时间分辨荧光免疫分析仪检测

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GB/T 4960.6-2008核科学技术术语.第6部分：核仪器仪表

GB/T 4960的本部分规定了核辐射探测器、通用核仪器、核设施仪表和控制、辐射防护仪器及核辐射应用仪器等核仪器的基本术语和定义。本部分适用于有关核仪器标准、合同、报告和技术规格书等技术文件的编写，文献翻译以及技术交流等。

GB/T 10630-1997放射性矿产地质术语分类与代码

本标准规定了放射性矿产地质术语分类与代码。 本标准适用于我国放射性矿产地质信息系统，也适用于放射性矿产地质工作的其他有关领域。

GB/T 27404-2008实验室质量控制规范.食品理化检测

本标准规定了食品理化检测实验室质量控制的管理要求、技术要求、过程控制要求和结果的质量保证要求。本标准适用于从事食品质量（包括感官和理化）、化学物质（包括有效成分、农兽药残留、食品添加剂、重金属、毒素、环境污染物等）检测的食品理化检测实验室的质量控制。其他学科领域的化学检测实验室亦可参照使用。

GB/T 33715-2017纳米技术 纳米技术职业场所健康和安全指南

本标准给出了与纳米技术相关的职业场所的健康和安全指南。本标准侧重于纳米材料职业制造和应用相关的健康和安全条例。本标准提供的信息可以帮助相关公司、研究人员、劳动者和其他人员在生产、操作、使用和处理纳米材料时防止产生对健康和安全不利的后果。这些建议广泛适用于一系列的纳米材料及应用。本标准是基于目前能够得到的关于纳米技术的信息，包括表征、健康效应、暴露评估和控制条例。

GB 51204-2016建筑电气工程电磁兼容技术规范

本规范适用于新建、扩建和改建的民用建筑和一般工业建筑的电气工程电磁兼容的设计、施工、检测及验收。

YY/T 1304.1-2015时间分辨荧光免疫检测系统 第1部分:半自动时间分辨荧光免疫分析仪

YY/T 1304的本部分规定了半自动时间分辨荧光免疫分析仪(以下简称分析仪)的术语和定义、要求和试验方法、标识、标签和使用说明书、包装、运输和贮存。本部分适用于单标记时间分辨荧光免疫分析。本部分不适用于双标记及多标记时间分辨荧光免疫分析。

YY/T 1304.2-2015时间分辨荧光免疫检测系统 第2部分:时间分辨荧光免疫分析定量测定试剂(盒)

YY/T 1304的本部分规定了时间分辨荧光免疫分析定量测定试剂(盒)(以下简称试剂盒)的术语和定义、要求和试验方法、标识、标签和使用说明书、包装、运输和贮存。本部分适用于单标记时间分辨荧光免疫分析。本部分不适用于双标记及多标记时间分辨荧光免疫分析。

YY/T 1533-2017全自动时间分辨荧光免疫分析仪

本标准规定了全自动时间分辨荧光免疫分析仪(以下简称分析仪)的要求、试验方法、标志、标签和使用说明书、包装、运输和贮存。本标准适用于全自动时间分辨荧光免疫分析仪。

YY/T 1582-2018胶体金免疫层析分析仪

本标准规定了胶体金免疫层析分析仪的要求、试验方法、标签和使用说明、包装、运输和贮存。本标准适用于通过测定胶体金试剂卡反应区条带的反射率对样品结果进行判读的仪器(以下简称分析仪)。本标准不适用于采用荧光标记或其他标记方法进行快速免疫测定的仪器。

NY/T 1896-2010兽药残留实验室质量控制规范

本标准规定了兽药残留实验室质量控制的管理要求、技术要求、过程控制要求、检测与检测方法要求和结果的质量保证要求。本标准适用于从事动物性产品中兽药(包括有毒有害化学品)残留检测实验室的质量控制。兽药残留研究实验室可参照使用。

NY/T 3050-2016羊奶真实性鉴定技术规程

本标准规定了聚合酶链式反应(PCR)方法、二维凝胶电泳(2-DE)法及酶联免疫吸附(ELISA)法，对生羊奶、超高温灭菌(UHT)液态羊奶和羊奶粉中掺入牛源性奶成分的定性检测方法。本标准第一法和第二法适用于生羊奶、UHT灭菌液态羊奶及羊奶粉；第三法适用于生羊奶。本标准第一法的检出限为：生羊奶中掺假2.0%生牛奶，生羊奶掺假0.2%牛奶粉，UHT液态羊奶掺假5.0%UHT液态牛奶，羊奶粉掺假2.0%牛奶粉；第二法的检出限为生羊奶掺假5.0%生牛奶，生羊奶掺假1.0%牛奶粉，UHT液态羊奶掺假5.0%UHT液态牛奶，羊奶粉掺假2.0%牛奶粉；第三法的检出限为生羊奶掺假0.1%生牛奶。

WS/T 360-2011流式细胞术检测外周血淋巴细胞亚群指南

本标准规定了流式细胞术检测外周血淋巴细胞亚群(T细胞、B细胞、NK细胞、CD4+T细胞和CD8+T细胞)的技术要点,包括标本采集和运输、免疫荧光染色技术、流式细胞仪检测和分析、结果报告和审核等方面。

SN/T 4095.1-2015实验室仪器设备期间核查管理规范

本部分规定了实验室仪器设备期间核查的通用要求。本部分适用于实验室仪器设备的期间核查。

SN/T 4601-2016进出口食品、化妆品检验术语

本标准界定了进出口食品、化妆品一般术语、制抽样术语、感官检验方法术语、理化检验方法术语、生物学检验方法术语、毒理学术语、风险分析术语、质量管理体系术语、出入境监督监管术语、标准术语、缩略语。本标准适用于进出口食品、化妆品标准的编写和出版，也适用于食品工业生产、科研、教学及其他有关领域。

DIN 58932-5-2007血液学.血液中血细胞浓度的测定.第5部分:血小板浓度的测定用参考方法

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

DIN EN ISO 7218-2014食品和动物饲料的微生物学.微生物学检验的通用要求和导则(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水质. 水中16种多环芳烃(PAH)的测定. 采用质量色谱检测的气相色谱分析法(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空气质量.环境空气中苯并(a)芘浓度测定用标准方法

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电磁兼容性(EMC).环境.公共中压供电系统中低频传导干扰及信号的兼容性等级

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电磁兼容性(EMC).试验和测量技术.混响室试验方法

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.