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Congenital Foix-chavany-marie Syndrome: Disease Bioinformatics

Research of Congenital Foix-chavany-marie Syndrome has been linked to Facial Paralysis, Diplegia, Deglutition Disorders, Anarthria Speech Disorder, Brain Ischemia. The study of Congenital Foix-chavany-marie Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Congenital Foix-chavany-marie Syndrome has been researched in relation to the Reflex Pathway. This pathway complements our catalog of research reagents for the study of Congenital Foix-chavany-marie Syndrome including antibodies and ELISA kits against CSF2, LAMC2, MID1.

Congenital Foix-chavany-marie Syndrome 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 Foix-chavany-marie Syndrome 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 180 products for the study of Congenital Foix-chavany-marie Syndrome that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-67769
Western Blot: MID1 Antibody [NBP1-67769] - Analysis of extracts from 293 cells, using. The lane on the right is treated with the synthesized peptide.Immunocytochemistry/Immunofluorescence: MID1 Antibody [NBP1-67769] - Analysis of HeLa cells, using. The picture on the right is treated with the synthesized peptide.

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

NBP2-42388
Western Blot: LAMC2 Antibody (CL2980) [NBP2-42388] - Lane 1: Marker [kDa] 460, 268, 238, 171, 117, 71, 55, 41, 31  Lane 2: Human cell line A-431Immunohistochemistry: LAMC2 Antibody (CL2980) [NBP2-42388] - Staining of human lymph node shows absence of immunoreactivity in lymphoid tissue (negative control).

Mouse Monoclonal
Species Human
Applications WB, IHC, IHC-P


Related Genes

Congenital Foix-chavany-marie Syndrome has been researched against:

Related Pathways

Congenital Foix-chavany-marie Syndrome has been linked to:

Related PTMs

Alternate Names

Congenital Foix-chavany-marie Syndrome is also known as Foix Chavany Marie Syndrome.