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Trisomy 17q22: Disease Bioinformatics

Research of Trisomy 17q22 has been linked to Trisomy, Hydrops Fetalis, Monosomy, Arthrogryposis, Developmental Delay (disorder). The study of Trisomy 17q22 has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Trisomy 17q22 including antibodies and ELISA kits against MB.

Trisomy 17q22 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 Trisomy 17q22 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 112 products for the study of Trisomy 17q22 that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: Myoglobin Antibody (5A2G8) [NB110-89456] - Analysis using Myoglobin mouse mAb against truncated Myoglobin recombinant protein(AA: 2-154).Immunohistochemistry-Paraffin: Myoglobin Antibody (5A2G8) [NB110-89456] - Analysis of paraffin-embedded human skeletal muscle tissue showing cytoplasmic localization using anti-Myoglobin antibody with DAB staining.

Mouse Monoclonal
Species Human
Applications WB, ELISA, IHC

Related Genes

Trisomy 17q22 has been researched against:

Related Pathways

Related PTMs

Alternate Names

Trisomy 17q22 is also known as Duplication 17q.