Anti-Rhodopsin Antibody [1D4]

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SKU:
STMA00048
Antibody Type:
Monoclonal
Applications:
WB
Applications:
IHC
Applications:
ICC/IF
Applications:
IP
Applications:
ELISA
Reactivity:
Vertebrate
Host Species:
Mouse
Isotype:
IgG1
  • Immunohistochemistry analysis using Mouse Anti-Rhodopsin Monoclonal Antibody, Clone 1D4 (STMA00048). Tissue: backskin. Species: Mouse. Fixation: Bouin's Fixative and paraffin-embedded. Primary Antibody: Mouse Anti-Rhodopsin Monoclonal Antibody (STMA00048) at 1:100 for 1 hour at RT. Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:50 for 1 hour at RT. Localization: Dull epidermal staining.
  • Western Blot analysis of Human Cell lysates showing detection of Rhodopsin protein using Mouse Anti-Rhodopsin Monoclonal Antibody, Clone 1D4 (STMA00048). Load: 15 µg. Block: 1.5% BSA for 30 minutes at RT. Primary Antibody: Mouse Anti-Rhodopsin Monoclonal Antibody (STMA00048) at 1:1000 for 2 hours at RT. Secondary Antibody: Sheep Anti-Mouse IgG: HRP for 1 hour at RT.
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Description

Rhodopsin Antibody [1D4]

Rhodopsin Antibody [1D4] is a mouse monoclonal antibody directed against Rhodopsin, offered by Assay Genie for research applications. Reported applications include WB, IHC, ICC/IF, IP and ELISA. Reported reactivity: Vertebrate. Supplied as IgG1, purified by Protein G.

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. This antibody is also available conjugated to ATTO 390, ATTO 488, ATTO 594, APC, Biotin, FITC, HRP, PerCP and RPE. Supplied in 100 µg. For research use only; not for diagnostic or therapeutic procedures.

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