BBS12 antibody

Catalog No. ABIN2854610

Product Details anti-BBS12 Antibody

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BBS12 antibody is un-conjugated

Application: Western Blotting (WB)

Cross-Reactivity: Human

Characteristics: Rabbit polyclonal antibody to BBS12 (Bardet-Biedl syndrome 12)
FLJ35630 antibody [C1C3]

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human BBS12. 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: HepG2

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % 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 BBS12

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

Alternative Name: Bardet-Biedl syndrome 12 (BBS12 Products)

Synonyms: Gm1805 antibody, Gm407 antibody, Gm721 antibody, RP23-137F6.2 antibody, RGD1561608 antibody, C4orf24 antibody, DKFZP468P0511 antibody, Bardet-Biedl syndrome 12 (human) antibody, Bardet-Biedl syndrome 12 antibody, Bardet-Biedl syndrome 12 L homeolog antibody, Bbs12 antibody, BBS12 antibody, bbs12 antibody, bbs12.L antibody

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.

Molecular Weight: 79 kDa

Gene ID: 166379

UniProt: Q6ZW61