Human Acetyl-CoA Acetyltransferase 1 (ACAA1) Protein

234€ (5 µg)
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935106861
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name
Human Acetyl-CoA Acetyltransferase 1 (ACAA1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx073272
tested applications
SDS-PAGE
Description
Acetyl-COA Acyltransferase is a recombinant enzyme.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Proteins and Peptides |
Immunogen Target | Acetyl-CoA Acetyltransferase 1 (ACAA1) |
Host | E. coli |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Origin | Human |
Expression | Recombinant |
Purity | > 95% (SDS-PAGE) |
Size 1 | 5 µg |
Size 2 | 20 µg |
Size 3 | 1 mg |
Form | Liquid |
Tested Applications | SDS-PAGE |
Availability | Shipped within 5-10 working days. |
Storage | Store below -18°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P09110 |
Alias | ACAA, Lnc-Myd88, PTHIO, THIO |
Background | Protein ACAA1 |
Status | RUO |
Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
Acetyl Coenzyme A Acyltransferase 1 (ACAA1), also known as thiolase, is a peroxisomal enzyme involved in the final step of beta-oxidation of very-long-chain fatty acids and branched-chain fatty acids. It catalyzes the thiolytic cleavage of 3-ketoacyl-CoA into acetyl-CoA and a shortened acyl-CoA, which is then further metabolized for energy production. ACAA1 is critical for lipid metabolism and plays an important role in energy homeostasis during fasting or periods of high energy demand. Dysregulation of ACAA1 activity can lead to metabolic disorders, such as Zellweger syndrome and other peroxisomal biogenesis disorders, characterized by impaired fatty acid oxidation and accumulation of toxic lipid intermediates. ACAA1 is also being studied for its role in the metabolic reprogramming of cancer cells, where it contributes to lipid catabolism and tumor progression.
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