m protein 中文意思是什麼

m protein 解釋
m蛋白成分
  • m : （pl. M's, m's）1. 英語字母表第十三字母。2. M 形狀的東西；【印刷】＝ em. 3. M （羅馬數字） 1000. MCML ＝ 1950.
  • protein : n. 【化學】朊，蛋白（質）。
  1. Sedegah m, hedstrom rc, hobart p, et al. protection against malaria by immunization with plasmid dna encoding circumsporozoite protein [ j ]. proc natl acad sci usa, 1994, 91 ( 21 ) : 9866

    劉彥文，余新炳，徐勁等.惡性瘧原蟲海南株環子孢子蛋白基因的克隆與表達[ j ] .中國人獸共患病雜志， 2000 ， 16 （ 1 ） : 8
  2. Hector r w, ingrid y, menendez m a, et al. increased expression of heat shock protein ? 70 protects a549 cells against hyperoxia j. am j physiol, 1998 oct ; 275 ( 4ptl ) : l836 ? 841

    肖貞良，孫耕耘，錢桂生.肺循環灌注對大鼠肺微血管內皮細胞分離和培養的影響j .中國病理生理雜志， 1999 ， 15 （ 11 ） ： 1053 ? 1054
  3. In this paper, a field strain of infectious bronchitis virus was isolated from proventriculus tissue, morphological observation by electron - microscope and the biological characterizations of the virus were studied, pairs of specific primers are designed and synthesized in correspondence with them, according to the published sequences of infectious bronchitis virus three structural protein ( spike protein s membrane protein m nucleocapsid protein n ) genes, the cdna of si gene, s2 gene, m gene. n gene of ib v isolate lx4 were amplified by rt - pcr and full sequences were first reported

    在此基礎上，根據國內外已發表的ibv基因序列，分別設計特異性引物，應用不同引物進行反轉錄合成cdna ，分片段對ibv的主要結構基因進行pcr擴增，並分別將各個目的片段克隆到puc19載體上，在大腸桿菌dh5中實現目的基因的分子克隆，經藍白斑篩選、限制性內切酶分析、 pcr鑒定，篩選出重組陽性質粒，並對各個目的基因片段進行序列測定，從而獲得ibv主要結構基因全序列。
  4. 4 termer m. humoral immune response in human tuberculosis : immunoglublines g, a and m directed against the purified 12 protein antigen of mycobacterial bovis bacillus calmette g verin. j c lin microbiol, 1988, 27 : 1714

    3黃蓉蓉.酶聯免疫吸附試驗檢測肺結核病人血清抗體的初步研究.中華結核和呼吸雜志， 1983 ， 6 ： 351
  5. One was based on the sbs sensitive membrane and " gas phase " immunoassay technology. by immobilized anti - tb or anti - trichinosis on the sbs membrane, it can be used to determine m. tuberculosis and trfohiflosjs. the other one was based on the protein a sensitive membrane and " liquid phase " immunoassay technoiogy

    一種是基於sbs膜固定抗體的壓電氣相兔疫技術，我們利用該技術首次對結核病和旋毛蟲病分別進行了快速診斷：另一種是基於蛋白a定向修飾抗體的壓電液相兔疫傳感技術，我們利用該技術首次對結核病進行了診斷。
  6. The sequence 56 analysis shows that there is a long open reading frame in it which encode a protein of 364 animo acid residues. the m protein include 47 basic amino acid, 30 acidic amino acid, which cause a basic estimated pi of 9. 7. phylogenetic tree based on ndv matrix protein gene shows that the b95 and v4 has the most close relationship than other ndv strain

    關于ndvm蛋白國內未見有報道，國外對此蛋白的研究也十分有限，本文克隆出了ndv株b95m蛋白基因的全序列，為m蛋白的表達及進一步研究其在病毒復制與致病中的作用機理打下了基礎。
  7. 97 % identities in amino acids respectively. the e. coli strain dh5 transformed recombinant plasmid phn was induced with 0. 6 mmol / m iptg for n gene expression. the expressed product was identified by sds - page and westem - blot test, a fusion protein about 47ku as we expected was found

    將含有重組質粒phn的菌株dh5在37條件下培養，以濃度為0 . 6mmol / liptg誘導，重組質粒n基因phn融合蛋白獲得了表達：經sds - page ， western - blot試驗，確定其表達的融合蛋白產物大小為預期的47ku 。
  8. Carville dg, dirmtrijevic n, walsh m, et al. thrombus precursor protein : marker of thrombosis early in the pathogenesis of myocardial infarction [ j ]. clin chem, 1996, 42 ( 9 ) : 1537

    諸俊，何曉東，葉書來，等.急性心肌梗死與不穩定心絞痛患者血栓前體蛋白和肌酸激酶的檢測[ j ] .中國動脈硬化雜志， 2002 ， 10 （ 2 ） ： 165 - 166
  9. The expression vector pse380 - / iy / was constructed and transformed into e. coli dh5a, expressing hyl gene by adding iptg into the broth. the expression of hyl gene showed a 120kda protein band on sds - page gel and was found to have capability to degrade ha molecules derived from a microorganism dissolved in 0. 1 m acetate buffer solution ( ph4. 0 )

    經轉化大腸桿菌dh5a和iptg誘導表達後用sds - page電泳分析，獲得一條約120kda的表達條帶； iptg誘導表達后提取原生質膜測定透明質酸分解酶活力，表明該hyl片段的產物能夠在體外分解細菌來源的ha 。採用兩種策略滅活hyl基因。
  10. Koshiyama m, fujii h, kinezaki m, et al. immunohistochemical expression of topoisomerase iialpha ( topo ilalpha ) and multidrug resistance - associated protein ( mrp ), plus chemosensitivity testing, as chemotherapeutic indices of ovarian and endometrial carcinomas [ j ]. anticaneer res, 2001, 21 ( 4b ) : 2925

    屠重棋，袁淑蘭，王艷萍，等.外周血淋巴細胞和骨肉瘤細胞體外化療藥敏相關性研究[ j ] .中國腫瘤臨床， 2003 ， 30 （ 3 ） : 194
  11. I ' m making a protein shake ' cause we ' re gonna need

    我在做蛋白質奶昔，因為我們需要
  12. Fusion expression of m - centrin in e. coil bl21 was performed by induction of fptg. fusion protein was digested by ppase and was purified by gst chelating affinity chromatography and ion exchange chromatography. the final products were checked by sds - page gel

    融合蛋白gst - m - centrin菌體經過超聲波裂解后得到的上清夜經過gst親和層析後用prescissionprotease （ ppase ）酶切，酶切產物再次經過gst親和層析和hitrapq陰離子交換層析兩步柱層析純化后，得到純度較高的的m - centrin 。
  13. Marie - therese. loones, sandra m. have investigated the developmental expression of heat shock proteins in the nervous system of the unstressed mouse embryo. the results suggested the biological importance of hsps in neuronal differentiation and migration, as well as in cell signaling, protein transport

    Marie - therese . loones ， sandram . dsouza分別研究了熱休克蛋白在小鼠胚胎期和出生后的神經系統發育過程中的分佈情況，推測hsps在神經發育過程中可能與神經細胞的分化、遷移以及神經細胞內的信號轉導和蛋白質的運輸有關。
  14. Radioimmunoassay was used to test the immune activity of m - insulin fusion protein

    放免法測定人胰島素突變體融合蛋白的活性。
  15. Biological activity of this fusion protein was detected by vsv / wish system, the result was 4. 104. 1 104iu / m =

    將篩選出來的重組菌株誘導144小時，取菌液上清液用vsv wish系統檢測重組蛋白的抗病毒活性為4
  16. Ptxb1 - hng and ptxb1 - m - insulin are expressed in e. coli successfully. after sds - page and densitometric scan analysis, the results show that the expression level of hng fusion protein is above 40 % and m - insulin fusion protein above 50 % of total bacterial proteins. western - blot result demonstrated m - insulin fusion protein had specific reaction with mouse anti human insulin antibody ( igg )

    Pbv220 ? hng在大腸桿菌中未檢測到表達，后兩個克隆在大腸桿菌bl21 （ de3 ）中獲得高效表達， hng及m - insulin融合蛋白表達量分別佔全菌蛋白的40及50左右；經western - blot鑒定m - insulin融合蛋白可以與小鼠抗人胰島素單克隆抗體（ igg ）發生抗原抗體結合反應。
  17. After sds - page and densitometric scan analysis, the expression level of hng fusion protein is above 40 % and m - insulin fusion protein above 50 %. western - blot result demonstrated m - insulin fusion protein had specific reaction with mouse anti human insulin antibody, we got hng fusion protein and m - insulin fusion protein with purity of above 80 %

    今士考個二目卜乙成功構建了ptxbi一hng及ptxbi一m一insulin原核表達克隆，並獲得了高效表達，經過純化得到純度人於80 %的融合蛋白，並對人胰島素突變體融合蛋白進行了初步活性測定。
  18. The results show that the optimal conditions of the expression of bl21 ( de3 ) - ptxbl - hng and bl21 ( de3 ) - ptxb1 - m - insuiin are : bl medium, 37, 200rpm for 4. 75h, then 1ptg was added to the medium to 0. 01mmol / l, induce for another 5h. 3. hng fusion protein and m - insulin fusion protein are expressed as inclusion bodies in e. coli

    工程菌表達條件的研究山西醫科大學2003屆碩士學位論文表達鑿l株blzi （ de3 ）一ptxbi一hng及bl21 （ de3 ）一ptxbi一介insulin均在bl培養基， 37oc 、 zoorpm搖床培養4小時45分時進入對數生民中後期，此時加入終濃度0 . olmlnol / l的i屍tg開始誘導，再持續培養5小時可達到最人表達量。
  19. 3 antimicrobiol substance and protein in the hemolymph of nymphae induced by m. anisopliae no antimicrobiol substance was detected in the hemolymph of nymphae by different kinds of micropathogens after injection with m. anisopliae, which meant that the fungus could not induce p. americanna to produce antimicrobiol substance. injection of fungal spores caused the decline of protein concentration ( pc ) at the begaining, but after that the pc increased rapidly

    3綠僵菌孢子對蜚蠊血淋巴中抗菌物質及蛋白質的誘導注射綠僵菌后的不同時期提取蜚蠊血淋巴，以多種不同類型的植物病原菌、昆蟲病原菌及腐生菌作為檢測菌，均未檢測出蜚蠊血淋巴中有抗菌物質存在，即綠僵菌不能誘導蜚蠊產生抗菌物質。
  20. Construction of porcine reproductive and respiratory syndrome virus m protein gene vaccine and immunological experiment on mice

    蛋白基因疫苗的構建及在小鼠的免疫試驗
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