ACAT1 antibody
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- Target See all ACAT1 Antibodies
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ACAT1 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Purification
- Affinity purified
- Immunogen
- ACAT1 antibody was raised using a synthetic peptide corresponding to a region with amino acids SYTRSKAAWEAGKFGNEVIPVTVTVKGQPDVVVKEDEEYKRVDFSKVPKL
- Top Product
- Discover our top product ACAT1 Primary Antibody
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- Application Notes
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - Comment
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ACAT1 Blocking Peptide, catalog no. 33R-8958, is also available for use as a blocking control in assays to test for specificity of this ACAT1 antibody
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ACAT1 antibody in PBS
- Concentration
- Lot specific
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- 4 °C/-20 °C
- Storage Comment
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 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. The gene encoding ACAT1 spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene 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
- 41 kDa (MW of target protein)
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