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Cone-rod Dystrophy And Amelogenesis Imperfecta: Disease Bioinformatics

Research of Cone-rod Dystrophy And Amelogenesis Imperfecta has been linked to Dystrophy, Retinitis Pigmentosa, Amelogenesis Imperfecta, Hypertrichosis, Retinal Dystrophies. The study of Cone-rod Dystrophy And Amelogenesis Imperfecta has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Cone-rod Dystrophy And Amelogenesis Imperfecta include Amelogenesis, Transport, Ion Transport, Metal Ion Transport, Ion Homeostasis. These pathways complement our catalog of research reagents for the study of Cone-rod Dystrophy And Amelogenesis Imperfecta including antibodies and ELISA kits against NEUROFIBROMATOSIS TYPE 1, RETINAL DYSTROPHY, CBS, NF1, CNNM4.

Cone-rod Dystrophy And Amelogenesis Imperfecta 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 Cone-rod Dystrophy And Amelogenesis Imperfecta 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 83 products for the study of Cone-rod Dystrophy And Amelogenesis Imperfecta that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-89280
Immunocytochemistry/Immunofluorescence: CNNM4 Antibody [NBP1-89280] - Staining of human cell line U-2 OS shows positivity in cytoskeleton (actin filaments).Immunohistochemistry-Paraffin: CNNM4 Antibody [NBP1-89280] - Staining of human appendix shows cytoplasmic and membranous positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications ICC/IF, IHC, IHC-P

1 Publication
NB300-155
Western Blot: Neurofibromin 1 Antibody [NB300-155] - Western Blot of (A, B, C above).Immunohistochemistry: Neurofibromin 1 Antibody [NB300-155] - NF1 protein labeling displays positive signal in the maturing and the hypertrophic cartilages but only faint labeling in the proliferative cartilage.

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

4 Publications
NBP2-57086
Western Blot: CNNM2 Antibody [NBP2-57086] - Western blot analysis in human cell line RT-4.Immunocytochemistry/Immunofluorescence: CNNM2 Antibody [NBP2-57086] - Staining of human cell line HEK 293 shows localization to vesicles.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF

NBP1-89281
Immunohistochemistry-Paraffin: CNNM1 Antibody [NBP1-89281] - Staining of human testis shows moderate cytoplasmic positivity in cells in seminiferus ducts and strong positivity in Leydig cells.

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

H00000875-M01
Western Blot: CBS Antibody (3E1) [H00000875-M01] - CBS monoclonal antibody (M01), clone 3E1. Analysis of CBS expression in MCF-7.Immunohistochemistry-Paraffin: CBS Antibody (3E1) [H00000875-M01] - Analysis of monoclonal antibody to CBS on formalin-fixed paraffin-embedded human hepatocellular carcinoma. Antibody concentration 3 ug/ml.

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

     1 Review

44 Publications

Related Genes

Cone-rod Dystrophy And Amelogenesis Imperfecta has been researched against:

Related Pathways

Cone-rod Dystrophy And Amelogenesis Imperfecta has been linked to:

Alternate Names

Cone-rod Dystrophy And Amelogenesis Imperfecta is also known as Cone-rod Congenital Amaurosis Associated With Congenital Hypertrichosis, Jalili Syndrome.