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Product Name Rhodopsin/RP4/RHO Chinese Name 视网膜色素变性蛋白4抗体 Alias CSNBAD1; MGC138309; MGC138311; OPN 2; OPN2; opsd; OPSD_HUMAN; Opsin 2; opsin 2; Opsin 2 rod pigment; Opsin-2; Opsin2; Retinitis Pigmentosa 4; Retinitis pigmentosa 4 autosomal dominant; RHO; Rhodopsin; RP 4; RP4. Research Area Cell biology Neurobiology Signal transduction Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Dog, Cow, Rabbit, ) Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 39kDa Cellular localization The cell membrane Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human Rhodopsin/RP4/RHO: 301-348/348 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail 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, Jul 2008]
Function:
Photoreceptor required for image-forming vision at low light intensity. Required for photoreceptor cell viability after birth. Light-induced isomerization of 11-cis to all-trans retinal triggers a conformational change leading to G-protein activation and release of all-trans retinal.
Subcellular Location:
Membrane. Synthesized in the inner segment (IS) of rod photoreceptor cells before vectorial transport to the rod outer segment (OS) photosensory cilia.
Tissue Specificity:
Rod shaped photoreceptor cells which mediates vision in dim light.
Post-translational modifications:
Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region.
DISEASE:
Retinitis pigmentosa 4.
Night blindness, congenital stationary, autosomal dominant 1.
Similarity:
Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.
Contains one covalently linked retinal chromophore.
SWISS:
P08100
Gene ID:
6010
Database links:
Entrez Gene: 6010 Human
Entrez Gene: 212541 Mouse
Omim: 180380 Human
SwissProt: P28681 Chinese Hamster
SwissProt: P08100 Human
SwissProt: P15409 Mouse
SwissProt: P49912 Rabbit
Unigene: 247565 Human
Unigene: 2965 Mouse
Unigene: 406156 Mouse
Unigene: 92530 Rat
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