RPE65 Recombinant Rabbit Monoclonal Antibody (7B10), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA549847-Each-of-1 | In Stock | ₹ 37,202.00 |
FEMA549847 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 37,202.00
GST (18%): ₹ 6,696.36
Total Price: ₹ 43,898.36
Antigen
RPE65
Classification
Recombinant Monoclonal
Concentration
1.6 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide, pH 7.4
Gene Accession No.
Q16518
Gene Symbols
RPE65
Immunogen
A synthesized peptide derived from human RPE65
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Applications
ELISA, Immunohistochemistry (Paraffin)
Clone
7B10
Conjugate
Unconjugated
Gene
RPE65
Gene Alias
65kDa, A930029L06Rik, all-trans-retinyl-palmitate hydrolase, BCO family, member 3, BCO3, LCA2, Lutein isomerase, membrane receptor p63, meso-zeaxanthin isomerase, modifier of retinal degeneration 1, Mord1, mRPE65, p63, RBP-binding membrane protein, rd12, retinal pigment epithelium 65, retinal pigment epithelium 65-like, retinal pigment epithelium abundant protein RPE65, retinal pigment epithelium specific protein 65, retinal pigment epithelium, 65 kDa, retinal pigment epithelium-specific 65 kDa protein, retinal pigment epithelium-specific 65kD protein, retinal pigment epithelium-specific protein (65kD), retinal pigment epithelium-specific protein 65kDa, retinal pigment epithelium-specific protein RPE65, Retinitis pigmentos, retinitis pigmentosa 20 (autosomal recessive), retinoid isomerohydrolase, retinoid isomerohydrolase RPE65, retinol isomerase, RP20, RPE65, rpe65 gene for retinal pigment epithelium-specific protein, RPE65, retinoid isomerohydrolase, sRPE65, truncated RPE65
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
6121
Content And Storage
-20°C or -80°C if preferred
Isotype
IgG
Related Products
Description
- RPE65 is a major protein of the retinal pigment epithelium (RPE)
- RPE65 is essential for the regeneration of rhodopsin in the visual cycle
- Mutations in RPE65 are responsible for certain forms of autosomal recessive severe retinal dystrophy, including Leber Congenital Amaurosis (LCA)
- Loss of function results in a block in retinoid processing required for the synthesis of 11-cis retinal and the accumulation of retinyl esters in the RPE.