"TNNI2" Related Products


Recombinant Human TNNI2, MYC/DDK-tagged

Cat.No.: TNNI2-16H
Product Overview: Recombinant Human TNNI2, transcript variant 2, fused with C-terminal MYC/DDK, was expressed in HEK293 cells.
Description: This gene encodes a fast-twitch skeletal muscle protein, a member of the troponin I gene family, and a component of the troponin complex including troponin T, troponin C and troponin I subunits. The troponin complex, along with tropomyosin, is responsible for the calcium-dependent regulation of striated muscle contraction. Mouse studies show that this component is also present in vascular smooth muscle and may play a role in regulation of smooth muscle function. In addition to muscle tissues, this protein is found in corneal epithelium, cartilage where it is an inhibitor of angiogenesis to inhibit tumor growth and metastasis, and mammary gland where it functions as a co-activator of estrogen receptor-related receptor alpha. This protein also suppresses tumor growth in human ovarian carcinoma. Mutations in this gene cause myopathy and distal arthrogryposis type 2B. Alternatively spliced transcript variants have been found for this gene.
Source: HEK293 cells
Species: Human
Molecular Mass: 21.2 kDa
Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration: >50 ug/mL as determined by microplate BCA method
Storage Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Gene Name: TNNI2 troponin I type 2 (skeletal, fast) [ Homo sapiens (human) ]
Official Symbol: TNNI2
Synonyms: TNNI2; troponin I type 2 (skeletal, fast); troponin I, skeletal, fast; troponin I, fast skeletal muscle; AMCD2B; DA2B; FSSV; troponin I fast twitch 2; troponin I; fast twitch skeletal muscle isoform
Gene ID: 7136
mRNA Refseq: NM_001145829
Protein Refseq: NP_001139301
MIM: 191043
UniProt ID: P48788
Chromosome Location: 11p15.5
Pathway: Muscle contraction; Striated Muscle Contraction
Function: contributes_to actin binding; protein binding; troponin T binding

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