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MF2L2 Rabbit Polyclonal Antibody, 100ul RNA Synthesis Mutations in SLC22A5 (solute carrier

SKU: 49537436821

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MF2L2 Rabbit Polyclonal Antibody, 100ul RNA Synthesis Mutations in SLC22A5 (solute carrier

Store: happygoluckyhtx.com · Domain: happygoluckyhtx.com

Description

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

as well as in disease processes

stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways

The encoded protein stabilizes the ORC and therefore aids in DNA replication

Members of this protein family have six EF-hand domains which bind calcium

MF2L2 Rabbit Polyclonal Antibody, 100ul RNA Synthesis Mutations in SLC22A5 (solute carrier

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