Nearest D (m) [DELTA]h Test Point day Station (m) BOCA 1646/ ALME (ERGNSS) 5431.138 69.579 207 ALMR (RAP) 5830.770 140.837 CUES 1646/ ALME (ERGNSS) 17656.927 -71.106 209 ALMR (RAP) 15931.600 0.152 PILI 1644/ COBA (ERGNSS) 19510.396 -209.286 191 CRDB (RAP) 16568.213 -215.345 RUBI 1643/ COBA (ERGNSS) 16824.827 45.782 190 CRDB (RAP) 9832.145 39.723 GRND 1645/ MALA (ERGNSS) 19732.142 -761.576 201 MLGA
(RAP) 22425.871 -765.748 TORR 1645/ MALA (ERGNSS) 18499.179 30.496 200 MLGA
(RAP) 22207.881 26.323 Table 3 Discrepancies in the local geodetic frame (East, North and Up components) by comparing ERGNSS and RAP post-processing solutions in ETRS89.
As an example, the known fact that BRs act synergistically with auxins to promote cell elongation 16] is nicely reflected in the MLGA drawn network (Figure 5(b)).
The MLGA method can also be successfully used to analyze gene interaction networks.
We use a well-known ribosomal gene complex [23-25] to illustrate the possibilities of MLGA to discover interesting structures in the correlation network.
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Oxoid MLGA (Membrane Lactose Glucuronide Agar) simplifies the membrane filtration method of E.coli and coliforms by reducing the number of filtration stages required from two to one and by reducing the need for further confirmation steps.
The chromogenic substrate in Oxoid MLGA, 5-bromo-4-chloro-3-indolyl-b-D-glucuronide (BCIG), is cleaved by the enzyme [beta]-glucuronidase and produces a blue chromophore that builds up within the bacterial cells.
Not only does Oxoid MLGA simplify the differentiation and enumeration of E.coli and coliforms by reducing the number of plates required but, since the chromogen is so specific, it also eliminates the need for further confirmation of green E.coli colonies.