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SNTG2 antibody

The Rabbit Polyclonal anti-SNTG2 antibody has been validated for WB. It is suitable to detect SNTG2 in samples from Human.
Catalog No. ABIN7465582

Quick Overview for SNTG2 antibody (ABIN7465582)

Target

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

Reactivity

  • 21
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Human

Host

  • 20
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Rabbit

Clonality

  • 21
Polyclonal

Conjugate

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

Application

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Western Blotting (WB)
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Syntrophin gamma 2. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: A549 , H1299

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    SNTG2 (Syntrophin, gamma 2 (SNTG2))

    Alternative Name

    syntrophin gamma 2

    Background

    Syntrophin gamma 2 , G2SYN , SYN5,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. [provided by RefSeq, Jul 2008]

    Molecular Weight

    60 kDa

    Gene ID

    54221

    UniProt

    Q9NY99
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