- Tel: 858.663.9055
Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.
Titration of the RHO antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 310-339 from human Rhodopsin was used as the immunogen for this RHO antibody.
Aliquot the RHO antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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