熱門關(guān)鍵詞: CO2搖床 凝膠成像系統(tǒng) 細(xì)胞培養(yǎng)耗材 乳酸分析儀 發(fā)酵罐 Rainin移液槍 振蕩培養(yǎng)箱 生物反應(yīng)器
細(xì)胞名稱: 人結(jié)腸癌細(xì)胞(STR鑒定正確)
細(xì)胞別稱:HT 29; HT29; ht-29細(xì)胞
細(xì)胞貨號:TCH-C213
規(guī)格:1×10?cells | T25 培養(yǎng)瓶
配套培養(yǎng)基貨號:TCH-G213
0512-62956104
ht-29細(xì)胞
細(xì)胞名稱: 人結(jié)腸癌細(xì)胞(STR鑒定正確)
細(xì)胞別稱:HT 29; HT29; ht-29細(xì)胞
貨號:TCH-C213
規(guī)格:1×10?cells | T25 培養(yǎng)瓶
價格:1500元 (干冰運輸需另加200元干冰費)
種屬來源:人
組織來源:結(jié)直腸
特 征:結(jié)直腸癌
細(xì)胞形態(tài):上皮細(xì)胞樣
生長特性:貼壁生長
培養(yǎng)體系:McCoy's 5A+10%FBS+1%P/S
配套培養(yǎng)基貨號:TCH-G213
傳代比例:1:3-1:6,每2-3天換液一次
傳代周期:48-72 h
培養(yǎng)條件:氣相:95%空氣+5%CO2,溫度:37℃
凍存條件:60%基礎(chǔ)培養(yǎng)基+30%FBS+10%DMSO,液氮儲存
質(zhì)量檢測:細(xì)菌、真菌、支原體檢測均為陰性
ht-29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)發(fā)生G。
蘇州阿爾法生物除了提供細(xì)胞系購買,細(xì)胞株購買,pc12細(xì)胞株,肺癌細(xì)胞株,ht-29細(xì)胞,血管內(nèi)皮細(xì)胞株,肝癌細(xì)胞株,腫瘤細(xì)胞株,胃癌細(xì)胞株,hela細(xì)胞株,胰島細(xì)胞株,s180細(xì)胞株,hela細(xì)胞株,動物細(xì)胞,干細(xì)胞外,還提供MEM培養(yǎng)基,DMEM,F12培養(yǎng)基,RPMI培養(yǎng)基等基礎(chǔ)培養(yǎng)基,干細(xì)胞培養(yǎng)基,培養(yǎng)基添加劑,間充質(zhì)干細(xì)胞培養(yǎng)基 ,完全培養(yǎng)基,低血清培養(yǎng)基,胎牛血清,雞血清等細(xì)胞培養(yǎng)試劑。
參考文獻:
"Didier ES, et al. Characterization of Encephalitozoon (Septata) intestinailis isolates cultured from nasal mucosa and bronchoalveolar lavage fluids of two AIDS patients. J. Eukaryot. Microbiol. 43: 34-43, 1996. PubMed: 8563708
Fogh J. Human tumor cells in vitro. New York: Plenum Press; 1975.
Chen TR, et al. WiDr is a derivative of another colon adenocarcinoma cell line, HT-29. Cancer Genet. Cytogenet. 27: 125-134, 1987. PubMed: 3472642
Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871
Goodfellow M, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 77210034
Adachi A, et al. Productive, persistent infection of human colorectal cell lines with human immunodeficiency virus. J. Virol. 61: 209-213, 1987. PubMed: 3640832
Fantini J, et al. Human colon epithelial cells productively infected with human immunodeficiency virus show impaired differentiation and altered secretion. J. Virol. 66: 580-585, 1992. PubMed: 1727501
Butzow R, et al. A 60-kD protein mediates the binding of transforming growth factor-beta to cell surface and extracellular matrix proteoglycans. J. Cell Biol. 122: 721-727, 1993. PubMed: 8335695
Trainer DL, et al. Biological characterization and oncogene expression in human colorectal carcinoma cell lines. Int. J. Cancer 41: 287-296, 1988. PubMed: 3338874
Hanski C, et al. Tumorigenicity, mucin production and AM-3 epitope expression in clones selected from the HT-29 colon carcinoma cell line. Int. J. Cancer 50: 924-929, 1992. PubMed: 1372882
Reiter LS, et al. The role of the urokinase receptor in extracellular matrix degradation by HT29 human colon carcinoma cells. Int. J. Cancer 53: 444-450, 1993. PubMed: 8381394
Barnett SW, et al. Characterization of human immunodeficiency virus type 1 strains recovered from the bowel of infected individuals. Virology 182: 802-809, 1991. PubMed: 2024498
Shabahang M, et al. 1,25-Dihydroxyvitamin D3 receptor as a marker of human colon carcinoma cell line differentiation and growth inhibition. Cancer Res. 53: 3712-3718, 1993. PubMed: 8393379"
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