WebMay 14, 2024 · Hypoaldosteronism, congenital, due to CMO I deficiency, 203400, Autosomal recessive (Familial hypoaldosteronism) (CYP11B2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) GTR Test ID Help Each Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is … WebA total of 41 tagSNPs (a minor allele frequency >0.05, with an r 2 threshold of 0.8) in the STAR, HSD3B1, HSD3B2, CYP17A1, CYP21A2, CYP11B1, and CYP11B2 genes have been identified in the HapMap Han Chinese population. The SNPs were genotyped using single-base extension detecting technology (iPLEX; Capital Bio Corporation, Beijing, …
Development of CYP11B1 and CYP11B2 assays utilizing
WebCYP11B2. General description of the gene and the encoded protein (s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas … Web35 CYP11B2 Silencer Select Pre-designed, Validated, and Custom siRNA in Standard, HPLC, and In-vivo Ready Purities. Popular ... Related Assays; Related Antibodies; Related Controls; Assay ID 161401 View Assay on Map … opticians marton middlesbrough
Cyp11b2 - PrimePCR Assay and Template Life Science Bio-Rad
WebConclusions: We conclude that APEX1 is a novel transcriptional repressor of CYP11B2 and that differential APEX1 binding at -1651 of CYP11B2 results in altered gene expression. This mechanism may contribute to the observed relationship between CYP11B2 genotype and aldosterone phenotype in a subgroup of hypertensive patients. (Circ Res. 2012;111: ... WebPrimePCR™ PreAmp for Probe Assay: CYP11B2, Human Reaction: 400 reactions Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for … Web杂环螺环化合物专利检索,杂环螺环化合物属于治疗内分泌系统疾病的药物专利检索,找专利汇即可免费查询专利,治疗内分泌系统疾病的药物专利汇是一家知识产权数据服务商,提供专利分析,专利查询,专利检索等数据服务功能。 portland general customer service number