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PMP22 Antibody

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

  • WB - PMP22 Antibody AP16083a
    PMP22 Antibody (Cat. #AP16083a) western blot analysis in human normal Uterus tissue lysates (35ug/lane).This demonstrates the PMP22 antibody detected the PMP22 protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q01453
Other Accession NP_696996.1, NP_000295.1, NP_696997.1
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 17891 Da
Antigen Region 102-130 aa
Additional Information
Gene ID 5376
Other Names Peripheral myelin protein 22, PMP-22, Growth arrest-specific protein 3, GAS-3, PMP22, GAS3
Target/Specificity This PMP22 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 102-130 amino acids from human PMP22.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsPMP22 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name PMP22
Synonyms GAS3
Function Might be involved in growth regulation, and in myelinization in the peripheral nervous system.
Cellular Location Cell membrane; Multi-pass membrane protein
Research Areas
Citations (0)

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This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies.


Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010) Kohl, B., et al. Am. J. Pathol. 176(3):1390-1399(2010) Kabzinska, D., et al. J. Appl. Genet. 51(2):203-209(2010) Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009) Stangler Herodez, S., et al. J. Int. Med. Res. 37(5):1626-1631(2009)

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$ 295.00
$ 99.00
Cat# AP16083a
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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