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Recombinant Human Cholesteryl ester transfer protein (CETP)

ACP24379

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP24379 Target NameCETP
Target SynonymsBPIFF; CETP; CETP_HUMAN; Cholesteryl ester transfer protein; Cholesteryl ester transfer protein plasma; HDLCQ10; Lipid transfer protein IFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range18-493
Protein LengthFull Length of Mature ProteinPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP11597
Background Information
  • Uniprot Id

    P11597

  • Target Species

    Human

  • Target Name

    CETP

  • Target Full Name

    Cholesteryl ester transfer protein

  • Target Function

    Involved in the transfer of neutral lipids, including cholesteryl ester and triglyceride, among lipoprotein particles. Allows the net movement of cholesteryl ester from high density lipoproteins/HDL to triglyceride-rich very low density lipoproteins/VLDL, and the equimolar transport of triglyceride from VLDL to HDL. Regulates the reverse cholesterol transport, by which excess cholesterol is removed from peripheral tissues and returned to the liver for elimination.

  • Target Involvement

    Hyperalphalipoproteinemia 1 (HALP1)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    BPI/LBP/Plunc superfamily, BPI/LBP family

  • Target Tissue Specificity

    Expressed by the liver and secreted in plasma.

  • Target Synonyms

    BPIFF; CETP; CETP_HUMAN; Cholesteryl ester transfer protein; Cholesteryl ester transfer protein plasma; HDLCQ10; Lipid transfer protein I

  • Target Background

    The protein encoded by this gene is found in plasma, where it is involved in the transfer of cholesteryl ester from high density lipoprotein (HDL) to other lipoproteins. Defects in this gene are a cause of hyperalphalipoproteinemia 1 (HALP1). Two transcript variants encoding different isoforms have been found for this gene.

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