PEX12 polyclonal antibody

Catalog # PAB18576

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Price

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Quantity

Size:100 ug
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of PEX12.

    Immunogen

    A synthetic peptide corresponding to amino acids at C-terminus of human PEX12.

    Sequence

    RSHQACPITGYP

    Host

    Goat

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:8000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — PEX12

    Entrez GeneID

    5193

    Protein Accession#

    NP_000277.1

    Gene Name

    PEX12

    Gene Alias

    PAF-3

    Gene Description

    peroxisomal biogenesis factor 12

    Omim ID

    601758

    Gene Ontology

    Hyperlink

    Gene Summary

    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). [provided by RefSeq

    Other Designations

    peroxin 12|peroxisome assembly factor 3|peroxisome assembly protein 12

  • Interactome
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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