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TPM2 antibody

The Rabbit Polyclonal anti-TPM2 antibody is suitable to detect TPM2 in samples from Human, Mouse and Rat. It has been validated for WB, IF, IHC (p) and FACS.
Catalog No. ABIN7882570
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TPM2 antibody (ABIN7882570)

Target

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

Reactivity

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  • 10
  • 5
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  • 2
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  • 2
  • 1
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Human, Mouse, Rat

Host

  • 52
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Rabbit

Clonality

  • 52
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Polyclonal

Conjugate

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

Application

  • 39
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  • 6
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  • 4
  • 4
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  • 1
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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Purpose

    Tropomyosin 2 Antibody / TPM2 / Tropomyosin beta

    Sequence

    KQAEDRCKQL EEEQQALQK

    Purification

    Antigen affinity purified

    Immunogen

    Amino acids KQAEDRCKQLEEEQQALQK from the human protein were used as the immunogen for the Tropomyosin 2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Tropomyosin 2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Tropomyosin 2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    TPM2 (Tropomyosin-2 (TPM2))

    Alternative Name

    Tropomyosin 2

    Background

    Beta-Tropomyosin, also known as tropomyosin beta chain is a protein that in humans is encoded by the TPM2 gene. 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.

    UniProt

    P07951
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