幾個日語遙控器方面的專業(yè)用語 請達人們幫忙翻譯一下～ 謝謝哦
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1.銘板（面貼） 2.紅外發(fā)射管 3.陶瓷諧振器 4.片阻 5.片容 6.插件電阻 7.導電膠 8. 紅膠（邦定用的） 9.黑膠（邦定封膠用的） 10.
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- 深圳華祥雨傘廠 2010-01-14 00:00:00
- プラグインのセラミック発振子 抵抗で
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- ↘*社會又如何 2010-01-27 00:00:00
- 1。ネームプレート（顏を貼り付け） 2。赤外線LED 3。セラミック発振子 4シート抵抗 5シート容量 6。プラグインの抵抗 7。導電性接著剤 8。レッドガム（ボンディングに使用） 9。レコード（接著シール使用） 10.
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- Q773975494 2010-01-11 00:00:00
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- 幾個日語遙控器方面的專業(yè)用語 請達人們幫忙翻譯一下～ 謝謝哦
- 1.銘板（面貼） 2.紅外發(fā)射管 3.陶瓷諧振器 4.片阻 5.片容 6.插件電阻 7.導電膠 8. 紅膠（邦定用的） 9.黑膠（邦定封膠用的） 10.
2010-01-10 06:10:42
466
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- 請專家?guī)兔Ψg一下，謝謝！
- 粒度檢測方法與優(yōu)缺點比較 粉末粒度分布的測量方法經過百余年的發(fā)展，據統計至少已經發(fā)展了上百種，但隨著科技的發(fā)展，有些方法被逐步淘汰，有些方法得到了改進和發(fā)展（如激光散射法、動態(tài)光散射等）， 并在生產、科研中得到了廣泛的應用，現在普遍使用的測量... 粒度檢測方法與優(yōu)缺點比較 粉末粒度分布的測量方法經過百余年的發(fā)展，據統計至少已經發(fā)展了上百種，但隨著科技的發(fā)展，有些方法被逐步淘汰，有些方法得到了改進和發(fā)展（如激光散射法、動態(tài)光散射等）， 并在生產、科研中得到了廣泛的應用，現在普遍使用的測量方法有篩分法、顯微圖像法、光透沉降法、激光散射（衍射）法等幾種，下面簡單介紹幾種常用的粒度測量方法。 ▲ 篩分法 是一種具有很長歷史的粒度測定方法，篩分法粒度測量是利用一組篩孔大小不同的標準篩將粉末進行篩分，然后對每個篩上樣品分別進行稱重，進而得到以質量為量綱的粒度分布數據，并可由分布結果計算出如Dv50等其它參數。篩分滶要特點是測量成本低廉，操作簡單，但存在著如重復性差，測量時間較長，不能對5um以下的顆粒進行測量等缺點。 ▲顯微圖像分析法 利用光學或電子顯微鏡及計算機圖像識別技術對顆粒粒度及粒度分布，顆粒形貌進行測量，分析的方法。這種方法不僅能夠測量粒度分布而且能夠直接觀察到顆粒的形狀，是目前唯yi的一種可目視的直觀測試方法，這種特點也是其它粒度測量儀器所不具備。這種方法的優(yōu)點是直觀、簡便、費用低，缺點是由于取樣量很少，為使測量結果代表性，必須增加待測顆粒的個數（一般認為測量顆粒的個數應在1000個以上），這就相應嗇了測量時間，及測試人員的工作強度，但由于能夠對顆粒形貌（如長徑比等）進行測量，目前也有廣泛應用。 ▲光透沉降法 沉降法粒度測試的理論基礎是斯托克司定律和比爾定律。前者給出顆粒沉降速度與粒徑的關系，后者闡明光透過率與粒徑重量的關系?？珊唵蔚拿枋鰹椋涸诔两狄褐?，有若干相同比重的顆粒，如果同一時刻，從同一位置開始下降，則不同直徑的顆粒到達測量區(qū)的時間是不同的，根據顆粒到達測量區(qū)的時間，及光強的強弱，就可以計算出顆粒的粒徑，及相應粒徑的顆粒在顆粒群中占有的比例。采用此種原理的測量儀器有比較長的使用歷史，但隨著科技的發(fā)展和測量手段的進步，此方法的缺點也日益突出，如測量時間長，重復性誤差大等。 ▲ 激光散射法 顆粒測量儀器是以富朗和菲衍射（Fraunhofer diffraction）和米氏散射（Mie scattering）為理論基礎。此理論可以簡單理解為沿直線傳播的平行激光束，在傳播過程中遇到顆粒的遮擋后，傳播方向發(fā)生了改變（即發(fā)生了衍射和散射現象），并且大顆粒使激光改變的角度小，小顆粒改變大。（實際上是由于顆粒的遮擋在無限遠處形成了一個愛里斑，愛里斑87%的能量集中在ZX亮環(huán)，且顆粒直徑越大，ZX環(huán)越小，顆粒直徑越小ZX亮環(huán)越大）。如果能在不同角度上接收光能， 對于相應的的角度，其光能是對應直徑的顆粒集合發(fā)生衍射（散射）造成的，相應其他角度上光能的強弱也就反應了對應直徑顆粒在整個顆粒集合中占有的比例。 ▲ 采用激光粒度測量儀器相對于光透沉降粒度測量儀器具有很多優(yōu)點： 1. 原理先進，并且由于測試過程中沒有需要預先設定的參數（如樣品比重、介質黏度、環(huán)境溫度等），及在測量過程中隨時改變的條件， 因此測量結果準確、可靠。 2. 測量速度快，測試時間與樣品粒度分布無關，典型測試過程一般小于一分鐘； 3. 每次測試，多次對樣品進行掃描，測試結果重復性好； 4. 進樣方式種類多，可適用于各種類樣品。 展開
2016-03-07 05:37:01
674
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- 幫忙翻譯下專業(yè)日語！
- 急用，謝謝！
2010-08-25 00:51:12
674
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- 幫忙翻譯一下化工方面的單詞 英語
- 堿值測定器試劑移液管錐形瓶酸式滴定管甲基黃溴甲酚綠混合指示劑鹽酸標準溶液摩爾/升酸式滴定管... 堿值 測定器 試劑 移液管 錐形瓶 酸式滴定管 甲基黃溴甲酚綠混合指示劑 鹽酸標準溶液 摩爾/升 酸式滴定管 展開
2010-01-17 06:38:39
676
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- 幫忙翻譯一下，謝謝
- IFRS13willhelpincreasetransparencywhenentitiesusemodelstomeasurefairvalue，particularlywhenusersneedmoreinformationaboutmeasurementuncertainty，suchaswhenthemarketforanasse... IFRS 13 will help increase transparency when entities use models to measure fair value， particularly when users need more information about measurement uncertainty， such as when the market for an asset or a liability has become less active. IFRS 13 requires entities to disclose information about the valuation techniques and inputs used to measure fair value， as well as information about the uncertainty inherent in fair value measurements (which was of particular concern during the global fi nancial crisis). Some of those disclosures， including the fair value hierarchy， were already introduced in March 2009 through an amendment to IFRS 7 Financial Instruments: Disclosures. Those disclosures have been relocated to IFRS 13. The requirements in IFRS 13 also incorporate the guidance in a FASB Staff Position (FSP) issued in April 2009. 展開
2012-04-29 01:58:49
511
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- 請幫忙翻譯一下，拜托
- A new kind of TiO2 nanotube array/Ni(OH)2 (TiO2/Ni(OH)2) composite electrode with the storage ability of light energy was prepared by the deposition of Ni(OH)2 on the TiO2 nanotube array， which was synthesized by anodizing Ti foils in an HF... A new kind of TiO2 nanotube array/Ni(OH)2 (TiO2/Ni(OH)2) composite electrode with the storage ability of light energy was prepared by the deposition of Ni(OH)2 on the TiO2 nanotube array， which was synthesized by anodizing Ti foils in an HF aqueous solution. SEM and XRD results showed that Ni(OH)2 particles were well distributed on high density， well-ordered and uniform TiO2 nanotube arrays. The photoelectrochemical properties of the TiO2/Ni(OH)2 electrode were investigated in NaHCO3/NaOH buffer solution (pH 10) by means of UV–vis absorption spectra， cyclic voltammogram (CV) and photocurrent measurements. It was found that the TiO2/Ni(OH)2 electrode was highly sensitive to light and exhibited excellent photoelectrochromic properties. Upon UV irradiation， the photogenerated holes by TiO2 nanotube arrays can oxidize Ni(OH)2 to NiOOH， and thus the TiO2/Ni(OH)2 electrode can be photo-charged by light。1. Introduction Among many visible light photocatalysts， TiO2nanostructures have attracted much attention due to high photocatalytic activ-ity， nontoxicity， chemical stability and huge potential applications [1–6]. The TiO2 nanotube array is one of most attention-getting TiO2nanostructures because of large surface area and outstanding charge transport properties. TiO2nanotube arrays can be utilized in dye-sensitized solar cells[7–9]， photocatalysis and hydrogen gas sensing [10]. So far， a variety of methods have been attempted to prepare TiO2 nanotube arrays， such as hydrothermal synthe-sis[11]， Langmuir–Blodgett technique [12]， solution casting [13] and anodization technique[10，14]， etc. Among these methods， the anodization technique has many advantages of low cost， low tem-perature and easy to be scaled up to large-area preparation. Recently， anewkindof photo-functional systemwith theenergy storage ability has been developed by coupling TiO2 photosen-sitive electrode with energy storage materials. In Takahashi and Tatsuma’swork[15]，aTiO2/Ni(OH)2bilayer thinfilmwas suggested for the oxidative energy storage. In this case， a redox-activep-type semiconductor Ni(OH)2is coupled withn-type TiO2photocatalyst to formap–njunction，WhenTiO2is illuminatedby light， holesgen-erated at the junction are separated from excited electrons， trans-ported into the bulk of Ni(OH)2and oxidized Ni(OH)2to NiOOH. Therefore， the oxidative energy storage system was constructed 展開
2012-11-13 20:08:52
530
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- 求日語 日文翻譯幫忙翻譯一下。。。萬分感謝
- 請求項2記載の透明硬脆材料のレーザ加工裝置において、前記半透過ミラー及び前記反射ミラーにおける凹面のそれぞれの焦點位置が、同位置となるよう配置したことを特徴とするレーザ加工裝置。
2014-03-16 13:43:20
637
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- 請各位大蝦幫忙翻譯一下：
- Withmorethan6millionnewmeasurementchannelssoldlastyear，NationalInstrumentsisaworldwideleaderinvirtualinstrumentation.Engineershaveusedvirtualinstrumentationformorethan25y... With more than 6 million new measurement channels sold last year， National Instruments is a worldwide leader in virtual instrumentation. Engineers have used virtual instrumentation for more than 25 years to bring the power of flexible software and PC technology to test， control， and design applications making accurate analog and digital measurements from DC to 2.7 GHz. This document provides an excellent introduction to virtual instrumentation as well as additional resources for continued research. What is virtual instrumentation? With virtual instrumentation， software based on user requirements defines general-purpose measurement and control hardware functionality. Virtual instrumentation combines mainstream commercial technologies， such as the PC， with flexible software and a wide variety of measurement and control hardware， so engineers and scientists can create user-defined systems that meet their exact application needs. With virtual instrumentation， engineers and scientists reduce development time， design higher quality products， and lower their design costs. 展開
2007-05-22 09:38:51
477
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- 請高手幫忙翻譯一下 3
- 2.2.1. Physical and physicochemical characterization The particle size distribution of the Ch-zeolite was determined using a laser diffraction equipment (CILASk 1064) and standard wet sieving (Mesh Tylerk series). Scanning electron mic... 2.2.1. Physical and physicochemical characterization The particle size distribution of the Ch-zeolite was determined using a laser diffraction equipment (CILASk 1064) and standard wet sieving (Mesh Tylerk series). Scanning electron microscopy (SEM-PHILIPSk XL20) was used for photomicrographs as well as to analyse the Ch-zeolite composition (Energy Dispersion X-ray， EDX). The sample was initially placed in a vacuum chamber for coating with a thin layer (few nanometers) of gold (Au). The specific surface area of the material was measured by the methylene blue technique and by nitrogen gas adsorption methods， with the latter also providing information about particle porosity. In the methylene blue adsorption method， aqueous solutions (50 ml) of methylene blue (100 mg l 1) were agitated using an orbital shaker (Marconik) for an hour at room temperature in the presence of different quantities of the Ch-zeolite (0.05–0.3 g). The suspensions were then allowed to settle for 23 h and the resulting supernatants were centrifuged at 5000 rpm before the analysis of the residual methylene blue concentration. Results obtained correspond to averaged values of three different experiments. The specific surface area was evaluated by the Langmuir model， assuming the formation， at high concentrations， of a dye monolayer and 1.08 nm2 molecule 1， for the cross-sectional area (Van den Hul and Lyklema， 1968). The Ch-zeolite specific surface area was evaluated by the nitrogen gas adsorption method， using automated equipment (Autosorb 1-Quantachrome Instrumentsk)， employing multipoint BET isotherm adsorption data fitting. Also from these data， the porosity of the material was evaluated through parameters such as volume of total pores (d < 206 nm)， surface area and volume of micropores (d < 2 nm; Micropore Analysis Method). Zeta potential measurements for the natural and ammonia loaded zeolite， as a function of medium pH， were determined using a Zeta Plusk equipment (Brookhaven Instruments). Suspensions (0.01% v/v) of the Ch-zeolite， previously sieved below 37 Am (400 Mesh Tylerk)， in a 10 3 mol l 1 solution of KNO3 were used and the medium pH was controlled with the addition of HNO3 (pH< 7) and KOH (pH>7)， separately. For the Ch-zeolite saturated with ammonia， suspensions of the material were prepared by the same procedure， except that the sample was loaded with 100 mg NH3–N l 1 of ammonia. 展開
2018-11-22 17:49:22
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- 測序方面的生物專業(yè)英文句子翻譯
- The cDNA and gene sequences currently available includes 31，741 unique sequences assembled from 217，519 high quality 454 sequencing reads.這句怎么翻譯？尤其是high quality 454 sequencing reads具體怎么翻譯
2012-10-02 13:55:39
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- 翻譯一下幾個生物專業(yè)詞匯apoptosis，microarray....
- 翻譯一下幾個生物專業(yè)詞匯apoptosis，microarray，phenotype.heterozygous，cortice，internalize，up-regulate，down-regulate，cyclopamine，vivo，catenin，cadherin... 翻譯一下幾個生物專業(yè)詞匯apoptosis，microarray，phenotype.heterozygous，cortice，internalize，up-regulate，down-regulate，cyclopamine，vivo，catenin，cadherin 展開
2006-05-16 02:18:53
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- 請翻譯一下這段英文1，謝謝
- Materials For the present study， the matrix was ABS supplied by Formosa Co. The reinforcements were polyacrylonitrile based high strength CFs. The properties of materials used were given in Table 1. Carbon fibre surface treatment Carbon fi... Materials For the present study， the matrix was ABS supplied by Formosa Co. The reinforcements were polyacrylonitrile based high strength CFs. The properties of materials used were given in Table 1. Carbon fibre surface treatment Carbon fibres were oxidised by boiling in HNO3 under reflux for 5 h (T5120uC). Afterwards， the nitric acid oxidised fibres were washed with distilled water to neutral pH. Fibre surface composition The fibres were characterised by X-ray photoelectron spectroscopy (ESCA 300， Scienta， Sweden) to determine the level of functionalisation of the modified fibres. An initial survey scan was performed to determine the detectable elements， followed by high resolution scans. The entire X-ray photoelectron spectrum was energy referenced to the C1s peak of graphite (bending energy5284?5 eV). Composite preparation Before processing， ABS pellets and CFs were dried in a vacuum oven for 4 h at 80uC. Composites containing 0， 5， 10， 15， 20， 25 and 30 wt-% SCF were prepared by melt mixing in a co-rotating twin screw extruder (Thermoprism TSE 16 TC， L/D:24). The ABS pellets and CFs were fed from the main and side feeders respectively. The molten composite obtained from the die of the extruder was water cooled and pelletised. The extrusion conditions were arranged， as shown in Table 2. The viscosity of the melt containing CFs depends on the viscosity of the polymer matrix as well as the processing temperature. To avoid unfavourable shearing conditions， the melt temperature is kept as high as possible regarding thermal degradation. Before PA6 was blended to promote interfacial adhesion， vacuum drying of the ABS and PA6 pellets was carried out at 80uC for 4 and 12 h respectively. The 0， 10， 20 and 30 wt-% PA6 containing batches were fed through the main feeder to the twin screw extruder. The extrudate was water cooled and chopped into small pellets. The produced ABS/PA6 pellets were vacuum dried again at 80uC for 12 h. To prepare the SCF reinforced ABS/PA6 composites， the blend was introduced into the twin screw extruder from the main feeder， and SCFs were fed from the side feeder. The twin screw extruder was operated at the same processing conditions used during the blend preparation. The extrudate was again water cooled and chopped into small pellets. The extrusion grades of resin were used to make the extrudate form fully. The specimens for the mechanical characterisation experiments were moulded using a laboratory scale injection moulding machine (microinjector， model 1998; Daca Instruments) at a barrel temperature of 230uC and mould temperature of 80uC. The injection moulding machine used in this study was a laboratory type microinjector. The principle of the operation is that the preweighed (，2?5 g) raw material is loaded into the cylindrical barrel and allowed to melt at a preset barrel temperature for 1 min.Then the molten plastic is pushed through an injection tip by a piston. 展開
2011-04-23 21:43:45
427
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- 誰能翻譯這段英文，化學專業(yè)方面的，很難
- This work examines the behaviour of fluorine modified b-PbO2 electrodes in the processes of O2 and O3 evolution in sulphuric acid. The electrochemical kinetic analyses of these processes are based on quasi-steady-state polarisation and impe... This work examines the behaviour of fluorine modified b-PbO2 electrodes in the processes of O2 and O3 evolution in sulphuric acid. The electrochemical kinetic analyses of these processes are based on quasi-steady-state polarisation and impedance data. The good agreement between the two sets of measurements allows some basic conclusions to be drawn. In particular， the O2 evolution process is always inhibited at F-doped PbO2 electrodes， and impedance results suggest possible changes in the mechanism， with electrodesorption of intermediates becoming more important as the concentration of the doping element increases. The interpretation of the data for the less positive potentials region invokes the specific adsorption of SO4 as a factor influencing the kinetics of O2 evolution. The current efficiency for O3 formation as a function of the amount of NaF added to the PbO2 growth solution reaches a maximum for a concentration of 0.01 mol dm 3. A plausible cause for the decrease on the higher concentration side is the discharge of adsorbed SO4 2 (or HSO4 ) eventually yielding persulphate. This reaction is known to be favoured in the presence of a relatively high amount of fluoride in the electrolyte. An analysis of the results of modified neglect of diatomic differential overlap (MNDO) calculations on Pb cluster models and of X-ray photoelectron spectroscopy (XPS) data suggests that the coverage by weakly adsorbed oxygen species (OH and H2O) is an important parameter that is influenced by F-doping. ? 1999 Elsevier Science Ltd. All rights reserved. 展開
2009-02-21 00:33:53
466
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- 請教英語高人，幫忙翻譯一下．急用，謝謝?。?！
- Theelementalcontentofrawmaterials，phosphogypsum，substrate(potassiumsalt)，products(superphosphateand“Amofoska”)，soil，andgrasswasdeterminedusingconventionalandepithermaln... The elemental content of raw materials， phosphogypsum， substrate (potassium salt)， products (superphosphate and “Amofoska”)， soil， and grass was determined using conventional and epithermal neutron activation analysis using the IBR-2 pulsed fast reactor at Frank Laboratory of Neutron Physics (FLNP)， Joint Institute for Nuclear Research (JINR)， Dubna， Russia. The analytical procedure was described elsewhere by Frontasyeva and Pavlov [15]. Quality control was based on the application of certified reference materials (CRMs): IAEA-336 (lichens)， IAEA-SDM (lake sediment) and IAEA-SL1 (soil). The certified values and the results obtained by NAA were compared (Table 2). Concentrations of most elements were in good agreement with the CRMs except for Ti， Ni， Ce， Eu， Dy and Rb， which differed from the certified value as follows: Ti - 41.7 %， Ni - 26.5 %， Ce - 24.3 %， Eu - 32.9 % and Dy - 33.3 % in IAEA-SL1 (soil) and Rb - 20.6 % in IAEA-336 (lichens). For the 21 elements in agreement with the certified values the bias observed was below 20 %. For 11 elements (Al， V， Mn， As， Br， Sc， Cr， Sm， Na， Co and Sb)， the bias ranged from 0.03 % to 5 %， for 5 elements (Fe， Zn， Ba， Th and Cs) the bias was greater than 5 % but lower than 10 %， and for 5 elements (La， Tb， Hf， Ta and U) the bias was determined to be between 10 % and 20 %. Samples of raw materials， phosphogypsum， substrate， products， soil (of about 0.1 g)， and grass (0.3 g) were irradiated in cadmium-screened channels 1 and 2 of the pneumatic “Regata” system described elsewhere by Frontasyeva and Pavlov [15]. In order to determine elements associated with long-lived radionuclides， samples were irradiated for 100 hours. Spectra of induced gamma activity were recorded after 4 and 20-24 days of cooling. Short irradiations， 5 minutes for grass samples and 60 seconds for the remaining samples， allowed determination of Al， Ca， Cl， I， K， Na， Mg， Mn， Ti and V. Gamma-ray spectra were recorded after 5 and 12 minutes after irradiation. Data processing was performed using software developed at FLNP JINR [16， 17]. All gamma-spectrometers and counting electronics were made at JINR [16]. The software developed at FLNP JINR for peak searching， peak fitting， and nuclide identification routines were used for processing the amplitude spectra [16]. In the case of the lack of analytical data， there was a half of the detection limit inserted for each analyte [18]. Principal component analysis (classical PCA and fuzzy PCA) was performed as a tool for searching the possible correlations between environmental and industrial samples that could implicate the impact of phosphatic fertilizer production on the environment adjacent to the plant. 請給一個比較能看懂的翻譯，謝謝. 展開
2007-06-03 08:49:34
477
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- 請高手翻譯一下有關測量設備的日語說法
- 低溫脆性試驗機. 硫變儀. 門尼儀. 垂直彈性儀. 電擊穿試驗機. 壓縮彈性儀 AKRON耐磨耗試驗機 換氣式熱空氣老化箱 這些設備用日語怎么說啊，請幫幫忙啊，謝謝
2010-06-27 19:53:21
579
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- 急求翻譯 請幫忙翻譯一下這篇英文資料，急用?。。?！
- Wells-BrookfieldCone/PlateRapidDeterminationOfAbsoluteViscosityIntroductionTheWells-BrookfieldCone/PlateViscometergivesresearchersasophisticatedinstrumentforroutinelydete... Wells-Brookfield Cone/Plate Rapid Determination Of Absolute Viscosity Introduction The Wells-Brookfield Cone/Plate Viscometer gives researchers a sophisticated instrument for routinely determining absolute viscosity of fluids in small sample volumes. Its cone and plate geometry provides the precision necessary for development of complete rheological data. Principle of Operation The Wells-Brookfield Cone/Plate Viscometer is a precise torque meter which is driven at discrete rotational speeds. The torque measuring system， which consists of a calibrated beryllium-copper spring connecting the drive mechanism to a rotating cone， senses the resistance to rotation caused by the presence of sample fluid between the cone and a stationary flat plate. The resistance to the rotation of the cone produces a torque that is proportional to the shear stress in the fluid. The amount of torque is indicated either on a dial or digital display， depending on model. This reading is easily converted to absolute centipoise units (mPa.s) from pre-calculated range charts. Alternatively， viscosity can be calculated from the known geometric constants of the cone， the rate of rotation， and the stress related torque. See Range Tables The correct relative position of cone and plate is obtained by following a simple mechanical procedure without the need for external gauges or supplementary instrumentation. The stationary plate forms the bottom of a sample cup which can be removed， filled with .5 ml to 2.0 ml of sample fluid (depending on cone in use)， and remounted without disturbing the calibration. The sample cup is jacketed and has tube fittings for connection to a constant temperature circulating bath. The system is accurate to within ?.0% of the working range. Reproducibility is to within ?.2%. Working temperature range is from 0oC to 100oC. 展開
2018-11-17 09:10:28
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- 幫忙介紹幾個主流的運動控制方面的開發(fā)板（評估板）
- 驅動要求：無感無刷直流電機，輸出電壓24V，電流Z大2，穩(wěn)定8-1。Z好是主流產品，有一些技術支持。我是初學者，謝謝關照... 驅動要求：無感無刷直流電機，輸出電壓24V，電流Z大2，穩(wěn)定8-1。 Z好是主流產品，有一些技術支持。我是初學者，謝謝關照 展開
2016-03-23 06:17:05
423
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- 請幫忙分析一下血細胞分析報告單，謝謝~
- 血細胞分析報告單參數報警結果參考范圍WBC白細胞數目4.9*10^9/L4.0-10.0LYMPH#淋巴細胞數目1.0*10^9/L0.6-4.1MID#中間細胞數目0.0*10^9/L0.1-1.8GRAN#中性粒細胞數目L3.9*10^9/L2.0-7... 血細胞分析報告單 參數 報警 結果 參考范圍 WBC白細胞數目 4.9*10^9/L 4.0-10.0 LYMPH#淋巴細胞數目 1.0*10^9/L 0.6-4.1 MID#中間細胞數目 0.0*10^9/L 0.1-1.8 GRAN#中性粒細胞數目 L 3.9*10^9/L 2.0-7.8 LYMPH%淋巴細胞百分比 21.4% 20.0-40.0 MID%中間細胞百分比 1.9% 1.0-15.0 GRAN%中性粒細胞百分比 H 76.7% 50.0-70.0 HGB血紅蛋白 141g/L 110-160 RBC紅細胞數目 5.04*10^12/L 3.50-5.50 HCT紅細胞壓積 H 52.0% 36.0-48.0 MCV平均紅細胞體積 H 103.3fL 80.0-99.0 MCH平均紅細胞血紅蛋白含量 27.9 26.0-35.0 MCHC平均紅細胞血紅蛋白濃度 L 271 300-380 RDW-CV紅細胞分布寬度變異系數 12.0% 11.5-14.5 RDW-SD紅細胞分布寬度標準差 49.5 35.0-56.0 PLT血小板數目 256*10^9 100-300 MPV平均血小板體積 8.2 7.4-10.4 PDW血小板分布寬度 H 17.5 15.0-17.0 PCT血小板壓積 0.209% 0.108-0.282 醫(yī)院醫(yī)生說我有點感冒，但是我沒有感冒的癥狀。有時候坐著就算慢慢地站起來也會眼前發(fā)黑，腦袋有充血的感覺，眼前黑幾分鐘，覺得是貧血，但是醫(yī)生說沒有貧血（請幫忙判斷一下）。還有我的指甲貼肉的部分異常紅，家里人的指甲貼肉部分都是偏白的，不知道這是什么原因（請解釋一下有沒有什么問題）。然后手腳總是冰冷的，有時候嘗試捂熱，但是捂不很熱，還出汗（請解釋一下這是什么原因）。謝謝！ 展開
2013-02-20 02:54:45
523
2
- 請高手高手高高手幫忙翻譯下面的設備名稱
- 請幫忙翻譯下：謝謝！斑點酶解系統自動斑點切取系統蛋白純化系統基因芯片掃描系統二維電泳梯度膠制備系統全自動電泳儀多通道懸液芯片系統體內可見光成像系統如果您翻譯的十分準確，我... 請幫忙翻譯下：謝謝！ 斑點酶解系統 自動斑點切取系統 蛋白純化系統 基因芯片掃描系統 二維電泳梯度膠制備系統 全自動電泳儀 多通道懸液芯片系統 體內可見光成像系統 如果您翻譯的十分準確，我將再加Z高分（好像是100分）。 我要英文，謝謝！ 展開
2009-07-21 06:02:17
773
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- 日語 <色牢度 >的讀音 。服裝方面的！謝謝
- 日語 <色牢度 >的讀音 。服裝方面的！謝謝
2011-05-17 14:16:01
501
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