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NU4LM Polyclonal Antibody, 20ul Peptide Library Humans homozygous for certain mutations

SKU: 11172602064

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NU4LM Polyclonal Antibody, 20ul Peptide Library Humans homozygous for certain mutationsCatalytic activity: NADH + ubiquinone = NAD(+) + ubiquinol.,disease: Defects in MT ND4 are a cause of Leber hereditary optic neuropathy (LHON)

Store: schmucketriebe.at · Domain: schmucketriebe.at

Description

Humans homozygous for certain mutations in this gene exhibit prolonged apnea after administration of the muscle relaxant succinylcholine

This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis

subcellular location:Lacks the PDZ domain

these tubes offer ease and efficiency in your lab work

NU4LM Polyclonal Antibody, 20ul Peptide Library Humans homozygous for certain mutationsCatalytic activity: NADH + ubiquinone = NAD(+) + ubiquinol.,disease: Defects in MT ND4 are a cause of Leber hereditary optic neuropathy (LHON)

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