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Persistent Hyperlysinemia: Disease Bioinformatics

Research of Persistent Hyperlysinemia has been linked to Hyperlysinemias, Cystinuria, Muscle Hypertonia, Convulsions, Lysinuric Protein Intolerance. The study of Persistent Hyperlysinemia has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Persistent Hyperlysinemia include Transport, Urea Cycle, Lysine Transport. These pathways complement our catalog of research reagents for the study of Persistent Hyperlysinemia including antibodies and ELISA kits against L2HGDH.

Top Research Reagents

We have 8 products for the study of Persistent Hyperlysinemia that can be applied to Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

NBP3-04540
Western Blot: L2HGDH Antibody [NBP3-04540] - Western blot analysis of extracts of Mouse heart, using L2HGDH Rabbit pAb (NBP3-04540) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.ICC/IF-L2HGDH Antibody [NBP3-04540] - Analysis of U2OS cells using L2HGDH antibody at dilution of 1:100. Blue: DAPI for nuclear staining.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, ICC/IF


Related Genes

Persistent Hyperlysinemia has been researched against:

Related Pathways

Persistent Hyperlysinemia has been linked to:

Related Diseases

Persistent Hyperlysinemia has been studied in relation to diseases such as:

Alternate Names

Persistent Hyperlysinemia is also known as Persistent Hyperlysinaemia.