Rho-related GTP-binding protein Antikörper (C-Term)

Produktnummer ABIN7269975

Der Kaninchen Polyklonal anti-Rho-related GTP-binding protein Antikörper (ABIN7269975) detektiert spezifisch Rho-related GTP-binding protein in WB und IHC. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für Rho-related GTP-binding protein Antikörper (C-Term) (ABIN7269975)

Target: Rho-related GTP-binding protein (RhO (pan))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Rho-related GTP-binding protein Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Produktdetails anti-Rho-related GTP-binding protein Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: Rhodopsin Rabbit pAb

Sequenz: NESFVIYMFV VHFTIPMIII FFCYGQLVFT VKEAAAQQQE SATTQKAEKE VTRMVIIMVI AFLICWVPYA SVAFYIFTHQ GSNFGPIFMT IPAFFAKSAA IYNPVIYIMM NKQFRNCMLT TICCGKNPLG DDEASATVSK TETSQVAPA

Kreuzreaktivität: Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human Rhodopsindopsin (NP_000530.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu Rho-related GTP-binding protein

Target: Rho-related GTP-binding protein (RhO (pan))

Andere Bezeichnung: RHO

Hintergrund: 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.,RHO,CSNBAD1,OPN2,RP4,rhodopsin,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),Neuroscience,RHO

Molekulargewicht: 38kDa

Gen-ID: 6010

UniProt: P08100