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Recombinant Human Protein-glutamine gamma-glutamyltransferase K (TGM1), Truncated

ACP23382

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP23382 Target NameTGM1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Protein LengthPartialPurity>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 IDP22735
Background Information
  • Uniprot Id

    P22735

  • Target Species

    Human

  • Target Name

    TGM1

  • Target Full Name

    Protein-glutamine gamma-glutamyltransferase K

  • Target Function

    Catalyzes the cross-linking of proteins and the conjugation of polyamines to proteins. Responsible for cross-linking epidermal proteins during formation of the stratum corneum. Involved in cell proliferation.

  • Target Involvement

    Ichthyosis, congenital, autosomal recessive 1 (ARCI1)

  • Target Subcellular Location

    Membrane; Lipid-anchor.

  • Target Protein Families

    Transglutaminase superfamily, Transglutaminase family

  • Target Synonyms

    ARCI1; Epidermal TGase; ICR2; KTG; LI; LI1; Protein glutamine gamma glutamyltransferase K; Protein-glutamine gamma-glutamyltransferase K; TG(K); TGase 1; TGASE; TGase K; TGase-1; TGK; TGM1; TGM1_HUMAN; Transglutaminase 1 (K polypeptide epidermal type I; protein glutamine gamma glutamyltransferase); Transglutaminase 1; Transglutaminase K; Transglutaminase; keratinocyte; Transglutaminase-1

  • Target Background

    The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE).

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