SOAT1 anticorps (AA 190-270)

N° du produit ABIN7213440

L’anticorps anti-SOAT1 Polyclonal Lapin est utilisé pour la détection de SOAT1 dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB, ELISA, IHC et IF.

Aperçu rapide pour SOAT1 anticorps (AA 190-270) (ABIN7213440)

Antigène: SOAT1 (Sterol O-Acyltransferase 1 (SOAT1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SOAT1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Détail du produit anti-SOAT1 anticorps

Épitope: AA 190-270

Fonction: Rabbit Anti-ACAT-1 Polyclonal Antibody

Specificité: ACAT-1 Polyclonal Antibody detects endogenous levels of ACAT-1 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the Internal region of human ACAT-1 at AA range: 190-270

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur SOAT1

Antigène: SOAT1 (Sterol O-Acyltransferase 1 (SOAT1))

Autre désignation: ACAT-1

Sujet: ACAT1, ACAT, MAT, Acetyl-CoA acetyltransferase, mitochondrial, Acetoacetyl-CoA thiolase, T2ACAT1 encodes a mitochondrially localized enzyme (acetyl-CoA acetyltransferase 1) that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in ACAT1 are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.

Poids moléculaire: 45kD

ID gène: 38

UniProt: P24752