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SNTG2 antibody (AA 100-430)

This Rabbit Polyclonal antibody specifically detects SNTG2 in WB, ELISA and FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7869875
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SNTG2 antibody (AA 100-430) (ABIN7869875)

Target

See all SNTG2 Antibodies
SNTG2 (Syntrophin, gamma 2 (SNTG2))

Reactivity

  • 22
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 21
  • 1
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SNTG2 antibody is un-conjugated

Application

  • 21
  • 13
  • 13
  • 7
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 2
    • 1
    • 1
    • 1
    AA 100-430

    Purpose

    Syntrophin gamma 2 Antibody / SNTG2

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids I100-R430) was used as the immunogen for the Syntrophin gamma 2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Syntrophin gamma 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 Syntrophin gamma 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

    SNTG2 (Syntrophin, gamma 2 (SNTG2))

    Alternative Name

    Syntrophin gamma 2

    Background

    This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described.

    UniProt

    Q9NY99
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