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Western blotAntibody data
- Antibody Data
- Antigen structure
- References [10]
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- Product number
- ABIN350798 - Provider product page
- Provider
- antibodies-online
- Proper citation
- Antibodies-Online Cat#ABIN350798, RRID:AB_10785804
- Product name
- anti-Rhodopsin (RHO) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide from c-terminal region of human Rhodopsin (OPSD, Opsin-2) conjugated to an immunogenic carrier protein was used as the antigen. The antigen is homologous in mouse and rat.
- Reactivity
- Human, Mouse
- Host
- Sheep
- Epitope
- C-Term
- Vial size
- 150 μL
- Storage
- Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability.
- Handling
- Avoid freeze and thaw cycles.
Submitted references Detection of vivax malaria sporozoites naturally infected in Anopheline mosquitoes from endemic areas of northern parts of Gyeonggi-do (Province) in Korea.
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
Sequence analysis of the 5.34-kb 5' flanking region of the human rhodopsin-encoding gene.
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347.
Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.
Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
Isolation and nucleotide sequence of the gene encoding human rhodopsin.
Lee HW, Shin EH, Cho SH, Lee HI, Kim CL, Lee WG, Moon SU, Lee JS, Lee WJ, Kim TS
The Korean journal of parasitology 2002 Jun;40(2):75-81
The Korean journal of parasitology 2002 Jun;40(2):75-81
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
Sieving PA, Richards JE, Naarendorp F, Bingham EL, Scott K, Alpern M
Proceedings of the National Academy of Sciences of the United States of America 1995 Jan 31;92(3):880-4
Proceedings of the National Academy of Sciences of the United States of America 1995 Jan 31;92(3):880-4
Sequence analysis of the 5.34-kb 5' flanking region of the human rhodopsin-encoding gene.
Bennett J, Sun D, Karikó K
Gene 1995 Dec 29;167(1-2):317-20
Gene 1995 Dec 29;167(1-2):317-20
Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347.
Macke JP, Hennessey JC, Nathans J
Human molecular genetics 1995 Apr;4(4):775-6
Human molecular genetics 1995 Apr;4(4):775-6
Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
Vaithinathan R, Berson EL, Dryja TP
Genomics 1994 May 15;21(2):461-3
Genomics 1994 May 15;21(2):461-3
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.
Macke JP, Davenport CM, Jacobson SG, Hennessey JC, Gonzalez-Fernandez F, Conway BP, Heckenlively J, Palmer R, Maumenee IH, Sieving P
American journal of human genetics 1993 Jul;53(1):80-9
American journal of human genetics 1993 Jul;53(1):80-9
Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.
Farrar GJ, Findlay JB, Kumar-Singh R, Kenna P, Humphries MM, Sharpe E, Humphries P
Human molecular genetics 1992 Dec;1(9):769-71
Human molecular genetics 1992 Dec;1(9):769-71
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
Sung CH, Davenport CM, Hennessey JC, Maumenee IH, Jacobson SG, Heckenlively JR, Nowakowski R, Fishman G, Gouras P, Nathans J
Proceedings of the National Academy of Sciences of the United States of America 1991 Aug 1;88(15):6481-5
Proceedings of the National Academy of Sciences of the United States of America 1991 Aug 1;88(15):6481-5
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
Dryja TP, McGee TL, Reichel E, Hahn LB, Cowley GS, Yandell DW, Sandberg MA, Berson EL
Nature 1990 Jan 25;343(6256):364-6
Nature 1990 Jan 25;343(6256):364-6
Isolation and nucleotide sequence of the gene encoding human rhodopsin.
Nathans J, Hogness DS
Proceedings of the National Academy of Sciences of the United States of America 1984 Aug;81(15):4851-5
Proceedings of the National Academy of Sciences of the United States of America 1984 Aug;81(15):4851-5
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