Thermo Fisher Scientific Bestrophin Polyclonal Antibody, FITC

Applications and Tested Dilutions

Product Specifications

Target Information

The retinal pigment epithelium (RPE) and choroid form a differentiated system of the eye that supports retinal health and function.
Best vitelliform macular dystrophy (Best disease) is an early-onset autosomal dominant condition characterized by the accumulation of lipofuscin-like material within and beneath the RPE, leading to progressive central vision loss.
This material appears as a yellow mass resembling an egg yolk that later darkens and becomes irregular, a process referred to as “scrambling the egg.”
Best disease often results from mutations in the Bestrophin gene, which encodes a protein with four transmembrane domains localized to the basolateral plasma membrane of RPE cells.
Human Bestrophin forms oligomeric chloride channels sensitive to intracellular calcium, and missense mutations can reduce or abolish Bestrophin-mediated membrane current.
The human Bestrophin gene encodes a 585 amino acid protein.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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