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CABP2 belongs to a subfamily of calcium binding proteins that share similarity to calmodulin. Additionally we are shipping and and many more products for this protein.
Genetic defects in CABP2 cause moderate-to-severe sensorineural hearing impairment.
Results show that CaBP1/caldendrin (show CABP1 ELISA Kits) and CaBP2 are not required for normal gross retinal and synapse morphology but are necessary for the proper transmission of light responses through the retina; CaBP1/caldendrin (show CABP1 ELISA Kits) and CaBP2 likely act by modulating presynaptic Ca(2 (show CA2 ELISA Kits)+)-dependent signaling mechanisms.
This gene belongs to a subfamily of calcium binding proteins that share similarity to calmodulin. Like calmodulin, these family members can likely stimulate calmodulin-dependent kinase II and the protein phosphatase calcineurin. Calcium binding proteins are an important component of calcium mediated cellular signal transduction.
calcium-binding protein 2