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T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜,T-47D cell
  • T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜,T-47D cell

T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

價(jià)格 詢價(jià)
包裝 1000000細(xì)胞數(shù) 2000000細(xì)胞數(shù)
最小起訂量 1000000細(xì)胞數(shù)
發(fā)貨地 上海
更新日期 2025-02-23
QQ交談 微信洽談

產(chǎn)品詳情

中文名稱:T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜英文名稱:T-47D cell
品牌: ATCC\RCB等產(chǎn)地: 國(guó)外
保存條件: 常溫培養(yǎng)或液氮凍存純度規(guī)格: T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜
產(chǎn)品類別: 化學(xué)試劑
種屬: 詳見產(chǎn)品資料組織: 詳見產(chǎn)品資料
細(xì)胞系: 詳見產(chǎn)品資料細(xì)胞形態(tài): 詳見產(chǎn)品資料
生長(zhǎng)狀態(tài): 詳見產(chǎn)品資料靶點(diǎn): 詳見產(chǎn)品資料
應(yīng)用: 詳見產(chǎn)品資料
2025-02-23 T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜 T-47D cell 1000000細(xì)胞數(shù)/RMB;2000000細(xì)胞數(shù)/RMB ATCC\RCB等 國(guó)外 常溫培養(yǎng)或液氮凍存 T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜 化學(xué)試劑

"T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

傳代比例:1:2-1:4(首次傳代建議1:2)

生長(zhǎng)特性:貼壁生長(zhǎng)

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(gè)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(guó),也在日本、美國(guó)和歐洲等多個(gè)國(guó)家和地區(qū)進(jìn)行。

換液周期:每周2-3次

KM-12 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:T8細(xì)胞、MZCRC1細(xì)胞、U-251 MG細(xì)胞

ME1 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:TE9細(xì)胞、Tb 1 Lu (NBL-12)細(xì)胞、NCI-H2228細(xì)胞

Hep G2-Luc 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:SUDHL-5細(xì)胞、A673細(xì)胞、Ls-174-T細(xì)胞

背景信息:最初是從一位54歲女性的乳房侵入性導(dǎo)管癌患者的胸腔積液中分離出來的;發(fā)現(xiàn)分化的上皮亞株(T-47D)有細(xì)胞質(zhì)連接和17-β-雌二醇及其他類固醇降血鈣素的受體,T-47D細(xì)胞表達(dá)WNT7B癌基因。

T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

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

貼壁細(xì)胞(adherent cells):該類細(xì)胞的生長(zhǎng)必須有可以貼附的支持物表面,細(xì)胞依靠自身分泌的或培養(yǎng)基中提供的貼附因子才能在該表面上生長(zhǎng),繁殖;當(dāng)細(xì)胞在該表面生長(zhǎng)后,一般形成兩種形態(tài),即成纖維樣細(xì)胞性或上皮樣細(xì)胞;其生長(zhǎng)過程分為游離期、貼壁期、潛伏期、對(duì)數(shù)期、平臺(tái)期和衰退期。懸浮細(xì)胞(suspension cell):不貼附于生長(zhǎng)物,細(xì)胞呈圓形,呈單個(gè)細(xì)胞或者細(xì)小細(xì)胞團(tuán),懸浮細(xì)胞生長(zhǎng)空間大,傳代方便,能夠大量增殖。

HCC1833 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:HBL-100細(xì)胞、NGEC細(xì)胞、HUT-125細(xì)胞

BT-20 Cells;背景說明:該細(xì)胞1958年由E.Y. Lasfargues 和 L. Ozzello 建系,源自一位74歲白人女性的乳腺癌組織。該細(xì)胞表達(dá)WNT3和WNT78。TNF alpha抑制該細(xì)胞生長(zhǎng)。該細(xì)胞雌激素受體陰性,但表達(dá)5'外顯子缺失的雌激素mRNA。;傳代方法:1:2—1:4傳代,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:Ramos (RA 1)細(xì)胞、H-1694細(xì)胞、MC-4細(xì)胞

WEHI-279 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:P31FUJ細(xì)胞、LICCF細(xì)胞、PC14細(xì)胞

3T3.T4 Cells(提供STR鑒定圖譜)

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

物種來源:人源、鼠源等其它物種來源

T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

形態(tài)特性:上皮細(xì)胞樣

貼壁細(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(shí)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(shí)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(shí),從組織消化下細(xì)胞。這種方法作用溫和,對(duì)細(xì)胞損傷較小,但是,價(jià)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(duì)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(shí)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(gè)人的使用經(jīng)常覺得對(duì)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(shí)。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(duì)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(tái)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。

NCI-H1819 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:NCIH2110細(xì)胞、KYSE 510細(xì)胞、CNE1細(xì)胞

SK-BR3 Cells;背景說明:這株細(xì)胞源自胸水。沒有病毒顆粒。亞顯微結(jié)構(gòu)特征包括微絲和橋粒,肝糖原顆粒,大溶酶體,成束的細(xì)胞質(zhì)纖絲。SK-BR-3細(xì)胞株過表達(dá)HER2/c-erb-2基因產(chǎn)物。;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:MKN-74細(xì)胞、DMS-114細(xì)胞、Tohoku Hospital Pediatrics-1細(xì)胞

RBL.2H3 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(zhǎng)滿。;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:BT20細(xì)胞、HCC 70細(xì)胞、GM346細(xì)胞

KYSE-520 Cells;背景說明:食管鱗癌;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:Bx-PC3細(xì)胞、S180細(xì)胞、H35細(xì)胞

PAN 02 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:MFM-223細(xì)胞、MTEC1細(xì)胞、RAW-264.7細(xì)胞

VMRC-LCD 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:M059K細(xì)胞、NBL-S細(xì)胞、NCI-H1522細(xì)胞

HIBEpiC 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:HEK 293A細(xì)胞、Normal Rat Kidney-52E細(xì)胞、H2107細(xì)胞

R 1610 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:E0771細(xì)胞、PA1細(xì)胞、MLE12細(xì)胞

MOLP-8 Cells;背景說明:漿細(xì)胞骨髓瘤;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:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:Hs 742.T細(xì)胞、HSC-4細(xì)胞、SNU475細(xì)胞

KMY1022 Cells;背景說明: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:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:OCILY-19細(xì)胞、CT26.CL25細(xì)胞、HCC0095細(xì)胞

Vero 76 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:SK-N-BE(1)細(xì)胞、HM細(xì)胞、PG-4 S+L-細(xì)胞

266 Bl 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(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:GM03671C細(xì)胞、KM-H2細(xì)胞、SACC-83細(xì)胞

ACC-3 Cells;背景說明:Acc-3細(xì)胞源自一位49歲男性的腺樣囊性癌。能表達(dá)角蛋白。;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:4T1-LUC細(xì)胞、HRA 19細(xì)胞、SUM-149細(xì)胞

ECC-12 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:RCC10細(xì)胞、SCL1細(xì)胞、Lec1細(xì)胞

CEM/0 Cells;背景說明:G.E. Foley 等人建立了類淋巴母細(xì)胞細(xì)胞株CCRF-CEM。 細(xì)胞是1964年11月從一位四歲白人女性急性淋巴細(xì)胞白血病患者的外周血白血球衣中得到。此細(xì)胞系從香港收集而來。;傳代方法:1:2傳代。3天內(nèi)可長(zhǎng)滿。;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:NCI-H1734細(xì)胞、GM01232E細(xì)胞、NTera-2D1細(xì)胞

VP303 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:Huh-7細(xì)胞、COLO 205細(xì)胞、MOLP-8細(xì)胞

WERI Cells;背景說明:WERI-Rb-I細(xì)胞株是1974年R.M. McFall 和 T.W. Sery建立的兩株人眼癌細(xì)胞系中的一株。 細(xì)胞能在Difco Bacto-Agar中存活但不形成克隆。 掃描電鏡顯示在表面囊泡,板狀偽足和微絨毛在數(shù)量上和頻率上的改變。 細(xì)胞分化研究,腫瘤治療的動(dòng)物模型和生化評(píng)價(jià)都涉及這株細(xì)胞。;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:圓形細(xì)胞聚集成葡萄狀;相關(guān)產(chǎn)品有:OV3121細(xì)胞、AHH1細(xì)胞、HAC-84細(xì)胞

Abcam A-431 ACSL4 KO Cells(提供STR鑒定圖譜)

Abcam Raji MAPK7 KO Cells(提供STR鑒定圖譜)

Bayer/BCIRL-SfNS1-0714-C36-TR Cells(提供STR鑒定圖譜)

BayGenomics ES cell line RRR653 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YTA130 Cells(提供STR鑒定圖譜)

CHA-hES47 Cells(提供STR鑒定圖譜)

DA01726 Cells(提供STR鑒定圖譜)

DD1560 Cells(提供STR鑒定圖譜)

GM01948 Cells(提供STR鑒定圖譜)

NCIH1876 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(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:OP-9細(xì)胞、HO1-N1細(xì)胞、NCI H2106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

SCC9 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:NCI-H2135細(xì)胞、CCD-841-CoTr細(xì)胞、NIH:OVCAR-10細(xì)胞

HDLM-2 Cells;背景說明: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:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:MHCC-97細(xì)胞、D407細(xì)胞、H2106細(xì)胞

Los Angeles Prostate Cancer-4 Cells;背景說明:前列腺癌;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:SF295細(xì)胞、HKBML細(xì)胞、HRVEC細(xì)胞

HCT 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(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:COV 434細(xì)胞、NCIH2170細(xì)胞、MSTO211H細(xì)胞

CCD19-Lu 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:UCD-MLA-144細(xì)胞、NG 108-15細(xì)胞、AAV-293細(xì)胞

MNNG Cells;背景說明:骨肉瘤;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:I90細(xì)胞、Clone 929細(xì)胞、SW 839細(xì)胞

T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

NCI-H226 Cells;背景說明:1980年分離建立。;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:Doubling time: ~50 hours (ATCC).細(xì)胞、H820細(xì)胞、RA細(xì)胞

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:Jurkat, Clone E6-1細(xì)胞、CCD18Co細(xì)胞、TSCCa細(xì)胞

HSC-3 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1 x 10^5 cells/10cm dish;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:NCIH2081細(xì)胞、Nb2細(xì)胞、HUCEC細(xì)胞

JAR Cells;背景說明:JAR細(xì)胞株來源于胎盤滋養(yǎng)層腫瘤;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:SkChA-1細(xì)胞、BL1339細(xì)胞、HEL-92.1.7細(xì)胞

293T/17 Cells;背景說明:胚腎;5型腺病毒及SV40轉(zhuǎn)化;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:SU-DHL-16細(xì)胞、IPEC1細(xì)胞、H1693細(xì)胞

RL-952 Cells;背景說明:這些細(xì)胞有α角蛋白,定義明確的連接復(fù)合體,張力絲和表面微絨毛。;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:B16細(xì)胞、BEND細(xì)胞、TE3A細(xì)胞

Hu-P-T4 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:COV362細(xì)胞、697細(xì)胞、Menschliche Und Tierische Zellkulture-3細(xì)胞

GM22771 Cells(提供STR鑒定圖譜)

HAP1 MMP17 (-) 1 Cells(提供STR鑒定圖譜)

Mia PACA 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(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:U118細(xì)胞、Ramos 1細(xì)胞、GM06141B細(xì)胞

IOSE-29 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:LTEP-a-2細(xì)胞、SNU-C2B細(xì)胞、MAntle cell VERona-1細(xì)胞

HCC941122 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:NCI-H1963細(xì)胞、Blotchy fibroblast-11細(xì)胞、H-1793細(xì)胞

SU86_86 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:HFL-I細(xì)胞、Melan-a細(xì)胞、L-Wnt3A細(xì)胞

MMAc-SF 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:HEB細(xì)胞、Kit-225-K6細(xì)胞、MB157細(xì)胞

P36 Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:3-1:8?jìng)鞔?,?3天換液1次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:星形的;相關(guān)產(chǎn)品有:MGSMC細(xì)胞、NCIH2227細(xì)胞、NHDF細(xì)胞

hTERT-HME-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(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:293-EBNA細(xì)胞、HGF-1細(xì)胞、KOPN-8細(xì)胞

SUDHL-4 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:懸浮;形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:NCI H345細(xì)胞、NW-MEL-38細(xì)胞、H-676B細(xì)胞

HQ00304 Cells(提供STR鑒定圖譜)

KCL034 Cells(提供STR鑒定圖譜)

MGM-S Cells(提供STR鑒定圖譜)

NK-92CI Cells(提供STR鑒定圖譜)

RB 5205 Cells(提供STR鑒定圖譜)

UCSD036i-4-5 Cells(提供STR鑒定圖譜)

ZR-75-1 VIII-17 Cells(提供STR鑒定圖譜)

HAP1 TMEM2 (-) 2 Cells(提供STR鑒定圖譜)

X63 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:MPASMC細(xì)胞、C8-D1A細(xì)胞、SU4細(xì)胞

HSC-T6 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:Hs742T細(xì)胞、MM6細(xì)胞、HOC-1細(xì)胞

SUPB15 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(zhǎng)滿。;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:SN12C-PM6細(xì)胞、HRPEpiC細(xì)胞、A 2058細(xì)胞

MAVER 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(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:HuH 6細(xì)胞、FL-83B細(xì)胞、P3.NS-1/1.Ag4.1細(xì)胞

L5178Y-R 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:mIMCD3細(xì)胞、RT-BM細(xì)胞、HK2細(xì)胞

L5178Y-R 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:mIMCD3細(xì)胞、RT-BM細(xì)胞、HK2細(xì)胞

C6 Cells;背景說明:膠質(zhì)細(xì)胞株C6是由Benda等用N-nitrosomethylurea誘導(dǎo)的大鼠膠質(zhì)瘤克隆,并經(jīng)過一系列的體外培養(yǎng)和動(dòng)物傳代交替后建成的。 當(dāng)細(xì)胞從低密度生長(zhǎng)到滿瓶時(shí),S-100產(chǎn)量增加10倍。;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:NCIH1975細(xì)胞、GNM細(xì)胞、MUTZ-3細(xì)胞

IPEC-1 Cells;背景說明:小腸;上皮細(xì)胞;自發(fā)永生;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(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:P3 (Jiyoye)細(xì)胞、CCRF/CEM/0細(xì)胞、SKNO1細(xì)胞

A-427 Cells;背景說明:肺腺癌;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:詳見產(chǎn)品說明書;相關(guān)產(chǎn)品有:D407細(xì)胞、Centre Antoine Lacassagne-62細(xì)胞、SL-1細(xì)胞

IBMF-7 Cells;背景說明: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:HSC/mHSC細(xì)胞、SW954細(xì)胞、L5178-R細(xì)胞

L1210 Cells;背景說明:該細(xì)胞源于用0.2%甲基膽蒽(溶解)涂抹雌性小鼠的皮膚誘發(fā)的腫瘤,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;相關(guān)產(chǎn)品有:HCA-7細(xì)胞、SVG p12細(xì)胞、TE9細(xì)胞

L-6 myoblast Cells;背景說明:該細(xì)胞是Yaffe在甲基膽蒽存在的情況下從大鼠大腿肌原代培養(yǎng)的最初兩代細(xì)胞中分離得到的;在培養(yǎng)基中融合形成多核的肌管和橫紋肌纖維,細(xì)胞融合的程度隨著代數(shù)的增加而下降,因此細(xì)胞應(yīng)低代次冷凍并周期性地重新克隆以選擇融合能力強(qiáng)的細(xì)胞。鼠痘病毒陰性。該細(xì)胞應(yīng)在達(dá)匯合狀態(tài)前傳代,以延緩細(xì)胞分化能力的喪失。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成肌細(xì)胞樣;相關(guān)產(chǎn)品有:P30-OHKUBO細(xì)胞、SKCO-1細(xì)胞、TALL-104細(xì)胞

Farage OL Cells;背景說明:Farage細(xì)胞源于一名患有彌漫性大B細(xì)胞淋巴瘤(DLBCL)白人女性的活檢淋巴組織,由HBen-Bassat建系。經(jīng)IL-4處理,該細(xì)胞CD21,CD22,CD54和CD58表達(dá)上調(diào),而CD21,CD22,andCD38表達(dá)下調(diào)。;傳代方法:1:3傳代,2-3天傳一代;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:F-36P細(xì)胞、SK-RC 52細(xì)胞、SK-MEL5細(xì)胞

T98 G Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:按1:3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:Colon38細(xì)胞、MMQ細(xì)胞、32D.cl3細(xì)胞

H2444 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:H1437細(xì)胞、NCI-H1568細(xì)胞、SW 48細(xì)胞

STAN193i-432C1 Cells(提供STR鑒定圖譜)

UWB1-289 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:A2780/CP細(xì)胞、HHFK細(xì)胞、DBTRG-05MG細(xì)胞

P3-X63Ag8 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:HCC 2185細(xì)胞、Reuber H35細(xì)胞、H460細(xì)胞

PF382 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:懸浮生長(zhǎng);形態(tài)特性:淋巴母細(xì)胞;相關(guān)產(chǎn)品有:FRTL-5 Cl 2細(xì)胞、RWPE1細(xì)胞、PC 61 5.3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(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:OVCA-420細(xì)胞、H4IIEC3細(xì)胞、ABE-8.1/2細(xì)胞

NCI-157 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:KP-N-RT細(xì)胞、NCIH378細(xì)胞、HCC0038細(xì)胞

NCI H226 Cells;背景說明:1980年分離建立。;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:Human Microvascular Endothelial Cell line-1細(xì)胞、HCC78細(xì)胞、BAR-T細(xì)胞

P3-X63-Ag 8.653 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:NCIH1618細(xì)胞、NBLS細(xì)胞、TGW細(xì)胞

CHO-Lec1 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:H1963細(xì)胞、H4-II-EC3細(xì)胞、A2780CP細(xì)胞

T-47D人乳腺管癌細(xì)胞全年復(fù)蘇|已有STR圖譜

Hs-343-T Cells;背景說明:詳見相關(guān)文獻(xiàn)介紹;傳代方法:1:2—1:3傳代;每周換液2-3次。;生長(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:FL83B細(xì)胞、RCK-8細(xì)胞、HCT FET細(xì)胞

A-375SM 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:HCa/16A3-F細(xì)胞、RPMI No. 1846細(xì)胞、CAOV3細(xì)胞

Hs1.Tes 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:hCMEC/D3細(xì)胞、NS1-Ag4/1細(xì)胞、KNS-42細(xì)胞

MDAMB435S Cells;背景說明:MDA-MB-435S是一種紡錘形的細(xì)胞,1976年由其親本(435)中篩選得到。435是從31歲的轉(zhuǎn)移性乳腺導(dǎo)管腺癌女性患者胸水中分離得到。當(dāng)用熒光染料對(duì)微管蛋白進(jìn)行染色時(shí)親本細(xì)胞顯現(xiàn)散布特征(II型)。最近通過cDNA陣列研究表明,親本(MDA-MB-435)可歸入黑素瘤起源。;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:紡錘形;相關(guān)產(chǎn)品有:Caco-2/BBe 1細(xì)胞、CHP-100細(xì)胞、SUDHL8細(xì)胞

ME-180 Cells;背景說明:這株細(xì)胞來源于一個(gè)細(xì)胞集落不規(guī)則沒有顯著角質(zhì)化的侵染性鱗狀細(xì)胞癌。 單層培養(yǎng)的細(xì)胞間可以觀察到帶狀連接,也注意到有細(xì)胞質(zhì)張力絲。 1970年發(fā)現(xiàn)支原體污染并去除。 腫瘤壞死因子(TNF)α抑制ME-180的生長(zhǎng)。 這株細(xì)胞含有人乳頭瘤病毒(HPV)DNA,與HPV-39的同源性高于HPV-18。;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:HEK/EBNA細(xì)胞、NCI-N87細(xì)胞、SKNBE(1)細(xì)胞

HT29 Cells;背景說明:該細(xì)胞是1964年由FoghJ用移植培養(yǎng)方法和含15%FBS的F12培養(yǎng)液從原發(fā)性腫瘤分離的。近來,已建株的培養(yǎng)細(xì)胞用含血清的McCoy's5a培養(yǎng)基培養(yǎng)。該細(xì)胞系在裸鼠中成瘤,也能在類固醇處理的地鼠中成瘤。該細(xì)胞可合成IgA、CEA、TGFβ結(jié)合蛋白和黏液素;表達(dá)尿激酶受體,但沒有檢測(cè)到血漿酶原活性;不表達(dá)CD4,但細(xì)胞表面表達(dá)半乳糖神經(jīng)酰胺(HIV的可能替代受體)。該細(xì)胞系癌基因c-myc、K-ras、H-ras、N-ras、Myb、sis、fos陽性;p53基因過表達(dá),并且在273位密碼子處發(fā);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:MFE280細(xì)胞、P116細(xì)胞、L132細(xì)胞

BayGenomics ES cell line RRP008 Cells(提供STR鑒定圖譜)

BayGenomics ES cell line YHC106 Cells(提供STR鑒定圖譜)

hCD40L-M90 Cells(提供STR鑒定圖譜)

PCRP-CDC5L-2C6 Cells(提供STR鑒定圖譜)

BQ1 Cells(提供STR鑒定圖譜)

HPS0322 Cells(提供STR鑒定圖譜)

" "PubMed=8562478

Wosikowski K., Regis J.T., Robey R.W., Alvarez M., Buters J.T.M., Gudas J.M., Bates S.E.

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Mullen P., Ritchie A., Langdon S.P., Miller W.R.

Effect of Matrigel on the tumorigenicity of human breast and ovarian carcinoma cell lines.

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Wosikowski K., Schuurhuis D.H., Kops G.J.P.L., Saceda M., Bates S.E.

Altered gene expression in drug-resistant human breast cancer cells.

Clin. Cancer Res. 3:2405-2414(1997)


PubMed=9671407; DOI=10.1038/sj.onc.1201814

Sweeney K.J., Swarbrick A., Sutherland R.L., Musgrove E.A.

Lack of relationship between CDK activity and G1 cyclin expression in breast cancer cells.

Oncogene 16:2865-2878(1998)


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=10862037; DOI=10.1002/1098-2264(200007)28:3<308::aid-gcc9>3.0.CO;2-B

Kytola S., Rummukainen J., Nordgren A., Karhu R., Farnebo F., Isola J.J., Larsson C.

Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping.

Genes Chromosomes Cancer 28:308-317(2000)


PubMed=11044355; DOI=10.1054/bjoc.2000.1458; PMCID=PMC2408781

Davidson J.M., Gorringe K.L., Chin S.-F., Orsetti B., Besret C., Courtay-Cahen C., Roberts I., Theillet C., Caldas C., Edwards P.A.W.

Molecular cytogenetic analysis of breast cancer cell lines.

Br. J. Cancer 83:1309-1317(2000)


PubMed=11343771; DOI=10.1016/S0165-4608(00)00387-3

Rummukainen J., Kytola S., Karhu R., Farnebo F., Larsson C., Isola J.J.

Aberrations of chromosome 8 in 16 breast cancer cell lines by comparative genomic hybridization, fluorescence in situ hybridization, and spectral karyotyping.

Cancer Genet. Cytogenet. 126:1-7(2001)


PubMed=11414198; DOI=10.1007/s004320000207

Lahm H., Andre S., Hoeflich A., Fischer J.R., Sordat B., Kaltner H., Wolf E., Gabius H.-J.

Comprehensive galectin fingerprinting in a panel of 61 human tumor cell lines by RT-PCR and its implications for diagnostic and therapeutic procedures.

J. Cancer Res. Clin. Oncol. 127:375-386(2001)


PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459

Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.

Short tandem repeat profiling provides an international reference standard for human cell lines.

Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)


PubMed=11687795; DOI=10.1038/ng754

Snijders A.M., Nowak N.J., Segraves R., Blackwood S., Brown N., Conroy J., Hamilton G., Hindle A.K., Huey B., Kimura K., Law S., Myambo K., Palmer J., Ylstra B., Yue J.P., Gray J.W., Jain A.N., Pinkel D., Albertson D.G.

Assembly of microarrays for genome-wide measurement of DNA copy number.

Nat. Genet. 29:263-264(2001)


PubMed=12353263; DOI=10.1002/gcc.10107

Popovici C., Basset C., Bertucci F., Orsetti B., Adelaide J., Mozziconacci M.-J., Conte N., Murati A., Ginestier C., Charafe-Jauffret E., Ethier S.P., Lafage-Pochitaloff M., Theillet C., Birnbaum D., Chaffanet M.

Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.

Genes Chromosomes Cancer 35:204-218(2002)


PubMed=12661003; DOI=10.1002/gcc.10196

Seitz S., Wassmuth P., Plaschke J., Schackert H.K., Karsten U., Santibanez-Koref M.F., Schlag P.M., Scherneck S.

Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines.

Genes Chromosomes Cancer 37:29-35(2003)


PubMed=12800145; DOI=10.1002/gcc.10218

Adelaide J., Huang H.-E., Murati A., Alsop A.E., Orsetti B., Mozziconacci M.-J., Popovici C., Ginestier C., Letessier A., Basset C., Courtay-Cahen C., Jacquemier J., Theillet C., Birnbaum D., Edwards P.A.W., Chaffanet M.

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene.

Genes Chromosomes Cancer 37:333-345(2003)


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

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

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

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


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=16417655; DOI=10.1186/bcr1370; PMCID=PMC1413994

Shadeo A., Lam W.L.

Comprehensive copy number profiles of breast cancer cell model genomes.

Breast Cancer Res. 8:R9.1-R9.14(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=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=17254797; DOI=10.1016/j.biologicals.2006.10.001

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

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

Biologicals 35:195-202(2007)


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=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)


PubMed=19727395; DOI=10.1371/journal.pone.0006888; PMCID=PMC2731225

Wadlow R.C., Wittner B.S., Finley S.A., Bergquist H., Upadhyay R., Finn S.P., Loda M., Mahmood U., Ramaswamy S.

Systems-level modeling of cancer-fibroblast interaction.

PLoS ONE 4:E6888-E6888(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)


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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=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)


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=21378333

Ford C.H.J., Al-Bader M., Al-Ayadhi B., Francis I.

Reassessment of estrogen receptor expression in human breast cancer cell lines.

Anticancer Res. 31:521-527(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=21912889; DOI=10.1007/s10637-011-9744-z

Sutherland H.S., Hwang I.Y., Marshall E.S., Lindsay B.S., Denny W.A., Gilchrist C., Joseph W.R., Greenhalgh D., Richardson E., Kestell P., Ding A., Baguley B.C.

Therapeutic reactivation of mutant p53 protein by quinazoline derivatives.

Invest. New Drugs 30:2035-2045(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=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)


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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=23325432; DOI=10.1101/gr.147942.112; PMCID=PMC3589544

Varley K.E., Gertz J., Bowling K.M., Parker S.L., Reddy T.E., Pauli-Behn F., Cross M.K., Williams B.A., Stamatoyannopoulos J.A., Crawford G.E., Absher D.M., Wold B.J., Myers R.M.

Dynamic DNA methylation across diverse human cell lines and tissues.

Genome Res. 23:555-567(2013)


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=23671654; DOI=10.1371/journal.pone.0063056; PMCID=PMC3646030

Lu Y.-H., Soong T.D., Elemento O.

A novel approach for characterizing microsatellite instability in cancer cells.

PLoS ONE 8:E63056-E63056(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=24456987; DOI=10.1186/1755-8166-7-8; PMCID=PMC3914704

Rondon-Lagos M., Verdun Di Cantogno L., Marchio C., Rangel N., Payan-Gomez C., Gugliotta P., Botta C., Bussolati G., Ramirez-Clavijo S.R., Pasini B., Sapino A.

Differences and homologies of chromosomal alterations within and between breast cancer cell lines: a clustering analysis.

Mol. Cytogenet. 7:8.1-8.14(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=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=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=27378269; DOI=10.1186/s12885-016-2452-5; PMCID=PMC4932681

Kangaspeska S., Hultsch S., Jaiswal A., Edgren H., Mpindi J.P., Eldfors S., Bruck O., Aittokallio T., Kallioniemi O.-P.

Systematic drug screening reveals specific vulnerabilities and co-resistance patterns in endocrine-resistant breast cancer.

BMC Cancer 16:378.1-378.17(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=29718670; DOI=10.1021/acs.jproteome.8b00165; PMCID=PMC6670293

Clark D.J., Hu Y.-W., Bocik W., Chen L.-J., Schnaubelt M., Roberts R.R., Shah P., Whiteley G.R., Zhang H.

Evaluation of NCI-7 cell line panel as a reference material for clinical proteomics.

J. Proteome Res. 17:2205-2215(2018)


PubMed=30787054; DOI=10.1158/1055-9965.EPI-18-1132; PMCID=PMC6548687

Hooker S.E. Jr., Woods-Burnham L., Bathina M., Lloyd S., Gorjala P., Mitra R., Nonn L., Kimbro K.S., Kittles R.A.

Genetic ancestry analysis reveals misclassification of commonly used cancer cell lines.

Cancer Epidemiol. Biomarkers Prev. 28:1003-1009(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)


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)


PubMed=31978347; DOI=10.1016/j.cell.2019.12.023; PMCID=PMC7339254

Nusinow D.P., Szpyt J., Ghandi M., Rose C.M., McDonald E.R. 3rd, Kalocsay M., Jane-Valbuena J., Gelfand E.T., Schweppe D.K., Jedrychowski M.P., Golji J., Porter D.A., Rejtar T., Wang Y.K., Kryukov G.V., Stegmeier F., Erickson B.K., Garraway L.A., Sellers W.R., Gygi S.P.

Quantitative proteomics of the Cancer Cell Line Encyclopedia.

Cell 180:387-402.e16(2020)"



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2025-02-23
¥1500
武漢尚恩生物技術(shù)有限公司
2023-12-18
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