時(shí)間分辨熒光免疫分析儀檢測

時(shí)間分辨熒光免疫分析儀檢測項(xiàng)目報(bào)價(jià)？??解決方案？??檢測周期？??樣品要求？

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GB/T 4960.6-2008核科學(xué)技術(shù)術(shù)語.第6部分：核儀器儀表

GB/T 4960的本部分規(guī)定了核輻射探測器、通用核儀器、核設(shè)施儀表和控制、輻射防護(hù)儀器及核輻射應(yīng)用儀器等核儀器的基本術(shù)語和定義。本部分適用于有關(guān)核儀器標(biāo)準(zhǔn)、合同、報(bào)告和技術(shù)規(guī)格書等技術(shù)文件的編寫，文獻(xiàn)翻譯以及技術(shù)交流等。

GB/T 10630-1997放射性礦產(chǎn)地質(zhì)術(shù)語分類與代碼

本標(biāo)準(zhǔn)規(guī)定了放射性礦產(chǎn)地質(zhì)術(shù)語分類與代碼。 本標(biāo)準(zhǔn)適用于我國放射性礦產(chǎn)地質(zhì)信息系統(tǒng)，也適用于放射性礦產(chǎn)地質(zhì)工作的其他有關(guān)領(lǐng)域。

GB/T 27404-2008實(shí)驗(yàn)室質(zhì)量控制規(guī)范.食品理化檢測

本標(biāo)準(zhǔn)規(guī)定了食品理化檢測實(shí)驗(yàn)室質(zhì)量控制的管理要求、技術(shù)要求、過程控制要求和結(jié)果的質(zhì)量保證要求。本標(biāo)準(zhǔn)適用于從事食品質(zhì)量（包括感官和理化）、化學(xué)物質(zhì)（包括有效成分、農(nóng)獸藥殘留、食品添加劑、重金屬、毒素、環(huán)境污染物等）檢測的食品理化檢測實(shí)驗(yàn)室的質(zhì)量控制。其他學(xué)科領(lǐng)域的化學(xué)檢測實(shí)驗(yàn)室亦可參照使用。

GB/T 33715-2017納米技術(shù) 納米技術(shù)職業(yè)場所健康和安全指南

本標(biāo)準(zhǔn)給出了與納米技術(shù)相關(guān)的職業(yè)場所的健康和安全指南。本標(biāo)準(zhǔn)側(cè)重于納米材料職業(yè)制造和應(yīng)用相關(guān)的健康和安全條例。本標(biāo)準(zhǔn)提供的信息可以幫助相關(guān)公司、研究人員、勞動(dòng)者和其他人員在生產(chǎn)、操作、使用和處理納米材料時(shí)防止產(chǎn)生對(duì)健康和安全不利的后果。這些建議廣泛適用于一系列的納米材料及應(yīng)用。本標(biāo)準(zhǔn)是基于目前能夠得到的關(guān)于納米技術(shù)的信息，包括表征、健康效應(yīng)、暴露評(píng)估和控制條例。

GB 51204-2016建筑電氣工程電磁兼容技術(shù)規(guī)范

本規(guī)范適用于新建、擴(kuò)建和改建的民用建筑和一般工業(yè)建筑的電氣工程電磁兼容的設(shè)計(jì)、施工、檢測及驗(yàn)收。

YY/T 1304.1-2015時(shí)間分辨熒光免疫檢測系統(tǒng) 第1部分:半自動(dòng)時(shí)間分辨熒光免疫分析儀

YY/T 1304的本部分規(guī)定了半自動(dòng)時(shí)間分辨熒光免疫分析儀(以下簡稱分析儀)的術(shù)語和定義、要求和試驗(yàn)方法、標(biāo)識(shí)、標(biāo)簽和使用說明書、包裝、運(yùn)輸和貯存。本部分適用于單標(biāo)記時(shí)間分辨熒光免疫分析。本部分不適用于雙標(biāo)記及多標(biāo)記時(shí)間分辨熒光免疫分析。

YY/T 1304.2-2015時(shí)間分辨熒光免疫檢測系統(tǒng) 第2部分:時(shí)間分辨熒光免疫分析定量測定試劑(盒)

YY/T 1304的本部分規(guī)定了時(shí)間分辨熒光免疫分析定量測定試劑(盒)(以下簡稱試劑盒)的術(shù)語和定義、要求和試驗(yàn)方法、標(biāo)識(shí)、標(biāo)簽和使用說明書、包裝、運(yùn)輸和貯存。本部分適用于單標(biāo)記時(shí)間分辨熒光免疫分析。本部分不適用于雙標(biāo)記及多標(biāo)記時(shí)間分辨熒光免疫分析。

YY/T 1533-2017全自動(dòng)時(shí)間分辨熒光免疫分析儀

本標(biāo)準(zhǔn)規(guī)定了全自動(dòng)時(shí)間分辨熒光免疫分析儀(以下簡稱分析儀)的要求、試驗(yàn)方法、標(biāo)志、標(biāo)簽和使用說明書、包裝、運(yùn)輸和貯存。本標(biāo)準(zhǔn)適用于全自動(dòng)時(shí)間分辨熒光免疫分析儀。

YY/T 1582-2018膠體金免疫層析分析儀

本標(biāo)準(zhǔn)規(guī)定了膠體金免疫層析分析儀的要求、試驗(yàn)方法、標(biāo)簽和使用說明、包裝、運(yùn)輸和貯存。本標(biāo)準(zhǔn)適用于通過測定膠體金試劑卡反應(yīng)區(qū)條帶的反射率對(duì)樣品結(jié)果進(jìn)行判讀的儀器(以下簡稱分析儀)。本標(biāo)準(zhǔn)不適用于采用熒光標(biāo)記或其他標(biāo)記方法進(jìn)行快速免疫測定的儀器。

NY/T 1896-2010獸藥殘留實(shí)驗(yàn)室質(zhì)量控制規(guī)范

本標(biāo)準(zhǔn)規(guī)定了獸藥殘留實(shí)驗(yàn)室質(zhì)量控制的管理要求、技術(shù)要求、過程控制要求、檢測與檢測方法要求和結(jié)果的質(zhì)量保證要求。本標(biāo)準(zhǔn)適用于從事動(dòng)物性產(chǎn)品中獸藥(包括有毒有害化學(xué)品)殘留檢測實(shí)驗(yàn)室的質(zhì)量控制。獸藥殘留研究實(shí)驗(yàn)室可參照使用。

NY/T 3050-2016羊奶真實(shí)性鑒定技術(shù)規(guī)程

本標(biāo)準(zhǔn)規(guī)定了聚合酶鏈?zhǔn)椒磻?yīng)(PCR)方法、二維凝膠電泳(2-DE)法及酶聯(lián)免疫吸附(ELISA)法，對(duì)生羊奶、超高溫滅菌(UHT)液態(tài)羊奶和羊奶粉中摻入牛源性奶成分的定性檢測方法。本標(biāo)準(zhǔn)第一法和第二法適用于生羊奶、UHT滅菌液態(tài)羊奶及羊奶粉；第三法適用于生羊奶。本標(biāo)準(zhǔn)第一法的檢出限為：生羊奶中摻假2.0%生牛奶，生羊奶摻假0.2%牛奶粉，UHT液態(tài)羊奶摻假5.0%UHT液態(tài)牛奶，羊奶粉摻假2.0%牛奶粉；第二法的檢出限為生羊奶摻假5.0%生牛奶，生羊奶摻假1.0%牛奶粉，UHT液態(tài)羊奶摻假5.0%UHT液態(tài)牛奶，羊奶粉摻假2.0%牛奶粉；第三法的檢出限為生羊奶摻假0.1%生牛奶。

WS/T 360-2011流式細(xì)胞術(shù)檢測外周血淋巴細(xì)胞亞群指南

本標(biāo)準(zhǔn)規(guī)定了流式細(xì)胞術(shù)檢測外周血淋巴細(xì)胞亞群(T細(xì)胞、B細(xì)胞、NK細(xì)胞、CD4+T細(xì)胞和CD8+T細(xì)胞)的技術(shù)要點(diǎn),包括標(biāo)本采集和運(yùn)輸、免疫熒光染色技術(shù)、流式細(xì)胞儀檢測和分析、結(jié)果報(bào)告和審核等方面。

SN/T 4095.1-2015實(shí)驗(yàn)室儀器設(shè)備期間核查管理規(guī)范

本部分規(guī)定了實(shí)驗(yàn)室儀器設(shè)備期間核查的通用要求。本部分適用于實(shí)驗(yàn)室儀器設(shè)備的期間核查。

SN/T 4601-2016進(jìn)出口食品、化妝品檢驗(yàn)術(shù)語

本標(biāo)準(zhǔn)界定了進(jìn)出口食品、化妝品一般術(shù)語、制抽樣術(shù)語、感官檢驗(yàn)方法術(shù)語、理化檢驗(yàn)方法術(shù)語、生物學(xué)檢驗(yàn)方法術(shù)語、毒理學(xué)術(shù)語、風(fēng)險(xiǎn)分析術(shù)語、質(zhì)量管理體系術(shù)語、出入境監(jiān)督監(jiān)管術(shù)語、標(biāo)準(zhǔn)術(shù)語、縮略語。本標(biāo)準(zhǔn)適用于進(jìn)出口食品、化妝品標(biāo)準(zhǔn)的編寫和出版，也適用于食品工業(yè)生產(chǎn)、科研、教學(xué)及其他有關(guān)領(lǐng)域。

DIN 58932-5-2007血液學(xué).血液中血細(xì)胞濃度的測定.第5部分:血小板濃度的測定用參考方法

The aim of the standard is to specify a reference method for the determination of thrombocytes in human blood.

DIN EN ISO 7218-2014食品和動(dòng)物飼料的微生物學(xué).微生物學(xué)檢驗(yàn)的通用要求和導(dǎo)則(ISO 7218-2007+Amd 1-2013).德文版本EN ISO 7218-2007+A1-2013

This standard gives general instructions for carrying out microbiological examinations in accordance with specific standards. To help to ensure the validity of the examinations. To ascertain the general techniques used for conducting the examinations are the same in all labs. To help to achieve homogeneous results.

DIN ISO 28540-2014水質(zhì). 水中16種多環(huán)芳烴(PAH)的測定. 采用質(zhì)量色譜檢測的氣相色譜分析法(GC-MS)的方法(ISO 28540-2011)

This International Standard specifies a method for the determination of at least 16 selected PAH (see Table 1) in drinking water and ground water in mass concentrations above 0,005 ìg/l and in surface water in mass concentrations above 0,01 ìg/l (for each individual compound). This International Standard can be used for samples containing up to 150 mg/l of suspended matter. This method is, with some modification, also suitable for the analysis of waste water. It is possible that this method is applicable to other PAH, provided the method is validated for each case.

BS EN 15549-2008空氣質(zhì)量.環(huán)境空氣中苯并(a)芘濃度測定用標(biāo)準(zhǔn)方法

This document specifies a measurement method for the determination of particulate benzo[a]pyrene (BaP) inambient air, which can be used in the framework of the Council Directive 96/62/EC [1] and the Directive2004/107/EC [2]. This document specifies performance characteristics and performance criteria for themeasurement method when it is used as a reference method. The performance characteristics of themeasurement method are based on a sampling period of 24 h.This document describes a measurement method which comprises sampling of BaP as part of the PM10particles, sample extraction and analysis by high performance liquid chromatography (HPLC) withfluorescence detector (FLD) or by gas chromatography with mass spectrometric detection (GC/MS). Themethod is applicable for the measurement of BaP in the concentration range from approx. 0,04 ng/m3 toapproximately 20 ng/m3.The lower limit of the applicable range depends on the noise level of the detector and the variability of thelaboratory filter blank.NOTE If the BaP concentration exceeds the calibration range the extract can be diluted.

BS EN 61000-2-12-2003電磁兼容性(EMC).環(huán)境.公共中壓供電系統(tǒng)中低頻傳導(dǎo)干擾及信號(hào)的兼容性等級(jí)

This part of IEC 61000 is concerned with conducted disturbances in the frequency range from 0 kHz to 9 kHz, with an extension up to 148,5 kHz specifically for mains signalling systems. It gives compatibility levels for public medium voltage a.c. distribution systems having a nominal voltage between 1 kV and 35 kV and a nominal frequency of 50 Hz or 60 Hz (see IEC 60038).\nCompatibility levels are specified for electromagnetic disturbances of the types which can be expected in public medium voltage power supply systems, for guidance in:\na) the limits to be set for disturbance emission into public power supply systems (including the planning levels defined in 3.1.5);\nb) the immunity limits to be set by product committees and others for the equipment exposed to the conducted disturbances present in public power supply systems.\nThe disturbance phenomena considered are:\n· voltage fluctuations and flicker;\n· harmonics up to and including order 50;\n· inter-harmonics up to the 50 harmonic;\n· voltage distortions at higher frequencies (above 50 harmonic);\n· voltage dips and short supply interruptions;\n· voltage unbalance;\n· transient overvoltages;\n· power frequency variation;\n· d.c. components;\n· mains signalling.\nMost of these phenomena are described in IEC 61000-2-1. In cases where it is not yet possible to establish compatibility levels, some information is provided.\nThe medium-voltage systems covered by this standard are public distribution systems supplying either:\na) private installations in which equipment is connected directly or through transformers, or\nb) substations feeding public low-voltage distribution systems.\nThe compatibility levels specified in this standard apply at the point of common coupling in the case of (a) and at the medium-voltage terminals of the substation in the case of (b). See Clause 4.

BS EN 61000-4-21-2011電磁兼容性(EMC).試驗(yàn)和測量技術(shù).混響室試驗(yàn)方法

This part of IEC 61000 considers tests of immunity and intentional or unintentional emissionsfor electric and/or electronic equipment and tests of screening effectiveness in reverberationchambers. It establishes the required test procedures for performing such tests. Only radiatedphenomena are considered.The objective of this part is to establish a common reference for using reverberationchambers to evaluate the performance of electric and electronic equipment when subjected toradio-frequency electromagnetic fields and for determining the levels of radio-frequencyradiation emitted from electric and electronic equipment.NOTE Test methods are defined in this part for measuring the effect of electromagnetic radiation on equipmentand the electromagnetic emissions from equipment concerned. The simulation and measurement ofelectromagnetic radiation is not adequate for quantitative determination of effects. The defined test methods areorganized with the aim to establish adequate reproducibility and repeatability of test results and qualitative analysisof effects.This part of IEC 61000 does not intend to specify the tests to be applied to a particularapparatus or system. Its main aim is to give a general basic reference to all concernedproduct committees of the IEC. The product committees should select emission limits and testmethods in consultation with CISPR. The product committees remain responsible for theappropriate choice of the immunity tests and the immunity test limits to be applied to theirequipment. Other methods, such as those covered in IEC 61000-4-3, CISPR 16-2-3 andCISPR 16-2-4 may be used.