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Recombinant Human Dipeptidyl aminopeptidase-like protein 6 (DPP6), Truncated

ACP23619

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP23619 Target NameDPP6
Target SynonymsDPP6Dipeptidyl aminopeptidase-like protein 6; DPPX; Dipeptidyl aminopeptidase-related protein; Dipeptidyl peptidase 6; Dipeptidyl peptidase IV-like protein; Dipeptidyl peptidase VI; DPP VIFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>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 IDP42658
Background Information
  • Uniprot Id

    P42658

  • Target Species

    Human

  • Target Name

    DPP6

  • Target Full Name

    A-type potassium channel modulatory protein DPP6

  • Target Function

    Promotes cell surface expression of the potassium channel KCND2. Modulates the activity and gating characteristics of the potassium channel KCND2. Has no dipeptidyl aminopeptidase activity.

  • Target Involvement

    Familial paroxysmal ventricular fibrillation 2 (VF2); Mental retardation, autosomal dominant 33 (MRD33)

  • Target Subcellular Location

    Cell membrane; Single-pass type II membrane protein.

  • Target Protein Families

    Peptidase S9B family

  • Target Tissue Specificity

    Expressed predominantly in brain.

  • Target Synonyms

    DPP6Dipeptidyl aminopeptidase-like protein 6; DPPX; Dipeptidyl aminopeptidase-related protein; Dipeptidyl peptidase 6; Dipeptidyl peptidase IV-like protein; Dipeptidyl peptidase VI; DPP VI

  • Target Background

    This gene encodes a single-pass type II membrane protein that is a member of the peptidase S9B family of serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Variations in this gene may be associated with susceptibility to amyotrophic lateral sclerosis and with idiopathic ventricular fibrillation. Alternative splicing results in multiple transcript variants.

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