- 精製する、純化する
WordNet
- become clean or pure or free of guilt and sin; "The hippies came to the ashram in order to purify"
- make pure or free from sin or guilt; "he left the monastery purified" (同)purge, sanctify
- remove impurities from, increase the concentration of, and separate through the process of distillation; "purify the water" (同)sublimate, make pure, distill
- treat or prepare so as to put in a usable condition; "refine paper stock"; "refine pig iron"; "refine oil"
- attenuate or reduce in vigor, strength, or validity by polishing or purifying; "many valuable nutrients are refined out of the foods in our modern diet"
- make more precise or increase the discriminatory powers of; "refine a method of analysis"; "refine the constant in the equation"
- reduce to a fine, unmixed, or pure state; separate from extraneous matter or cleanse from impurities; "refine sugar" (同)rectify
- the quality of excellence in thought and manners and taste; "a man of intellectual refinement"; "he is remembered for his generosity and civilization" (同)civilization, civilisation
- the result of improving something; "he described a refinement of this technique" (同)elaboration
- a ceremonial cleansing from defilement or uncleanness by the performance of appropriate rites (同)purgation
- the act of cleaning by getting rid of impurities
- the act of purging of sin or guilt; moral or spiritual cleansing; "purification through repentance"
- (baseball) the fourth position in the batting order (usually filled by the best batter on the team) (同)cleanup position, cleanup spot
- freeing from noxious matter; "filtration is a purifying agent"
PrepTutorEJDIC
- (…を除いて)…‘を'清める,きれいにする,浄化する《+『名』+『of』+『名』》;(…から)…‘を'除いてきれいにする《+『名』+『from』+『名』》 / きれいになる
- …‘を'『精製する』,精錬する / 〈言葉・態度など〉‘を'『洗練する』,上品にする,優雅にする
- 〈U〉精製,精錬 / 〈U〉洗練,上品,優雅 / 〈C〉改良点,工夫 / 〈C〉(…の)極致《+『of』+『名』》
- 清めること,浄化
- 掃除,清掃 / (汚職・ギャンブルなどの)一掃,浄化 / 《俗》大もうけ / (野球で)走者を一掃する
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/07/02 15:23:27」(JST)
wiki en
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 悪性腫瘍に関連した凝固亢進状態の病因 pathogenesis of the hypercoagulable state associated with malignancy
- 2. 血液透析に使用される水の混入物質 contaminants in water used for hemodialysis
- 3. 血漿分画製剤および組換えDNA産生凝固因子 plasma derivatives and recombinant dna produced coagulation factors
- 4. アデノウイルスの病因およびベクター使用 adenovirus pathogenesis and vector applications
- 5. トロンボポエチンの生物学および生理学 biology and physiology of thrombopoietin
English Journal
- EXPRESSION, PURIFICATION, AND CHARACTERIZATION OF COLD-ADAPTED INORGANIC PYROPHOSPHATASE FROM PSYCHROPHILIC Shewanella sp. AS-11.
- Ginting EL, Iwasaki S, Maeganeku C, Motoshima H, Watanabe K.Author information a Department of Applied Biochemistry and Food Science , Saga University , Saga , Japan.AbstractIn the presence of divalent cations, inorganic pyrophosphatase is activated to hydrolyze inorganic pyrophosphate to inorganic phosphate. Here, we clone, express, purify, and characterize inorganic pyrophosphatase from the psychrophilic Shewanella sp. AS-11 (Sh-PPase). The recombinant Sh-PPase was expressed in Escherichia coli BL21 (DE3) at 20°C using pET16b as an expression vector and purified from the cell extracts by a combination of ammonium sulfate fractionation and anion-exchange chromatography. Sh-PPase was found to be a family II PPase with a subunit molecular mass of 34 kD that preferentially utilizes Mn(2+) over Mg(2+) ions for activity. The functional characteristics of Sh-PPase, such as activity, temperature dependency, and thermal inactivation, were greatly influenced by manganese ions. Manganese ion activation increased the enzyme's activity at low temperatures; therefore, it was required to gain the cold-adapted characteristics of Sh-PPase.
- Preparative biochemistry & biotechnology.Prep Biochem Biotechnol.2014 Jul 4;44(5):480-92. doi: 10.1080/10826068.2013.833114.
- In the presence of divalent cations, inorganic pyrophosphatase is activated to hydrolyze inorganic pyrophosphate to inorganic phosphate. Here, we clone, express, purify, and characterize inorganic pyrophosphatase from the psychrophilic Shewanella sp. AS-11 (Sh-PPase). The recombinant Sh-PPase was ex
- PMID 24397719
- Facts and myths of antibacterial properties of silk.
- Kaur J, Rajkhowa R, Afrin T, Tsuzuki T, Wang X.Author information Australian Future Fibres Research & Innovation Centre, Institute for Frontier Materials, Deakin University, Geelong, VIC 3216, Australia.AbstractSilk cocoons provide protection to silkworm from biotic and abiotic hazards during the immobile pupal phase of the lifecycle of silkworms. Protection is particularly important for the wild silk cocoons reared in an open and harsh environment. To understand whether some of the cocoon components resist growth of microorganisms, in vitro studies were performed using gram negative bacteria Escherichia coli (E. coli) to investigate antibacterial properties of silk fiber, silk gum, and calcium oxalate crystals embedded inside some cocoons. The results show that the previously reported antibacterial properties of silk cocoons are actually due to residues of chemicals used to isolate/purify cocoon elements, and properly isolated silk fiber, gum, and embedded crystals free from such residues do not have inherent resistance to E. coli. This study removes the uncertainty created by previous studies over the presence of antibacterial properties of silk cocoons, particularly the silk gum and sericin. © 2013 Wiley Periodicals, Inc. Biopolymers 101: 237-245, 2014.
- Biopolymers.Biopolymers.2014 Mar;101(3):237-45. doi: 10.1002/bip.22323.
- Silk cocoons provide protection to silkworm from biotic and abiotic hazards during the immobile pupal phase of the lifecycle of silkworms. Protection is particularly important for the wild silk cocoons reared in an open and harsh environment. To understand whether some of the cocoon components resis
- PMID 23784754
- Novel core-shell Cerium(IV)-immobilized magnetic polymeric microspheres for selective enrichment and rapid separation of phosphopeptides.
- Wang ZG1, Cheng G1, Liu YL1, Zhang JL2, Sun DH3, Ni JZ4.Author information 1State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Changchun 130022, China; University of Chinese Academy of Sciences, Beijing 100049, China.2State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Changchun 130022, China. Electronic address: zjl@ciac.ac.cn.3Changchun Institute Technology, Changchun 130012, China.4State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Changchun 130022, China; College of Life Science, Shenzhen University, Shenzhen 518060, China.AbstractIn this work, novel magnetic polymeric core-shell structured microspheres with immobilized Ce(IV), Fe3O4@SiO2@PVPA-Ce(IV), were designed rationally and synthesized successfully via a facile route for the first time. Magnetic Fe3O4@SiO2 microspheres were first prepared by directly coating a thin layer of silica onto Fe3O4 magnetic particles using a sol-gel method, a poly(vinylphosphonic acid) (PVPA) shell was then coated on the Fe3O4@SiO2 microspheres to form Fe3O4@SiO2@PVPA microspheres through a radical polymerization reaction, and finally Ce(IV) ions were robustly immobilized onto the Fe3O4@SiO2@PVPA microspheres through strong chelation between Ce(IV) ions and phosphate moieties in the PVPA. The applicability of the Fe3O4@SiO2@PVPA-Ce(IV) microspheres for selective enrichment and rapid separation of phosphopeptides from proteolytic digests of standard and real protein samples was investigated. The results demonstrated that the core-shell structured Fe3O4@SiO2@PVPA-Ce(IV) microspheres with abundant Ce(IV) affinity sites and excellent magnetic responsiveness can effectively purify phosphopeptides from complex biosamples for MS detection taking advantage of the rapid magnetic separation and the selective affinity between Ce(IV) ions and phosphate moieties of the phosphopeptides. Furthermore, they can be effectively recycled and show good reusability, and have better performance than commercial TiO2 beads and homemade Fe3O4@PMAA-Ce(IV) microspheres. Thus the Fe3O4@SiO2@PVPA-Ce(IV) microspheres can benefit greatly the mass spectrometric qualitative analysis of phosphopeptides in phosphoproteome research.
- Journal of colloid and interface science.J Colloid Interface Sci.2014 Mar 1;417:217-26. doi: 10.1016/j.jcis.2013.11.004. Epub 2013 Nov 19.
- In this work, novel magnetic polymeric core-shell structured microspheres with immobilized Ce(IV), Fe3O4@SiO2@PVPA-Ce(IV), were designed rationally and synthesized successfully via a facile route for the first time. Magnetic Fe3O4@SiO2 microspheres were first prepared by directly coating a thin laye
- PMID 24407680
- Aspartic acid incorporated monolithic columns for affinity glycoprotein purification.
- Armutcu C1, Bereli N1, Bayram E1, Uzun L1, Say R2, Denizli A3.Author information 1Hacettepe University, Department of Chemistry, Biochemistry Division, Ankara, Turkey.2Anadolu University, Department of Chemistry, Biochemistry Division, Eskişehir, Turkey.3Hacettepe University, Department of Chemistry, Biochemistry Division, Ankara, Turkey. Electronic address: denizli@hacettepe.edu.tr.AbstractNovel aspartic acid incorporated monolithic columns were prepared to efficiently affinity purify immunoglobulin G (IgG) from human plasma. The monolithic columns were synthesised in a stainless steel HPLC column (20cm×5mm id) by in situ bulk polymerisation of N-methacryloyl-l-aspartic acid (MAAsp), a polymerisable derivative of l-aspartic acid, and 2-hydroxyethyl methacrylate (HEMA). Monolithic columns [poly(2-hydroxyethyl methacrylate-N-methacryloyl-l-aspartic acid) (PHEMAsp)] were characterised by swelling studies, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The monolithic columns were used for IgG adsorption/desorption from aqueous solutions and human plasma. The IgG adsorption depended on the buffer type, and the maximum IgG adsorption from aqueous solution in phosphate buffer was 0.085mg/g at pH 6.0. The monolithic columns allowed for one-step IgG purification with a negligible capacity decrease after ten adsorption-desorption cycles.
- Colloids and surfaces. B, Biointerfaces.Colloids Surf B Biointerfaces.2014 Feb 1;114:67-74. doi: 10.1016/j.colsurfb.2013.08.008. Epub 2013 Oct 8.
- Novel aspartic acid incorporated monolithic columns were prepared to efficiently affinity purify immunoglobulin G (IgG) from human plasma. The monolithic columns were synthesised in a stainless steel HPLC column (20cm×5mm id) by in situ bulk polymerisation of N-methacryloyl-l-aspartic acid (MAAsp),
- PMID 24161508
Japanese Journal
- Isolation and characterization of hematopoietic stem cells in teleost fish
- Developmental and Comparative Immunology 58, 86-94, 2016-05-01
- NAID 120005771110
- マイクロバブルによる染色廃液の浄化法
- 福井工業高等専門学校研究紀要. 自然科学・工学 (49), 109-115, 2016-03
- NAID 120005764754
- 将来への帰還、過去への投企―エチエンヌ・スーリオの、創造する「ノスタルジー」
- 人間科学研究 (12), 49-66, 2016-03
- NAID 120005750918
- 現代インドネシアにおけるザカート実践の多様性とその管理の二形態
- イスラーム世界研究 9, 265-273, 2016-03
- NAID 120005749877
Related Links
- Rational製品：Rational PurifyPlus。アプリケーションの信頼性と性能を改善するために 必要なランタイム分析ツールが全て揃ったツールセット、Rational PurifyPlusの製品 概要をご紹介致します。
- A runtime analysis solution to help developers write reliable code. Two crucial functions make this possible: memory corruption detection and memory leak detection.
Related Pictures
★リンクテーブル★
| リンク元 | 「refine」「refinement」「精製」「purification」「cleanup」 |
| 拡張検索 | 「copurify」「co-purify」 |
「refine」
- v.
- 精製する、洗練させる、精巧にする
「refinement」
「精製」
- 英
- purification、refinement、cleanup、purify、refine
- 関
- 洗練、精巧、改良、緻密化、純化
「purification」
「cleanup」
「copurify」
- 同時精製する、共精製する
「co-purify」
- 同時精製する