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Ammonia was quantified enzymatically using a UV assay (No 1112732035; Boehringer Manheim, R-Biopharm AG, Germany).
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In agreement with this hypothesis, using a UV crosslinking assay, we observed little difference between crosslinking of SF2/ASF and ΔNSF2/ASF to IgM M1-M2 pre-mRNA, whereas the ΔRS protein bound less efficiently to IgM M1-M2 than did either SF2/ASF or ΔNSF2/ASF; however, when the N-terminal extension was deleted from ΔRS, its binding to the pre-mRNA was greatly enhanced (Figure 3B).
The HPLC assay was conducted using a UV detection wavelength of 259 nm.
Using a PCR-based genotyping assay that directly visualised CEB1 alleles on long-read agarose gels using a UV transilluminator, direct analysis of PCR products has provided a robust alternative, allowing fine resolution and sizing of mutations.
Gels were viewed using a UV trans-illuminator.
The concentration of RNA was determined using a UV spectrophotometer.
DNA was visualized using a UV transilluminator and photographed.
The drug content was determined using a UV method.
The UV power output was measured using a UV light meter with a peak sensitivity at 340 nm (LUYOR, UV 340B, China).
For a DSLR, consider using a UV filter.
Sections were observed using a UV-fluorescence microscope.
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