人 TPM1 (NM_000366) cDNA克隆

Accession: NM_000366
基因名称: TPM1
基因别名: CMH3; TMSA; CMD1Y; LVNC9; C15orf13; HTM-alpha
基因描述: Homo sapiens tropomyosin 1 (alpha) (TPM1), transcript variant 5, mRNA.
种属: Human
CDS区长度: 855 (查看编码区序列)
翻译后氨基酸长度: 284 (查看氨基酸序列)
Transcript Variant: This variant (5) contains an alternate, in-frame exon and uses an alternate in-frame splice site and upstream stop codon, compared to variant 1. It encodes isoform 5, which has a different C-terminus, compared to isoform 1.
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G109019 人 TPM1 (NM_000366) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]