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Glucosidase, Beta, Acid (GBA) (C-Term) Peptid

GBA Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN977306
  • Target Alle GBA Produkte
    GBA (Glucosidase, Beta, Acid (GBA))
    Protein Region
    C-Term
    Spezies
    Human
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    EGSQRVGLVA SQKNDLDAVA LMHPDGSAVV VVLNRSSKDV PLTIKDPAVG
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-GBA Antibody. 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
    GBA (Glucosidase, Beta, Acid (GBA))
    Synonyme
    GBA1 Peptide, GCB Peptide, GLUC Peptide, BETA-GLUCOSIDASE Peptide, T12J13.8 Peptide, T12J13_8 Peptide, beta glucosidase 25 Peptide, PSPTO3318 Peptide, PSPTO4290 Peptide, GC Peptide, GCase Peptide, betaGC Peptide, glucosylceramidase beta Peptide, beta glucosidase 25 Peptide, beta-glucosidase Peptide, Beta-glucosidase Peptide, glucosidase, beta, acid Peptide, glucosylceramidase Peptide, bglX-2 Peptide, GBA Peptide, BGLU25 Peptide, PSPTO_3318 Peptide, bglX Peptide, bglA4 Peptide, Gba Peptide, LOC100399524 Peptide, bglA.2 Peptide, bglX-2 Peptide
    Hintergrund
    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.

    Alias Symbols: GBA1, GCB, GLUC

    Protein Size: 536
    Molekulargewicht
    59 kDa
    Gen-ID
    2629
    NCBI Accession
    NM_000157, NP_000148
    UniProt
    P04062
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