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富士比奥

Fujirebio是IVD测试领域的全球领导者,拥有50多年的构想,开发,生产和全球范围内的IVD产品商业化经验。这些范围从专业测试到涵盖品种的全自动常规临床实验室测试解决方案...
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新冠肺炎富士比奥

临床实验室

Flu A/B & SARS-CoV-2 Real-Time RT-PCR Test
DIAPEXQ流感A/B&SARS-COV-2

DiaPlexQ Flu A/B&SARS-COV-2是一项实时RT-PCR检验,用于从鼻咽拭子中SARS-COV-2的achenza A/B病毒和N和ORF1A基因的HA基因定性检测。
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SARS-COV-2(ORF1A,N,RDRP)实时RT-PCR测试
DIAPEXQ SARS-COV-2(ORF1A,N,RDRP)

DIAPEXQ SARS-COV-2(ORF1A,N,RDRP)is a Real-time RT-PCR test for the qualitative detection of SARS-CoV-2 nucleic acids in various sample types.
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自动降压素(PCT)测试
Lumipulse G B•R•A•H•M•S PCT

Lumipulse G B•R•A•H•M•S PCT immunoreaction cartridges are for in vitro diagnostic (IVD) use with a two-step sandwich immunoassay method on the LUMIPULSE G system for the quantitative determination of procalcitonin (PCT) in human serum and plasma. The CE marked test is the most sensitive fully automated PCT test and the assay utilizes proven CLEIA (chemiluminescent enzyme immunoassay) technology with results that in up to 35 minutes.
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COVID-19荧光RT等热测定
IAMP COVID 19 SANO分析

IAMP Covid-19 Sano分析是一种基于Atila专有等温扩增技术的实时荧光RT均质测定。CE标记的测定旨在用于从SARS-COV-2中定性检测鼻咽拭子中的核酸,口咽拭子和唾液标本,这些人从疑问患有COVID-19的感染符号和感染症状的人身上。
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SARS-COV-2 S-IGG抗体测定法
lumipulse g sars-cov-2 s-igg

lumipulse g sars-cov-2 s-iggis an assay system, including a set of immunoassay reagents, for the quantitative measurement of IgG-type antibodies SARS-CoV-2 spike protein (SARS-CoV-2 S-IgG) in specimens based on CLEIA technology. The CE marked assay system has a specific two-step immunoassay method and runs on the LUMIPULSE G System with results available in up to 30 minutes.
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SARS-CoV-2 Antigen Test
lumipulse g sars-cov-2 ag

CE标记的Lumipulse G SARS-COV-2 Ag设计用于与Lumipulse G系统一起在体外诊断(IVD)中,用于在人鼻咽或唾液中检测和定量测量SARS-COV-2抗原。该测定法被用作确认SARS-COV-2感染的诊断工具,并利用经过验证的Cleia(化学发光酶免疫测定)技术,可在35分钟内提供结果。
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SARS-COV-2 AG对照
Lumipulse® SARS-CoV-2 Ag Controls

CE标记的Lumipulse®SARS-COV-2 AG对照旨在用作测定的质量控制材料,以监视Lumipulse G系统上SARS-COV-2抗原分析实验室测试程序的精确度。
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BNP控制
Lumipulse® BNP Control

CE标记的Lumipulse®BNP控制旨在用作测定的质量控制,以监视Lumipulse G系统上人类B型纳特里赛肽(BNP)分析的实验室测试程序的精确度。
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AMH Immunoreaction Cartridges
Lumipulse® G AMH (anti-Müllerian hormone)

CE标记的Lumipulse®GAMH(抗肿瘤激素)免疫反应弹药用于在Lumipulse G系统中用于体外诊断(IVD),用于在基于两步的Lumipulse的两步免疫测定方法中对AMH进行全自动化的定量测量G系统。该测定法利用了经过验证的Cleia(化学发光酶免疫测定)技术,其结果可在35分钟内获得。
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LH Immunoreaction Cartridges
Lumipulse® G LH (Luteinizing Hormone)

The CE marked Lumipulse® G LH (Luteinizing Hormone) immunoreaction cartridges are intended for in vitro diagnostic (IVD) use with the LUMIPULSE G System for the quantitative measurement of luteinizing hormone (LH) in serum or plasma. The assay utilizes proven CLEIA (ChemiLuminescent Enzyme Immunoassay) technology with results that are available in up to 35 minutes.
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HIV p24 Antigen Test
INNOTEST® HIV Antigen mAb

The CE marked INNOTEST® HIV Antigen mAb is an enzyme immunoassay for the qualitative detection of HIV p24 antigen in human serum, plasma, and cell culture supernatant. The kit contains reagents for confirmation of HIV p24 antigens in repeatedly reactive samples.
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COVID-19测试
iAMP COVID-19 Detection Kit

CE标记的IAMP COVID-19检测试剂盒设计用于在没有预处理的鼻或口咽拭子上对SARS-COV-2(COVID-19)的定性核酸检测。使用等温扩增和实时荧光检测,该套件需要有限的动手时间,并且仅在75至90分钟内提供快速的样品至上。
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SARS-COV-2分析
ESPLINE® SARS-CoV-2

The CE marked ESPLINE® SARS-CoV-2 is a cassette-style immunochromatographic assay for in vitro diagnostic (IVD) use for the detection of SARS-CoV-2 antigen directly from nasopharyngeal swab fluid. It can detect SARS-CoV-2 within 30 minutes using a simple procedure without any special instruments and is intended for use as an aid in the diagnosis of SARS-CoV-2 infection.
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关于富士比奥

Fujirebio是IVD测试领域的全球领导者,拥有50多年的构想,开发,生产和全球范围内的IVD产品商业化经验。这些范围从专业测试到涵盖品种的全自动常规临床实验室测试解决方案y of disease states.
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免疫测试

免疫测试

Model: Inno-Lia HIV I/II分数(20T)
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描述:

CE标记为Inno-LIA®HIVI/II评分免疫印迹分析旨在确认和区分人血清和血浆中对HIV-1,HIV-1组O和HIV-2抗体的抗体。The INNO-LIA HIV I/II Score test contains recombinant proteins and synthetic peptides from HIV-1 and HIV-2 as well as a synthetic peptide from HIV-1 group O.
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标签:[[临床实验室这是给予的, [快速测试这是给予的
Full Description 特征

Description

CE标记为Inno-LIA®HIVI/II评分免疫印迹分析旨在确认和区分人血清和血浆中对HIV-1,HIV-1组O和HIV-2抗体的抗体。Inno-LIA HIV I/II分数测试包含来自HIV-1和HIV-2的重组蛋白和合成肽,以及来自HIV-1组O的合成肽。这些仔细选择的抗原以最佳浓度涂在最佳的浓度上,作为在离散线上,作为离散线的,带有塑料背面的尼龙带。Request Information

特征

•所有可通过一条条检测到的主要HIV菌株:HIV-1,HIV-2和HIV-1组O
• Optimal specificity in screened-negative blood donors: 96.7% (290/300)
• High sensitivity in BBI panels
•简短和隔夜的程序
•颜色编码的试剂
•现成的试剂
•要监视的四个控制线1)非特异性反应性,2)添加样品,3)和4)颜色开发步骤
• Fully automated strip processing possible using TENDIGO™, Auto-LIA™ 48, Auto-LiPA™ 48 or AutoBlot 3000(H)
• Objective, automated reading and interpretation of the strips possible using LiRAS® for Infectious DiseasesRequest Information

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