GLAZE 发表于 2025-3-21 16:51:25
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http://reply.papertrans.cn/19/1888/188711/188711_2.pngesoteric 发表于 2025-3-22 00:37:55
https://doi.org/10.1007/b102447Expression; Mammalia; biotechnology; gene expression; phenotype; protein; translation极小量 发表于 2025-3-22 08:01:28
978-1-4757-6990-6Springer Science+Business Media New York 1992勉励 发表于 2025-3-22 09:33:24
https://doi.org/10.1007/978-3-531-91015-4, or a gene) are examined in great detail through a series of narrowly defined questions and experimental protocols. This approach can illuminate many phenotypic characteristics of complex systems, including whole organisms, if those phenotypes are the direct consequence of a single gene’s function.傲慢人 发表于 2025-3-22 14:38:08
http://reply.papertrans.cn/19/1888/188711/188711_6.pnglattice 发表于 2025-3-22 18:56:57
https://doi.org/10.1007/978-3-531-91015-4nd peroxisome where n-alkane is metabolized. Host-vector systems are needed in order to investigate this phenomenon at the molecular level. Since . does not have plasmids, the isolation of an ARS site from the genome of C maltosa was attempted so as to construct vectors. Several host-vector systemsBINGE 发表于 2025-3-22 21:38:03
https://doi.org/10.1007/978-3-531-91015-4 with some branching via (3-1,6- linkages (2). The glucan network in the yeast cell wall, due to its rigidity, is an essential structure in preventing lysis of the protoplast in a hypotonic environment. Several microorganisms have been reported to produce extracellular enzymes capable of lysing yeas半圆凿 发表于 2025-3-23 02:29:12
https://doi.org/10.1007/978-3-531-91015-4eview). The two a-crystallins (αA and (αB) are present in all vertebrates, and arose from duplication of a common ancestral gene. The αA gene is expressed in a lens-specific manner, while the αB gene is expressed in numerous tissues (see 24 for review). A combination of transgenic mouse (28), mutage束以马具 发表于 2025-3-23 06:54:15
https://doi.org/10.1007/978-3-531-91015-4 in a pUC expression vector. Insertion of a synthetic oligonucleotide duplex containing a ribosomal binding sequence at 5’ upstream to ATG start codon resulted in a recombinant plasmid which expressed catalytically active TS-DHFR in . The expression of Plasmodium enzyme was demonstrated as follows: