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

Catalog No. ABIN7269975

The Rabbit Polyclonal anti-Rho-related GTP-binding protein antibody (ABIN7269975) specifically detects Rho-related GTP-binding protein in WB and IHC. The antibody is reactive with Human samples.

Quick Overview for Rho-related GTP-binding protein antibody (C-Term) (ABIN7269975)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Rho-related GTP-binding protein antibody is un-conjugated

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

Product Details anti-Rho-related GTP-binding protein Antibody

Binding Specificity: C-Term

Purpose: Rhodopsin Rabbit pAb

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

Cross-Reactivity: Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Rho-related GTP-binding protein

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

Alternative Name: RHO

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

Molecular Weight: 38kDa

Gene ID: 6010

UniProt: P08100