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TPM2 antibody (AA 1-254)

This Rabbit Polyclonal antibody specifically detects TPM2 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN1885852

Quick Overview for TPM2 antibody (AA 1-254) (ABIN1885852)

Target

See all TPM2 Antibodies
TPM2 (Tropomyosin-2 (TPM2))

Reactivity

  • 56
  • 29
  • 10
  • 5
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 51
  • 5
Rabbit

Clonality

  • 51
  • 5
Polyclonal

Conjugate

  • 19
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TPM2 antibody is un-conjugated

Application

  • 38
  • 17
  • 13
  • 13
  • 10
  • 6
  • 6
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 8
    • 5
    • 4
    • 2
    • 1
    • 1
    AA 1-254

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 254 of Tropomyosin 2
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    TPM2 (Tropomyosin-2 (TPM2))

    Alternative Name

    Tropomyosin 2

    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.

    Molecular Weight

    33 kDa

    Gene ID

    7169

    NCBI Accession

    NM_213674, NP_998839
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