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Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptid

PEX12 Reaktivität: Human Wirt: Synthetic WB
Produktnummer ABIN5518157
  • Target Alle PEX12 Produkte
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 3
    Synthetic
    Applikation
    Western Blotting (WB)
    Sequenz
    SIMFLVLLPY LKVKLEKLVS SLREEDEYSI HPPSSRWKRF YRAFLAAYPF
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
    Hintergrund
    This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS).

    Alias Symbols: PAF-3, PBD3A

    Protein Size: 167
    Gen-ID
    5193
    NCBI Accession
    NM_000286, NP_000277
    UniProt
    O00623
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