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Usher Syndrome, Type 1a: Disease Bioinformatics

Research of Usher Syndrome, Type 1a has been linked to Usher Syndrome, Complete Hearing Loss, Retinal Degeneration, Deafness Congenital, Retinitis Pigmentosa. The study of Usher Syndrome, Type 1a has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Usher Syndrome, Type 1a include Cellular Localization, Localization. These pathways complement our catalog of research reagents for the study of Usher Syndrome, Type 1a including antibodies and ELISA kits against DFNB31, GPR98, USH2A, RHO, GRK1.

Usher Syndrome, Type 1a 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 Usher Syndrome, Type 1a 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 155 products for the study of Usher Syndrome, Type 1a that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

H00025861-Q01
12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human

NLS1729
Immunohistochemistry-Paraffin: GPR98 Antibody [NLS1729] - Anti-GPR98 / VLGR1 antibody IHC of human Skin, Melanoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.Immunohistochemistry-Paraffin: GPR98 Antibody [NLS1729] - Analysis of anti-GPR98 / VLGR1 antibody with human kidney, renal tubules.

Rabbit Polyclonal
Species Human, Equine
Applications WB, IHC, IHC-P

NBP1-47602
Western Blot: Rhodopsin Antibody (1D4) [NBP1-47602] - Analysis of Human Cell lysates showing detection of Rhodopsin protein using Mouse Anti-Rhodopsin Monoclonal Antibody, Clone 1D4. Load: 15 ug protein. Block: 1.5% BSA for 30 minutes at RT. Primary Antibody: Mouse Anti-Rhodopsin Monoclonal Antibody at 1:1000 for 2 hours at RT. Secondary Antibody: Sheep Anti-Mouse IgG: HRP for 1 hour at RT.Immunocytochemistry/Immunofluorescence: Rhodopsin Antibody (1D4) [NBP1-47602] - Analysis using Mouse Anti-Rhodopsin Monoclonal Antibody, Clone 1D4. Tissue: backskin. Species: Mouse. Fixation: Bouins Fixative and paraffin-embedded. Primary Antibody: Mouse Anti-Rhodopsin Monoclonal Antibody at 1:100 for 1 hour at RT. Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:50 for 1 hour at RT. Localization: Dull epidermal staining.

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

2 Publications
NB120-2776
Immunocytochemistry/Immunofluorescence: GRK1 Antibody (D11) [NB120-2776] - Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes at room temperature and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a Rhodopsin Kinase 1a/b Monclonal Antibody (D11) at a dilution of 1:200 and incubated overnight in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody for 45 minutes at room temperature in the dark. F-actin (red) was stained with a fluorescent phalloidin and nuclei (blue) were stained with DAPI.Immunocytochemistry/Immunofluorescence: GRK1 Antibody (D11) [NB120-2776] - Immunolocalization of GRK1a/b in bovine retina

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


Related Genes

Usher Syndrome, Type 1a has been researched against:

Related Pathways

Usher Syndrome, Type 1a has been linked to:

Related Diseases

Usher Syndrome, Type 1a has been studied in relation to diseases such as:

Alternate Names

Usher Syndrome, Type 1a is also known as Retinitis Pigmentosa And Congenital Deafness.