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Peroxisomal Biogenesis Factor 19 (PEX19) (C-Term) Peptide

PEX19 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN5673442

Quick Overview for Peroxisomal Biogenesis Factor 19 (PEX19) (C-Term) Peptide (ABIN5673442)

Target

PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Origin

Human

Source

  • 4
Synthetic

Application

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

    C-Term

    Sequence

    RFEMVLDLMQ QLQDLGHPPK ELAGEMPPGL NFDLDALNLS GPPGASGEQC

    Characteristics

    This is a synthetic peptide designed for use in combination with anti- PEX19 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.
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Storage

    -20 °C

    Storage Comment

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

    PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

    Background

    This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). 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. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.

    Alias Symbols: PXF, HK33, PMP1, PMPI, PXMP1, PBD12A, D1S2223E

    Protein Size: 261

    Gene ID

    5824

    NCBI Accession

    NM_001193644, NP_001180573
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