Rhodopsin / RHO

RHO antibody LS-C188582 is an unconjugated mouse monoclonal antibody to bovine RHO (Rhodopsin). Validated for IF, IHC, IP and WB.

Antibodies Primary

Article No

LS-C188582-0.1

Species Reactivity

cow/bovine

Size

0.1 ml

Clone

1D4

Source / Host

mouse

Shipping Information

RT

Application

IF, IHC, IP, WB

Article No

LS-C188582-0.1

Species Reactivity

cow/bovine

Size

0.1 ml

Clone

1D4

Source / Host

mouse

Shipping Information

RT

Application

IF, IHC, IP, WB

Specifications

NCBI Number 6010
Application IF, IHC, IP, WB
Article No LS-C188582-0.1
Country Availability SE, FI, DK, NO, FO, GL
Clone 1D4
Clone Type monoclonal
Conjugation Unconjugated
Description RHO antibody LS-C188582 is an unconjugated mouse monoclonal antibody to bovine RHO (Rhodopsin). Validated for IF, IHC, IP and WB.
Recommended Dilution IHC-P (1:100), WB (1:1000)
Supplier LifeSpan Biosciences
Entrez Gene ID 6010
Gene Symbol RHO
Immunogen Bovine rhodopsin.
Isotype IgG1
Notes RHO antibody LS-C188582 is an unconjugated mouse monoclonal antibody to bovine RHO (Rhodopsin). Validated for IF, IHC, IP and WB.
Alias Names RHO, CSNBAD1, OPN2, Rhodopsin, RP4, Opsin 2, rod pigment, Opsin-2
Product Type Antibodies Primary
Purification Protein G Purified
Shipping Information RT
Size 0.1 ml
Source / Host mouse
Species Reactivity cow/bovine
Storage -20°C
Substrate / Buffer 10mM HEPES, pH 7.5, 150mM NaCl, 0.09% Sodium Azide, 50% Glycerol, 0.01% BSA
Technical Specifications Recognizes rhodopsin, a pigment of the retina responsible for the formation of photoreceptor cells and the first events in the perception of light. Rhodopsin consists of the protein opsin and a reversibly bound cofactor, retinal, a photoreactive chromophore. Upon light absorption the 11-cis-retinal is isomerized to all-trans retinal, leading to a change in the shape of rhodopsin. The change activates the associated G protein and triggers a second messenger cascade, eventually resulting in the transmission of a nerve impulse to the brain. The trans-retinal is released and converted back into 11-cis-retinal for re-entry into the cycle. Defects in the gene cause various retinopathies such as retinitis pigmentosa and X-linked congenital stationary night blindness.
Product Page Updated 2024-04-12T06:35:05.844Z
Volume 0.1 ml

Documentation

Shipping info
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