Rhodopsin Antikörper (AA 299-348)
Kurzübersicht für Rhodopsin Antikörper (AA 299-348) (ABIN1532407)
Target
Alle Rhodopsin (RHO) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 299-348
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Verwendungszweck
- Rhodopsin Antibody
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Spezifität
- Rhodopsin Polyclonal Antibody detects endogenous levels of Rhodopsin protein.
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Aufreinigung
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Reinheit
- > 95 %
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Immunogen
- The antiserum was produced against synthesized peptide derived from human Rhodopsin. AA range:299-348
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Isotyp
- IgG
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Applikationshinweise
- WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:5000.. IF 1:50-200
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Store at -20°C/1 year
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Haltbarkeit
- 12 months
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: "Rhodopsin in plasma from patients with diabetic retinopathy - development and validation of digital ELISA by Single Molecule Array (Simoa) technology." in: Journal of immunological methods, Vol. 446, pp. 60-69, (2017) (PubMed).
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- Rhodopsin (RHO)
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Andere Bezeichnung
- Rhodopsin
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Substanzklasse
- Chemical
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Hintergrund
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Synonyms: RHO, OPN2, Rhodopsin, Opsin-2
Background: 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],
Gene Name: RHO
Protein Name: Rhodopsin
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Molekulargewicht
- 39 kDa
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Gen-ID
- 6010
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OMIM
- 180380
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UniProt
- P08100
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Pathways
- WNT Signalweg, Sensory Perception of Sound, Regulation of G-Protein Coupled Receptor Protein Signaling, Phototransduction
Target
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