NU2M Polyclonal Antibody, 20ul Antibody Humanization We offer custom DNA oligo

We offer custom DNA oligo synthesis options including but not limited to standard oligos

Defects in this gene are associated with Fuchs endothelial corneal dystrophy and posterior polymorphous corneal dystrophy type 2

suggesting that the function of this gene may be signal repression

beta 2 has a more restricted tissue distribution

SKP2 encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif

NU2M Polyclonal Antibody, 20ul Antibody Humanization We offer custom DNA oligoCatalytic activity: NADH + ubiquinone = NAD(+) + ubiquinol.,disease: Defects in MT ND2 are a cause of Leber hereditary optic neuropathy (LHON)