人 INS (NM_000207) cDNA克隆

Accession: NM_000207
基因名称: INS
基因别名: ILPR; IRDN; IDDM2; MODY10
基因描述: Homo sapiens insulin (INS), transcript variant 1, mRNA.
种属: Human
CDS区长度: 333 (查看编码区序列)
翻译后氨基酸长度: 110 (查看氨基酸序列)
Transcript Variant: This transcript (1) represents the shortest variant. Variants 1-3 encode the same protein.
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G102910 人 INS (NM_000207) cDNA克隆 pDONR223 2ug质粒 点击询价

After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]