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MAB5428-25UG Anti-Retinal Pigment Epithelium 65

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MAB5428-25UG
25 μg  
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Overview

Replacement Information
Description
Catalogue NumberMAB5428-25UG
Brand Family Chemicon®
Trade Name
  • Chemicon
DescriptionAnti-Retinal Pigment Epithelium 65
Alternate Names
  • RPE65
References
Product Information
FormatPurified
Control
  • Eye
PresentationPurified immunoglobulin. Liquid in 0.02M phosphate buffer, pH 7.6, 0.25M NaCl, and 0.1% sodium azide.
Quality LevelMQ100
Applications
ApplicationAnti-Retinal Pigment Epithelium 65 Antibody detects level of Retinal Pigment Epithelium 65 & has been published & validated for use in ELISA, IH, IP & WB.
Key Applications
  • ELISA
  • Immunohistochemistry
  • Immunoprecipitation
  • Western Blotting
Application NotesWestern blot: 1:5,000-1:20,000 on bovine RPE membranes using ECL. Suggested dilution buffer is TBS containing 10% calf serum, 0.25% T-20, 1M D-glucose with 10% glycerol. Suggested blocking buffer is TBS containing 2% BSA and 0.5% Tween 20. Preferred gel percentage is 10%.

Immunohistochemistry on frozen tissue sections: 1:250-1:500

Immunoprecipitation: 20 μg of antibody in a reaction volume of 500 μL.

Immunoaffinity purification

ELISA

Optimal working dilutions must be determined by end user.
Biological Information
ImmunogenBovine RPE microsomal membranes.
Clone401.8B11.3D9
ConcentrationPlease refer to lot specific datasheet.
HostMouse
SpecificityReacts with Retinal Pigment Epithelium 65 (RPE65). On bovine RPE membranes the antibody recognizes a protein with a molecular weight of ~65 kDa.
IsotypeIgG
Species Reactivity
  • Bovine
  • Human
  • Mouse
  • Xenopus
Antibody TypeMonoclonal Antibody
Entrez Gene Number
Entrez Gene SummaryThis gene encodes a protein which is located in the retinal pigment epithelium and is involved in the production of 11-cis retinal and in visual pigment regeneration. There are two forms of this protein, a soluble form called sRPE65, and a palmitoylated, membrane-bound form known as mRPE65. mRPE65 serves as the palmitoyl donor for lecithin retinol acyl transferase (LRAT), the enzyme that catalyzes the vitamin A to all trans retinol step of the chromophore regeneration process. Both mRPE65 and sRPE65 also serve as regulatory proteins, with the ratio and concentrations of these molecules playing a role in the inhibition of 11-cis retinal synthesis. Mutations in this gene have been associated with Leber congenital amaurosis type 2 (LCA2) and retinitis pigmentosa.
Gene Symbol
  • RPE65
  • mRPE65
  • rd12
  • LCA2
  • p63
  • RP20
  • sRPE65
Purification MethodProtein A Purfied
UniProt Number
UniProt SummaryFUNCTION: SwissProt: Q16518 # Plays important roles in the production of 11-cis retinal and in visual pigment regeneration. The soluble form binds vitamin A (all-trans-retinol), making it available for LRAT processing to all-trans-retinyl ester. The membrane form, palmitoylated by LRAT, binds all-trans-retinyl esters, making them available for IMH (isomerohydrolase) processing to all-cis- retinol. The soluble form is regenerated by transferring its palmitoyl groups onto 11-cis-retinol, a reaction catalyzed by LRAT (By similarity).
SIZE: 533 amino acids; 60948 Da
SUBCELLULAR LOCATION: Cytoplasm (By similarity). Cell membrane; Lipid-anchor (By similarity). Note=Attached to the membrane by a lipid anchor when palmitoylated (membrane form), soluble when unpalmitoylated (By similarity).
TISSUE SPECIFICITY: Retinal pigment epithelium specific.
PTM: Palmitoylation by LRAT regulates ligand binding specificity; the palmitoylated form (membrane form) specifically binds all- trans-retinyl-palmitate, while the soluble unpalmitoylated form binds all-trans-retinol (vitamin A) (By similarity).
DISEASE: SwissProt: Q16518 # Defects in RPE65 are the cause of Leber congenital amaurosis type 2 (LCA2) [MIM:204100]. LCA designates a clinically and genetically heterogeneous group of childhood retinal degenerations, generally inherited in an autosomal recessive manner. Affected infants have little or no retinal photoreceptor function as tested by electroretinography. LCA represents the most common genetic cause of congenital visual impairment in infants and children. & Defects in RPE65 are the cause of retinitis pigmentosa type 20 (RP20) [MIM:180069]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP20 inheritance is autosomal dominant.
SIMILARITY: SwissProt: Q16518 ## Belongs to the carotenoid oxygenase family.
Molecular Weight~ 65 kDa
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality AssuranceTested
Usage Statement
  • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage ConditionsMaintain for 1 year at 2–8°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Packaging Information
Material Size25 μg
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalog Number GTIN
MAB5428-25UG 04054839337574

Documentation

Anti-Retinal Pigment Epithelium 65 Certificates of Analysis

TitleLot Number
Anti-Retinal Pigment Epithelium 65 - 3180443 3180443
Anti-Retinal Pigment Epithelium 65 - 3508358 3508358
Anti-Retinal Pigment Epithelium 65 - 3862811 3862811
Anti-Retinal Pigment Epithelium 65 - 3893433 3893433
Anti-Retinal Pigment Epithelium 65 - 3928048 3928048
Anti-Retinal Pigment Epithelium 65 - 3949799 3949799
Anti-Retinal Pigment Epithelium 65 - 4037479 4037479
Anti-Retinal Pigment Epithelium 65 MONOCLONAL ANTIBODY 3070778
Anti-Retinal Pigment Epithelium 65 MONOCLONAL ANTIBODY 3089128
Anti-Retinal Pigment Epithelium 65 MONOCLONAL ANTIBODY Q2912150

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