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>   首页   >   产品   >   一抗   >   代谢   >   HGD Antibody (monoclonal) (M10)   

HGD Antibody (monoclonal) (M10)

Mouse monoclonal antibody raised against a partial recombinant HGD.

     
  • 3 - HGD Antibody (monoclonal) (M10) AT2362a
    Immunofluorescence of monoclonal antibody to HGD on HeLa cell . [antibody concentration 10 ug/ml]
  • 10 - HGD Antibody (monoclonal) (M10) AT2362a
    Detection limit for recombinant GST tagged HGD is approximately 0.3ng/ml as a capture antibody.
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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
IF, E
Primary Accession Q93099
Other Accession NM_000187
Reactivity Human
Host mouse
Clonality monoclonal
Isotype IgG2b Kappa
Clone Names 3G4
Calculated MW 49964 Da
Additional Information
Gene ID 3081
Other Names Homogentisate 1, 2-dioxygenase, Homogentisate oxygenase, Homogentisic acid oxidase, Homogentisicase, HGD, HGO
Target/Specificity HGD (NP_000178, 377 a.a. ~ 445 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution IF~~1:50~200
E~~N/A
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsHGD Antibody (monoclonal) (M10) 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 the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.

REFERENCES

Alkaptonuria Introne WJ, et al. , 1993. PMID 20301627.Human variation in alcohol response is influenced by variation in neuronal signaling genes. Joslyn G, et al. Alcohol Clin Exp Res, 2010 May. PMID 20201926.Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria. Vilboux T, et al. Hum Mutat, 2009 Dec. PMID 19862842.R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE. Abdulrazzaq YM, et al. Ann Hum Genet, 2009 Jan. PMID 18945288.Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560.

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