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NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier
NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier
NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier
NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier

NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier

SKU: 33971863172

4.8
SEK162.00 SEK186.00

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NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier

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Description

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

When an extracellular ligand binds to a G-protein-linked receptor

As a type II hair keratin

Calmodulin-binding protein which may function as scaffolding or signaling protein and may play a role in dendritic Ca(2+) signaling

NAB1 Rabbit Polyclonal Antibody, 50ul Primary Antibodies Mutations in SLC22A5 (solute carrier

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