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SLMAP antibody (AA 25-607)

The Rabbit Polyclonal anti-SLMAP antibody (ABIN7872886) specifically detects SLMAP in WB, ELISA and FACS. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7872886
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SLMAP antibody (AA 25-607) (ABIN7872886)

Target

See all SLMAP Antibodies
SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivity

  • 9
  • 3
  • 2
  • 1
Human, Mouse

Host

  • 5
  • 4
  • 1
  • 1
Rabbit

Clonality

  • 8
  • 3
Polyclonal

Conjugate

  • 11
This SLMAP antibody is un-conjugated

Application

  • 11
  • 7
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 25-607

    Purpose

    SLMAP Antibody / Sarcolemmal membrane-associated protein

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids D25-E607) was used as the immunogen for the SLMAP antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SLMAP 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 SLMAP 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

    SLMAP (Sarcolemma Associated Protein (SLMAP))

    Alternative Name

    SLMAP

    Background

    Sarcolemmal membrane-associated protein is a protein that in humans is encoded by the SLMAP gene. This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

    UniProt

    Q14BN4
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