Bestrophin-1 Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: RA22381-50, RA22381-100
Citations, Manuals and MSDS Available upon request.
Background: bestrophin 1 (BEST1) Homo sapiens This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008],
Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage Instructions: -20°C/1 year
Recommended dilutions: Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Alternative Names: Bestrophin-1 (TU15B;Vitelliform macular dystrophy protein 2)
Applications: WB; IHC-p; IF (paraffin section)
Species Cross-Reactivity: Human; Rat; Mouse
GeneID (Human): 7439
Protein MW (KDa): 67
SWISS: O76090
Source: Rabbit
Research Use Only