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Purine Nucleoside Phosphorylase (PNP) (Middle Region) Peptide

PNP Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN980823

Aperçu rapide pour Purine Nucleoside Phosphorylase (PNP) (Middle Region) Peptide (ABIN980823)

Antigène

PNP (Purine Nucleoside Phosphorylase (PNP))

Origine

Humain

Source

  • 2
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-NP antibody (Catalog #: ARP48474_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    PNP (Purine Nucleoside Phosphorylase (PNP))

    Classe de substances

    Viral Protein

    Sujet

    Defects in NP are the cause of nucleoside phosphorylase deficiency (NP deficiency). It leads to a severe T-cell immunodeficiency with neurologic disorder in children. The specific function of NP is not yet known.This gene encodes an enzyme which reversibly catalyzes the phosphorolysis of purine nucleosides. The enzyme is trimeric, containing three identical subunits. Mutations which result in nucleoside phosphorylase deficiency result in defective T-cell (cell-mediated) immunity but can also affect B-cell immunity and antibody responses. Neurologic disorders may also be apparent in patients with immune defects. A known polymorphism at aa position 51 that does not affect enzyme activity has been described. A pseudogene has been identified on chromosome 2. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: MGC117396, MGC125915, MGC125916, PNP, PRO1837, PUNP, NP

    Protein Interaction Partner: APLP1,C1orf103,C7orf64,CCDC90B,NCALD,TFAM,TFB2M,TP53,ZHX1,APLP1,C1orf103,C7orf64,CCDC90B,TP53,ZHX1

    Protein Size: 289

    Poids moléculaire

    32 kDa

    ID gène

    4860

    NCBI Accession

    NM_000270, NP_000261

    UniProt

    P00491
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