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After purification, the samples were quantified using a Nano Drop spectrophotometer (Nano Drop Technologies, Wilmington, DE, USA).
Total protein levels of the samples were quantified using Bradford analysis prior to gel loading.
All the samples were quantified using picodrop spectrophotometer (Picodrop Limited, UK), aliquoted in triplicates to avoid DNA damage during repeated freeze thawing and stored at −20°C.
Total protein levels of the samples were quantified using Bradford analysis and a total of 100 µg protein were loaded in each lane.
The samples were quantified using the nCounter Digital Analyzer.
The samples were quantified using a validated HPLC method [ 11].
Similar(40)
The radioactivity of the samples was quantified using a gamma counter (Packard Instruments).
The DNA in the samples was quantified using an ND-1000 Spectrophotometer (NanoDrop Technologies Inc., USA).
The total protein content of the samples was quantified using a 2-D Quant kit.
The TBARS content of the samples was quantified using a standard curve generated using malondialdehyde (MDA) at 532 nm [ 24].
The presence of viral DNA in the samples was quantified using a previously described general CaPV real-time PCR.
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