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微生物群體多樣性測序分析原理

科技 更新时间:2024-09-28 01:29:06

微生物群體多樣性測序分析原理(IF7.328)1

微生物群體多樣性測序分析原理(IF7.328)2

文章主題:

3D生物打印海藻酸鹽凝膠細菌納米纖維素(BNC)支架與RSC96細胞的生物相容性評價

Biocompatibility evaluation of a 3D-bioprinted alginate-GelMA-bacteria nanocellulose (BNC) scaffold laden with oriented-growth RSC96 cells

影響因子(IF):7.328

作者單位:北京大學口腔醫院

微生物群體多樣性測序分析原理(IF7.328)3

PCR Array數據結果

Figure 9. a) PCR array heatmap of 92 genes. b-g) Quantitative comparison of ASCL1, POU3F3, NEUROG1, DLL1, NOTCH1 and ERBB2 gene expression on day 7 analysed by the 2-△△Ct method using GAPDH as the internal control. Dates were represented as the mean ± SD (n = 3). (*p < 0.05, **p < 0.01 and ***p < 0.001)

沃吉基因PCR Array方法描述

……Ninety-two mRNA constructs encoding neuroregeneration-related genes were detected using a rat neurogenesis PCR array (Wcgene Biotech, Shanghai, China) according to the manufacturer's protocol (n = 3). Gene expression profiles were analysed according to the manufacturer's protocol (Wcgene Biotech, Shanghai, China), and data were analysed using software from Wcgene Biotech. Genes with fold change greater or less than 2.0 were considered biologically significant.……

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