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Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive: Disease Bioinformatics

Emery-dreifuss autosomal recessive muscular dystrophy is a rare syndrome that primarily affects cardiac muscles and muscles used for movement. Symptoms of Emery-dreifuss autosomal recessive muscular dystrophy such as restriction of movement of certain joints such as the elbows, ankles, and neck and muscle wasting in the upper arms and lower legs appear in early childhood and worsen over time. By adulthood, most individuals with the disorder have heart problems such as cardiac conduction defects and arrhythmias. Emery-dreifuss autosomal recessive muscular dystrophy is caused by mutations in the LMNA gene and is inherited in an autosomal recessive manner. There is no cure for Emery-dreifuss autosomal recessive muscular dystrophy.

Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive 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 Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 223 products for the study of Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NB100-56649
Western Blot: Lamin A + C Antibody [NB100-56649] - Analysis of human Lamin A + C in 15 ug of HeLa cell lysate using NB100-56649 at 1:1000.Immunocytochemistry/Immunofluorescence: Lamin A + C Antibody [NB100-56649] - Lamin A/C antibody was tested in A431 cells at 1:100 against DyLight 488 (Green). Alpha tubulin and nuclei were counterstained against DyLight 568 (Red) and DAPI (Blue).

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, Flow-IC

5 Publications
NBP2-59783
Western Blot: Lamin B1 Antibody (CL3929) [NBP2-59783] - Analysis in human cell line MCF-7.Immunocytochemistry/Immunofluorescence: Lamin B1 Antibody (CL3929) [NBP2-59783] - Staining of A-431 cells showing specific staining of nuclear membrane in green. Microtubule and nuclear probes are visualized in red and blue, respectively (where available). Antibody staining is shown in green.

Mouse Monoclonal
Species Human
Applications WB, ICC/IF, IHC

2 Publications

Related Genes

Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive has been researched against:

Alternate Names

Muscular Dystrophy, Emery-dreifuss, Autosomal Recessive is also known as Autosomal Recessive Emery-dreifuss Muscular Dystrophy.