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COG7 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant COG7.

     
  • IF - COG7 Antibody (monoclonal) (M01) AT1580a
    Immunofluorescence of monoclonal antibody to COG7 on HeLa cell. [antibody concentration 10 ug/ml]
    detail
  • WB - COG7 Antibody (monoclonal) (M01) AT1580a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (110.44 KDa) .
    detail
  • WB - COG7 Antibody (monoclonal) (M01) AT1580a
    Western Blot analysis of COG7 expression in transfected 293T cell line by COG7 monoclonal antibody (M01), clone 3G4-1B3.

    Lane 1: COG7 transfected lysate(65 KDa).
    Lane 2: Non-transfected lysate.
    detail
  • E - COG7 Antibody (monoclonal) (M01) AT1580a
    Detection limit for recombinant GST tagged COG7 is 0.03 ng/ml as a capture antibody.
    detail
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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, IF, E
Primary Accession P83436
Other Accession BC037563
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG1 kappa
Clone Names 3G4-1B3
Calculated MW 86344 Da
Additional Information
Gene ID 91949
Other Names Conserved oligomeric Golgi complex subunit 7, COG complex subunit 7, Component of oligomeric Golgi complex 7, COG7
Target/Specificity COG7 (AAH37563, 1 a.a. ~ 770 a.a) full-length 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.
PrecautionsCOG7 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

The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.

References

A new mutation in COG7 extends the spectrum of COG subunit deficiencies. Zeevaert R, et al. Eur J Med Genet, 2009 Sep-Oct. PMID 19577670.Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing. Laufman O, et al. EMBO J, 2009 Jul 22. PMID 19536132.A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. Morava E, et al. Eur J Hum Genet, 2007 Jun. PMID 17356545.COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins. Steet R, et al. Mol Biol Cell, 2006 May. PMID 16510524.COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation. Shestakova A, et al. Traffic, 2006 Feb. PMID 16420527.

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$ 350.00
Cat# AT1580a
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Availability: 7-10 days
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