BBS12 anticorps (AA 25-100) (Cy3)

N° du produit ABIN1409553

Détail du produit anti-BBS12 anticorps (Cy3)

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

Épitope: AA 25-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BBS12 est conjugé à/à la Cy3

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

Homologie: Human,Mouse,Cow,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human BBS12

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur BBS12

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

Autre désignation: BBS12 (BBS12 Produits)

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

Sujet:

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.