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This is because the absorption and scattering labels are detected at the same wavelength as the excitation wavelength and are seen against a high background of light coming directly from the source.
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Normally the red-shifted fluorescence of single molecule labels is detected.
Briefly, the DNA backbone and fluorescent labels were detected, integrated, and converted into single-molecule genome maps.
Antibody labeling was detected using a chemiluminescence detection kit (Biological Industries, Kibbutz Beit Haemek, Israel).
Antibody labeling was detected using the chemiluminiscence detection kit (Biological Industries, Israel).
Antibody labeling was detected using an enhanced chemiluminescence detection kit (Biological Industries, Kibbutz Beit Haemek, Israel).
No labeling was detected with sense 35S-labeled riboprobes used as control of the hybridization specificity.
When fluorescence-labeled siRNA were applied i.c.v. in rats no label was detected in brain tissue in spite of the use of cell detergents to improve the delivery.
No labeling was detected in blood, suggesting that MWCNT were not absorbed from gastrointestinal tract in detectable concentrations [97], lymphatic system and liver were not analyzed.
Appearance of label was detected beginning around 10 20 days after the start of labeling.
However, neither ALK gene rearrangements nor ALK protein labeling was detected in LGMS (0/9).
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