RHO polyclonal antibody
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More Files
- More Functions
Immunocytochemistry
Immunocytochemistry (ICC) staining of HEK293 human embryonic kidney cells transfected (A) or untransfected (B) with RHO. Using RHO polyclonal antibody (Cat # PAB26439).
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of RHO.
Immunogen
A synthetic peptide corresponding to 19 amino acids at 2nd extracellular domain of human RHO.
Host
Rabbit
Reactivity
Human, Monkey, Mouse, Pig, Rabbit, Rat
Specificity
BLAST analysis of the peptide immunogen showed no homology with other human proteins.
Form
Liquid
Purification
Immunoaffinity chromatography
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1-3 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -80°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunocytochemistry
Immunocytochemistry (ICC) staining of HEK293 human embryonic kidney cells transfected (A) or untransfected (B) with RHO. Using RHO polyclonal antibody (Cat # PAB26439). -
Gene Info — RHO
Entrez GeneID
6010Protein Accession#
P08100Gene Name
RHO
Gene Alias
CSNBAD1, MGC138309, MGC138311, OPN2, RP4
Gene Description
rhodopsin
Omim ID
180380Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
opsin 2, rod pigment|retinitis pigmentosa 4, autosomal dominant|rhodopsin (opsin 2, rod pigment) (retinitis pigmentosa 4, autosomal dominant)
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Interactome
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Disease
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