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>   首页   >   产品   >   一抗   >   癌症   >   GYG1 Antibody (monoclonal) (M08)   

GYG1 Antibody (monoclonal) (M08)

Mouse monoclonal antibody raised against a partial recombinant GYG1.

     
  • 1 - GYG1 Antibody (monoclonal) (M08) AT2303a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (33.77 KDa) .
  • 1 - GYG1 Antibody (monoclonal) (M08) AT2303a
    GYG1 monoclonal antibody (M08), clone 2C10. Western Blot analysis of GYG1 expression in PC-12 ( (Cat # AT2303a )
  • 1 - GYG1 Antibody (monoclonal) (M08) AT2303a
    GYG1 monoclonal antibody (M08), clone 2C10. Western Blot analysis of GYG1 expression in HepG2 ( (Cat # AT2303a )
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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
Primary Accession P46976
Other Accession NM_004130
Reactivity Human, Rat
Host mouse
Clonality monoclonal
Isotype IgG1 Kappa
Clone Names 2C10
Calculated MW 39384 Da
Additional Information
Gene ID 2992
Other Names Glycogenin-1, GN-1, GN1, GYG1, GYG
Target/Specificity GYG1 (NP_004121, 1 a.a. ~ 73 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.
PrecautionsGYG1 Antibody (monoclonal) (M08) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas

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

BACKGROUND

This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.

REFERENCES

Glycogenin-1 deficiency and inactivated priming of glycogen synthesis. Moslemi AR, et al. N Engl J Med, 2010 Apr 1. PMID 20357282.Glycogenin protein and mRNA expression in response to changing glycogen concentration in exercise and recovery. Wilson RJ, et al. Am J Physiol Endocrinol Metab, 2007 Jun. PMID 17311895.Interaction between glycogenin and glycogen synthase. Skurat AV, et al. Arch Biochem Biophys, 2006 Dec 1. PMID 17055998.Towards a proteome-scale map of the human protein-protein interaction network. Rual JF, et al. Nature, 2005 Oct 20. PMID 16189514.Increases in glycogenin and glycogenin mRNA accompany glycogen resynthesis in human skeletal muscle. Shearer J, et al. Am J Physiol Endocrinol Metab, 2005 Sep. PMID 15870102.

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