ACAT1 antibody (C-Term)

Catalog No. ABIN391807

Product Details anti-ACAT1 Antibody

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

Binding Specificity: AA 296-329, C-Term

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ACAT1 antibody is un-conjugated

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

Predicted Reactivity: Pr

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

Immunogen: 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

Application Details

Application Notes: WB: 1:2000. WB: 1:1000. WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Expiry Date: 6 months

Target Details for ACAT1

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

Alternative Name: ACAT1 (ACAT1 Products)

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

Background: 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.

Molecular Weight: 45200

Gene ID: 38

NCBI Accession: NP_000010

UniProt: P24752