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Electron microscopy may help to resolve this question.
35 Adding phenol to the classic Congo red dye and using fluorescence microscopy or electronic microscopy may help improve the sensitivity of this technique for the detection of amyloid deposits.
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Using atomic scale in situ transmission electron microscopy (TEM) [82] during the reaction process may help in observing and understanding the nucleation process certainly.
Use of improved experimental approaches, ideally confocal fluorescence microscopy or light sheet microscopy of intact aerial tissues, as well as further optimized ABACUS1 lines, may help in elucidating spatiotemporal patterns of ABA levels in the leaf.
Further super-resolution fluorescence microscopy experiments either using microinjected, or photoactivatable-, photoswitchable FP-tagged protein may help elucidate how α-synuclein is trafficked in cells providing more data on the physiological function and dysfunction of this important IDP.
In vivo confocal microscopy may show hyperreflective filaments, corresponding to filamentous fungi including Alternaria, and thus may help to establish an early diagnosis [9]; however, this technique is not widely available.
As our confocal microscopy studies showed some colocalization of MP and CpG within DC compartments, this may help explain the increased cytokine production and antigen-dependent CD4+ T-cell response when DCs were costimulated.
3D-reconstruction may help us refine the classification of lung adenocarcinoma by adding detailed spatial/structural information to 2D light microscopy evaluation.
It may help others.
Deceptive marketing may help.
The change may help.
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