Analytical Data
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Gene name
ACSS3
- Application
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Alternative Names
Acyl-CoA synthetase short-chain family member 3
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Species
Human
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Source
E. coli
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Tag
N- His
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q9H6R3
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Expression Region
30-686aa
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Molecular Weight
77.9 kDa
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
ACSS3 (Acetyl-CoA Synthetase 3) is a crucial enzyme that plays a significant role in the metabolic pathway of acetate utilization, particularly in the context of energy production and cell signaling. Research on ACSS3 has gained prominence due to its involvement in various physiological processes, including fatty acid metabolism, thermogenesis, and the regulation of mitochondrial function. As a mitochondrial enzyme, ACSS3 catalyzes the conversion of acetate into acetyl-CoA, which is vital for biosynthetic pathways and energy generation. Dysregulation of ACSS3 has been implicated in a range of metabolic disorders, including obesity, diabetes, and certain types of cancer. Understanding the structure and function of the ACSS3 protein is essential for elucidating its role in metabolic regulation and its potential as a therapeutic target. Recent studies have focused on the enzymatic mechanisms of ACSS3, its regulatory pathways, and its interactions with other key metabolic enzymes. Additionally, the exploration of ACSS3's role in cellular responses to nutritional changes and its contribution to the development of metabolic diseases has opened new avenues for research. Overall, the study of ACSS3 is not only critical for comprehending fundamental metabolic processes but also holds promising implications for the development of interventions in metabolic diseases and the enhancement of metabolic health.
