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Congenital Muscular Hypertrophy-cerebral Syndrome: Disease Bioinformatics

Research of Congenital Muscular Hypertrophy-cerebral Syndrome has been linked to Cornelia De Lange Syndrome, Genetic Diseases, X-linked, Developmental Disabilities, Growth Retardation, Congenital Anomaly Of Face. The study of Congenital Muscular Hypertrophy-cerebral Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Congenital Muscular Hypertrophy-cerebral Syndrome including antibodies and ELISA kits against SMC1A, NIPBL, SMC3.

Congenital Muscular Hypertrophy-cerebral 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 Muscular Hypertrophy-cerebral 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 63 products for the study of Congenital Muscular Hypertrophy-cerebral Syndrome that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NB100-204
Immunohistochemistry-Paraffin: SMC1 Antibody [NB100-204] - FFPE section of mouse colon carcinoma CT26. Antibody: Affinity purified rabbit anti-SMC1 used at a dilution of 1:5,000 (0.2ug/ml). Detection: DABImmunohistochemistry-Paraffin: SMC1 Antibody [NB100-204] -  FFPE section of human ovarian carcinoma. Antibody: Affinity purified rabbit anti-SMC1 used at a dilution of 1:5,000 (0.2ug/ml). Detection: DAB

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Simple Western, ELISA

33 Publications
H00025836-M01
Western Blot: NIPBL Antibody (3B9) [H00025836-M01] - Detection against Immunogen (37.73 KDa).Immunocytochemistry/Immunofluorescence: NIPBL Antibody (3B9) [H00025836-M01] - Analysis of monoclonal antibody to NIPBL on HeLa cell. Antibody concentration 10 ug/ml.

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

NB100-207
Western Blot: SMC3 Antibody [NB100-207] - Whole cell lysate (10 ug) from HEK293T, HeLa, Jurkat, LNCaP, U2OS, A-549, TCMK-1, and NIH 3T3 cells prepared using NETN lysis buffer. Antibody: Affinitypurified rabbit anti-SMC3 antibody  used for WB at 0.04 ug/ml. Detection:Chemiluminescence with an exposure time of 3 seconds.Immunohistochemistry-Paraffin: SMC3 Antibody [NB100-207] -  Section of mouse renal cell carcinoma. Antibody: Affinity purified rabbit anti-SMC3  used at 1:5,000 (0.2ug/ml). Detection: DAB

Rabbit Polyclonal
Species Human, Mouse, C. elegans
Applications WB, IHC, IHC-P

8 Publications

Related Genes

Congenital Muscular Hypertrophy-cerebral Syndrome has been researched against:

Related Diseases

Congenital Muscular Hypertrophy-cerebral Syndrome has been studied in relation to diseases such as:

Alternate Names

Congenital Muscular Hypertrophy-cerebral Syndrome is also known as X-linked Cornelia De Lange Syndrome.