Acetyl-CoA Acetyltransferase 1 (ACAT1) Peptide
ACAT1
Reactivity: Human
Host: Synthetic
BP, WB, IHC
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- Target See all ACAT1 products
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-ACAT1 antibody (Catalog #: ARP54278_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Synonyms
- ACAT Peptide, MAT Peptide, T2 Peptide, THIL Peptide, RATACAL Peptide, 6330585C21Rik Peptide, Acat Peptide, fd16h07 Peptide, fd20g06 Peptide, wu:fd16h07 Peptide, wu:fd20g06 Peptide, zgc:86832 Peptide, acat1-a Peptide, acetyl-CoA acetyltransferase 1 Peptide, acetyl-Coenzyme A acetyltransferase 1 Peptide, acetyl-CoA acetyltransferase 1 L homeolog Peptide, ACAT1 Peptide, Acat1 Peptide, acat1 Peptide, acat1.L Peptide
- Background
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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.This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. This gene 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: ACAT, MAT, T2, THIL
Protein Interaction Partner: EIF1B
Protein Size: 427 - Molecular Weight
- 41 kDa
- Gene ID
- 38
- NCBI Accession
- NM_000019, NP_000010
- UniProt
- P35610
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