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Rhodopsin Polyclonal Antibody

Product Specifications

Background

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.

CAS Number

9007-83-4

Synonyms

RHO; OPN2; Rhodopsin; Opsin-2

Host

Rabbit

Reactivity

Human;Mouse;Rat

Immunogen

Synthesized peptide derived from the Internal region of human Rhodopsin.

Clonality

Polyclonal

Applications

WB, ELISA

Stability

-20°C for one year

Concentration

1 mg/ml

Molecular Weight

39028

Antibody Type

Primary antibody

Isotype

IgG

Available Sizes

Frequently Asked Questions

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