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DOI:10.1080/1040-840291046731 6

The A326S mutant of Gialpha1 as an approximation of the receptor-bound state

As explained in two excellent recent reviews [18, 88] and illustrated in Figure 4, the hypomagnesaemia is due to the induction of a loss of function mutation in the epithelial Mg2+ channel TRPM6 (transient receptor potential cation channel, subfamily M, member 6), one of the main tubular magnesium channels in the distal collecting tubular cells

The BrdU labelled DNA conjugate was detected using the anti-BrdU-POD-Fab fragment and treated with TMB substrate to form a colour complex (Roche, Canada)
