Acetyl-CoA Acetyltransferase 1 (ACAT1) Peptid
ACAT1
Reaktivität: Säugetier
Wirt: Synthetic
BP, WB, IHC
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- Target Alle ACAT1 Produkte
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Protein-Typ
- Synthetic
- Spezies
- Säugetier
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequenz
- GHQDVMVAGG MESMSNVPYV MNRGSTPYGG VKLEDLIVKD GLTDVYNKIH
- Produktmerkmale
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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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- Applikationshinweise
- Optimal conditions should be determined by the investigator
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handhabung
- Avoid repeated freeze/thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20 °C long term.
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- Target
- ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
- Synonyme
- 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
- Hintergrund
- 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.
- Molekulargewicht
- 41 kDa
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