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Separated spots were located using an ultraviolet analyzer with 254 nm wavelength (WFH-203B, Shanghai Jing Branch Industrial Co., Ltd., China).
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The change in ultraviolet absorption at 340 nm was measured immediately, using an ultraviolet spectrophotometer.
Peaks were detected using an ultraviolet detector at 210 nm.
The plasmid concentration was evaluated using an ultraviolet spectrophotometer.
The concentration of RNA was determined using an ultraviolet spectrophotometer.
The DNA bands were observed using an ultraviolet transilluminator.
The purity and integrity of the RNA was confirmed using an ultraviolet spectrometer before use.
overnight by capillary elution and subjected to ultraviolet crosslinking at 120 000 μJ cm−2 using an ultraviolet Stratalinker 1800 (Stratagene, La Jolla, CA, USA).
The concentration and purity of the extracted total RNA was measured using an ultraviolet spectrophotometer.
The OD value was detected using an ultraviolet spectrophotometer (752S, Lengguang Tech. Co., Shanghai, China).
Total RNA was isolated and quantified using an ultraviolet spectrophotometer (Pharmacia) following the manufacturer's instructions.
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