EZElisa™ Human Putative microR
NA 17 host Gene Protein（MIR17HG）ELISA试剂盒-EZElisa™ Human Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit- 询价
- Biogradetech
- 美国
- A-QEK06052-96wells
- 2025年07月10日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
运输过程中保存：2-8℃
- 保质期：
1年
- 英文名：
EZElisa™ Human Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit
- 库存：
100
- 供应商：
艾美捷科技
EZElisa™ Human Putative microRNA 17 host Gene Protein（MIR17HG）ELISA试剂盒，EZElisa™ Human Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit， Putative microRNA 17 host Gene Protein（MIR17HG）ELISA试剂盒, Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit
产品名称：EZElisa™人巨噬细胞炎性蛋白3 β（MIP 3b）ELISA试剂盒-EZElisa™ Human Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit
产品货号：A-QEK06052-96wells
产品规格：96wells
Enzyme Immunoassay for the estimation of Putative microRNA 17 host Gene Protein (MIR17HG) in serum and plasma, tissue homogenates and other biological fluids.
种属：Human
检测方法：比色法
检测范围：
该EZElisa™ Human Putative microRNA 17 host Gene Protein（MIR17HG）ELISA KitELISA的特点包括：即用即用的操作步骤标准化和高重复性批次之间的一致性准确性和精确性经过七个点的验证，符合金环标准质量ELISA的要求，这是Biogradetech质量的基准标志。EZElisa™ ELISA试剂盒用于评估样品中的特定生物标志物，样品可以是血清
运输过程中保存：2-8℃
点击：EZElisa™人巨噬细胞炎性蛋白3 β（MIP 3b）ELISA试剂盒-EZElisa™ Human Putative microRNA 17 host Gene Protein (MIR17HG) ELISA Kit更多Biogradetech产品信息价格，货期，产品说明，百度搜“艾美捷科技”进入官网网站，查看具体产品且快速下单。
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文献和实验, and normalized microRNA expression data have been submitted to the Gene Expression Omnibus with accession number GSE16421. Fig. 1 Differential microRNA expression in human melanoma (ME-15) and hepatoma (HuH7) cells. microRNA expression levels were compared
in the promoters of both mouse and human BIC genes. Putative NF-{kappa}B sites are present in the upstream region of the BIC promoter, and previous studies on the increased production of miR-155 in B cells have implicated NF-{kappa}B (15). This transcription factor
MicroRNA Regulation of Growth Factor Receptor Signaling in Human Cancer Cells
that bind to the 3′-untranslated region of target mRNAs, are now recognized to play key roles in the regulation of gene expression, particularly in tumor development and metastasis. We have shown that miRNA-7 (miR-7) and miRNA-331-3p (miR-331-3p) directly
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