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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

4.4
SEK162.00 SEK185.00

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

Store: matisco.be · Domain: matisco.be

Description

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

Regulator of G protein signaling 4 belongs to this family

|induction:By interferon gamma and interferon beta

ATP5C1 encodes a subunit of mitochondrial ATP synthase

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

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