Sentence examples for excess detection from inspiring English sources

It is possible that the WGA and low level of parasitaemia lead to a failure of one allele to amplify by PCR, and therefore an excess detection rate of pseudo-homozygotes.

The excess detection antibody was removed after 1 hr and a horseradish peroxidase-conjugated antibody (anti-rabbit Ig-HRP) was added to the wells for 30 min. Following a final washing step to remove the excess anti-rabbit Ig-HRP, a substrate was added and absorbance was read at 450nm.

Excess detection mix was removed by washing the slides in 4 × SSC, 0.05% Igepal for 3 × 3 minutes.

Grids were washed 4 times with PBS-BSA buffer at room temperature to remove excess detection antibody.

After blocking with 5% bovine serum albumin in 0.2% Tween 20/4XSSC (4XT), detection was performed using anti-digoxigenin fluorescein (sheep) (Roche) at 37°C in a humid chamber for 30 min. Excess detection reagents were washed at 45°C in 4XT.

T1 2 is immediately above excess 210Pb detection limit (A.D. 1860).

T1 2 is immediately above the excess 210Pb detection limit (A.D. 1860).

Stars indicate horizons at the excess 210Pb detection limit and the 137Cs maximum (McHugh et al. 2016).

In the case of radioisotopes, horizons in the two cores that excess 210Pb detection limits (A.D. 1860) and the maximum for 137Cs (A.D. 1963; Peirson 1971) were referred to in previous studies (McHugh et al. 2016) (Figs. 2 and 3).

Figure 1C presents χ max/ χ'inf versus VC DNA-coil concentration (0 4.5 pM) for 250 nm beads conjugated with 40-, 60-, and 100-fold excess of detection oligonucleotides.

Figure 1A and B show χ max/ χ'inf versus VC DNA-coil concentration in two different concentration ranges; 0 1.5 and 0 13.5 pM, respectively, for 100 nm beads prepared varying the excess of detection oligonucleotides with respect to the total number of beads.