BBS12 antibody (AA 25-100) (AbBy Fluor® 594)

Catalog No. ABIN2810188

The Rabbit Polyclonal anti-BBS12 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect BBS12 in samples from Human.

Quick Overview for BBS12 antibody (AA 25-100) (AbBy Fluor® 594) (ABIN2810188)

Target: BBS12 (Bardet-Biedl Syndrome 12 (BBS12))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BBS12 antibody is conjugated to AbBy Fluor® 594

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

Product Details anti-BBS12 Antibody (AbBy Fluor® 594)

Binding Specificity: AA 25-100

Predicted Reactivity: Human,Mouse,Cow,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BBS12

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 BBS12

Target: BBS12 (Bardet-Biedl Syndrome 12 (BBS12))

Alternative Name: BBS12

Background:

Synonyms: Bardet Biedl syndrome 12 protein, Bardet-Biedl syndrome 12 human, Bardet-Biedl syndrome 12 protein homolog, BBS12 gene, C4orf24, FLJ35630, FLJ41559, Gm1805, Gm407, Gm721, RP23-137F6.2,BBS12_HUMAN.

Background: The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene.