Human Acetyl Coenzyme A Acetyltransferase 1 (ACAT1) Protein

Este producto es parte de ACAT - Acetyl Coenzyme A Acetyltransferase
Human Acetyl Coenzyme A Acetyltransferase 1 (ACAT1) Protein
234€ (5 µg)

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Name
Human Acetyl Coenzyme A Acetyltransferase 1 (ACAT1) Protein
Category
Proteins and Peptides
Provider
Abbexa
Reference
abx073370
Tested Applications
SDS-PAGE

Description

Acetyl-Corecombinant enzyme A acetyltransferase 1 is a recombinant enzyme.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Proteins and Peptides
Immunogen Target
Acetyl CoProtein A Acetyltransferase 1 (ACAT1)
Host
E. coli
Assay Type
Activity: Not tested
Sequence Fragment: 34-427 AA
Tag: N-terminal His tag
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Origin
Human
Observed MW
43.8 kDa
Expression
Recombinant
Purity
> 95% (SDS-PAGE)
Purification
Purified by proprietary chromatographic techniques.
Size 1
5 µg
Size 2
20 µg
Size 3
1 mg
Form
Liquid
Tested Applications
SDS-PAGE
Buffer
20 mM Tris-HCl buffer (pH 7.5), 0.1M NaCl, 10% glycerol and 1 mM DTT.
Availability
Shipped within 5-10 working days.
Storage
Store at 4°C if the entire vial will be used within 2-4 weeks. Store at -20 °C for long term storage. For long term storage, it is recommended to add a carrier protein (0.1% HSA or BSA). Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P24752
Alias
ACAT,MAT,T2,THIL,Acetoacetyl-CoA thiolase
Background
Protein ACAT1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Concentration: 1 mg/ml

Background

ACAT1, also known as mitochondrial acetoacetyl-CoA thiolase, is an enzyme localized in the mitochondria that catalyzes the reversible conversion of two molecules of acetyl-CoA into acetoacetyl-CoA, a critical step in ketone body synthesis and cholesterol metabolism. It is involved in energy production during periods of fasting or carbohydrate restriction by contributing to ketogenesis. ACAT1 also plays a role in the breakdown of branched-chain amino acids, linking it to amino acid metabolism. Dysregulation or mutations in the ACAT1 gene have been implicated in rare metabolic disorders such as beta-ketothiolase deficiency, which is characterized by the inability to properly metabolize ketogenic amino acids and fatty acids, leading to metabolic acidosis. Recent studies have also suggested a potential role for ACAT1 in cancer metabolism, where its activity is linked to metabolic reprogramming in tumor cells.

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