SNTG2 antibody

Catalog No. ABIN7465582

The Rabbit Polyclonal anti-SNTG2 antibody is suitable to detect SNTG2 in samples from Human. It has been validated for WB.

Quick Overview for SNTG2 antibody (ABIN7465582)

Target: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SNTG2 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SNTG2 Antibody

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 Details

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

Handling

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 Details for SNTG2

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