TBL2 Polyclonal Antibody, 100ul sgRNA Oligos It contains a set of

It contains a set of putative metal binding motifs with similarity to that seen in a family of membrane desaturases-hydroxylases

Mutations in this gene have been reported to be associated with nonsyndromic hearing loss

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Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor

TBL2 Polyclonal Antibody, 100ul sgRNA Oligos It contains a set ofTBL2 encodes a member of the beta transducin protein family. Most proteins of the beta transducin family are involved in regulatory functions. transducin beta like 2 is possibly involved in some intracellular signaling pathway. TBL2 is deleted in Williams Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11. 3.