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Hyperimidodipeptiduria: Disease Bioinformatics

Research of Hyperimidodipeptiduria has been linked to Deficiency Of Prolidase, Ulcer, Skin Ulcer, Infective Disorder, Proteinuria Of Undiagnosed Cause. The study of Hyperimidodipeptiduria has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hyperimidodipeptiduria include Transport, Cell Growth, Pathogenesis, Excretion. These pathways complement our catalog of research reagents for the study of Hyperimidodipeptiduria including antibodies and ELISA kits against ELN, PEPD.

Hyperimidodipeptiduria 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 Hyperimidodipeptiduria 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 27 products for the study of Hyperimidodipeptiduria that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: PEPD Antibody (1D5-H3) [H00005184-M01] - PEPD monoclonal antibody (M01), clone 1D5-H3 Analysis of PEPD expression in HepG2.Immunocytochemistry/Immunofluorescence: PEPD Antibody (1D5-H3) [H00005184-M01] - Analysis of monoclonal antibody to PEPD on HepG2 cell. Antibody concentration 10 ug/ml.

Mouse Monoclonal
Species Human
Applications WB, ELISA, ICC/IF

Immunohistochemistry: Elastin Antibody [NBP1-80710] - Staining of human skin shows distinct positivity in extracellular fibers.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

2 Publications

Related Genes

Hyperimidodipeptiduria has been researched against:

Related Pathways

Hyperimidodipeptiduria has been linked to:

Related PTMs

Hyperimidodipeptiduria has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Hyperimidodipeptiduria is also known as Iminodipeptiduria.