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  2. Monoclonal

SMC-177

Rhodopsin Antibody, Clone 1D4

Cannot supply to this region.

SKU:
SMC-177
Additional Names:
OPN2, opsd, opsin 2, opsin 2 rod pigment, opsin2, RHO, RP4, MGC138309, Retinitis Pigmentosa 4
Application:
ELISA, IHC, WB, IF, ICC, IP
Concentration:
1 mg/ml
Species Reactivity:
Bovine
Purification:
Protein G Purified
Storage Conditions:
-20[o]C
Supplier:
StressMarq Biosciences
Host:
Mouse
ABP:
IMP-GEN-2015-06 < 10% Serum <100ml
Buffer:
PBS pH7.4, 50% glycerol, 0.09% sodium azide
Immunogen:
Bovine Rhodopsin
Clone:
1D4
Uniprot:
P02699
Synonyms:
rhodopsin;rhodopsin (opsin 2, rod pigment) (retinitis pigmentosa 4, autosomal dominant)
Extra Details:
Rhodopsin is a light-sensitive G protein-coupled receptor (GPCR) found in the rod photoreceptor cells of the retina. It plays a central role in the phototransduction cascade, converting light into electrical signals essential for vision in low-light conditions. Beyond its classical role in visual processing, rhodopsin has emerged as a key player in retinal neurodegeneration. Mutations in the RHO gene encoding rhodopsin are a leading cause of autosomal dominant retinitis pigmentosa (adRP), a progressive neurodegenerative disorder characterized by photoreceptor cell death and vision loss. Misfolded rhodopsin accumulates in the endoplasmic reticulum, triggering cellular stress responses, including the unfolded protein response (UPR) and apoptosis. Rhodopsin dysfunction also affects mitochondrial dynamics, oxidative stress regulation, and autophagy-pathways commonly implicated in broader neurodegenerative diseases such as Alzheimer's and Parkinson's. Its involvement in protein misfolding and trafficking makes rhodopsin a valuable model for studying proteostasis and neurodegeneration. As a well-characterized GPCR with known structural and functional properties, rhodopsin serves as a powerful tool for investigating the molecular mechanisms underlying neuronal survival, degeneration, and therapeutic intervention strategies in neurodegenerative research.
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