foreign protein 中文意思是什麼
foreign protein
解釋
異處蛋白-
Diphtheria antitoxin is a foreign protein.
白喉抗毒素是異性蛋白。 -
The expression efficiency difference between ped5 and pcdhfrl, a vector utilizing cmv enhancer / promoter ( pcmv - ie ) for foreign protein production, was analyzed using human interferon - p ( ifn - ) gene and human secreted alkaline phosphatase ( seap ) gene as reporters. when analyzed in transient expression, ped5 showed a little more protein produciton than pcdhfrl. however, in continuous expression, when serum concentration was lessened to slow down cell proliferation, ped5 expressed 3. 1 times more reporter proteins than pcdhfrl, which implied that pef - io was less affected by cell cycle status in contrast to pcmv - ie, making ped5 a good expression vector for foreign protein production
應用人-干擾素（ ifn - ）和人分泌型堿性磷酸酶（ seap ）基因作為報告基因，對含有巨細胞病毒即早期啟動子（ p _ （ cmv - ie ） ）的表達載體pcdhfr1和ped5表達外源蛋白的能力進行了比較，發現對于瞬時表達， ped5略好於pcdhfr1 ；在穩定表達中，通過降低血清濃度，使細胞增殖緩慢，這時ped5表達外源蛋白的能力較pcdhfr1高3 . 1倍。 -
The new synthesized protein was led to endoplastic reticulum cavity by eukaryotic secretory signal peptide sequence and then anchored to innerwall of endoplastic reticulum by kdel sequence, which interdicted the process of protein entering golgi body and cytoplasm, and then avoided heterogeneous glycosylation modification of foreign protein and prolonged the disappearance of half life of protein in organism. 2
真核分泌信號肽序列可以引導新合成的蛋白質進入內質網腔， kdel序列將進入內質網腔的蛋白質錨定在內質網內壁上，從而阻斷了蛋白質進入高爾基體和細胞質的過程，進而避免了外源蛋白質的異源糖基化修飾，延長了蛋白質在生物體內的半衰期。 -
Mass spectrometry of synthetic hw - ma and rgd - hw are in full agreement with those speculated theoretically, which proves the success of peptide synthesis and refold. on isolated mouse phrenic nerve - diaphragm preparations, hw - ma can block the neuromuscular transmission in 35 minutes or so ( l 10 - 5 g / ml ), its biological activity shows 73 % decrease comparing with biological activity of native hwtx - i. it proves t hat the protein engineering of synthetic chimera hwtx - i has gained success to some extent, although it did not achieve our expectations. thus it proved that hwtx - i can be using as natural scaffold for protein engineering. and also emphasized the importance of " local stereo circumstances " of activity site when the foreign activity site was transferred into a natural scaffold
濃度為1 / 1059 / ml的hw一ma突變體能可逆阻斷小白鼠隔神經書高肌的接頭傳遞，阻斷時一間為35min左右，與天然hwtx一i比較，生物學活性下降3一4倍，說明合成的突變體改造獲得了一定的成功，盡管與我們預期的目標有一定的差距，從而證明hwtx一i可以作為蛋白質工程研究的天然分子骨架，同時也強調了往天然分子骨架中轉移外源活性位點時維持活性位點「局部立體環境」的重要性。 -
It has not only many advantages of the prokaryotic expression system such as growing quickly, manipulating easily, strong power to express and control foreign protein, but also the ability to make foreign protein modified in post - translation. so pichia pastoris gene expression system is more appropriate to express many eukoryotic proteins than prokaryotic system and has attracted more and more people " s attention on it
它不僅具有原核表達系統生長快速，操作簡單，外源基因表達量大並受到嚴格調控等特點，還具有真核生物特有的蛋白質翻譯后修飾的功能，表達真核生物蛋白質具有原核表達系統無法比擬的優越性。 -
27kd protein bands were detected in transgenic plants by western blot analysis, and the results showed that the foreign lea3 gene could express in transgenic strawberry plants
Westernblot分析，在轉化植株中檢測到了27kd雜交帶，表明在轉化草莓體內有外源基因翻譯產物的積累。 -
In order to screen the precious high protein and the low protein germplasm resources, this experiment determined the grain protein content of 564 wheat core germplasm materials from domestic or foreign countries with near - infrared da7200 method, and screened many precious high protein or low protein germplasm resources
摘要為了篩選高蛋白和低蛋白的種質為資源，以國內外564份小麥核心種質為材料，用da7200近紅外儀測定籽粒蛋白質含量，比較分析了國內外種質資源蛋白質含量的高低，篩選出一批寶貴的高蛋白和低蛋白的種質資源。 -
It is concluded that " green fluorescent protein gene has been integrated and expressed in at least 2 transgenic fish, it is also showed that foreign gene integrating positions and copy numbers are differ in different individuals
對于基因組上整合有gfp基因的2尾轉化個體， gfp基因在基因組上的整合位點和拷貝數並不相同，說明gfp基因作為外源基因在轉基因個體上的整合位點和拷貝數是非確定性的。 -
The expression of recombinant infectious bursal disease ( ibdv ) vp2 gene in transgenic tobacco was studied. it revealed that the vp2 produced in transgenic tobacco could react with serum specific for ibdv. these results were the basic of investigating the immunological function of foreign protein vp2 produced in transgenic plants and bolstered the concept of using transgenic plants for a novel, edible, safe vaccine production
研究了傳染性法氏囊病病毒抗原蛋白基因ibdvvp2在煙草中的表達情況，證明轉基因煙草中產生了能與ibdv特異抗血清反應的ibdv抗原蛋白，為研究轉基因植物中生產的外源蛋白vp2的免疫學功能奠定了基礎，並為利用轉基因植物生產可食疫苗提供了實驗依據。 -
Baculovirus is a kind of double - stranded circle large dna virus, which has been developed as an environment sound pesticide and a powerful vector of foreign protein expression as well as a potential vector of gene therapy
桿狀病毒是一類雙鏈環狀dna病毒，作為生物防治殺蟲劑及高效外源蛋白表達載體得到廣泛研究。近來有許多學者致力於桿狀病毒作為基因治療載體的研究。 -
30000 t y fine quality alcohol project and 30000t y protein feed project. the excellent quality and service were highly commended by the foreign clients
一承接年產10000 500000噸優級酒精工程新建及技術改造總體設計建設等工作gb10343 2002 -
This implied that the 31 kd initiated from atg codon of pres2 gene, the 30 kd encoded by the s gene was glycosylated form of s protein, the 25 kd initiated from atg codon of the pres2 gene was disassembled form of 31 kd and the 28 kd was a glycosylated form of25kd. under optimal condition the expression level of foreign gene was considerably affected on hosts ( silkworm race ), the highest difference of expression level in various races can reach up to 8 times
推測31kd處的條帶為起始於presz起始密碼子atg的表達產物，同時具有pres ： z和s抗原性， 30kd處的雜交條帶為起始於s基因起始密碼子atg表達產物的糖基化形式， 25kd的條帶可能是中蛋白的降解產物，而28kd的條帶可能25kd條帶的糖基化形式。 -
After inducement by methanol, the soluble part of trail was secreted into supernatant. a high - level strain named as gtr48 with more than 38 % of total protein secreted was screened. the foreign protein expressed amount to 10mg / l by estimate
我們篩選到一株高表達的菌株gtr48 ，經過甲醇誘導之後trail基因表達量占總的酵母分泌蛋白的38以上，並且初步估計其表達量可以達到每升十幾毫克以上。 -
Effects of different leader peptides on the foreign peptide displayed on gene 8 protein of filamentous phage
不同的引導肽對絲狀噬菌體基因8蛋白展示外源多肽的影響 -
Through three rounds of screening, seventeen clones were selected and used in competitive test. the mab ge3 could specifically inhibit eight out of seventeen clones from binding to swine antisera. based on the amin acid sequences deduced from the foreign sequence inserted in the phage, it was indicated that all clones shared the core sequence - p / ekphf, that was similar to aa50 ~ aa55 domain of n protein of prrsv
從第三輪親和篩選的噬菌體中隨機挑取17個克隆進行功能鑒定，結果表明8個克隆與mabge3具有較強的特異性結合力並可以被prrsv陽性血清阻斷，測序發現7個克隆具有核心序列： p ekphf ，該序列與prrsvn蛋白aa50 aa55 （ p ekphf ）具有較高的同源性。
分享友人