試劑片 的英文怎麼說
中文拼音 [shìjìpiān]
試劑片
英文
analoids-
Tao feng changzhou chemical company located in the jiangsu international plastics city, is in changzhou city, the river additives ltd. and jurong city tao reagent production plant product sales window, the major products : toluene, pure benzene, xylene, n - octanol, ethyl acetate, acetic acid small fat, silicone oil, aniline, poly - succinimide, benzene triazole derivatives, isopropanolamine, ethanolamine, alkylation two aniline, scale inhibitor, promoting agents, antioxidants, ppd, defoamer, metal deactivator, hx - 3308 scale and corrosion inhibitor, hx03 - 12 diesel flow improver, parathion octyl - zinc chloride bridge acid, chlorine bridge anhydride, chlorobenzene, double - dicyclopentadiene, norbornene anhydride
常州濤峰化工有限公司座落在江蘇國際塑化城，是常州市夏溪助劑有限公司和句容市龍濤試劑廠生產的產品的銷售窗口，主要經營產品：甲苯、純苯、二甲苯、辛醇、乙酸乙脂、乙酸丁脂、硅油、二苯胺、雙聚丁二酰亞胺、苯三唑衍生物、異丙醇胺、乙醇胺、烷基二苯胺、防垢劑、促進劑、抗氧劑、降凝劑、消泡劑、金屬鈍化劑、 hx - 3308阻垢緩蝕劑、 hx03 - 12柴油流動改進劑、硫磷丁辛基鋅鹽、氯橋酸、氯橋酸酐、氯苯、雙聚環戊二烯、降冰片烯二酸酐等。Through measuring the value of infrared radiation when the complex decoy is burning, it is concluded that the complex decoy ' s energy of infrared radiation is much more than the substrate ' s. through researching the performance of microwave radar ' s transmission and refection within the band of 3mm and 8mm, it is proved that the interference with radar is feasible
在復合誘餌劑的性能測試方面：對制備出的復合誘餌劑燃燒時的紅外輻射展開研究，發現了復合誘餌劑的紅外輻射能量比基片的紅外輻射能量有很大的增加；開展了對3mm 、 8mm波段毫米波雷達的透射與反射性能試驗，證明了該誘餌劑干擾雷達波是可行的。Determination of end carboxyl content in pet chip using photometric method was discussed, the optimiza tion of measuring condition and parameters such as sample weight, concentration of titrant, blank of solvent were stud ied
論述採用光度法測定聚酯切片的端羧基，對稱樣量、滴定劑的濃度、溶劑的空白等測試條件和參數進行優化選擇。Since the dichromated gelatin has a higher diffraction efficiency in all holographic recording materials, the aim of this research is to use dichromated gelatin as the recording material and to make use of the principle of holography to design holographic optical components, especially in fabrication procedure of dichromated gelatin film and in experimental technique to form a high diffraction efficiency using different angular exposure method
為了產生優質的聚焦能力與效率，本研究採用目前具有最高繞射效率（ 80 ~ 90 % ）的重鉻酸明膠材料作為感光劑，除了自行調制藥劑比例成分，並依嚴格的製作步製成重鉻酸明膠全像片外，並採用不同角度重覆曝光方式改良干涉式波帶板無法自動追蹤的缺點，經過多次試驗與改進，藉以形成具備高繞射效率和自動追蹤功能的全像光學波帶板。Products : rectifers, high silicon cast iron anodes, mmo anodes ( rod, tubularribbon ), titanium conductor bar, sacrificial anodes ( aluminum, magnesiumzinc ）, magnesiumzinc ribbon anodes, zinc grounding cell, reference electrodes, test postjunction boxes, thermite ( corrtech exothermic weld metal ) mold, cathodic protection system utilizing solar energy, cp data remote monitoring system, and other accessories
我們的產品：恆電位儀、高硅鑄鐵陽極、鈦基混合金屬氧化物陽極（帶狀、棒狀、管狀） 、鈦導電片、鋅合金陽極、鎂合金陽極、鋁合金陽極、鋅帶鎂帶、長效硫酸銅參比電極、高純鋅參比電極、鋅接地電池、陰極保護測試樁、鋁熱焊模具和焊劑、太陽能陰極保護系統、陰極保護參數遠程監測控制系統等全系列陰極保護系統配套產品。Textile floor coverings - burning behavior - tablet test at ambient temperature
鋪地紡織品燃燒性能在室溫下片劑試驗Extraction of large - fragment genomic dna in order to gain dna template of pcr amplification ( long pcr amplification and salvage pcr amplification ) which was high purity and large fragment, three methods were used to extract genomic dna of bacillus subtilis, i. e. low melting - point agarose embedding method, sds - proteinase k - phenol chloroform extraction method and bacterial genomic dna extraction kit method. the genomic dna of bacillus subtilis were gained by these methods, and the operated programs of the methods were improved. the results showed that the genomic dna extracted by low melting - point agarose embedding method were obviously biggest than that of another two methods
大片段基因組dna的提取為了獲得用於pcr擴增（長距離pcr擴增和分段pcr擴增）的高純度、大片段（至少為pcr產物長度的4倍）的dna模板，應用三種方法：低熔點瓊脂糖包埋法， sds -蛋白酶k -酚氯仿抽提法和細菌基因組dna提取試劑盒法，分別提取獲得了枯草桿菌基因組dna ，並對3種方法的操作程序進行了不同程度的改進，結果表明：低熔點瓊脂糖包埋法提取的基因組dna片段明顯大於后兩種方法，採用0 . 5瓊脂糖凝膠電泳3h ，仍然跑不出加樣孔。The results of the experiments indicates that concentration of aminosilane influences the fluorescence background of glass slide, and some factors affect immobile ratio of oligonucleotide probe, such as aminosilane treatment time, aldehyde treatment time, uv crosslinking energy, washing temperature and time
研究表明，氨基化試劑濃度對玻片熒光背景有影響，氨基化試劑處理時間、醛基化處理時間、紫外交聯能量和洗滌溫度和時間等工藝因素影響寡核苷酸探針的固定率。Constructing cdna expressing library of erythrocytic plasmodium falciparum from hainan : the total rna was obtained by using. triplix kit. a modified oligo ( dt ) primer ( cds ffi pcr primer ) was used in the single - stranded ( ss ) dna synthesis reaction. the ss - dna was reversely transcripted from total rna. double - stranded ( ds ) cdna was amplified by long - distance ( ld ) pcrafter the digestion with proteinase k and sfi i, the cdna with no less than 200bp was collected and purified by glass - milk kitthe library was constructed after the ligation of cdna to tiplex2 phage particle packaged with the packaging extract system in vitro. a high titer and high recombinant ratio of cdna library was constructed
構建惡性瘧原蟲海南株紅內期cdna表達文庫提取紅內期惡性瘧原蟲海南株總rna ，直接以總rna為模板使用cdna文庫構建試劑盒，首先反轉錄合成ss一dna ，再擴增合成ds一dna （ cdna ） ，對擴增產物用蛋白酶k消化及左z丁i酶切，抽提蛋白、去除rna后，用玻璃奶試劑盒純化、回收20obp以上的片斷，經與載體連接再用蛋白包裝物包裝后形成未擴增文庫，最後擴增完成惡性瘧原蟲海南株紅內期cdna表達文庫的構建。3. based on the bond test for 33 concrete specimens and gfrp and bending test for 15 beams strengthening with gfrp, surface preparation of concrete, type of epoxy adhesives, thickness of adhesives, hardening time of adhesives, cure condition after strengthening are considered, and the effect on concrete structures strengthening with gfrp causing by construction behavior was analyzed. 4
根據gfrp片材加固混凝土結構在施工中常涉及到的一些相關因素，如混凝土基層表面處理情況、所選用的粘結劑類型、塗抹粘結劑的厚度、加固的方式以及養護狀況，進行了33個混凝土試件與gfrp片材的剪切粘結試驗，並進行了採用gfrp片材加固的15根混凝土梁的抗彎試驗，分析了與施工性能相關的因素對gfrp片材加固混凝土結構效果的影響。Extenders for paints - specifications and methods of test - natural talc chlorite in lamellar form
塗料填充劑.規范和試驗方法.片狀天然滑石亞氯酸鹽The review has been written to introduce new developments of environment - friendly synthesis of pinacols in aqueous media, including microwave irradiation, ultrasound irradiation, solvent - free, electrosynthesis and photochemical synthesis
綜述了近年來片吶醇綠色合成研究的新進展，主要包括微波、超聲波、固相合成、電合成、光化學合成等新技術、新試劑在該反應中的應用。Take a portion of a well isolated colony from each of the dishes and streak onto a filter paper moistened with the oxidase reagent or use commercially available test kits according to the recommendations of the supplier
用鉑環或無菌吸管從接種盤上取一個隔離很好的菌落的一部分，並在已用氧化酶試劑浸濕過的濾紙上（或使用商業可直接使用的試劑片）劃線。Films of the cnx nanotube were produced by thermal decomposition on fe - coated si substrates, and their low field emission properties have been investigated. a high - emission current density of 1. 28ma / cm2 for an applied field of 2. 54v / u m was achieved, implying cnx nanotubes have better electron field emitter properties than the films of carbon tubes and bcn tubes do under same experiment conditions
860熱解乙二胺，在沉積有鐵催化劑的矽片上生長出cn _ x納米管薄膜，並進行了低場致電子發射特性測試，外加電場2 . 54v / m時，發射電流達到1 . 28ma / cm ~ 2 ，比相同實驗條件下制備出的碳管、硼碳氮管薄膜的場致電子發射性能優越。Standard test method for determining the bacteria - eliminating effectiveness of hygienic handwash and handrub agents using the fingerpads of adult subjects
用成人受驗者的指形墊片測定衛生洗手和擦手劑除菌效果的標準試驗方法By taking the method of dish culture and the method of sticking up filter and through comparing the circle of inhibiting bacterium, some kinds of medicament to inhibit trichoderma viride and bacillus subtilis were selected
摘要試驗採用平皿培養法和濾紙片法，通過比較抑菌圈直徑大小，初步篩選出幾種能夠抑制木霉和枯草芽孢桿菌生長的藥劑。After electrophorised on 1 % agarose gel, the pcr production was purified with agarose gel dna extraction kit. the segment was ligated with vector pmd18 - t and then was tranformed into the competent cell of dh5 a. a construction mstnd - pmd18t was generated by inserting the sequence of 254bp into pmd18 - t vector and selecting the sense clones. positive clone was identified by three ways : endonuclease digestion, pcr and sequencing. the result showed that the cloned sequence coincides with the designed sequence. this construction was digested with nco i and xho i and ligated the pet28a ( + ) vector digested with the same enzymes using dna ligation kit. the production of ligation reaction was transformed into the competent cell of bl21 ( de3 ). after 12 - 16 hours of culture, several colnes appeared on the plate. some positive clones were selected to extract their plasmid. these plasmids were digested by nco i and xho i and indentified by pcr. a contraction, mstnd - pet28a was generated. the result showed that the cloned sequence coincides with the designed sequence
F _ 1長38bp ， r _ 1長36bp ，其它片段均40bp長， f _ 1和r _ 1片段兩端分別加上限制性內切酶nco和xho的識別位點序列。用成對單鏈片段進行延伸反應，然後用其他單鏈片段作為引物，進行pcr擴增，用dna快速純化回收試劑盒回收所得254bppcr產物，與pmd18 - t載體連接、轉化dh _ 5 。受體菌感受態細胞，利用藍白斑遺傳學篩選法篩選陽性克隆，提取其質粒，採用nco和xho雙酶切鑒定，獲得了254bp的片段；用pmd18 - t載體上的特異引物rv - m和m13 - 47進行pcr鑒定，獲得300bp的片段。Genome dna of all blood samples were extracted by using erythrocyte lysis solution and pcr buffer / nonionic detergent / proteinase k. a 109bp fragment was amplified from the human genome dna. 2. in 166 han samples, 19 ( 11. 45 % ) heterozygous genotypes of codon 54 mutant allele were found by pcr - sscp
用紅細胞裂解液和pcr緩沖液非離于去污劑蛋白酶k兩種自配試劑成功地提取了所收標本的人白細胞基因組dna ，並以此為模板成功擴增出預期的109hpmbl目的基因片段。4 ) fragement recovery of pcr products pcr products were separated on a 1. 5 % agarose gel. the expected fragment was recovered by using pcr fragment recovery kit according to the manufacturers instructions
4 、凝膠回收應用pcr目的基因片段回收試劑盒對擴增陽性pcr產物進行凝膠回收，純化目的dna片段。Ii ) two fragments ( about 240bp and 130bp ) were amplified from human keratinocytes total rna by rt - pcr. the recombinant pm - hpabl and pm - hpabs plasmids were constructed by inserting 240bp and 130bp pcr products into pmd 18 - t vector, respectively. the recombinants were identified by restriction enzyme analysis and dna sequencing, iii ) two orfs ( > 100bp ) were found in the insert sequence of pm - hpabl
應用smartpcr試劑盒和簡並引物從人皮膚角質形成細胞cdna中擴增到長分別為24obp和13obp左右的2種片段，將它們插入pmd18一t載體，用酶切法初步篩選陽性重組子pm . hrabl和pm一hrabs ，對陽性重組子進一步作測序鑒定。分享友人