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Congenital Muscular Dystrophy (disorder): Disease Bioinformatics

Research of Congenital Muscular Dystrophy (disorder) has been linked to Dystrophy, Muscular Dystrophy, Coronary Microvascular Disease, Fukuyama Type Congenital Muscular Dystrophy, Myopathy. The study of Congenital Muscular Dystrophy (disorder) has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Muscular Dystrophy (disorder) include Glycosylation, Pathogenesis, Localization, Regeneration, Myelination. These pathways complement our catalog of research reagents for the study of Congenital Muscular Dystrophy (disorder) including antibodies and ELISA kits against MEROSIN, ALPHA-DYSTROGLYCAN, DY, GLYCOSYLTRANSFERASE, BETA-DYSTROGLYCAN.

Top Research Reagents

We have 795 products for the study of Congenital Muscular Dystrophy (disorder) that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

FKTN Antibody (7J5N6)

NBP3-15472

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

Laminin alpha 2 Antibody (2D4)

H00003908-M01

Mouse Monoclonal
Species Human
Applications WB, ELISA, IHC

7 Publications

Collagen VI alpha 1 Antibody

NB120-6588

$Western Blot: Collagen VI alpha 1 Antibody [NB120-6588] - Purification and imaging of collagen VI microfibrils from bovine cornea. Reducing SDS-PAGE (left hand panel) and western blot (right hand panel) of the central fraction of the void peak. Collagen VI chains were detected using a polyclonal rabbit anti collagen VI antibody. Arrows highlight bands at approximately 250 kDa, which corresponds to the alpha3 chain, and at 120 kDa which corresponds to alpha1 and alpha2 chains. Image collected and cropped by CiteAb from the following publication (www.linkinghub.elsevier.com/retrieve/pii/S1742706116306912) licensed under a CC-BY license.$