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>   首页   >   产品   >   一抗   >   信号转导   >   COG7 Antibody (C-term)   

COG7 Antibody (C-term)

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - COG7 Antibody (C-term) AP18478b
    COG7 Antibody (C-term) (Cat. #AP18478b) western blot analysis in mouse lung tissue lysates (35ug/lane).This demonstrates the COG7 antibody detected the COG7 protein (arrow).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, E
Primary Accession P83436
Other Accession NP_705831.1
Reactivity Human, Mouse
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 86344 Da
Antigen Region 725-753 aa
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 This COG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 725-753 amino acids from the C-terminal region of human COG7.
Dilution WB~~1:1000
E~~Use at an assay dependent concentration.
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.
PrecautionsCOG7 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name COG7
Function Required for normal Golgi function.
Cellular Location Golgi apparatus membrane; Peripheral membrane protein
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

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

Zeevaert, R., et al. Eur J Med Genet 52(5):303-305(2009)
Laufman, O., et al. EMBO J. 28(14):2006-2017(2009)
Morava, E., et al. Eur. J. Hum. Genet. 15(6):638-645(2007)
Steet, R., et al. Mol. Biol. Cell 17(5):2312-2321(2006)
Shestakova, A., et al. Traffic 7(2):191-204(2006)

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