Wnt-16 Polyclonal Antibody, 50ul RNA Synthesis In complex with XRCC6 and

In complex with XRCC6 and XRCC5 (Ku80)

A missense mutation in this gene causes myoclonus dystonia

The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes

45 µm pore size and a PVDF membrane

It may exert its effects via protein-protein interactions with other transcriptional regulators rather than via direct binding of DNA

Wnt-16 Polyclonal Antibody, 50ul RNA Synthesis In complex with XRCC6 andThe WNT gene family consists of structurally related genes which encode secreted signaling proteins. Protein Wnt 16 have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. WNT16 is a member of the WNT gene family. It contains two transcript variants diverging at the 5' termini. These two variants are proposed to be the products of separate promoters and not to