TPM2 Polyclonal Antibody

• 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.

• Description:

  This is a TPM2 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• 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 al

• Swiss Prot:

  P07951

• Accession Number:

  NP_998839

• Reactivity:

  Human

• Immunogen:

  Synthetic peptide of human TPM2

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  WB, IHC, ELISA

• Purification Method:

  Affinity purification

• Assay Type:

  Antibody

• Concentration:

  0.4 mg/mL

• Dilution:

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

• Buffer:

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

• Storage Conditions:

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

• Calculated Molecular Weight:

  33 kDa

• Host or Source:

  Rabbit

• Isotype:

  IgG