Acetyl-CoA Acetyltransferase 1 (ACAT1) Peptide
ACAT1
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
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- Antigène Tous les produits ACAT1
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Type de proteíne
- Synthetic
- Origine
- Mammifères
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- GHQDVMVAGG MESMSNVPYV MNRGSTPYGG VKLEDLIVKD GLTDVYNKIH
- Attributs du produit
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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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- Indications d'application
- 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
- Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20 °C long term.
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- Antigène
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Synonymes
- 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
- Sujet
- 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.
- Poids moléculaire
- 41 kDa
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