Theradiag于1986年创立,初致力于分发体外诊断,特别是针对自身免疫性疾病。
Autoimmunity:根据您的需求进行创新
自身免疫性疾病是心血管疾病和癌症发病后的第三个原因。这是一组在临床表现和相关器*面不同的疾病,但它们具有相同的机制:针对生物体中通常存在的物质或组织的免疫系统疾病。
产生针对身体组分的自身抗体。它们的检测是一些自身免疫性疾病的诊断和有时预后的重要工具。
凭借其在自身免疫诊断试剂盒开发方面的专业知识,Theradiag提供了一整套试剂,控制和自动化系统,可用于诊断自身免疫性疾病的诊断:
Atradiag专注于您的需求,开发适合您实验室活动的创新技术产品:
FIDIS™
由Theradiag开发的基于xMAP®技术的FIDIS TM试剂盒可在一次分析中同时检测同一样品中的多种分析物。与传统的IFA或ELISA格式相比,FIDIS™技术及其在CARIS™平台上的自动化使得实验室能够以比传统套件格式更快,更低的成本执行分析并具有良好可靠性。Theradiag开发了一系列全面的商业化xMAP技术测试,用于诊断自身免疫病理学,并继续提供传染性血清学和人体细胞因子测量的扩展小组。
如果一个免疫荧光仍然是筛选自身抗体的参考试验。Theradiag提供免疫荧光测试,以筛选和鉴定主要的自身抗体(ANA,ANCA,TS,器官特异性自身抗体)和优化的方案,以便于结果解释和简化CARIS™仪器系列的适应性。
ELISA
Theradiag提供全面的成熟ELISA检测。这些测试中的大多数都提供了标准化的协议,并共享了几种常用试剂,有利于简单有效的自动化。该标准化允许用户在同一平板上同时进行多个测试,从而大化ELISA测定。
CHORUS™
Chorus™系统是一款紧凑型多参数分析仪,专门用于以单位为基础的ELISA检测,使用即用型检测设备。凭借其在自身免疫和传染性血清学方面的*测试和完整的可追溯性,Chorus™系统允许执行常规分析和不常见的参数,具有适的灵活性和安全性。
免疫印迹
我们的免疫印迹试验允许同时检测针对生化表征并固定在条带上的几种抗原的抗体。这些测定使得能够容易且快速地基于个体或串联鉴定重要数量的抗体。
CH 86010 ANA-8
CH 86014 Screen
CH 86016 Sm
CH 86018 SS-A
CH 86024 SS-B
CH 86026 Scl-70
CH 86028 Cenp-B
CH 86030 Jo-1
CH 86032 dsDNA-G
CH 86038 RF-G
CH 86040 RF-M
CH 86046 Cardiolipin G
CH 86048 Cardiolipin M
CH 86050 Beta 2 Glicoproteina G
CH 86052 Beta 2 Glicoproteina M
CH 86054 Gliadin A
CH 86056 Gliadin G
CH 86058 tTg-A
CH 86060 tTg G
CH 86062 ASCA A
CH 86066 PR3
CH 86068 MPO
CH 86070 GBM
CH 86072 a-Tg
CH 86074 a-TPO
CH 86084 AMA M2
CH 86088 U1_70
CH 86090 Intrinsic Factor
CH 86092 snRNP-C
CH 86094 ANTI-CCP
免疫荧光
HME ANA HEp-2
HME - SérumsdecontrôleANA
HME - Autresréactifs
Instructions for use
Immunofluorescence
BDI C020S_IFU_dsDNA C+strong
ME 0248-0296-0201-0202 Crithidia luciliae
ME 902.2 et 902.8 Conjugués IgG
ELISA
HM002 DNA-LISA PEROX
HM008 ENA-LISA PEROX
Immunoblot
HM015 DNA-DOT
HM042 ENA-DOT 7
FIDIS™
MX005 FIDIS dsDNA
MX117 FIDIS Connective Profile
Chorus™
CH 86010 ANA-8 S
CH 86016 Sm
CH 86018-SS-A
CH 86024 SS-B
CH 86026 Scl-70CH86028 Cenp-B
CH 86030 Jo-1
CH 86032 dsDNA-G
CH 86088 U1-70
CH 86092 snRNP-C
Instruction for use
Immunofluorescence
ME 0131- Keratin Coupes d’oesophage de rat
ELISA
HM028PE FR-LISA IgM
HM028HPE FR-LISA IgM
FCCP600 DIASTAT Anti-CCP (quantitatif)
FIDIS ™
MX103 FIDIS Rheuma-RF
MX104 FIDIS anti-CCP
Instruction for use
Immunofluorescence
BDI C004S CQ+ MITOCHONDRIES TITRATION 1X0.5ml
BDI C005S_IFU_Smooth muscle control strong
BDI C006S_IFU_GPC control strong
ME 1248-1296-0831-0832 Triple substrat
ME 902.2 et 902.8 Conjugués IgG
Sérums de contrôle ME
Immunoblot
HM043 CYTO-DOT 4
FIDIS™
MX030-48 MX030-96 FIDIS Cyto-Panel
Instruction for use
Immunofluorescence
BDI C023S CQ Titrage cANCA 0,5 mL
Immunoblot
HM025 ANCA-MBG-DOT
FIDIS™
MX007 FIDIS Vasculitis
Instruction for use
Immunofluorescence
BDI C026S_IFU_Endomysial C+
ME 0648-0696-0604ESD-0608ESD Endomysium
ME 0904 Conjugué IgA
Sérums de contrôle ME
FIDIS™
MX109-110 FIDIS Celiac DPG
Instruction for use
ELISA
HM001PE & HM006PE CARDIOLISA IgG IgM PEROX
HM007PE PHOSPHO-LISA IgG IgM PEROX
HM018 BETA2-LISA PEROX
AI 10209 AIDA P-Ethanolamine-GM
AI 10229 AIDA Prothrombin-GM
AI 10234 AIDA APS Profile-GM
AI 10240 AIDA Annexin V-GM
FIDIS™
MX012-013 FIDIS APS
Instruction for use
ELISA
RLTRE 96.3 Anti RTSH
FIDIS™
MX002 FIDIS Thyro
Instruction for use
FIDIS™
MX030-48 MX030-96 FIDIS Cyto-Panel
Instruction for use
Immunofluorescence
BDI-C023S-CQ-Titrage-cANCA-05-mL
Brochure
Diabetes mellitus type 1
Instruction for use
Immunofluorescence
BDI K4815 Coffret ICAc
ELISA
RLGDE 96 Anti-GAD
RLIAE 96 Anti-IA2
RL ZNT8 96D
Instruction for use
Immunofluorescence
ME 902.2 et 902.8 Conjugués IgG
ME 0904 Conjugué FITC IgA
Sérums de contrôle ME
BDI C009S Basement membrane control strong (Titre fort)
ELISA
RLACH/96 Anti AChR
Instruction for use
Extracellular simplex kits
MX HG01121 FIDIS Multispecies TGF-B1
Pre-mixed multiplex kits
MX HC2509 FIDIS Hu Cytokine 25-plex
MX HC0306 FIDIS Hu Cytokine Death Receptor 3-Plex
MX HC0502 FIDIS Hu cytokine Th1-Th2 5-plex
MX HC0503 FIDIS Hu CytokineInflammatory 5-plex
MX HC0507 FIDIS Hu Cytokine II 5-Plex
MX HC1001 FIDIS Hu Cytokine 10-plex
MX HC106001 FIDIS Hu Chemokine 10-plex
Coffrets de tampon
MX HB0001 FIDIS Extracellular Protein Buuffer Reagent kit
质量控制
在对实验室质量控制的监管要求不断增加的背景下,Theradiag通过提供全套质量控制工具来帮助您监测诊断测试在自动免疫方面的性能。
IMMUNO-TROL:*的自身免疫多参数质量控制
IMMUNO-TROL是自动免疫中*的多参数控制。它们旨在确保一系列自身免疫免疫测定方法(DOT,ELISA和FIDIS)的日常对照评估。
液体控制和随时可用,它们可以随着时间的推移验证和监控您的技术,以及控制您的分析系统性能。这些控制是普遍的,并且与使用的试剂无关。现在有5种不同的免疫控制产品,方便的形式为2 x 0.5 ml,涵盖了主要的自身免疫参数。
Fiche IMMUNO-TROL
QUAL-IMAGE:通过电子手段识别免疫荧光模式。
QUAL-IMAGE是由Theradiag开发的一种新型教育工具,致力于实验室员工资格认证和自动免疫的在职培训。
QUAL-IMAGE通过发送高分辨率图片提出免疫荧光模式识别,为培训,评估和优化员工技能提供创新方法。
有四种方案可用于HEp-2细胞,三基质,人粒细胞和食道组织的模式识别。
QUAL-IMMUN:外部质量控制计划
QUAL-IMMUN是与CTCB (图卢兹临床生物学质量控制中心)合作提出的自身免疫外部质量控制计划。Theradiag将其在样品制造方面的专业知识和CTCB 的经验和独立性用于处理结果。
每个计划每年包括两次调查,每次调查有3个样本。四个程序涵盖了自动免疫的主要指标(ANA,ENA,TS,APS,FR,CCP ......)。
每次咨询的结果都会提交给参与者,并附有统计报告,并附有自动免疫专家的意见。
QUAL-IMMUN是一种重要的测量工具,可以:
由于分子生物学在临床实验室中至关重要,因此,Theradiag专注于适用于大面积的遗传测试的商业化,例如传染病,肿瘤学,预测医学或治疗诊断学的诊断。分子生物学为实验室提供了方便和时间,与传统方法相比,具有更高的灵敏度和可靠性。
通过2010年与Asuragen达成的合作伙伴关系,Theradiag展示了这一快速增长领域的发展意愿,Asuragen专注于分子生物学测试的开发,包括致力于诊断脆性X染色体综合征的AmplideX™产品系列,对患者的监测用于慢性粒细胞白血病(BCR / ABL1转录物的定量)和癌基因领域的其他产物,例如KRAS / BRAF基因分型。
Theradiag通过收购microRNA平台巩固了分子生物学的这一发展战略,以便在未来几年内将其自己的分子生物学试剂盒商业化。
The AmplideX™ FMR1 PCR Kit (CE IVD) is an in vitro diagnostic device for use in clinical laboratories to amplify and detect the CGG repeat region in the 5′-untranslated region of the fragile X mental retardation-1 (FMR1) gene. This product is intended as an aid in diagnosis of fragile X syndrome and associated disorders, e.g. tremor and ataxia syndrome (FX-TAS) and primary ovarian insufficiency (FXPOI), through determination of CGG repeat length up to 200 CGG and detection of alleles greater than 200 CGG. The test consists in a polymerase chain reaction (PCR) of genomic DNA purified from whole blood followed by fragment sizing on a capillary electrophoresis and conversion of product size to the number of CGG repeats.
Fast reporting and reduced manipulation time
Theradiag presents the new AmplideX® FMR1 mPCR reagents which employs an innovative PCR-only approach for the detection of methylation status in the FMR1 gene. These reagents reveal the extent of methylation of each individual allele in both male and female samples, and thus definitively eliminate the need to run tedious and time consuming Southern blots.
Internet link
No More Southern Blots
Instructions for use
ASU76008 AmplideX FMR1
ASU49442 AmplideX FMR1 mPCR
Multimedia
AmplideX FMR1 Technical video
Publications
Articles
Posters
xTAG® GPP – Gastrointestinal pathogens detection
The xTAG® Gastrointestinal Pathogens Panel (GPP) kit is a multiplex molecular assay allowing the identification of several gastrointestinal pathogens: virus, bacteria and parasites.
This assay is based on the xMAP® technology of Luminex® and detects 15 targets in one reaction. This new tool allows the identification of pathogens responsible for Hospital Acquired Infections (HAI) such as C. difficile or Norovirus, foodborne illness agents like E. coli or Salmonella, and common causes of diarrhea, such as Rotavirus A, Campylobacter, and Shigella.
The assay comprises 4 steps from a stool sample:
The xTAG GPP allows to:
The results are read on Luminex® platform 100/200™ or MAGPIX®. A dedicated software analyzes the raw data for an easy analysis.
*Reagents not included
Brochures
xTAG GPP leaflet
Multimedia
Technical video
Publications
Articles
Posters
The xTAG® Respiratory Viral Panel (RVP) kit is a multiplexe molecular tool allowing the identification of the most common respiratory viruses.
This assay is based on the xMAP technology of Luminex and detects 9 viruses and their subtypes i.e20 targets in one tube. Viruses are responsible for 80% of the respiratory tract infections and can cause death in children, elderly and immunocompromised patients. This new tools was designed to allow a faster patient’s management and to avoid the spreading of the infections.
The assay works in 4 steps from nasopharyngeal swabs, nasal aspirates and bronchioalveolar lavages:
The results are read on Luminex® platform 100/200™ or MAGPIX®. A dedicated software analyzes the raw data for an easy analysis.
*Reagent not included
Brochure
xTAG RVP FAST V2 leaflet
Multimedia
Technical video
Publications
articles
Posters & Abstracts
The BCR/ABL1 Quant™ test is a quantitative in vitro diagnostic product to monitor the BCR-ABL1 to ABL1 ratio by RT-qPCR on whole blood of diagnosed Ph+ CML patients expressing e13a2, e14a2 or e1a2 fusion transcripts as an aid in the assessment of complete cytogenetic response, major molecular response, minimal residual disease and relapse.
The test starts with total RNA in a reverse transcription (RT), followed by multiplex real-time quantitative PCR (qPCR) amplification and quantification of BCR-ABL1 (e13a2, e14a2 and e1a2) fusion transcripts and the ABL1 transcript.
Theradiag also offer RNA calibrators for the standardization of the BCR/ABL1 quantification assays. These 4 calibrators are distributed on 5 logs for a better estimation of the major molecular response.
Brochures
ASU76005 BCR/ABL1 Quant
Internet link
Where Are You On The IS ?
Multimedia
Vidéo technique BCR/ABL1 Quant test
Publications
Articles
Posters
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