产品名称 Bestrophin 1 (BEST1) (C-Term) Antibody from ANTIBODIES-ONLINE GmbH
产品货号 ABIN1841874
产品价格 现货询价,电话:010-67529703
产品规格 100 µL
产品品牌 ANTIBODIES-ONLINE GmbH
产品概述
产品详情
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Antigenic SpecificityBestrophin 1 (BEST1) (C-Term)
Clonepolyclonal
Host SpeciesRabbit
Reactive Specieshuman
Isotypen/a
Formatserum
Size100 µL
Concentrationn/a
ApplicationsImmunohistochemistry (IHC),Western Blotting (WB)
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DescriptionFUNCTION: Forms calcium-sensitive chloride channels. Highly permeable to bicarbonate. Subcellular location: Cell membrane, Multi-pass membrane protein. Basolateral cell membrane Tissue specificity: Predominantly expressed in the basolateral membrane of the retinal pigment epithelium. Defects in BEST1 are the cause of vitelliform macular dystrophy type 2 (VMD2) also known as Best macular dystrophy (BMD). VMD2 is an autosomal dominant form of macular degeneration that usually begins in childhood or adolescence. VMD2 is characterized by typical 'egg-yolk' macular lesions due to abnormal accumulation of lipofuscin within and beneath the retinal pigment epithelium cells. Progression of the disease leads to destruction of the retinal pigment epithelium and vision loss. Defects in BEST1 are the cause of retinitis pigmentosa type 50 (RP50). Defects in BEST1 are a cause of adult-onset vitelliform macular dystrophy (AVMD). Defects in BEST1 are the cause of bestrophinopathy autosomal recessive (ARB). Defects in BEST1 are the cause of vitreoretinochoroidopathy autosomal dominant (ADVIRC).Synonyms: TU15B, Vitelliform macular dystrophy protein 2, BEST1, VMD2
ImmunogenA synthetic peptide from c-terminal region of human Bestrophin 1 conjugated to an immunogenic carrier protein was used as the antigen.
Other NamesCG6264|Dbest|Dmel\\CG6264|anon-WO0118547.380|best|dBest1|dbest1|dmBest1|BEST1|VMD2|best-1|ARB|BEST|BMD|RP50|TU15B|Bmd|Vmd2|mBest1
Gene, Accession #Gene ID: 7439
Catalog #ABIN1841874
Price
Order / More InfoBestrophin 1 (BEST1) (C-Term) Antibody from ANTIBODIES-ONLINE GmbH
Product Specific Referencesn/a
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