ACAT1 anticorps (C-Term)

N° du produit ABIN391807

Détail du produit anti-ACAT1 anticorps

Antigène: ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Épitope: AA 296-329, C-Term

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACAT1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Homologie: Pr

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This ACAT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 296-329 amino acids from the C-terminal region of human ACAT1.

Clone: RB14644

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:2000. WB: 1:1000. WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur ACAT1

Antigène: ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Autre désignation: ACAT1 (ACAT1 Produits)

Synonymes: anticorps ACAT, anticorps MAT, anticorps T2, anticorps THIL, anticorps RATACAL, anticorps 6330585C21Rik, anticorps Acat, anticorps fd16h07, anticorps fd20g06, anticorps wu:fd16h07, anticorps wu:fd20g06, anticorps zgc:86832, anticorps acat1-a, anticorps acetyl-CoA acetyltransferase 1, anticorps acetyl-Coenzyme A acetyltransferase 1, anticorps acetyl-CoA acetyltransferase 1 L homeolog, anticorps ACAT1, anticorps Acat1, anticorps acat1, anticorps acat1.L

Sujet: ACAT1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in the gene encoding ACAT1 are associated with the alpha-methylacetoaceticaciduria disorder,an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.

Poids moléculaire: 45200

ID gène: 38

NCBI Accession: NP_000010

UniProt: P24752