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By using this method, the quantity of isolated SWNTs deposited can be controlled by varying the deposition time.
The sample preparation determines quality and quantity of isolated colorants.
The quality and quantity of isolated pDNA were determined using spectrophotometer (Epoch Microplate Spectrophotometer, Take3 Micro-Volume Plate, BioTek, Bad Friedrichshall, Germany) and agarose gel electrophoresis.
Integrity and quantity of isolated RNA were assessed using a RNA Pico chip on an Agilent Bioanalyzer 2100 (Agilent Technologies) (Additional file 7: Table S5).
The quantity of isolated total RNA was checked for integrity by 2 % agarose gel electrophoresis as well as on an Agilent 2100 Bioanalyzer.
Quality and quantity of isolated total RNA and miRNA were determined using an Agilent 2100 Bioanalyzer for RNA (Agilent Technologies, Santa Clara, CA).
Similar(41)
Quantity and quality of isolated RNA was measured and evaluated by UV spectrophotometer and gel electrophoresis.
The quantity and quality of isolated RNA was determined by spectrophotometry.
The quantity and quality of isolated mRNA were assessed using a NanoDrop ND-1000 specThermo Scientificermo Scientific, Delaware, USA).
The quantity and quality of isolated RNA were tested by measuring absorbance and capillary gel electrophoresis using the 2100Bioanalyzer and RNA 6000 Pico Kit (Agilent Inc., Santa Clara, CA, USA).
Interestingly, we found that, at least within the range of amounts of material tested, chromatin extraction maintains an almost perfect linearity in terms of quantities of isolated chromatin.
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