HGD Antibody (SR1835) - BSA Free

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Western Blot: HGD Antibody (SR1835) [NBP3-22463] - Western blot analysis using NBP3-22463 in HepG2 cell lysate.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ICC/IF, IHC
Clone
SR1835
Clonality
Monoclonal
Host
Rabbit
Conjugate
Unconjugated
Format
BSA Free

Order Details

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Catalog# & Formulation Size Price

HGD Antibody (SR1835) - BSA Free Summary

Description
Novus Biologicals Rabbit HGD Antibody (SR1835) - BSA Free (NBP3-22463) is a recombinant monoclonal antibody validated for use in IHC, WB and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
Additional Information
Recombinant Monoclonal Antibody
Immunogen
A synthesized peptide derived from human HGD (Uniprot #: Q93099)
Specificity
Detects endogenous levels of total HGD
Source
HEK293
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Gene
HGD
Purity
Affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 1:50-1:200
  • Immunohistochemistry 1:50-1:200
  • Western Blot 1:500-1:2000
Theoretical MW
48 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS, pH 7.4, 150mM NaCl, 50% glycerol.
Preservative
0.02% Sodium Azide
Purity
Affinity purified

Alternate Names for HGD Antibody (SR1835) - BSA Free

  • 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.

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

WB Video Protocol
ICC/IF Video Protocol

FAQs for HGD Antibody (NBP3-22463) (0)

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol HGD