SNTG2 antibody (AA 181-280) (AbBy Fluor® 555)

Catalog No. ABIN1389059

The Rabbit Polyclonal anti-SNTG2 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect SNTG2 in samples from Human.

Quick Overview for SNTG2 antibody (AA 181-280) (AbBy Fluor® 555) (ABIN1389059)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SNTG2 antibody is conjugated to AbBy Fluor® 555

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-SNTG2 Antibody (AbBy Fluor® 555)

Binding Specificity: AA 181-280

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SNTG2

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for SNTG2

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

Alternative Name: SNTG2/Syntrophin 5

Background:

Synonyms: G2SYN, Gamma2-syntrophin, SNTG2, SYN5, Syntrophin-5, Syntrophin5, Syntrophin 5, Syntrophin gamma 2, SNTG2_HUMAN.

Background: 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.