TPM2 Antibody

TPM2

Alpha tropomyosin antibody; AMCD1 antibody; Arthrogryposis multiplex congenital distal type 1 antibody; Beta tropomyosin antibody; Beta-tropomyosin antibody; Cytoskeletal tropomyosin TM30 antibody; DA1 antibody; DA2B antibody; epididymis secretory protein Li 273 antibody; FLJ41118 antibody; Heat stable cytoskeletal protein 30 kDa antibody; HEL-S-273 antibody; hscp30 antibody; HTM alpha antibody; hTM5 antibody; MGC14582 antibody; MGC3261 antibody; MGC72094 antibody; NEM1 antibody; NEM4 antibody; Nemaline myopathy type 4 antibody; OK/SW cl.5 antibody; Sarcomeric tropomyosin kappa antibody; TM 5 antibody; TM3 antibody; TM30 antibody; TM30nm antibody; TMSA antibody; TMSB antibody; TPM 1 antibody; TPM 3 antibody; TPM1 alpha antibody; TPM1 kappa antibody; TPM2 antibody; TPM2_HUMAN antibody; TRK antibody; Tropomyosin 1 alpha antibody; Tropomyosin 1 alpha chain antibody; Tropomyosin 1 alpha chain isoform 6 antibody; Tropomyosin 2 (beta) antibody; Tropomyosin 2 antibody; Tropomyosin 3 antibody; Tropomyosin alpha 3 chain antibody; Tropomyosin alpha striated muscle isoform antibody; Tropomyosin beta chain antibody; Tropomyosin gamma antibody; Tropomyosin skeletal muscle beta antibody; Tropomyosin-2 antibody

Synthetic peptide of human TPM2

This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Antigen affinity purification

Signal Transduction

Synthetic peptide of Human TPM2