Difference between revisions of "Part:BBa K1350003:Experience"
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This is a part of Alkaline cellulase.We obtain the gene through the PCR method and recombine it in plasmid pET-28a which has strong expression ability, and we transform the recombinant plasmid in a strong protein expression system—— BL21 Escherichia coli ,then put in iptg artificially to induce alkaline cellulase. | This is a part of Alkaline cellulase.We obtain the gene through the PCR method and recombine it in plasmid pET-28a which has strong expression ability, and we transform the recombinant plasmid in a strong protein expression system—— BL21 Escherichia coli ,then put in iptg artificially to induce alkaline cellulase. | ||
| − | + | ===Application in deinking production=== | |
| − | =Mechanical synergy theory= | + | |
| − | [[File:Mechanism. | + | ====Mechanical synergy theory==== |
| + | <center>[[File:Mechanism.jpg|150px]]</center> | ||
===User Reviews=== | ===User Reviews=== | ||
Latest revision as of 18:43, 16 October 2014
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K1350003
This is a part of Alkaline cellulase.We obtain the gene through the PCR method and recombine it in plasmid pET-28a which has strong expression ability, and we transform the recombinant plasmid in a strong protein expression system—— BL21 Escherichia coli ,then put in iptg artificially to induce alkaline cellulase.
Application in deinking production
Mechanical synergy theory
User Reviews
UNIQ78a44ae14488fed3-partinfo-00000000-QINU UNIQ78a44ae14488fed3-partinfo-00000001-QINU