TPM2 Polyclonal Antibody | E-AB-12435

TPM2 Polyclonal Antibody | E-AB-12435 | Gentaur UK, US & Europe Distribution

Type: Polyclonal Antibody

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

Application: WB, IHC, ELISA

Reactivity: Human

Host: Rabbit

Isotype: IgG

Reserch Areas: Signal Transduction

Background: 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. TPM2 has been shown to interact with RRAD, PDLIM7 and TPM1.

Concentration: 0.4 mg/mL

Storage: Store at -20°C. Avoid freeze / thaw cycles.

Immunogen: Synthetic peptide of human TPM2

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification Method: Affinity purification

Dilution: WB 1:500-1:2000, IHC 1:50-1:200

Clone: N/A

Conjugation: Unconjugated

Molecular Weight(Calculated): 33 kDa

Molecular Weight(Observed): N/A