Recombinant Human SNTB2 cell lysate

• Cat.No.: SNTB2-1657HCL

Specification

• Description: Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes.
• Species: Human
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot

Gene Information

• Gene Name: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2) [ Homo sapiens ]
• Official Symbol: SNTB2
• Synonyms: SNTB2; syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2); D16S2531E, SNT2B2, SNTL, syntrophin, beta 2 (dystrophin associated protein A1, 59kD, basic component 2); beta-2-syntrophin; EST25263; SNT3; syntrophin-3; 59 kDa dystrophin-associated protein A1 basic component 2; dystrophin-associated protein A1, 59kD, basic component 2; SNTL; SNT2B2; D16S2531E
• Gene ID: 6645
• mRNA Refseq: NM_006750
• Protein Refseq: NP_006741
• MIM: 600027
• UniProt ID: Q13425
• Chromosome Location: 16q22.1
• Function: actin binding; calmodulin binding; protein binding