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首頁 > 細(xì)胞 > 人源細(xì)胞系 > 人皮膚惡性黑色素瘤細(xì)胞(SK-MEL-28)
人皮膚惡性黑色素瘤細(xì)胞(SK-MEL-28)
¥800.00元
細(xì)胞貨號(hào): CL0284
細(xì)胞種屬: 人源細(xì)胞系
細(xì)胞別名: SK-Mel-28; SK.MEL.28; SK-MEL 28; SK MEL-28; SK MEL 28; SK Mel 28; SKMel-28; SKMEL-28; SK-MEL28; SK-Mel28; SK Mel28; SKMEL28; SKMel28; SKmel28; SKML-28; SK28; AU-Mel; P-36; P36
發(fā)貨規(guī)格: 1×10?
供體信息: 51歲男性
腫瘤類型: 皮膚黑色素瘤
組織來源: 皮膚
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背景信息
培養(yǎng)建議
其他信息
  • 蛋白表達(dá): p53 positive
  • 同工酶: PGM3, 1, PGM1, 1, ES-D, 1, AK-1, 1-2, GLO-1, 2, G6PD, B
  • 致瘤性: Yes, in nude mice. Forms malignant melanoma (large round cell type)
  • 抗原表達(dá): Blood Type A; Rh+; HLA A11, A26, B40, DRw4
  • 突變信息: BRAF V600E mut: V600E type BRAF Mutation was determined by DNA based methods (sequencing, RT-PCR) and protein based methods (Western Blot), N-Ras wt
  • 核型: modal number = 90; range = 81 to 96. This is a hypotetraploid human cell line with the modal chromosome number of 90, occurring in 50% of cells. The rate of cells with a higher ploidy was 3.6%. This cell line has a very complex karyotype. There were 18 or more marker chromosomes that were common to most cells. Markers der(1)t(1;2) (p36.1;q21), del(1) (q2101) and several others had two copies per cell and t(2p14q), t(3q7p) and others had a single copy per cell. The Y/autosome translocation marker was identified as der(20)t(Y;20) (q11.23;q13.3) and had two copies per cell. The inclusion of a short segment of the euchromatic Yq11.23 was confirmed by the Southern blot DNA analysis. There were two normal X chromosomes per cell; Normal Y, N1 and N11 were absent; N19 had five or more copies per cell.
人皮膚惡性黑色素瘤細(xì)胞
Catalog No CL0284
Product information
  • 蛋白表達(dá): p53 positive
  • 同工酶: PGM3, 1, PGM1, 1, ES-D, 1, AK-1, 1-2, GLO-1, 2, G6PD, B
  • 致瘤性: Yes, in nude mice. Forms malignant melanoma (large round cell type)
  • 抗原表達(dá): Blood Type A; Rh+; HLA A11, A26, B40, DRw4
  • 突變信息: BRAF V600E mut: V600E type BRAF Mutation was determined by DNA based methods (sequencing, RT-PCR) and protein based methods (Western Blot), N-Ras wt
  • 核型: modal number = 90; range = 81 to 96. This is a hypotetraploid human cell line with the modal chromosome number of 90, occurring in 50% of cells. The rate of cells with a higher ploidy was 3.6%. This cell line has a very complex karyotype. There were 18 or more marker chromosomes that were common to most cells. Markers der(1)t(1;2) (p36.1;q21), del(1) (q2101) and several others had two copies per cell and t(2p14q), t(3q7p) and others had a single copy per cell. The Y/autosome translocation marker was identified as der(20)t(Y;20) (q11.23;q13.3) and had two copies per cell. The inclusion of a short segment of the euchromatic Yq11.23 was confirmed by the Southern blot DNA analysis. There were two normal X chromosomes per cell; Normal Y, N1 and N11 were absent; N19 had five or more copies per cell.
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