Difference between revisions of "Part:BBa K1350003:Experience"
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===Applications of BBa_K1350003=== | ===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. | 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. | ||
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| + | <br>===Application in deinking production=== | ||
| + | ==Mechanical synergy theory== | ||
| + | [[File:Mechanism.jpg]] | ||
===User Reviews=== | ===User Reviews=== | ||
Revision as of 18:40, 16 October 2014
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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
UNIQ3f05e8f24fed9f2f-partinfo-00000000-QINU UNIQ3f05e8f24fed9f2f-partinfo-00000001-QINU