"J82人膀胱移行癌細(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
CAMA Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3—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)胞貼壁斑塊;緊湊,很少匯合;相關(guān)產(chǎn)品有:CAL 51細(xì)胞、TSU-Pr1細(xì)胞、H929細(xì)胞
SNU886 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:Huh 7.5細(xì)胞、SNU-719細(xì)胞、Hu-P-T3細(xì)胞
MOVAS Cells;背景說(shuō)明:主動(dòng)脈平滑肌;SV40轉(zhuǎn)化;C57BL/6;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:SUM159PT細(xì)胞、KHYG細(xì)胞、M-O7e細(xì)胞
背景信息:電子顯微鏡下未觀察到橋粒但觀察到數(shù)目不同的粗面內(nèi)質(zhì)網(wǎng)和突出微絲。 含ras (H-ras)癌基因。
J82人膀胱移行癌細(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)
ATCC細(xì)胞庫(kù)(American Type Culture Colection),該中心一直致力于細(xì)胞分類、鑒定和保藏工作。ATCC是全球最大的生物資源保藏中心,ATCC通過(guò)行業(yè)標(biāo)準(zhǔn)產(chǎn)品、服務(wù)和創(chuàng)新解決方案支持全球?qū)W術(shù)、政府、生物技術(shù)、制藥、食品、農(nóng)業(yè)和工業(yè)領(lǐng)域的科學(xué)進(jìn)步。ATCC提供的服務(wù)和定制解決方案包括細(xì)胞和微生物培養(yǎng)、鑒定、生物衍生物的開(kāi)發(fā)和生產(chǎn)、性能測(cè)試和生物資源保藏服務(wù)。美國(guó)國(guó)家標(biāo)準(zhǔn)協(xié)會(huì)(ANSI)認(rèn)可了ATCC標(biāo)準(zhǔn)開(kāi)發(fā)組織,并制定了標(biāo)準(zhǔn)協(xié)議,以確保生物材料的可靠性和可重復(fù)性。ATCC的使命是為了獲取、鑒定、保存、開(kāi)發(fā)、標(biāo)準(zhǔn)化和分發(fā)生物資源和生物信息,以提高和應(yīng)用生物科學(xué)知識(shí)。
T 84 Cells;背景說(shuō)明:T84細(xì)胞株是從一位72歲男性結(jié)腸癌患者的肺轉(zhuǎn)移灶建立的可移植人類癌細(xì)胞株。 腫瘤組織皮下接種于BALB/c裸鼠,并連續(xù)進(jìn)行移植。 [26072] 在裸鼠身上的移植過(guò)程中,細(xì)胞株始終保持結(jié)腸癌的原始組織性狀。 [26072] 在無(wú)胸腺小鼠中傳代23代后建立了T84細(xì)胞株。 這些細(xì)胞單層生長(zhǎng)到飽和并在接觸細(xì)胞間展現(xiàn)出緊密連接和橋粒。 [1155] 有很多關(guān)于多肽類激素和神經(jīng)遞質(zhì)并維持定向電解質(zhì)傳輸?shù)氖荏w。 [1155] 這株細(xì)胞展現(xiàn)了接觸細(xì)胞中的緊密連接和橋粒。 [1155] 角蛋白免疫過(guò)氧化物酶染色陽(yáng)性。;傳代方法:1:2-1:4傳代;每周2次。;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞,多角;相關(guān)產(chǎn)品有:SACC83細(xì)胞、Strain L-929細(xì)胞、BCP1細(xì)胞
X63-AG 8.653 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:LAN-5細(xì)胞、OVCAR433細(xì)胞、H-157細(xì)胞
Vero E6 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:HL-60細(xì)胞、OCIAML3細(xì)胞、HOS TE 85細(xì)胞
3082T1 Cells(提供STR鑒定圖譜)
來(lái)源說(shuō)明:細(xì)胞主要來(lái)源ATCC、ECACC、DSMZ、RIKEN等細(xì)胞庫(kù)
物種來(lái)源:人源、鼠源等其它物種來(lái)源
J82人膀胱移行癌細(xì)胞全年復(fù)蘇|已有STR圖譜
形態(tài)特性:上皮細(xì)胞樣
細(xì)胞傳代培養(yǎng)實(shí)驗(yàn):體外培養(yǎng)的原代細(xì)胞或細(xì)胞株要在體外持續(xù)地培養(yǎng)就必須傳代,以便獲得穩(wěn)定的細(xì)胞株或得到大量的同種細(xì)胞,并維持細(xì)胞種的延續(xù)。培養(yǎng)的細(xì)胞形成單層匯合以后,由于密度過(guò)大生存空間不足而引起營(yíng)養(yǎng)枯竭,將培養(yǎng)的細(xì)胞分散,從容器中取出,以1:2或1:3以上的比率轉(zhuǎn)移到另外的容器中進(jìn)行培養(yǎng),即為傳代培養(yǎng);細(xì)胞“一代”指從細(xì)胞接種到分離再培養(yǎng)的一段期間,與細(xì)胞世代或倍增不同。在一代中,細(xì)胞培增3~6次。細(xì)胞傳代后,一般經(jīng)過(guò)三個(gè)階段:游離期、指數(shù)增生期和停止期。常用細(xì)胞分裂指數(shù)表示細(xì)胞增殖的旺盛程度,即細(xì)胞群的分裂相數(shù)/100個(gè)細(xì)胞。一般細(xì)胞分裂指數(shù)介于0.2%~0.5%,腫瘤細(xì)胞可達(dá)3~5%;細(xì)胞接種2~3天分裂增殖旺盛,是活力ZuiHAO時(shí)期,稱指數(shù)增生期(對(duì)數(shù)生長(zhǎng)期),適宜進(jìn)行各種試驗(yàn)。實(shí)驗(yàn)步驟:1.將長(zhǎng)成的培養(yǎng)細(xì)胞從二氧化碳培養(yǎng)箱中取出,在超凈工作臺(tái)中倒掉瓶?jī)?nèi)的培養(yǎng),加入少許消化。(以面蓋住細(xì)胞為宜),靜置5~10分鐘。2.在倒置鏡下觀察被消化的細(xì)胞,如果細(xì)胞變圓,相互之間不再連接成片,這時(shí)應(yīng)立即在超凈臺(tái)中將消化倒掉,加入3~5ml新鮮培養(yǎng),吹打,制成細(xì)胞懸。3.將細(xì)胞懸吸出2ml左右,加到另一個(gè)培養(yǎng)瓶中并向每個(gè)瓶中分別加3ml左右培養(yǎng),蓋HAO瓶塞,送回二氧化碳培養(yǎng)箱中,繼續(xù)進(jìn)行培養(yǎng)。一般情況,傳代后的細(xì)胞在2小時(shí)左右就能附著在培養(yǎng)瓶壁上,2~4天就可在瓶?jī)?nèi)形成單層,需要再次進(jìn)行傳代。
Hs-600-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,2-3天換液1次。;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:H-1781細(xì)胞、TMK1細(xì)胞、FM88細(xì)胞
H 9 Cells;背景說(shuō)明:H9細(xì)胞是HUT78(ATCCTIB161)的克隆系(Callo,RC,etal)。細(xì)胞表面帶有CD3、CD4標(biāo)記。研究表明,該細(xì)胞系對(duì)人體免疫缺陷病毒(HIV-1)敏感,可用于檢測(cè)、分離和增殖HIV-1,也可用于其它人類Tcell病毒的研究。;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:Tadarida brasiliensis 1 lung細(xì)胞、BE(2)C細(xì)胞、P3/NS1/1-Ag4.1細(xì)胞
L-Wnt3A 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:Hk-2細(xì)胞、Hs1.Tes細(xì)胞、MUGCHOR1細(xì)胞
DF-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:成纖維母細(xì)胞樣;相關(guān)產(chǎn)品有:H1184細(xì)胞、UPCI:SCC090細(xì)胞、NCIH727細(xì)胞
MOLP-8 Cells;背景說(shuō)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(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:Hs 742.T細(xì)胞、HSC-4細(xì)胞、SNU475細(xì)胞
KALS1 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:多邊形;相關(guān)產(chǎn)品有:NCIH209細(xì)胞、2BS細(xì)胞、Cloudman S91 melanoma細(xì)胞
Mel-RM Cells;背景說(shuō)明:黑色素瘤;神經(jīng)節(jié)轉(zhuǎn)移;男性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:MDAMB436細(xì)胞、DR2R1610細(xì)胞、SCC 4細(xì)胞
AN3 CA Cells;背景說(shuō)明:AN3CA細(xì)胞建系于1964年。它衍生于子宮內(nèi)膜癌患者淋巴結(jié)轉(zhuǎn)移組織,具有癌細(xì)胞的基本特性,能在體外長(zhǎng)期傳代培養(yǎng),接種實(shí)驗(yàn)動(dòng)物產(chǎn)生明顯腫瘤。但細(xì)胞的生物學(xué)特性及超微結(jié)構(gòu)尚未深入研究,僅發(fā)現(xiàn)該細(xì)胞系促黑激素合成為陰性。細(xì)胞常用于人子宮內(nèi)膜癌細(xì)胞生物學(xué)及其相關(guān)特性研究。;傳代方法:1:2傳代;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:上皮樣;相關(guān)產(chǎn)品有:BV-2細(xì)胞、Ishikawa細(xì)胞、COLO 679細(xì)胞
NCI/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:FM-88細(xì)胞、DC 2.4細(xì)胞、L-cell細(xì)胞
LS 1034 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:1:3傳代,每周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:MNNG-HOS (TE 85, clone F-5)細(xì)胞、LY細(xì)胞、OVCA 433細(xì)胞
PT67 Cells;背景說(shuō)明:逆轉(zhuǎn)錄病毒包裝細(xì)胞;雄性;NIH Swiss;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:CWR22Rv1細(xì)胞、OCILY3細(xì)胞、CCD841CoN細(xì)胞
NCI-H2170 Cells;背景說(shuō)明:該細(xì)胞1989年建系,源自一位患有肺鱗狀細(xì)胞癌的男性,該患者不吸煙;傳代方法:1:3—1:6傳代,3—5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:Intestinal Porcine Epithelial Cell line-J2細(xì)胞、BHT101細(xì)胞、COLO-824細(xì)胞
COLO201 Cells;背景說(shuō)明:該細(xì)胞源自一位70歲白人男性,CSAp (CSAp-)和CEA陰性。;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:懸浮+貼壁;形態(tài)特性:淋巴細(xì)胞;相關(guān)產(chǎn)品有:Duke University 4475細(xì)胞、BC-PAP細(xì)胞、Karpas422細(xì)胞
CAL148 Cells;背景說(shuō)明:乳腺癌;胸腔積液轉(zhuǎn)移;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:Hs895T細(xì)胞、QG-56細(xì)胞、SKOV-433細(xì)胞
EVSAT Cells;背景說(shuō)明:乳腺癌;腹水轉(zhuǎn)移;女性;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(zhǎng)特性:貼壁;形態(tài)特性:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:MB49細(xì)胞、HCC0044細(xì)胞、PVEC細(xì)胞
NSI/1-Ag4-1 Cells;背景說(shuō)明:這是P3X63Ag8(ATCCTIB-9)的一個(gè)不分泌克隆。Kappa鏈合成了但不分泌。能抗0.1mM8-氮雜鳥(niǎo)嘌呤但不能在HAT培養(yǎng)基中生長(zhǎng)。據(jù)報(bào)道它是由于缺失了3-酮類固醇還原酶活性的膽固醇營(yíng)養(yǎng)缺陷型。檢測(cè)表明肢骨發(fā)育畸形病毒(鼠痘)陰性。;傳代方法:1:2傳代,3天內(nèi)可長(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:NCI-H2066細(xì)胞、Nthy-ori 3.1細(xì)胞、alpha TC1 clone 6細(xì)胞
TK-1 Cells;背景說(shuō)明:淋巴瘤;AKR/Cum;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:TM3細(xì)胞、PC-3M細(xì)胞、GLC-15細(xì)胞
159-2 Cells(提供STR鑒定圖譜)
Abcam HeLa HGF KO Cells(提供STR鑒定圖譜)
AG22105 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line RRF328 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line XG533 Cells(提供STR鑒定圖譜)
C0736 Cells(提供STR鑒定圖譜)
CW60182 Cells(提供STR鑒定圖譜)
DA06462 Cells(提供STR鑒定圖譜)
GM01013 Cells(提供STR鑒定圖譜)
MJ Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:每周換液兩次;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:RN細(xì)胞、NCI-SNU-119細(xì)胞、Jurkat-FHCRC細(xì)胞
KMBC Cells;背景說(shuō)明:膽管癌;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:MKN-28細(xì)胞、TE 85 ClF-5細(xì)胞、Neukoplast細(xì)胞
H2009 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:貼壁生長(zhǎng);形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:MCF7細(xì)胞、OC-316細(xì)胞、HEK293-H細(xì)胞
Granta 519 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:HET-1A細(xì)胞、J 774A.1細(xì)胞、Central Adrenergic TH-expressing a細(xì)胞
BNL.1ME A.7R.1 Cells;背景說(shuō)明:肝;上皮細(xì)胞;BALB/c;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:NCI-H740細(xì)胞、NCI-SNU-C1細(xì)胞、3T3-Swiss albino細(xì)胞
Y79 Cells;背景說(shuō)明:1971年1月,該細(xì)胞由ReidTW及其同事從病人右眼切除的腫瘤進(jìn)行原代培養(yǎng)建立而成,此病人有很強(qiáng)的視網(wǎng)膜母細(xì)胞瘤的母系家族遺傳性。該細(xì)胞的超微結(jié)構(gòu),如核膜內(nèi)折、三層膜結(jié)構(gòu)、大的被膜小泡、環(huán)孔板、微管、中心粒、基粒等都與原始腫瘤相似。;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,成簇生長(zhǎng);相關(guān)產(chǎn)品有:CHL-1細(xì)胞、MAVER細(xì)胞、NCI-H211細(xì)胞
McA-RH 8994 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:A-375細(xì)胞、Baby Hamster Kidney-21細(xì)胞、SCL II細(xì)胞
AG06814-M Cells;背景說(shuō)明:LeonardHayflick建系;有限傳代細(xì)胞系;壽命為50±10代(倍增時(shí)間24h);來(lái)自妊娠3個(gè)月的正常胚胎肺組織。該細(xì)胞系是第一個(gè)用于人制備的人二倍體細(xì)胞;培養(yǎng)基中添加TNFα可以加快細(xì)胞生長(zhǎng)。;傳代方法:1:2-1:4傳代;2-3天換液1次;生長(zhǎng)特性:貼壁生長(zhǎng);形態(tài)特性:成纖維細(xì)胞樣;相關(guān)產(chǎn)品有:J774 A.1細(xì)胞、SNU-761細(xì)胞、Walker/LLC-WRC256細(xì)胞
J82人膀胱移行癌細(xì)胞全年復(fù)蘇|已有STR圖譜
IGROV 1 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:HDF-a細(xì)胞、NCI-Hut 125細(xì)胞、OLN-93細(xì)胞
GDM-1 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:MCF7-GFP細(xì)胞、B16 melanoma F10細(xì)胞、UWB1289細(xì)胞
16-HBE 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:MN60細(xì)胞、Transformed Human Liver Epithelial-2細(xì)胞、IPLB-Sf21-AE細(xì)胞
IB-RS-2 Cells;背景說(shuō)明: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:CNE細(xì)胞、RIMEC細(xì)胞、MDA-MB-435-S細(xì)胞
NCI-SNU-1 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:懸浮聚集;形態(tài)特性:上皮細(xì)胞;相關(guān)產(chǎn)品有:HCC-78細(xì)胞、MGSMC細(xì)胞、MH7A細(xì)胞
MSTO211H Cells;背景說(shuō)明:MSTO-211H細(xì)胞株是1985年從一位肺二相間皮瘤患者的胸水中建株的。這個(gè)病人接受過(guò)多種藥物聯(lián)合前期化療。MSTO-211H細(xì)胞具有高親和力的EGF結(jié)合位點(diǎn),并表達(dá)神經(jīng)元特異性烯醇酶(NSE)及人絨毛膜促性腺激素(HCG)的α與β亞基。未檢測(cè)到左旋多巴胺脫羧酶(DDC),邦巴辛與神經(jīng)tensin。細(xì)胞過(guò)表達(dá)c-myc原癌基因,并沒(méi)有觀察到基因重排或擴(kuò)增。V-src,v-abl,v-erbB,c-raf1,Ha-ras,Ki-ras,和N-ras的表達(dá)呈陽(yáng)性。未檢測(cè)到N-m;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)胞樣;相關(guān)產(chǎn)品有:NFS-60細(xì)胞、SUM-159PT細(xì)胞、CATH-a細(xì)胞
NE-1 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:159 PT細(xì)胞、MGC803細(xì)胞、HSC-6細(xì)胞
GM23862 Cells(提供STR鑒定圖譜)
HAP1 MYT1 (-) 2 Cells(提供STR鑒定圖譜)
SVEC 4-10 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:H-711細(xì)胞、RMG-1細(xì)胞、GLC-82細(xì)胞
Fetal Bovine Heart Endothelial 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:HT22細(xì)胞、U 266細(xì)胞、PLCPRF5細(xì)胞
OCI-Ly 8 Cells;背景說(shuō)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(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:K562/ADP細(xì)胞、MOLT3細(xì)胞、MDA-MB-436細(xì)胞
WSU-DLCL2 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:RL-95-2細(xì)胞、MIO-M1細(xì)胞、CEM/C1細(xì)胞
NK 10a Cells;背景說(shuō)明:1967年,該細(xì)胞系KleinE和KleinG建系,源于一名16歲患有Burkitt's淋巴瘤的黑人男性,beta-2-微球蛋白陰性,表達(dá)EBNA,VCA,sIg。該細(xì)胞攜帶EB病毒,是一個(gè)典型的B淋巴母細(xì)胞系,可用于白血病發(fā)病機(jī)制的研究。;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:NCIH1734細(xì)胞、alpha TC1.6細(xì)胞、MPP-89細(xì)胞
Ramos G6.C10 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法: 維持細(xì)胞濃度在2×105/ml-1×106/ml;根據(jù)細(xì)胞濃度每2-3天補(bǔ)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:SW-579細(xì)胞、T-ALL-1細(xì)胞、MDA-MB-175VII細(xì)胞
LS 174T Cells;背景說(shuō)明:LS 174T是LS 180 (ATCC CL 187)結(jié)腸腺癌細(xì)胞株的胰蛋白酶化變種。 它比親本更易傳代,象LS 180一樣生成大量的癌胚抗原(CEA)。 電鏡研究表明有豐富的微絲和細(xì)胞質(zhì)粘液素液泡。 直腸抗原3陽(yáng)性。 p53抗原表達(dá)陰性,但mRNA表達(dá)陽(yáng)性。 與ATCC CL-187來(lái)源于同一個(gè)腫瘤。LS 174T細(xì)胞角蛋白染色陽(yáng)性。 癌基因c-myc, N-myc, H-ras, N-ras, Myb, 和 fos的表達(dá)呈陽(yáng)性。 癌基因k-ras和sis的表達(dá)未做檢測(cè)。;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:HS 445T細(xì)胞、P3-NS1/1-Ag4-1細(xì)胞、L 540細(xì)胞
CT-26 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:Immortal Pig Intestinal-2I細(xì)胞、Hs-606-T細(xì)胞、A2780/Taxol細(xì)胞
HQ01628 Cells(提供STR鑒定圖譜)
KERA-LC14 Cells(提供STR鑒定圖譜)
MIN07i-33113.2D Cells(提供STR鑒定圖譜)
NOBAH-1 Cells(提供STR鑒定圖譜)
RC654 Cells(提供STR鑒定圖譜)
TXM-34 Cells(提供STR鑒定圖譜)
UM-SCC-8 Cells(提供STR鑒定圖譜)
HAP1 WWOX (-) 2 Cells(提供STR鑒定圖譜)
CHO-K1 Cells;背景說(shuō)明:1957年,PuckTT從成年中國(guó)倉(cāng)鼠卵巢的活檢組織建立了CHO細(xì)胞,CHO-K1是CHO的一個(gè)亞克隆。CHO-K1的生長(zhǎng)需要脯酸。;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:V 79細(xì)胞、MCF 7細(xì)胞、NCI-HUT-69細(xì)胞
HEL299 Cells;背景說(shuō)明:紅白細(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:SKOV3細(xì)胞、SK.OV.3細(xì)胞、TGBC11T細(xì)胞
WERIRb1 Cells;背景說(shuō)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:Clone 15 HL-60細(xì)胞、HCC0070細(xì)胞、Ly18細(xì)胞
HCC78 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:SK-N-SH細(xì)胞、SK-MEL2細(xì)胞、SW-837細(xì)胞
DC 2.4 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:526細(xì)胞、HFLS-OA細(xì)胞、NBL-S細(xì)胞
DC 2.4 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:526細(xì)胞、HFLS-OA細(xì)胞、NBL-S細(xì)胞
A9 (Hamprecht) Cells;背景說(shuō)明:皮下結(jié)締組織;自發(fā)永生;雄性;C3H/An;傳代方法:1:2-1:3傳代;每周換液2-3次。;生長(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:HLF細(xì)胞、CFSC-2G細(xì)胞、HEK293S細(xì)胞
B16F0 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:HEK-293-FT細(xì)胞、NCI H2106細(xì)胞、MLA144細(xì)胞
alpha TC1.6 Cells;背景說(shuō)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(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:HO1N1細(xì)胞、MIN-6細(xì)胞、BC-024細(xì)胞
CL11 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:HuH6細(xì)胞、P3-X63.Ag8.653細(xì)胞、HL7702細(xì)胞
DF-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:成纖維母細(xì)胞樣;相關(guān)產(chǎn)品有:H1184細(xì)胞、UPCI:SCC090細(xì)胞、NCIH727細(xì)胞
DF1 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:成纖維母細(xì)胞樣;相關(guān)產(chǎn)品有:MD Anderson-Metastatic Breast-468細(xì)胞、H838細(xì)胞、MC3T3-E1 Subclone 14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、COLO 699細(xì)胞、E6-1細(xì)胞
A549ATCC 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:H-1435細(xì)胞、SJCRH30細(xì)胞、RGB細(xì)胞
H-23 Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;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:上皮樣;相關(guān)產(chǎn)品有:L 363細(xì)胞、SK-N-BE(2C)細(xì)胞、NCI-H187細(xì)胞
STAN368i-894C2 Cells(提供STR鑒定圖譜)
ATDC-5 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:詳見(jiàn)產(chǎn)品說(shuō)明書(shū);相關(guān)產(chǎn)品有:KMST-6細(xì)胞、OVCAR-3細(xì)胞、MBMEC細(xì)胞
JG Cells;背景說(shuō)明:腎小球旁 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:SCC9細(xì)胞、High5細(xì)胞、MFE-296細(xì)胞
MMAc.SF 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:PIEC細(xì)胞、NCIH2452細(xì)胞、CDC/EU.HMEC-1細(xì)胞
HFLS-OA Cells;背景說(shuō)明:滑膜;關(guān)節(jié)炎成纖維 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:HFF-1細(xì)胞、L5178-R細(xì)胞、COV 434細(xì)胞
SN12C Cells;背景說(shuō)明:詳見(jiàn)相關(guān)文獻(xiàn)介紹;傳代方法:2x10^4 cells/ml;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:H727細(xì)胞、D283-MED細(xì)胞、TJ905細(xì)胞
CFSC-8B 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-6 myoblast細(xì)胞、HCAEC細(xì)胞、M20 [Human melanoma]細(xì)胞
H2107 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:上皮細(xì)胞;相關(guān)產(chǎn)品有:38C-13細(xì)胞、HIT T-15細(xì)胞、KB細(xì)胞
aNK Cells;背景說(shuō)明:NK細(xì)胞;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:OVCA8細(xì)胞、BNL 1ME A.7R.1細(xì)胞、NALM-6-M1細(xì)胞
J82人膀胱移行癌細(xì)胞全年復(fù)蘇|已有STR圖譜
X63Ag8-653 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:HCMEC(BL12-H)細(xì)胞、HCCLM3細(xì)胞、GNM細(xì)胞
OLN 93 Cells;背景說(shuō)明:膠質(zhì)細(xì)胞;自發(fā)永生;Wistar;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:Co320細(xì)胞、H-1693細(xì)胞、Transformed Human Liver Epithelial-3細(xì)胞
NCI-H1650 Cells;背景說(shuō)明:該細(xì)胞是從一名27歲白人男性(10年煙齡)支氣管肺泡癌患者的胸腔積液中分離得到的。;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)胞樣;相關(guān)產(chǎn)品有:P30/0HK細(xì)胞、L5178YR細(xì)胞、Hepa-RG細(xì)胞
B104 [Rat neuroblastoma] Cells;背景說(shuō)明:神經(jīng)母細(xì)胞瘤;BDIX;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:C57/B6-L細(xì)胞、H1770細(xì)胞、HECCL-1細(xì)胞
3T3-L1 ad Cells;背景說(shuō)明:3T3-L1是從3T3細(xì)胞(Swissalbino)中經(jīng)克隆分離得到的連續(xù)傳代的亞系。該細(xì)胞從快速分裂到匯合和接觸性抑制狀態(tài)經(jīng)歷了前脂肪細(xì)胞到脂肪樣細(xì)胞的轉(zhuǎn)變。該細(xì)胞鼠痘病毒陰性;可產(chǎn)生甘油三酯,高濃度血清可增強(qiáng)細(xì)胞內(nèi)脂肪堆積。;傳代方法:1:2傳代;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:IEC18細(xì)胞、DoHH2細(xì)胞、H2196細(xì)胞
MyLa 2059 Cells;背景說(shuō)明:皮膚;T淋巴細(xì)胞瘤;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:BC3H1細(xì)胞、L 428細(xì)胞、A-10細(xì)胞
BayGenomics ES cell line RRH063 Cells(提供STR鑒定圖譜)
BayGenomics ES cell line XH180 Cells(提供STR鑒定圖譜)
ES[MC1R(20):tetEomes(35)] Cells(提供STR鑒定圖譜)
N115-BU-7 Cells(提供STR鑒定圖譜)
Ubigene MC-38 Siglec15 KO Cells(提供STR鑒定圖譜)
MB-IS Cells(提供STR鑒定圖譜)
" "PubMed=77569; DOI=10.1111/j.1399-0039.1978.tb01259.x
Espmark J.A., Ahlqvist-Roth L., Sarne L., Persson A.
Tissue typing of cells in culture. III. HLA antigens of established human cell lines. Attempts at typing by the mixed hemadsorption technique.
Tissue Antigens 11:279-286(1978)
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=687519; DOI=10.1038/bjc.1978.164; PMCID=PMC2009694
O'Toole C.M., Price Z.H., Ohnuki Y., Unsgaard B.
Ultrastructure, karyology and immunology of a cell line originated from a human transitional-cell carcinoma.
Br. J. Cancer 38:64-76(1978)
PubMed=6244232
Williams R.D.
Human urologic cancer cell lines.
Invest. Urol. 17:359-363(1980)
PubMed=6220172
Dracopoli N.C., Fogh J.
Polymorphic enzyme analysis of cultured human tumor cell lines.
J. Natl. Cancer Inst. 70:469-476(1983)
PubMed=6823318; DOI=10.1038/301429a0
O'Toole C.M., Povey S., Hepburn P.J., Franks L.M.
Identity of some human bladder cancer cell lines.
Nature 301:429-430(1983)
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=4057431; DOI=10.1016/S0022-5347(17)47713-5
Bishai M.B., Kagawa S., Narayan K.S., Jones L.W., Kirk D.
Growth of a malignant human urothelial cell line (J82) in a serum-free medium (HMRI-1) developed previously for normal human urothelium.
J. Urol. 134:1287-1290(1985)
PubMed=3518877; DOI=10.3109/07357908609038260
Fogh J.
Human tumor lines for cancer research.
Cancer Invest. 4:157-184(1986)
PubMed=3708594
Masters J.R.W., Hepburn P.J., Walker L., Highman W.J., Trejdosiewicz L.K., Povey S., Parkar M., Hill B.T., Riddle P.N., Franks L.M.
Tissue culture model of transitional cell carcinoma: characterization of twenty-two human urothelial cell lines.
Cancer Res. 46:3630-3636(1986)
PubMed=3413074; DOI=10.1073/pnas.85.16.6042; PMCID=PMC281901
Pereira-Smith O.M., Smith J.R.
Genetic analysis of indefinite division in human cells: identification of four complementation groups.
Proc. Natl. Acad. Sci. U.S.A. 85:6042-6046(1988)
PubMed=2594029; DOI=10.1056/NEJM198912213212501
Yandell D.W., Campbell T.A., Dayton S.H., Petersen R., Walton D., Little J.B., McConkie-Rosell A., Buckley E.G., Dryja T.P.
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.
N. Engl. J. Med. 321:1689-1695(1989)
PubMed=7787250
Cooper M.J., Haluschak J.J., Johnson D., Schwartz S., Morrison L.J., Lippa M., Hatzivassiliou G., Tan J.
p53 mutations in bladder carcinoma cell lines.
Oncol. Res. 6:569-579(1994)
PubMed=8077054; DOI=10.1002/ijc.2910580512
Xu B.H., Gupta V., Singh S.V.
Characterization of a human bladder cancer cell line selected for resistance to mitomycin C.
Int. J. Cancer 58:686-692(1994)
PubMed=9137463
Debal V., Breillout F., Manfait M.
Concomitant decrease of resistance and modifications of the cytoskeleton after all-trans retinoic acid and phorbol ester treatments in a navelbine-resistant bladder carcinoma cell line.
Anticancer Res. 17:1147-1154(1997)
PubMed=9850064
Markl I.D.C., Jones P.A.
Presence and location of TP53 mutation determines pattern of CDKN2A/ARF pathway inactivation in bladder cancer.
Cancer Res. 58:5348-5353(1998)
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=11921286; DOI=10.1002/gcc.10050
Williams S.V., Sibley K.D., Davies A.M., Nishiyama H., Hornigold N., Coulter J., Kennedy W.J., Skilleter A., Habuchi T., Knowles M.A.
Molecular genetic analysis of chromosome 9 candidate tumor-suppressor loci in bladder cancer cell lines.
Genes Chromosomes Cancer 34:86-96(2002)
PubMed=12127398; DOI=10.1016/S0165-4608(01)00648-3
Strefford J.C., Lillington D.M., Steggall M., Lane T.M., Nouri A.M.E., Young B.D., Oliver R.T.D.
Novel chromosome findings in bladder cancer cell lines detected with multiplex fluorescence in situ hybridization.
Cancer Genet. Cytogenet. 135:139-146(2002)
PubMed=14762065; DOI=10.1101/gr.2012304; PMCID=PMC327104
Bignell G.R., Huang J., Greshock J., Watt S., Butler A.P., West S., Grigorova M., Jones K.W., Wei W., Stratton M.R., Futreal P.A., Weber B., Shapero M.H., Wooster R.
High-resolution analysis of DNA copy number using oligonucleotide microarrays.
Genome Res. 14:287-295(2004)
PubMed=15846775; DOI=10.1002/gcc.20166
Williams S.V., Adams J., Coulter J., Summersgill B.M., Shipley J.M., Knowles M.A.
Assessment by M-FISH of karyotypic complexity and cytogenetic evolution in bladder cancer in vitro.
Genes Chromosomes Cancer 43:315-328(2005)
PubMed=16885334; DOI=10.1158/0008-5472.CAN-06-1182
Lopez-Knowles E., Hernandez S., Malats N., Kogevinas M., Lloreta J., Carrato A., Tardon A., Serra C., Real F.X.
PIK3CA mutations are an early genetic alteration associated with FGFR3 mutations in superficial papillary bladder tumors.
Cancer Res. 66:7401-7404(2006)
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=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=23401075; DOI=10.1002/path.4176
Guo Y.-N., Chekaluk Y., Zhang J.-M., Du J.-Y., Gray N.S., Wu C.-L., Kwiatkowski D.J.
TSC1 involvement in bladder cancer: diverse effects and therapeutic implications.
J. Pathol. 230:17-27(2013)
PubMed=24367658; DOI=10.1371/journal.pone.0084411; PMCID=PMC3867501
Ross R.L., Burns J.E., Taylor C.F., Mellor P., Anderson D.H., Knowles M.A.
Identification of mutations in distinct regions of p85 alpha in urothelial cancer.
PLoS ONE 8:E84411-E84411(2013)
PubMed=24035680; DOI=10.1016/j.eururo.2013.08.057
Hurst C.D., Platt F.M., Knowles M.A.
Comprehensive mutation analysis of the TERT promoter in bladder cancer and detection of mutations in voided urine.
Eur. Urol. 65:367-369(2014)
PubMed=25997541; DOI=10.1186/s12864-015-1450-3; PMCID=PMC4470036
Earl J., Rico D., Carrillo-de-Santa-Pau E., Rodriguez-Santiago B., Mendez-Pertuz M., Auer H., Gomez G., Grossman H.B., Pisano D.G., Schulz W.A., Perez-Jurado L.A., Carrato A., Theodorescu D., Chanock S.J., Valencia A., Real F.X.
The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies.
BMC Genomics 16:403.1-403.16(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=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=27270441; DOI=10.1038/onc.2016.172; PMCID=PMC5140783
Nickerson M.L., Witte N., McGee Im K., Turan S., Owens C.R., Misner K., Tsang S.X., Cai Z.-M., Wu S., Dean M., Costello J.C., Theodorescu D.
Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response.
Oncogene 36:35-46(2017)
PubMed=29732388; DOI=10.3233/BLC-180167; PMCID=PMC5929350
Zuiverloon T.C.M., de Jong F.C., Costello J.C., Theodorescu D.
Systematic review: characteristics and preclinical uses of bladder cancer cell lines.
Bladder Cancer 4:169-183(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)"
關(guān)鍵字: J82人膀胱移行癌細(xì)胞全年復(fù)蘇|已有ST;傳代細(xì)胞;復(fù)蘇細(xì)胞;實(shí)驗(yàn)細(xì)胞;科研細(xì)胞;
上海冠導(dǎo)生物工程有限公司,先后從ATCC、DSMZ、ECACC、RIKEN、PromoCell、ScienCell、JCRB等國(guó)內(nèi)外細(xì)胞庫(kù)引進(jìn)細(xì)胞2000余株。以此為契機(jī),公司組建了冠導(dǎo)細(xì)胞庫(kù),我司細(xì)胞均由資深細(xì)胞培養(yǎng)工程師進(jìn)行培養(yǎng)。我司可以提供的細(xì)胞有:①細(xì)胞系②原代細(xì)胞③穩(wěn)轉(zhuǎn)株④耐藥株⑤標(biāo)記細(xì)胞⑥細(xì)胞配套試劑等。