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Hydroxykynureninuria: Disease Bioinformatics

Research of Hydroxykynureninuria has been linked to Inborn Errors Of Metabolism, Pellagra, Metabolic Diseases, Kidney Calculi, Tyrosine Transaminase Deficiency Disease. The study of Hydroxykynureninuria has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hydroxykynureninuria include Excretion, Glycolysis. These pathways complement our catalog of research reagents for the study of Hydroxykynureninuria including antibodies and ELISA kits against KYNU.

Hydroxykynureninuria Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hydroxykynureninuria below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 19 products for the study of Hydroxykynureninuria that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Immunohistochemistry-Paraffin: Kynureninase Antibody (1H1) [NBP2-45579] - staining of paraffin-embedded Human lymphoma tissue using anti-KYNU mouse monoclonal antibody. ; heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)Immunohistochemistry: Kynureninase Antibody (1H1) [NBP2-45579] - Analysis of Adenocarcinoma of Human breast tissue.

Mouse Monoclonal
Species Human
Applications IHC, IHC-P

Related Genes

Hydroxykynureninuria has been researched against:

Related Pathways

Hydroxykynureninuria has been linked to:

Related PTMs

Alternate Names

Hydroxykynureninuria is also known as hydroxykynureninuria, kynureninase deficiency, xanthurenic aciduria.