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anti-Rat (Rattus) Rhodopsin antibody for Immunohistochemistry

Recommended Rhodopsin Antibody (supplied by: Log in to see )

Antigen
Rhodopsin (RHO) Antibodies
  • 1F9
  • 143283_at
  • BEST:GH11778
  • CG4550
  • CG5192
  • CG5279
  • CG9668
  • CG10888
  • CSNBAD1
  • DMELRH1
  • DMELRH3
  • DMELRH4
  • DMELRH5
  • DMELRH6
  • Dmel\\CG4550
  • Dmel\\CG5192
  • Dmel\\CG5279
  • Dmel\\CG9668
  • Dmel\\CG10888
  • Dm Rh1
  • DmRh1
  • Dm Rh3
  • Dm Rh4
  • Dm Rh5
  • Dm Rh6
  • DRh1
  • FBgn0002940
  • FBgn0003249
  • FBgn0003250
  • fi06d11
  • kfh-rh
  • NinaE
  • Nina E
  • Noerg1
  • opn2
  • Opn2
  • OPN2
  • ops
  • Ops
  • opsin
  • ora
  • PIGRHO1
  • R
  • R8
  • RDP1
  • Rh
  • Rh-1
  • RH1
  • rh1
  • Rh1
  • Rh1(ninaE)
  • Rh1/ninaE
  • rh1/ninaE
  • RH3
  • rh3
  • RH4
  • rh4
  • RH5
  • rh5
  • RH6
  • rh6
  • RHO
  • rhodopsin
  • RP4
  • rp4
  • wu:fi06d11
  • xrho
  • zfo2
  • zfrho
Reactivity
Human, Mouse (Murine), Rat (Rattus)
152
38
22
12
4
3
2
1
1
1
Host
Mouse
180
35
3
1
Clonality
Monoclonal
Conjugate
This Rhodopsin antibody is un-conjugated
10
10
8
8
6
6
6
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
4
2
2
Application
Immunohistochemistry (IHC)
209
142
137
136
117
107
46
4
4
1
1
Supplier
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Catalog No. ABIN1741937
$ 478.57
Plus shipping costs $45.00
Relevance Score ABIN Application Conjugate Host Isotype Epitope Supplier Clonality References Details
0.0011340706 ABIN1532407 IHC ELISA WB Rabbit IgG AA 299-348 Log in to see Polyclonal
0.0011340706 ABIN1580458 ICC IF IHC WB Mouse IgG1 Log in to see B630 2
0.0011340706 ABIN210506 IHC WB Mouse IgG1 N-Term Log in to see
0.0011340706 ABIN1820678 IF IHC WB Mouse IgG Log in to see SPM301
0.0011340706 ABIN1103993 ICC IP IHC ELISA WB Mouse IgG1 Log in to see Rho 4D2
0.0011340706 ABIN447325 IHC (fro) IHC (p) IHC WB Sheep Log in to see Polyclonal
0.0011340706 ABIN1585613 IHC ELISA WB Mouse IgG1 Log in to see 1D4
0.0011340706 ABIN1842255 ICC IF IHC WB Mouse IgG1 Log in to see A531 2

Top referenced anti-Rhodopsin antibody for Immunohistochemistry

Similar anti-Rhodopsin Antibodies

Application / Reactivity Rat (Rattus) Human Mouse (Murine)
Western Blotting (WB) 13 Antibodies 22 Antibodies 5 Antibodies
Immunoprecipitation (IP) 1 Antibodies 1 Antibodies 1 Antibodies
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)) 6 Antibodies 6 Antibodies 1 Antibodies
Immunohistochemistry (IHC) 9 Antibodies 11 Antibodies 6 Antibodies
Immunohistochemistry (Frozen Sections) (IHC (fro)) 1 Antibodies 1 Antibodies 1 Antibodies
Immunofluorescence (IF) 5 Antibodies 5 Antibodies 1 Antibodies
Immunocytochemistry (ICC) 3 Antibodies 5 Antibodies

General

Antigen Rhodopsin (RHO) Antibodies
Reactivity Human, Mouse (Murine), Rat (Rattus)
(152), (38), (22), (12), (4), (3), (2), (1), (1), (1)
Host Mouse
(180), (35), (3), (1)
Clonality (Clone)
Monoclonal   ( )
Conjugate This Rhodopsin antibody is un-conjugated
(10), (10), (8), (8), (6), (6), (6), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (4), (2), (2)
Application Immunohistochemistry (IHC)
(209), (142), (137), (136), (117), (107), (46), (4), (4), (1), (1)
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Product Details anti-Rhodopsin Antibody

Target Details Rhodopsin Application Details Handling Images
Specificity Specific for the approx. 39 kDa rhodopsin protein.
Purification Protein G purified culture supernatant.
Immunogen Purified native bovine rhodopsin.
Clone 1D4

Target Details Rhodopsin

Product Details anti-Rhodopsin Antibody Application Details Handling Images back to top
Antigen
Alternative Name Rhodopsin (RHO Antibody Abstract)
Background Synonyms:
Rhodopsin, RHO
Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding.
Molecular Weight 39 kDa
Gene ID 509933
UniProt P02699
Pathways WNT Signaling

Application Details

Product Details anti-Rhodopsin Antibody Target Details Rhodopsin Handling Images back to top
Application Notes Recommended Dilution:
IHC approx. 1:100
Restrictions For Research Use only

Handling

Product Details anti-Rhodopsin Antibody Target Details Rhodopsin Application Details Images back to top
Format Liquid
Storage 4 °C
Storage Comment Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Images

Product Details anti-Rhodopsin Antibody Target Details Rhodopsin Application Details Handling back to top
Supplier Images
Immunohistochemistry (IHC) image for anti-Rhodopsin antibody (RHO) (ABIN1741937) Immunohistochemical staining of mouse retinal section showing specificimmunolabeling ...