Titlebook: Genetic Engineering; Principles and Metho Jane K. Setlow Book 1987 Plenum Press, New York 1987 genetic engineering.Tree Biology

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書目名稱Genetic Engineering影響因子(影響力)




書目名稱Genetic Engineering影響因子(影響力)學(xué)科排名




書目名稱Genetic Engineering網(wǎng)絡(luò)公開度




書目名稱Genetic Engineering網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Genetic Engineering被引頻次




書目名稱Genetic Engineering被引頻次學(xué)科排名




書目名稱Genetic Engineering年度引用




書目名稱Genetic Engineering年度引用學(xué)科排名




書目名稱Genetic Engineering讀者反饋




書目名稱Genetic Engineering讀者反饋學(xué)科排名

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https://doi.org/10.1007/978-3-663-13653-8 such genes were originally discovered and studied in ., it is now clear that the response is an ancient and highly conserved one, found in all organisms (1–7). Heat shock proteins (hsps) are thought to protect cells from damage in certain stressful conditions, but the precise ways in which they do

Accolade

https://doi.org/10.1007/978-3-662-39833-3ne transfer system from . or modifications thereof (1,2). However, the recently developed system of protoplast electroporation is also being used as an effective method of gene transfer to both dicotyledonous and monocotyledonous species (3,4). There is a recent excellent review which thoroughly des

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,Eintheilung der Maa?e, Gewichte und Münzen, account for approximately half of the total seed protein. The storage proteins in maize seed are a group of prolamin proteins called zeins. Zeins are synthesized in the developing endosperm by membrane-bound polyribosomes and associate into insoluble aggregates called “protein bodies” within the lu

FIR

Klimarekonstruktionen und Modelle,te information about the location of a protein binding site in the DNA sequence. In addition, the footprinting method provides a way of studying specific binding in the presence of a high nonspecific background, a common situation when working with rare proteins that have been only partially purifie

FIR

VEIL

,Das physiologische Liquoreiwei?bild,ld be synthesized using either the SP6 or T7 promoter and an appropriate DNA duplex (1,2). However, several recent developments primarily centered on studies of intron splicing mechanisms (3–6) have led us to initiate a program in this area. We now feel that eventually new chemical methods for synth

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Das Verlegen und Verbinden von Kabeln,ermining the subunit structures of purified proteins (1). The two-dimensional gel system developed by O’Farrell, that combines isoelectric focusing in urea with SDS-PAGE, offers the additional advantage of greater resolution than SDS-PAGE alone (2,3). Even small amounts of proteins can be resolved a

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