微生物群体多样性测序分析原理(IF7.328)

发布日期:2024-12-22 01:38:59     作者:硪心寒     手机:https://m.xinb2b.cn/life/lgz294103.html     违规举报



文章主题:

3D生物打印海藻酸盐凝胶细菌纳米纤维素(BNC)支架与RSC96细胞的生物相容性评价

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

影响因子(IF):7.328

作者单位:北京大学口腔医院


PCR Array数据结果

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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