recombination protein 中文意思是什麼
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Inspection for the biological activities of recombination protein of ? ctla4 extracellular domain in vitro : we investigated the role of ctla4e in t cell proliferation of mlr with 3h - tdr incorporation
重組人ctla4胞外區蛋白體內生物學活性研究： l ）觀察ctla4胞外區蛋白在小鼠變應性鼻炎中的作用。 -
The topics include : structure and function of genes, chromosomes and genomes, biological variation resulting from recombination, mutation, and selection, population genetics, use of genetic methods to analyze protein function, gene regulation and inherited disease
主題包括：基因、染色體與基因組的結構和功能；來自於基因重組、突變和篩選的生物變異；族群遺傳學；運用遺傳學的方法分析蛋白質的功能，基因的調控和遺傳性疾病。 -
Primary strucure and identification of a home - keeping protein ( a73 ) were obtained by maldi - tof / ms and databases. protein a73 is a dna repair protein, named recn, which is indispensable protein in genetic recombination and recombination repair
（ 2 ）不同生長期的rt19的蛋白表達數量和種類約有80是相同的，證實rt19在正常的生理過程中大部分蛋白的表達是穩定的，即為持家蛋白（如a73 ） 。 -
The recombination vectors were transformed into host strain of bl21 and induced with iptg. all the recombinant protein was expressed into inclusion body. the recombinant protein was identified with sds - page and westen - blot and purified through elution method. the muticlone antibody was got by immuning the rabbit with the purified protein
把重組質粒轉化入表達受體菌bl21 ，經iptg誘導后都獲得了表達，且都以包涵體的表達形式存在，用sds - page和western - blot的方法對重組蛋白進行了鑒定。 -
In the research of transgenic fish, green fluorescent protein gene was sub - cloned to downstream of carp p - actin gene promoter that was cloned in pucusa by molecular recombination technology. thus pagfp plasmid was constructed successfully. the recombination was determined by digestion of restriction enzyme and sequencing
實驗通過分子重組技術，採用定向克隆法將綠色熒光蛋白基因亞克隆到puc118a上鯉魚-肌動蛋白基因啟動子下游，構建成能在真核生物體內表達的表達載體pagfp ，經雙酶酶切法序列鑒定后，回收帶啟動子和目的基因片段。 -
The recombination expression vector, ppic9 - e2, was linearized by sal i and electroporated into p. pastoris gs115. recombinant p. pastoris gs115, designated gs115 - ppic9 - e2, was identified by pcr and the product of the pcr was analyzed by sequencing before its expression for csfv e2 protein
重組表達載體ppic9 - e2經sal酶切線性化后，電轉化整合到畢赤酵母gs115基因組上，經pcr鑒定和pcr產物測序分析，陽性轉化子命名為gs115 - ppic9 - e2 。 -
After ultrafiltration and rough separation with ammonium sulfate and anion - exchange chromatography, the recombination protein of ctla4 extracelluar domain was rectified from the ferment supernatants
表達菌甲醇誘導發酵；發酵上清液經超濾、硫酸胺粗分級分離以及陰離于交換層析，純化出ctla4胞外區蛋白。 -
The results were as following : 1. construction and identifcation of recombinant plant expression vector pbi ! 2i - th by dna recombination technology, sweet protein thaumatin gene was cloned into plant expression vector pbii2i. recombinant plasmid pbii2i - th was constructed successfully by enzyme cutting and electrophoresis
甜蛋白thaumatin基因植物表達質粒pbi _ （ 121 ） - th的構建與鑒定利用dna重組技術，將植物甜蛋白thaumatin基因克隆至植物表達載體pbi _ （ 121 ）中，通過酶切、電泳，鑒定thaumatin基因已成功構建到植物表達質粒pbi _ （ 121 ）中。 -
Expression in bone marrow mesenchymal cells transfected by bone morphogenetic protein 7 gene recombination and its significance
重組骨形態發生蛋白7基因轉染骨髓間充質幹細胞及其在該細胞中的表達 -
With the development of dna recombination technology, there are also some reports about the expression of recombined ifn protein by prokaryotic expression system, but the expressed proteins often consist in the form of inclusion body = the operations about extracting and purifying proteins are very complicated, biological activity of proteins are not high
隨著dna重組技術的發展，國內外亦有利用原核表達系統表達重組ifn蛋白的報道，但表達的目的蛋白常以包涵體形式存在，提取純化操作步驟復雜、蛋白活性不高。
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