of human breast and colorectal cancers.

Science 318:1108-1113(2007)

PubMed=18516279; DOI=10.1016/j.molonc.2007.02.004; PMCID=PMC2391005

Kenny P.A., Lee G.Y., Myers C.A., Neve R.M., Semeiks J.R., Spellman P.T., Lorenz K., Lee E.H., Barcellos-Hoff M.H., Petersen O.W., Gray J.W., Bissell M.J.

The morphologies of breast cancer cell lines in three-dimensional assays correlate with their profiles of gene expression.

Mol. Oncol. 1:84-96(2007)

PubMed=18277095; DOI=10.4161/cbt.7.5.5712

Berglind H., Pawitan Y., Kato S., Ishioka C., Soussi T.

Analysis of p53 mutation status in human cancer cell lines: a paradigm for cell line cross-contamination.

Cancer Biol. Ther. 7:699-708(2008)

PubMed=18386134; DOI=10.1007/s10585-008-9169-z

Hughes L., Malone C., Chumsri S., Burger A.M., McDonnell S.

Characterisation of breast cancer cell lines and establishment of a novel isogenic subclone to study migration, invasion and tumourigenicity.

Clin. Exp. Metastasis 25:549-557(2008)

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=19582160; DOI=10.1371/journal.pone.0006146; PMCID=PMC2702084

Kao J., Salari K., Bocanegra M., Choi Y.-L., Girard L., Gandhi J., Kwei K.A., Hernandez-Boussard T., Wang P., Gazdar A.F., Minna J.D., Pollack J.R.

Molecular profiling of breast cancer cell lines defines relevant tumor models and provides a resource for cancer gene discovery.

PLoS ONE 4:E6146-E6146(2009)

DOI=10.25904/1912/1434

Morrison B.J.

Breast cancer stem cells: tumourspheres and implications for therapy.

Thesis PhD (2010); Griffith University; Brisbane; Australia

PubMed=19593635; DOI=10.1007/s10549-009-0460-8

Hollestelle A., Nagel J.H.A., Smid M., Lam S., Elstrodt F., Wasielewski M., Ng S.S., French P.J., Peeters J.K., Rozendaal M.J., Riaz M., Koopman D.G., ten Hagen T.L.M., de Leeuw B.H.C.G.M., Zwarthoff E.C., Teunisse A.F.A.S., van der Spek P.J., Klijn J.G.M., Dinjens W.N.M., Ethier S.P., Clevers H.C., Jochemsen A.G., den Bakker M.A., Foekens J.A., Martens J.W.M., Schutte M.

Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines.

Breast Cancer Res. Treat. 121:53-64(2010)

PubMed=20070913; DOI=10.1186/1471-2407-10-15; PMCID=PMC2836299

Tsuji K., Kawauchi S., Saito S., Furuya T., Ikemoto K., Nakao M., Yamamoto S., Oka M., Hirano T., Sasaki K.

Breast cancer cell lines carry cell line-specific genomic alterations that are distinct from aberrations in breast cancer tissues: comparison of the CGH profiles between cancer cell lines and primary cancer tissues.

BMC Cancer 10:15.1-15.10(2010)

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

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

Signatures of mutation and selection in the cancer genome.

Nature 463:893-898(2010)

PubMed=21778573; DOI=10.3233/BD-2010-0307; PMCID=PMC3532890

Chavez K.J., Garimella S.V., Lipkowitz S.

Triple negative breast cancer cell lines: one tool in the search for better treatment of triple negative breast cancer.

Breast Dis. 32:35-48(2010)

DOI=10.4172/2157-7145.S2-005

Fang R.-X., Shewale J.G., Nguyen V.T., Cardoso H., Swerdel M.R., Hart R.P., Furtado M.R.

STR profiling of human cell lines: challenges and possible solutions to the growing problem.

J. Forensic Res. 2 Suppl. 2:5-5(2011)

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=22585861; DOI=10.1158/2159-8290.CD-11-0224; PMCID=PMC5057396

Marcotte R., Brown K.R., Suarez Saiz F.J., Sayad A., Karamboulas K., Krzyzanowski P.M., Sircoulomb F., Medrano M., Fedyshyn Y., Koh J.L.-Y., van Dyk D., Fedyshyn B., Luhova M., Brito G.C., Vizeacoumar F.J., Vizeacoumar F.S., Datti A., Kasimer D., Buzina A., Mero P., Misquitta C., Normand J., Haider M., Ketela T., Wrana J.L., Rottapel R., Neel B.G., Moffat J.

Essential gene profiles in breast, pancreatic, and ovarian cancer cells.

Cancer Discov. 2:172-189(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=23151021; DOI=10.1186/1471-2164-13-619; PMCID=PMC3546428

Grigoriadis A., Mackay A., Noel E., Wu P.-J., Natrajan R., Frankum J., Reis-Filho J.S., Tutt A.

Molecular characterisation of cell line models for triple-negative breast cancers.

BMC Genomics 13:619.1-619.14(2012)

PubMed=23601657; DOI=10.1186/bcr3415; PMCID=PMC3672661

Riaz M., van Jaarsveld M.T.M., Hollestelle A., Prager-van der Smissen W.J.C., Heine A.A.J., Boersma A.W.M., Liu J.-J., Helmijr J.C.A., Ozturk B., Smid M., Wiemer E.A.C., Foekens J.A., Martens J.W.M.

miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs.

Breast Cancer Res. 15:R33.1-R33.17(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=24009699; DOI=10.1371/journal.pone.0072704; PMCID=PMC3751845

Liu X., Nie H., Zhang Y.-B., Yao Y.-F., Maitikabili A., Qu Y.-P., Shi S.-L., Chen C.-Y., Li Y.

Cell surface-specific N-glycan profiling in breast cancer.

PLoS ONE 8:E72704-E72704(2013)

PubMed=24094812; DOI=10.1016/j.ccr.2013.08.020; PMCID=PMC3931310

Timmerman L.A., Holton T., Yuneva M., Louie R.J., Padro M., Daemen A., Hu M., Chan D.A., Ethier S.P., van 't Veer L.J., Polyak K., McCormick F., Gray J.W.

Glutamine sensitivity analysis identifies the xCT antiporter as a common triple-negative breast tumor therapeutic target.

Cancer Cell 24:450-465(2013)

PubMed=24162158; DOI=10.1007/s10549-013-2743-3; PMCID=PMC3832776

Prat A., Karginova O., Parker J.S., Fan C., He X.-P., Bixby L.M., Harrell J.C., Roman E., Adamo B., Troester M.A., Perou C.M.

Characterization of cell lines derived from breast cancers and normal mammary tissues for the study of the intrinsic molecular subtypes.

Breast Cancer Res. Treat. 142:237-255(2013)

PubMed=24176112; DOI=10.1186/gb-2013-14-10-r110; PMCID=PMC3937590

Daemen A., Griffith O.L., Heiser L.M., Wang N.J., Enache O.M., Sanborn Z., Pepin F., Durinck S., Korkola J.E., Griffith M., Hur J.S., Huh N., Chung J., Cope L., Fackler M.J., Umbricht C.B., Sukumar S., Seth P., Sume V.P., Jakkula L.R., Lu Y.-L., Mills G.B., Cho R.J., Collisson E.A., van 't Veer L.J., Spellman P.T., Gray J.W.

Modeling precision treatment of breast cancer.

Genome Biol. 14:R110.1-R110.14(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=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=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=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=25892236; DOI=10.1016/j.celrep.2015.03.050; PMCID=PMC4425736

Lawrence R.T., Perez E.M., Hernandez D., Miller C.P., Haas K.M., Irie H.Y., Lee S.-I., Blau C.A., Villen J.

The proteomic landscape of triple-negative breast cancer.

Cell Rep. 11:630-644(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=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=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=28287265; DOI=10.1021/acs.jproteome.6b00470; PMCID=PMC5557415

Yen T.-Y., Bowen S., Yen R., Piryatinska A., Macher B.A., Timpe L.C.

Glycoproteins in claudin-low breast cancer cell lines have a unique expression profile.

J. Proteome Res. 16:1391-1400(2017)

PubMed=28889351; DOI=10.1007/s10549-017-4496-x

Saunus J.M., Smart C.E., Kutasovic J.R., Johnston R.L., Kalita-de Croft P., Miranda M., Rozali E.N., Vargas A.C., Reid L.E., Lorsy E., Cocciardi S., Seidens T., McCart Reed A.E., Dalley A.J., Wockner L.F., Johnson J., Sarkar D., Askarian-Amiri M.E., Simpson P.T., Khanna K.K., Chenevix-Trench G., Al-Ejeh F., Lakhani S.R.

Multidimensional phenotyping of breast cancer cell lines to guide preclinical research.

Breast Cancer Res. Treat. 167:289-301(2018)

PubMed=29671673; DOI=10.1080/24701394.2018.1461852

Hedberg A., Knutsen E., Lovhaugen A.S., Jorgensen T.E., Perander M., Johansen S.D.

Cancer-specific SNPs originate from low-level heteroplasmic variants in human mitochondrial genomes of a matched cell line pair.

Mitochondrial DNA A. DNA Mapp. Seq. Anal. 30:82-91(2019)

PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675

Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.

An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.

Cancer Res. 79:1263-1273(2019)

PubMed=30971826; DOI=10.1038/s41586-019-1103-9

Behan F.M., Iorio F., Picco G., Goncalves E., Beaver C.M., Migliardi G., Santos R., Rao Y., Sassi F., Pinnelli M., Ansari R., Harper S., Jackson D.A., McRae R., Pooley R., Wilkinson P., van der Meer D.J., Dow D., Buser-Doepner C.A., Bertotti A., Trusolino L., Stronach E.A., Saez-Rodriguez J., Yusa K., Garnett M.J.

Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.

Nature 568:511-516(2019)"