EnCor Biotechnology

Mouse Monoclonal Antibody to Rhodopsin Cat# MCA-A531

$250.00
Description

      The MCA-A531 antibody was made against purified rhodopsin isolated from bovine retina (5). The epitope resides in the N-terminal 32 amino acids of rhodopsin (5). We document that the antibody works well for western blotting and for IF, ICC and IHC (for IHC see data under "Additional Info" tab). Another monoclonal antibody to rhodopsin developed in the same way and with an epitope mapped to the same region is MCA-B630. Both have been widely used in peer-reviewed studies (see here and here).

Amount: 100µL of 1mg/mL
Amount: 100µL of 1mg/mL
Immunofluorescent analysis of mouse retina section stained with mouse mAb to rhodopsin, MCA-A531, dilution 1:2,000, in green, and costained with rabbit pAb to GAP43, RPCA-GAP43, dilution 1:1,000 in red. The blue is Hoechst staining of nuclear DNA. Rhodopsin antibody reveals rhodopsin protein in rod cell membranes located in outer segments of photoreceptors layer (OS) of retina. GAP43 antibody stains axons of neuronal cells in the inner plexiform layer (IPL), where it was present in three distinct bands.
Western blot analysis of retina lysates from different species using mouse mAb to rhodopsin, MCA-A531, dilution 1:5,000 in green: [1] protein standard (red), [2] rat [3] mouse and [4] cow retina lysates. Strong band at 35kDa corresponds to rhodopsin protein. Bands about 70kDa and 140kDa result from the known tendency of rhodopsin to aggregate on SDS-PAGE gels.

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Name: Rhodopsin, mouse monoclonal, Cat# MCA-A531
Immunogen: Purified bovine rhodopsin
HGNC Name: RHO
UniProt: P08100
Molecular Weight: 35kDa
Host: Mouse
Isotype: IgG1
Species Cross-Reactivity: Human, rat, mouse, cow, pig, horse
RRID: AB_2572378
Format: Purified antibody at 1mg/mL in 50% PBS, 50% glycerol plus 5mM NaN3
Applications: WB, IF/ICC, IHC
Recommended Dilutions: WB:1:5,000. IF/ICC: 1:1,000-1:2,000. IHC: 1:2,000-1:4,000.
Storage: Store at 4°C for short term, for longer term at -20°C.

      Rhodopsin is the protein in the mammalian retina responsible for the light sensitivity of rod cells which are in turn responsible for vision in low light levels (1-4). Somewhat surprisingly, the rhodopsin protein turned out to be a typical member of the seven transmembrane G protein-coupled receptor (GPCR) superfamily. Whereas other GPCRs initiate signaling on binding a specific ligand, rhodopsin exists with a ligand already bound, specifically the vitamin A related substance retinal. The light causes a conformational change in the receptor bound retinal, which causes a conformational change to the rhodopsin molecule. This change in rhodopsin conformation then results in altered G protein signalling in the rod cell and ultimately to low light vision.



Chromogenic immunostaining of a 4% PFA fixed paraffin embedded rat retina section with mouse mAb to rhodopsin, MCA-A531, dilution 1:2,000, detected with DAB (brown) using the Vector Labs ImmPRESS method and reagents with citra buffer retrieval. Hematoxylin (blue) was used as the counterstain. MCA-A531 strongly labels the rod cells within the photoreceptor layer of the retina. This antibody has not been tested in NBF fixed material. Mouse select image for larger view.



Immunofluorescent analysis of pig retina section stained with mouse monoclonal antibody to rhodopsin, MCA-A531, in green, and costained with rabbit polyclonal antibody to Neurofilament-Medium, NF-M, RPCA-NF-M, in red. The blue is Hoechst staining of nuclear DNA. Rhodopsin antibody reveals rhodopsin protein in rod cell membranes located in outer segments of photoreceptors layer (ROS) of retina. RPCA-NF-M detects NF-M protein in the optic nerve fiber layer of the retina (ONFL). Mouse select image for larger view.

1. Molday RS. Photoreceptor membrane proteins, phototransduction, and retinal degenerative disease. The Frienwald lecture. Invest Ophthalmol Vis Sci. 39:2491-513 (1998).
2. Yau, KW. Phototransduction Mechanism in Retinal Rods and Cones. The Frienwald lecture. Invest Ophthalmol Vis Sci. 35:9-32 (1994).
3. Wilden U, Hall SW, Kühn H. Phosphodiesterase activation by photoexcited rhodopsin is quenched when rhodopsin is phosphorylated and binds the intrinsic 48-kDa protein of rod outer segments. Proc Natl Acad Sci USA 83:1174-8 (1986).
4. Smith WC, et al. Identification of regions of arrestin that bind to rhodopsin. Biochemistry Mar 38:2752-61 (1999).
5. Adamus G, et al. Use of peptides to select for anti-rhodopsin antibodies with desired amino acid sequence specificities. Pept. Res. 1:42-7 (1988).

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