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

N° du produit ABIN7269975

Cet anticorps anti-Rho-related GTP-binding protein est un anticorps Lapin Polyclonal détectant Rho-related GTP-binding protein dans WB et IHC. Adapté pour Humain.

Aperçu rapide pour Rho-related GTP-binding protein anticorps (C-Term) (ABIN7269975)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Rho-related GTP-binding protein est non-conjugé

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

Détail du produit anti-Rho-related GTP-binding protein anticorps

Épitope: C-Term

Fonction: Rhodopsin Rabbit pAb

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

Réactivité croisée: Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Rho-related GTP-binding protein

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

Autre désignation: RHO

Sujet: 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

Poids moléculaire: 38kDa

ID gène: 6010

UniProt: P08100