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

Produktnummer ABIN1537109

Der Kaninchen Polyklonal Anti-Rho-related GTP-binding protein-Antikörper wurde für WB validiert. Er ist geeignet, Rho-related GTP-binding protein in Proben von Human, Ratte und Maus zu detektieren.

Kurzübersicht für Rho-related GTP-binding protein Antikörper (C-Term) (ABIN1537109)

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

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

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

Applikation: Western Blotting (WB)

Klon: RB36659

Produktdetails anti-Rho-related GTP-binding protein Antikörper

Bindungsspezifität: AA 310-339, C-Term

Homologie: Pr

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This RHO antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 310-339 amino acids from the C-terminal region of human RHO.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:2000. WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: RHO Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu Rho-related GTP-binding protein

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

Andere Bezeichnung: RHO

Substanzklasse: Chemical

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.

Molekulargewicht: 38893

Gen-ID: 6010

NCBI Accession: NP_000530

UniProt: P08100