BFSP1 Rabbit Polyclonal Antibody, 50ul Micro Centrifuge Tubes KCNV2 encodes a member of

KCNV2 encodes a member of the potassium voltage-gated channel subfamily V

are the force-generating proteins responsible for the sliding movement in axonemes

Defects in TRPS1 are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III

PNN (Pinin

unspliced transcript in endothelial cells has been described

BFSP1 Rabbit Polyclonal Antibody, 50ul Micro Centrifuge Tubes KCNV2 encodes a member ofThis gene encodes a lens specific intermediate filament like protein named filensin. The encoded protein is expressed in lens fiber cells after differentiation has begun. This protein functions as a component of the beaded filament which is a cytoskeletal structure found in lens fiber cells. Mutations in this gene are the cause of autosomal recessive cortical juvenile onset cataract. Alternate splicing results in multiple transcript variants.