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

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

SKU: 49537436821

4.9
SEK123.75 SEK164.75

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

Store: schmucketriebe.at · Domain: schmucketriebe.at

Description

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

have been identified but their biological validity has not been established

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

leading to its own activation

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

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