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Recombinant Human Insulin (INS)

ACP00635

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP00635 Target NameINS
FormLiquid or Lyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
PurityGreater than 85% 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 IDP01308
Background Information
  • Uniprot Id

    P01308

  • Target Species

    Human

  • Target Name

    INS

  • Target Full Name

    Insulin

  • Target Function

    Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.

  • Target Involvement

    Hyperproinsulinemia (HPRI); Diabetes mellitus, insulin-dependent, 2 (IDDM2); Diabetes mellitus, permanent neonatal (PNDM); Maturity-onset diabetes of the young 10 (MODY10)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Insulin family

  • Target Synonyms

    IDDM; ILPR; IRDN; IDDM1; IDDM2; PNDM4; MODY10; Insulin

  • Target Background

    This gene encodes insulin, a peptide hormone that plays a vital role in the regulation of carbohydrate and lipid metabolism. After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified, including insulin-dependent diabetes mellitus, permanent neonatal diabetes diabetes mellitus, maturity-onset diabetes of the young type 10 and hyperproinsulinemia. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region.

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