酶樣的 的英文怎麼說
中文拼音 [yàngde]
酶樣的
英文
zymoid-
Aleurone grain ( aleurone body ) a modified vacuole found in the embryo and endosperm of seeds and containing mostly reserve proteins, but also phytic acid and various enzymes associated with mobilization ( digestion ) of these reserves
糊粉粒(糊粉體) :在種子胚或胚乳中發現的經過修飾的液泡,裡面包含許多儲藏蛋白,植酸和各種各樣的酶。Fourthly, according to the activity, collect, dialyse, freeze, dry respectively the sod protein through deae - sepharose column chromatog - raphy ; process the sod protein through sephacryl s - 200 column chromatography with the preceding method. at last, process the pure sod protein with same functional enzyme electrophoresis and active dye, isoelectric focusing electrophoresis and sds - page
將粗酶液過deae -瓊脂糖柱層析,得三個活力峰,分別收集、透析、乾燥濃縮后;再上sephacryls - 200凝膠柱層析,按與deae -瓊脂糖柱層析后同樣的方法收集處理。A double - strand cdna fragment of dh ( diapause hormone ) gene was obtained from kt - pcr amplification. the fragment was digested by two restriction enzyme nde 1 / ecor 1 and then was joined with pet - 30a ( + ) plasmid which was digested by nde 1 / ecor 1 too. then the outcome was transformed into escherichia coli bl21
Pcr產物經nde / ecor雙酶切后,與同樣雙酶切的pet - 30a ( + )質粒連接並轉化至大腸桿菌( escherichiacoli ) bl21中,經檢測篩選,成功得到陽性克隆。Only prokaryotes, such as bacteria, lack lysosomes.
只有細菌這樣的原核生物才沒有溶酶體。A great number of enzyme and bacterial preparation with a wide variety of trade names have been marketed as agents.
各種各樣的商品名的酶和細菌製品,已經作為試劑銷售。Its amino acid sequence exhibits significant homology with those of other thrombin - like snake venom enzymes. based on the homology, the catalytic residues and disulfide bridges of gloshedobin were deduced to be as follows : his43, asp88, ser182 and asp176 ; and disulfide bridges, cys7 - 141, cys 28 - 44, cys 76 - 234, cys120 - 188, cys152 - 167 and cys178 - 213
以同樣的方法,得到長白山白眉蝮蛇( gloydiusussuriensis )毒類凝血酶基因,並比較了它與大連蛇島蝮蛇類凝血酶基因序列的差別,發現兩者的同源性高達98 ,只有三個氨基酸不同: gln ~ ( 66 )( 3 ) pah " levels in maricultural site tvere much higher than that in the adjacent non - maricultural site, and it showed that mariculture was one of the contributors of marine pah " pollution in seal atef. 2 western xiamen harbort ( 1 ) pah " levels in surface seat " ater and sediment of the survey site " ere quite severe
5系統研究了鱸魚、真鯛體內不同器官、組織的生化指標? ?過氧化氫酶( cat ) 、超氧化物歧化酶( sod ) 、脂質過氧化( lpo )指標,結合水體及生物樣的pah污染分析結果,探討了這些指標對水環境pah污染的指示作用。By means of pcr, the signal peptide dna sequence was deleted. for study of the limited factors in expression of pro - urokinase, the pro - uk gene was divided into three fragments, and they were expressed in
最後用同樣的方法提高全長人尿激酶原cdna在大腸桿菌中的表達量,使其表達量達到全菌蛋白的5 % 。A pair of primers were designed and synthesized based on the published ge gene sequence of prv - rice strain for amplifying ge gene of prv min - a, yielding a 1. 7kb band. the segment was linked to puc19 plasma dna by means of t4 dna ligase, transformed into e. coli jm109 permissive cells, and incubated on lb fray containg amp, x - gal and iptg. small amount of plasma was extracted by base cleavaging for enzyme digest analysis and pcr, resulting in recombinant plasma puge dna containing prv ge
用t _ 4dna連接酶使ge基因與經bamhi 、 kpni同樣雙酶切的puc19質粒dna連接;用連接產物轉化大腸桿菌jml09感受態細胞,置含amp 、 x - gal和iptg的lb平板上培養12 20小時;挑取白色菌落於選擇性培養基擴大培養,堿裂解法小量提取質粒dna ,並進行酶切分析鑒定,結果獲得整合有prvge基因的重組質粒pugedna ,並與其它prv分離株進行ge基因序列同源性分析。These feedback mechanisms often make it difficult to determine the order of e - vents in a signalling cascade, since a small level of mpf activity is sufficient to activate most of the pathways involved in oocyte maturation
但是,這樣的反饋增加了對爪蟾卵成熟過程的調控機制探索的困難,反饋的存在使得人們不能確定信號傳導的順序。在反饋網路中,很難決定激酶的上下游關系。In vitro diagnostic medical devices - measurement of quantities in biological samples - metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials
體外診斷醫療器材.生物試樣的數值測量.校準儀和控制材料賦值的酶催化濃度計量溯源性An enzyme method for analysis of soluble - glucan in polysaccharides of agaricus blazei murill has been studied in this paper
摘要探討了酶法測定姬松茸多糖中-葡聚糖含量的方法,測得它的-葡聚糖含量在3 . 7 % ~ 3 . 9 %之間,標樣的平均回收率為86 . 8 % 。The same ability has been reported for some lymphocyte gpi - linked enzymes following lymphocyte actiation [ 43 ]
某些淋巴細胞gpi連接酶隨著淋巴細胞的活化具有同樣的能力,這已經被報道過43 。Such deficiencies cause lysosomal storage disorders, such as gaucher ' s disease, and replacement of the gene is an effective treatment
這樣的缺陷引起溶酶體堆積病(例如,高歇病) ,基因置換是一種有效的療法。Hydrophobicity analysis predicted a 36 - residue hydrophobic signal peptide for secretion in the n - terminus, and no transmembrane region was present, suggesting it might be a type of secretory protein. some generic and atipical n - glycosylation sites were present in clsp, suggesting that the protein might represent a glycoprotein. the clsp protein contained one cub ( clr / cls, an embryonic sea urchin protein uegf, and bone morphogenetic protein i ) domain from 39th to 164th ammo acids, which is known to be involved in protein - protein or protein - substrate interaction, and a trypsin - like serine protease domain positioned from 244th to 483rd amino acids
Clsp分子具有補體樣絲氨酸蛋白酶的多種結構特徵,包括36個氨基酸組成的疏水信號膚,一個cub ( clr / cls , anembryonicseaurehinproteinuegf , andbonemorphogeneticproteinl )結構域和一個胰酶樣絲氨酸蛋白酶結構域( t汀psin一likeserineproteasedomain )和幾個保守的糖基化位點等,沒有發現有跨膜區的存在。After determining the properties of the enzyme x - 22, white lime and fly ash, and testing the functions of the stabilizers, both single and together used, the most fitful mix ratio is determined. and then all kinds of the performance are tested and satisfy the requirement of the specification. the mechanism of stabilization and the strength creasing of the mixture are studied with the help of the results of xrd and sem photos
在定量實驗中,確定了堅土酶、熟石灰、粉煤灰的含量,對其單獨作用和復合作用進行了測試,並且最終確定了穩定混合料的最佳實驗配比,然後在最佳配合比情況下測定混合料的各項指標,滿足規范提出的要求,並結合x ?衍射( xrd )和掃描電鏡( sem )分析,闡述了試樣的穩定和強度增長機理。Howeer, under these circumstances cholinesterase would enter the salia by simple diffusion and therefore actiity should be correlated with saliary flow rate
在這樣的情況下乙酰膽堿酯酶將以簡單擴散的方式進入唾液,因此它的活性必將和唾液流量速率相關。The last, to the other seven kinds of substrates, dna did n ' t have any catalytic activity. on the contrast, pod had apparent activity to these substrates. the studies showed that dna has the peroxidase - like activity, but this activity is unlike pod which is protein
上述研究表明: dna具有過氧化物酶樣的活性,但是又不同於一般的蛋白質性質的酶,因為它與蛋白質性質的辣根過氧化物酶的催化性質有明顯差異。However, one weakness of quantitative simulation is the difficulties of determining parameters with existing experimental results ; and the dynamical behavior of the system will change with different parameter sets. thus it is necessary to construct qualitative models to complement the quantitative models. we constructed the qualitative model with gna ( genetic network analyzer ) and analyze
而且我們提出了可以用來檢驗pka的作用是通過cdc25 , mytl還是聯合作用的實驗理論依據,這樣的電腦模擬為繼續進行下一步的試驗提供了一個思路,如果精確的測量在mpf激活過程中各個不同的激酶的活性,就能夠鑒別pka的具體作用機制,我們還研究了mapk的作用。The 1. 488kb dna fragment was sequenced and ligated to pbi121 vector and transformed into otsa deficient of e. coli strains ( ff4169 ). otsa gene is in charge of trehalose - 6 - phosphate synthesis in e. coli. in growth curve experiment, the transformants that carried the 1. 488kb dna fragment grew well in minimum medium, which contains 0. 5mol / l nacl, while control strains could n ' t endure it
提取釀酒酵母的總dna ,以此為模板,採用pcr的方法從釀酒酵母中克隆出了1 . 488kb的海藻糖合成酶基因tps1片段,通過xba和sma雙酶切,與同樣經過xba和sma雙酶切的puc118載體質粒連接,轉入大腸桿菌dh5中,通過藍白斑篩選重組子。分享友人