Acetyl-CoA Acetyltransferase 1 (ACAT1) Peptide
ACAT1
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
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- Target See all ACAT1 products
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- GHQDVMVAGG MESMSNVPYV MNRGSTPYGG VKLEDLIVKD GLTDVYNKIH
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of ACAT1 antibody,
Alternative Names: ACAT1 control peptide, ACAT1 antibody Blocking Peptide, Anti-ACAT1 Blocking Peptide, Acetyl-Coenzyme A Acetyltransferase 1 Blocking Peptide, ACAT Blocking Peptide, MAT Blocking Peptide, T2 Blocking Peptide, THIL Blocking Peptide, ACAT1, ACAT-1, ACAT 1, ACAT-1 Blocking Peptide, ACAT 1 Blocking Peptide
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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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
- 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
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