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

SKU: 11172602064

4.4
USD97.20 USD126.20

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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)

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Description

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

these tubes offer ease and efficiency in your lab work

This gene is highly expressed in testis and the protein is localized to the nucleus

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

subcellular location:Lacks the PDZ domain

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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