Rho-related GTP-binding protein Antikörper (C-Term)
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- Target Alle Rho-related GTP-binding protein (RhO (pan)) Antikörper anzeigen
- Rho-related GTP-binding protein (RhO (pan))
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Bindungsspezifität
- C-Term
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Reaktivität
- Human, Maus, Ratte, Rind (Kuh), Meerschweinchen, Kaninchen, Schaf, Hund
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Rho-related GTP-binding protein Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Sequenz
- AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE
- Homologie
- Cow: 93%, Dog: 86%, Guinea Pig: 93%, Human: 100%, Mouse: 86%, Rabbit: 93%, Rat: 93%, Sheep: 93%
- Produktmerkmale
- This is a rabbit polyclonal antibody against RHO. It was validated on Western Blot.
- Aufreinigung
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human RHO
- Top Product
- Discover our top product RhO (pan) Primärantikörper
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- Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
- Kommentare
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Antigen size: 348 AA
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Target
- Rho-related GTP-binding protein (RhO (pan))
- Andere Bezeichnung
- RHO (RhO (pan) Produkte)
- Substanzklasse
- Chemical
- Hintergrund
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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.
Alias Symbols: CSNBAD1, MGC138309, MGC138311, OPN2, RP4
Protein Interaction Partner: DERL1, EDEM1, VCP, UBC, HSPA4, DNAJB2, RHO, PPP2CA, GRK5, GRK6, ARR3, GNGT1, SAG, GRK1, PRKCA, ADRBK1,
Protein Size: 348 - Molekulargewicht
- 39 kDa
- Gen-ID
- 6010
- NCBI Accession
- NM_000539, NP_000530
- UniProt
- P08100
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