HGD Antibody (2C10)

Images

 
Immunocytochemistry/ Immunofluorescence: HGD Antibody (2C10) [H00003081-M09] - Analysis of monoclonal antibody to HGD on HeLa cell. Antibody concentration 10 ug/ml
Immunoprecipitation: HGD Antibody (2C10) [H00003081-M09] - Analysis of HGD transfected lysate using anti-HGD monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with HGD rabbit polyclonal antibody.
Sandwich ELISA: HGD Antibody (2C10) [H00003081-M09] - Detection limit for recombinant GST tagged HGD is 1 ng/ml as a capture antibody.

Product Details

Summary
Product Discontinued
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Order Details


    • Catalog Number
      H00003081-M09
    • Availability
      Product Discontinued

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HGD Antibody (2C10) Summary

Description
Quality control test: Antibody Reactive Against Recombinant Protein.
Immunogen
HGD (NP_000178, 377 a.a. ~ 445 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. CFEKASKVKLAPERIADGTMAFMFESSLSLAVTKWGLKASRCLDENYHKCWEPLKSHFTPNSRNPAEPN
Specificity
HGD - homogentisate 1,2-dioxygenase (homogentisate oxidase) (2C10)
Isotype
IgG2b Kappa
Clonality
Monoclonal
Host
Mouse
Gene
HGD
Purity
IgG purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • ELISA
  • Immunocytochemistry/ Immunofluorescence
  • Immunoprecipitation
  • Sandwich ELISA
Application Notes
It has been used for ELISA.

Packaging, Storage & Formulations

Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
In 1x PBS, pH 7.4
Preservative
No Preservative
Purity
IgG purified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for HGD Antibody (2C10)

  • AKU
  • EC 1.13.11.5
  • HGOFLJ94126
  • homogentisate 1,2-dioxygenase (homogentisate oxidase)
  • homogentisate 1,2-dioxygenase
  • homogentisate oxidase
  • Homogentisate oxygenase
  • Homogentisic acid oxidase
  • homogentisicase

Background

Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

ICC/IF Video Protocol

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Bioinformatics

Gene Symbol HGD
Entrez
Uniprot