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Pim-2 Polyclonal Antibody, 100ul Cell Culture & Maintenance Mutations in this gene cause

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Pim-2 Polyclonal Antibody, 100ul Cell Culture & Maintenance Mutations in this gene causePIM2 encodes a protooncogene that acts as a serine threonine protein kinase. Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival.

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Description

Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP)

subunit:Interacts with FMRP

While all three are adapter proteins in signal transduction pathways

Rho family

The encoded protein is one of the components of a calcium channel

Pim-2 Polyclonal Antibody, 100ul Cell Culture & Maintenance Mutations in this gene causePIM2 encodes a protooncogene that acts as a serine threonine protein kinase. Studies determined the encoded protein functions to prevent apoptosis and to promote cell survival.

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