Mouse monoclonal to BestrophinBest macular dystrophy (BMD) or vitelliform macular dystrophy (VMD2), is an autosomal form of macular degeneration, characterized by a depressed light peak in the electrooculogram (EOG). It is inherited and has an early onset. Bestrophin is a 68 kDa basolateral plasma membrane protein encoded by the VMD2 gene. Bestrophin's function is still unknown, but data suggests that it is a chloride channel that plays a role in generating the altered EOG in Best disease patients. In addition, Bestrophin is a useful biochemical and histological marker of RPE (retinal pigment epithelial cells) cells.
Immunogen
Partial recombinant protein [KDHMDPYWALENRDEAHS]
Key Feature
Clonality
Monoclonal
Isotype
IgG1
Host Species
Mouse
Tested Applications
ICC/IFIHC-FIHC-PIPWB
Western Blot: 1:1000, Immunocytochemistry/Immunofluorescence Assay dependent, Immunohistochemistry-Frozen, Immunohistochemistry-Paraffin, Immunoprecipitation.:
Species Reactivity
HumanMonkey
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Gene Synonyms
BEST VMD2 Bestrophin 7439 O76090 153700 TU15B BMD ARB RP50
Target
Bestrophin
Tissue Specificity
This antibody is specific for Bestrophin.
Light Chain Type
kappa
Application
Application
Western Blot: Bestrophin 1 Antibody (E6-6) - Detection of Bestrophin (68 kDa) from human RPE cell lysate.