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Recombinant Human Pancreatic triacylglycerol lipase (PNLIP)

ACP23975

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP23975 Target NamePNLIP
Target Synonymslipase, pancreatic; LIPP_HUMAN; Pancreatic lipase; Pancreatic triacylglycerol lipase; PL; PNLIP; PNLIPD; PTL; Triacylglycerol acylhydrolaseFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range17-465
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 IDP16233
Background Information
  • Uniprot Id

    P16233

  • Target Species

    Human

  • Target Name

    PNLIP

  • Target Full Name

    Pancreatic triacylglycerol lipase

  • Target Function

    Plays an important role in fat metabolism. It preferentially splits the esters of long-chain fatty acids at positions 1 and 3, producing mainly 2-monoacylglycerol and free fatty acids, and shows considerably higher activity against insoluble emulsified substrates than against soluble ones.

  • Target Involvement

    Pancreatic lipase deficiency (PNLIPD)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    AB hydrolase superfamily, Lipase family

  • Target Synonyms

    lipase, pancreatic; LIPP_HUMAN; Pancreatic lipase; Pancreatic triacylglycerol lipase; PL; PNLIP; PNLIPD; PTL; Triacylglycerol acylhydrolase

  • Target Background

    This gene encodes a member of the lipase family of proteins. The encoded enzyme is secreted by the pancreas and hydrolyzes triglycerides in the small intestine, and is essential for the efficient digestion of dietary fats. Inhibition of the encoded enzyme may prevent high-fat diet-induced obesity in mice and result in weight loss in human patients with obesity. Mutations in this gene cause congenital pancreatic lipase deficiency, a rare disorder characterized by steatorrhea.

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