Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) Peptid

GRHPR Reaktivität: Human Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN977671

Kurzübersicht für Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) Peptid (ABIN977671)

Target

GRHPR (Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR))

Spezies

Human

Quelle

  • 3
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-GRHPR antibody (Catalog #: ARP48317_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.

    Aufreinigung

    Purified
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    GRHPR (Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR))

    Hintergrund

    GRHPR is an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene.This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. 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: GLXR, PH2, GLYD

    Protein Interaction Partner: LSM1,LSM1

    Protein Size: 328

    Molekulargewicht

    36 kDa

    Gen-ID

    9380

    NCBI Accession

    NM_012203, NP_036335

    UniProt

    Q9UBQ7
Sie sind hier:
Chat with us!