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Series concentrations of formaldehyde were prepared well previous as the standards.
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Platinum-based catalysts for the room temperature removal of formaldehyde are prepared on ceria and other supports (TiO2, Al2O3 and ZrO2) for comparison, starting from chloride and nitrate precursors.
A stock solution of 1 M formaldehyde was prepared in water and freshly diluted in SIF.
The formaldehyde was prepared from depolymerised paraformaldehyde as described (Farr and Nakane, 1981).
A 0.37% (by weight) solution of formaldehyde was prepared by dissolving paraformaldehyde in Dulbecco's Phosphate Buffered Saline without calcium or magnesium (PBS) pH 7.4.
MEL cells were cross-linked with 1% formaldehyde and nuclei were prepared from approximately 1 2×10 cells.
Melamine-resorcinol-formaldehyde (MR) aerogels were prepared by the sol-gel polymerization of formaldehyde with melamine and resorcinol using NaOH as catalyst, followed by freeze-drying.
Liver slices that were incubated for 0, 48 or 72 h in the presence or absence of PFD, were fixed with formaldehyde, and paraffin sections were prepared.
A single-cell suspension from fetal liver isolated from E14.5 embryos was cross linked with 0.4% formaldehyde and nuclear extracts were prepared.
Seventy-two hours post transduction the cells were cross-linked with 1% formaldehyde and chromatin fractions were prepared exactly as described previously.
Intact, pronase-treated, trypsin-treated, and formaldehyde-treated rabbit erythrocytes were prepared.
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