CABP4 Polyclonal Antibody

CABP4 (Calcium Binding Protein 4) is a Protein Coding gene. Diseases associated with CABP4 include Cone-Rod Synaptic Disorder, Congenital Nonprogressive and Congenital Stationary Night Blindness, Type 2B. Among its related pathways are Visual Cycle in Retinal Rods. CABP4 encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in CABP4 are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for CABP4.

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Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000; ELISA 1:5000-20000