ARG10776
anti-Bestrophin antibody
anti-Bestrophin antibody for Confocal microscopy (Confocal),ELISA,ICC/IF,Immunohistochemistry,Immunoprecipitation,Western blot,Dot blot and Human,Mouse,Rat
Overview
Product Description | Rabbit Polyclonal antibody recognizes Bestrophin |
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Tested Reactivity | Hu, Ms, Rat |
Tested Application | Confocal, Dot, ELISA, ICC/IF, IHC, IP, WB |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | Bestrophin |
Antigen Species | Human |
Immunogen | Synthetic peptide from Human Bestrophin. |
Conjugation | Un-conjugated |
Alternate Names | Vitelliform macular dystrophy protein 2; RP50; BMD; TU15B; VMD2; Bestrophin-1; ARB; BEST |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Affinity purified. |
Buffer | Tris-Glycine Buffer (pH 7.4 - 7.8), Hepes, 0.02% Sodium azide, 30% Glycerol and 0.5% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 30% Glycerol and 0.5% BSA |
Concentration | 0.5 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | BEST1 |
Gene Full Name | bestrophin 1 |
Background | 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] |
Function | Forms calcium-sensitive chloride channels. Highly permeable to bicarbonate. [UniProt] |
Highlight | Related products: Bestrophin antibodies; Anti-Rabbit IgG secondary antibodies; Related news: Gene therapy for retinitis pigmentosa (RP) |
Calculated MW | 68 kDa |
PTM | Phosphorylated by PP2A. |