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Congenital Eustachian Tube Anomaly: Disease Bioinformatics

Research of Congenital Eustachian Tube Anomaly has been linked to Otitis Media, Crest Syndrome, Congenital Heart Defects, Ear Inflammation, Cicatrix. The study of Congenital Eustachian Tube Anomaly has been mentioned in research publications which can be found using our bioinformatics tool below. Congenital Eustachian Tube Anomaly has been researched in relation to the Transposition Pathway. This pathway complements our catalog of research reagents for the study of Congenital Eustachian Tube Anomaly including antibodies and ELISA kits against SS18L1.

Congenital Eustachian Tube Anomaly 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 Congenital Eustachian Tube Anomaly 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 4 products for the study of Congenital Eustachian Tube Anomaly that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP2-20486
Western Blot: SS18L1 Antibody [NBP2-20486] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 10% SDS PAGE gel, diluted at 1:1000.Immunocytochemistry/Immunofluorescence: SS18L1 Antibody [NBP2-20486] - Immunofluorescence analysis of paraformaldehyde-fixed A431, using antibody at 1:500 dilution.

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


Related Genes

Congenital Eustachian Tube Anomaly has been researched against:

Related Pathways

Congenital Eustachian Tube Anomaly has been linked to:

Related PTMs

Alternate Names

Congenital Eustachian Tube Anomaly is also known as Eustachian Tube Anomalies.