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Recombinant Human Apolipoprotein C-II (APOC2)

ACP04880

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP04880 Target NameAPOC2
FormLiquid or Lyophilized powderExpression SystemYeast
Expression Range23-101aaMol Weight10.9kDa
Protein LengthFull Length of Mature ProteinPurityGreater than 90% as determined by 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 IDP02655
Background Information
  • Uniprot Id

    P02655

  • Target Species

    Human

  • Target Name

    APOC2

  • Target Full Name

    Apolipoprotein C-II

  • Target Function

    Component of chylomicrons, very low-density lipoproteins (VLDL), low-density lipoproteins (LDL), and high-density lipoproteins (HDL) in plasma. Plays an important role in lipoprotein metabolism as an activator of lipoprotein lipase. Both proapolipoprotein C-II and apolipoprotein C-II can activate lipoprotein lipase. In normolipidemic individuals, it is mainly distributed in the HDL, whereas in hypertriglyceridemic individuals, predominantly found in the VLDL and LDL.

  • Target Involvement

    Hyperlipoproteinemia 1B (HLPP1B)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Apolipoprotein C2 family

  • Target Tissue Specificity

    Liver and intestine.

  • Target Research Area

    Metabolism

  • Target Synonyms

    APC 2; APC2; Apo CII; Apo-CII; APOC 2; ApoC II; ApoC-II; APOC2; APOC2 protein; APOC2_HUMAN; ApoCII; Apolipoprotein C II; Apolipoprotein C II precursor; Apolipoprotein C2; ApolipoproteinCII; MGC75082; ProapoC-II; Proapolipoprotein C-II

  • Target Background

    This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is secreted in plasma where it is a component of very low density lipoprotein. This protein activates the enzyme lipoprotein lipase, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring upstream apolipoprotein C-IV (APOC4) gene.

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