BBS12 anticorps (AA 25-100)

N° du produit ABIN1387365

Cet anticorps anti-BBS12 est un anticorps Lapin Polyclonal détectant BBS12 dans WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p) et ICC. Adapté pour Humain.

Aperçu rapide pour BBS12 anticorps (AA 25-100) (ABIN1387365)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BBS12 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Détail du produit anti-BBS12 anticorps

Épitope: AA 25-100

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: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur BBS12

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

Autre désignation: BBS12

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.