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CDSN Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a partial recombinant CDSN.

     
  • WB - CDSN Antibody (monoclonal) (M01) AT1486a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (31.24 KDa) .
    detail
  • E - CDSN Antibody (monoclonal) (M01) AT1486a
    Detection limit for recombinant GST tagged CDSN is approximately 0.03ng/ml as a capture antibody.
    detail
  • SPECIFICATION
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Product Information
Application
  • 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
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, E
Primary Accession Q15517
Other Accession NM_001264
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG2a Kappa
Clone Names 6F11
Calculated MW 51607 Da
Additional Information
Gene ID 1041
Other Names Corneodesmosin, S protein, CDSN
Target/Specificity CDSN (NP_001255, 306 a.a. ~ 355 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsCDSN Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)
citation

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Background

This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. During maturation of the cornified layers, the protein undergoes a series of cleavages, which are thought to be required for desquamation. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6.

References

Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease. Oji V, et al. Am J Hum Genet, 2010 Aug 13. PMID 20691404.A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin. Caubet C, et al. FASEB J, 2010 Sep. PMID 20448140.Common genetic variation and the control of HIV-1 in humans. Fellay J, et al. PLoS Genet, 2009 Dec. PMID 20041166.High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. Barcellos LF, et al. PLoS Genet, 2009 Oct. PMID 19851445.Fine mapping of the psoriasis susceptibility locus PSORS1 supports HLA-C as the susceptibility gene in the Han Chinese population. Fan X, et al. PLoS Genet, 2008 Mar 21. PMID 18369457.

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$ 350.00
Cat# AT1486a
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Availability: 7-10 days
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