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Another approach potentially successful in BTJ regeneration is gel drying.
The complete hydrolysis of TEOS was achieved by oxalic acid, which also controlled the gel drying.
The conditions varied were type of hydrated zirconia gel, drying temperature before sulfation, calcination temperature after sulfation.
In this framework, a peculiar behavior was observed for CS-MMT, with the microspheres standing both against contraction during CO2 gel drying and under hydrothermal conditions.
The designed plant included acid hydrolysis of peels, filtration of the hydrolyzed suspension, alcoholic precipitation of pectin, gel pressing, gel drying, and pectin size reduction.
In this work, a supercritical carbon dioxide (SC-CO2) gel drying process was proposed to obtain CH scaffolds and, for the first time, the simultaneous elimination of unreacted glutaraldehyde (GTA), taking advantage of its solubility in supercritical mixtures.
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The fragmented DNA was then eletrophoresed on a 20% urea-polyacrylamide gel, dried and autoradiographed.
Gels were dried using DryEase Min-gel drying system (Invitrogen, UK), scanned and semiquantitative densitometry was performed on raw digitized images using SigmaScan Pro5 software (SPSS, Chicago, IL).
Bound complexes were separated on 6% polyacrylamide gels, dried and visualized on X-ray film.
Reactions were separated on 10% native polyacrylamide gels, dried and detected by phosphorimage analysis.
Total genomic DNA was extracted from silica-gel dried leaves following Alexander et al. [ 83].
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