Sentence examples for much weaker fluorescence from inspiring English sources
On the other hand, in Fig. 2B, an unmodified tip (bare tip without treatments in Fig. 1) that had been incubated with the same fluorescent antibodies showed much weaker fluorescence on the cantilever and a totally dark tip region which indicated no nonspecific adsorption of antibodies on the tip.
Strong fluorescent intensity was observed in microspores of the transgenic plants, whereas much weaker fluorescence intensity was detected in wild type (Fig. 5A-a, b and 5B).
E. coli harboring pPhaCAB (left side of the plate) had bright fluorescence under UV light (302 nm) in contrast to E. coli containing pBluescript II SK+ vector (right side of the plate) exhibiting a much weaker fluorescence than above.
Both 1 and 2 emit a much weaker fluorescence than that of the control compound 3 lacking of the binding units reflecting that a PET process originated from the C-3 thiourea group to the plural pyrenyl pendant groups is operative.
In contrast, much weaker fluorescence emission was observed from the bacteria incubated with the hydrogel at pH = 7.4.
A very strong fluorescence signal in the tumor was detected; however the organs, for example, liver and kidney, delineated much weaker fluorescence intensity.
After H2O2 treatment, the protoplasts of the WT plants displayed diffuse and much weaker fluorescent signals, but the protoplasts derived from the transgenic plants retained their intense fluorescence activity.
As shown in Figure 8 (lower panel), untreated A549 cells show much weaker green fluorescence than chem-AgNP-treated cells.
Unfortunately, fluorescence intensity of motor terminals exogenously labeled with GFP-HcBoNTx/A was much weaker than the endogenous fluorescence of motor terminals in thy1.2YFP16 mice.
Specifically, the intensity of fluorescence driven by the second cistron of the pAP2 vector [ 5] was consistently much weaker than the intensity of fluorescence driven by the second cistron of the pMigR vector [ 6], despite the fact that both utilize the EMCV-derived IRES.
In contrast, EYFP-fluorescence was much weaker, which can be explained by the fact that in particles of TB4-UL83-EYFP only part of ppUL83 is fused to EYFP as shown by immunoblot.
