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NCS1 Rabbit Polyclonal Antibody, 20ul Recombinant Protein Defects in RB1 are a

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NCS1 Rabbit Polyclonal Antibody, 20ul Recombinant Protein Defects in RB1 are aThis gene is a member of the neuronal calcium sensor gene family which encode calcium binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein coupled receptor phosphorylation in a calcium dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different

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Description

Defects in RB1 are a cause of childhood cancer retinoblastoma (RB)

subfamily F

and at a relatively lower level in thymus and bone marrow

This gene is a member of the melanoma antigen gene (MAGE) family

NCS1 Rabbit Polyclonal Antibody, 20ul Recombinant Protein Defects in RB1 are aThis gene is a member of the neuronal calcium sensor gene family which encode calcium binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein coupled receptor phosphorylation in a calcium dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different

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