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Astor Scientific  |  SKU: ASTP8915

Human ACAT1 (Acetyl-Coa Acetyltransferase, Mitochondrial) - Recombinant Protein

Molecule: ACAT1
Species: Human
Expression System: E.coli
Tag: N-6His
Expression Range: 111-427aa
$429.99 $549.99
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SDS-PAGE analysis of Human ACAT1 (Acetyl-Coa Acetyltransferase, Mitochondrial) - Recombinant Protein, showing >85% purity under 15% SDS-PAGE (Reduced)
Astor Scientific

Human ACAT1 (Acetyl-Coa Acetyltransferase, Mitochondrial) - Recombinant Protein

$429.99 $549.99

Product Overview

Product Name Recombinant Human Acetyl Coenzyme A Acetyltransferase 1 (ACAT1) Protein
Product Overview This recombinant human Acetyl Coenzyme A Acetyltransferase 1 (ACAT1) protein includes amino acids 111-427aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5% trehaloseprior to lyophilization.
Target Uniprot Id P24752
Recommended Name Acetyl-CoA acetyltransferase, mitochondrial
Gene Name ACAT1
Synonyms acetyl-CoA acetyltransferase 1, ACAT, MAT, T2, THIL
Species Human
Predicted Molecular Mass 37 kDa
Expression System E.coli
Expression Range 111-427aa
Tag N-6His
Purity >85%
Formulation Lyophilized
Buffer Phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5%Trehalose
Storage Condition 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C.
Reconstitution Instruction Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%.
Applications Positive Control; Immunogen; SDS-PAGE; WB
Research Area Metabolism
Target Function This is one of the enzymes that catalyzes the last step of the mitochondrial beta-oxidation pathway, an aerobic process breaking down fatty acids into acetyl-CoA. Using free coenzyme A/CoA, catalyzes the thiolytic cleavage of medium- to long-chain 3-oxoacyl-CoAs into acetyl-CoA and a fatty acyl-CoA shortened by two carbon atoms. The activity of the enzyme is reversible and it can also catalyze the condensation of two acetyl-CoA molecules into acetoacetyl-CoA. Thereby, it plays a major role in ketone body metabolism.
Subcellular Location Mitochondrion.
Protein Family Thiolase family
Associated Diseases 3-ketothiolase deficiency (3KTD)

Size

  • 100ug
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