Cat: IPD-X37334

Recombinant Human ACAT2 Protein,His & Myc

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Analytical Data

  • Gene name

    ACAT2

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Acetyl-CoA transferase-like protein Cytosolic acetoacetyl-CoA thiolase

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His & C- Myc

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9BWD1

  • Expression Region

    1-397aa

  • Molecular Weight

    48.8 kDa

  • Endotoxin

    < 1.0 EU per μg protein as determined by the LAL method.

  • Form

    Freeze-dried powder

  • Buffer formulation

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • Reconstitution

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • Customization

    Site-directed mutagenesis Custom tag design Custom buffer formulation Custom full-length protein production

  • 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.

  • 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.

  • 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.

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Protein Description

ACAT2, or Acyl-CoA:cholesterol acyltransferase 2, is an important enzyme involved in cholesterol esterification, playing a crucial role in lipid metabolism and homeostasis. It catalyzes the conversion of free cholesterol and fatty acyl-CoA into cholesterol esters, which are essential for cellular functions, including membrane structure, energy storage, and signaling. Dysregulation of ACAT2 has been implicated in various diseases, such as atherosclerosis, obesity, and neurodegenerative disorders. Given its significance in lipid metabolism, ACAT2 has emerged as a potential therapeutic target for the treatment of these conditions. The study of recombinant ACAT2 proteins allows for detailed investigations into the enzyme's structure, function, and regulatory mechanisms. Producing ACAT2 recombinantly enables researchers to explore its biochemical properties, assess its interactions with potential inhibitors, and develop assays for high-throughput screening of drug candidates. Furthermore, understanding ACAT2's role in cellular cholesterol homeostasis and its involvement in pathological processes can elucidate the underlying mechanisms of lipid-related diseases and facilitate the identification of novel therapeutic strategies. As research continues to uncover the complexities of lipid metabolism, ACAT2 remains a compelling focus within the field of metabolic disease research, with increasing relevance in the pursuit of effective treatments for associated health issues.

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