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theradiag自身免疫和遺傳學(xué)的產(chǎn)品列表

 更新時(shí)間:2018-09-11 點(diǎn)擊量:1472

Theradiag于1986年創(chuàng)立,初致力于分發(fā)體外診斷,特別是針對(duì)自身免疫性疾病。

自動(dòng)免疫

Autoimmunity:根據(jù)您的需求進(jìn)行創(chuàng)新

自身免疫性疾病是心血管疾病和癌癥發(fā)病后的第三個(gè)原因。這是一組在臨床表現(xiàn)和相關(guān)器*面不同的疾病,但它們具有相同的機(jī)制:針對(duì)生物體中通常存在的物質(zhì)或組織的免疫系統(tǒng)疾病。

產(chǎn)生針對(duì)身體組分的自身抗體。它們的檢測(cè)是一些自身免疫性疾病的診斷和有時(shí)預(yù)后的重要工具。

憑借其在自身免疫診斷試劑盒開發(fā)方面的專業(yè)知識(shí),Theradiag提供了一整套試劑,控制和自動(dòng)化系統(tǒng),可用于診斷自身免疫性疾病的診斷:

  • 質(zhì)量和性能確保可靠的結(jié)果并定位診斷。
  • 創(chuàng)新,通過整合個(gè)性化診斷和患者監(jiān)測(cè)的新參數(shù),不斷擴(kuò)展我們的標(biāo)記組。
  • 服務(wù),通過可靠的支持和我們的授權(quán)培訓(xùn)中心為您提供我們的專業(yè)知識(shí)。

Atradiag專注于您的需求,開發(fā)適合您實(shí)驗(yàn)室活動(dòng)的創(chuàng)新技術(shù)產(chǎn)品:

FIDIS™

由Theradiag開發(fā)的基于xMAP®技術(shù)的FIDIS TM試劑盒可在一次分析中同時(shí)檢測(cè)同一樣品中的多種分析物。與傳統(tǒng)的IFA或ELISA格式相比,F(xiàn)IDIS™技術(shù)及其在CARIS™平臺(tái)上的自動(dòng)化使得實(shí)驗(yàn)室能夠以比傳統(tǒng)套件格式更快,更低的成本執(zhí)行分析并具有良好可靠性。Theradiag開發(fā)了一系列全面的商業(yè)化xMAP技術(shù)測(cè)試,用于診斷自身免疫病理學(xué),并繼續(xù)提供傳染性血清學(xué)和人體細(xì)胞因子測(cè)量的擴(kuò)展小組。

如果一個(gè)免疫熒光仍然是篩選自身抗體的參考試驗(yàn)。Theradiag提供免疫熒光測(cè)試,以篩選和鑒定主要的自身抗體(ANA,ANCA,TS,器官特異性自身抗體)和優(yōu)化的方案,以便于結(jié)果解釋和簡(jiǎn)化CARIS™儀器系列的適應(yīng)性。

ELISA

Theradiag提供全面的成熟ELISA檢測(cè)。這些測(cè)試中的大多數(shù)都提供了標(biāo)準(zhǔn)化的協(xié)議,并共享了幾種常用試劑,有利于簡(jiǎn)單有效的自動(dòng)化。該標(biāo)準(zhǔn)化允許用戶在同一平板上同時(shí)進(jìn)行多個(gè)測(cè)試,從而大化ELISA測(cè)定。

CHORUS™

Chorus™系統(tǒng)是一款緊湊型多參數(shù)分析儀,專門用于以單位為基礎(chǔ)的ELISA檢測(cè),使用即用型檢測(cè)設(shè)備。憑借其在自身免疫和傳染性血清學(xué)方面的*測(cè)試和完整的可追溯性,Chorus™系統(tǒng)允許執(zhí)行常規(guī)分析和不常見的參數(shù),具有的靈活性和安全性。

免疫印跡

我們的免疫印跡試驗(yàn)允許同時(shí)檢測(cè)針對(duì)生化表征并固定在條帶上的幾種抗原的抗體。這些測(cè)定使得能夠容易且快速地基于個(gè)體或串聯(lián)鑒定重要數(shù)量的抗體。

Chorus™自身免疫性疾病

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

Connectivitis – ANA

免疫熒光

HME ANA HEp-2

HME - SérumsdecontrôleANA

HME - Autresréactifs

Connectivitis – ENA

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

Rheumatoid Arthritis

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

Auto-Immune Liver Diseases

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

Vasculitis

Instruction for use

Immunofluorescence

BDI C023S CQ Titrage cANCA 0,5 mL

Immunoblot

HM025 ANCA-MBG-DOT

FIDIS™

MX007 FIDIS Vasculitis

Celiac disease

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

Antiphospholipids syndrome

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

Auto-Immune Thyroiditis

Instruction for use

ELISA

RLTRE 96.3 Anti RTSH

FIDIS™

MX002 FIDIS Thyro

Pernicious anemia

Instruction for use

FIDIS™

 MX030-48 MX030-96 FIDIS Cyto-Panel

Inflammatory Bowel Disease (IBD)

Instruction for use

Immunofluorescence

BDI-C023S-CQ-Titrage-cANCA-05-mL

Diabetes mellitus type 1

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

Other organ-specific autoantibodies

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

Cytokines

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

質(zhì)量控制 - 自動(dòng)免疫

質(zhì)量控制

在對(duì)實(shí)驗(yàn)室質(zhì)量控制的監(jiān)管要求不斷增加的背景下,Theradiag通過提供全套質(zhì)量控制工具來幫助您監(jiān)測(cè)診斷測(cè)試在自動(dòng)免疫方面的性能。

 

IMMUNO-TROL:*的自身免疫多參數(shù)質(zhì)量控制

IMMUNO-TROL是自動(dòng)免疫中*的多參數(shù)控制。它們旨在確保一系列自身免疫免疫測(cè)定方法(DOT,ELISA和FIDIS)的日常對(duì)照評(píng)估。

液體控制和隨時(shí)可用,它們可以隨著時(shí)間的推移驗(yàn)證和監(jiān)控您的技術(shù),以及控制您的分析系統(tǒng)性能。這些控制是普遍的,并且與使用的試劑無關(guān)?,F(xiàn)在有5種不同的免疫控制產(chǎn)品,方便的形式為2 x 0.5 ml,涵蓋了主要的自身免疫參數(shù)。

Fiche IMMUNO-TROL

 

QUAL-IMAGE:通過電子手段識(shí)別免疫熒光模式。

QUAL-IMAGE是由Theradiag開發(fā)的一種新型教育工具,致力于實(shí)驗(yàn)室員工資格認(rèn)證和自動(dòng)免疫的在職培訓(xùn)。

QUAL-IMAGE通過發(fā)送高分辨率圖片提出免疫熒光模式識(shí)別,為培訓(xùn),評(píng)估優(yōu)化員工技能提供創(chuàng)新方法。

有四種方案可用于HEp-2細(xì)胞,三基質(zhì),人粒細(xì)胞和食道組織的模式識(shí)別。

 

QUAL-IMMUN:外部質(zhì)量控制計(jì)劃

QUAL-IMMUN是與CTCB (圖盧茲臨床生物學(xué)質(zhì)量控制中心)合作提出的自身免疫外部質(zhì)量控制計(jì)劃。Theradiag將其在樣品制造方面的專業(yè)知識(shí)和CTCB 的經(jīng)驗(yàn)和獨(dú)立性用于處理結(jié)果。

每個(gè)計(jì)劃每年包括兩次調(diào)查,每次調(diào)查有3個(gè)樣本。四個(gè)程序涵蓋了自動(dòng)免疫的主要指標(biāo)(ANA,ENA,TS,APS,F(xiàn)R,CCP ......)。

每次咨詢的結(jié)果都會(huì)提交給參與者,并附有統(tǒng)計(jì)報(bào)告,并附有自動(dòng)免疫專家的意見。

QUAL-IMMUN是一種重要的測(cè)量工具,可以:

  • 確認(rèn)您的劑量方法的性能
  • 在一組同行中比較您的結(jié)果

遺傳學(xué)

由于分子生物學(xué)在臨床實(shí)驗(yàn)室中至關(guān)重要,因此,Theradiag專注于適用于大面積的遺傳測(cè)試的商業(yè)化,例如傳染病,腫瘤學(xué),預(yù)測(cè)醫(yī)學(xué)或治療診斷學(xué)的診斷。分子生物學(xué)為實(shí)驗(yàn)室提供了方便和時(shí)間傳統(tǒng)方法相比,具有更高的靈敏度和可靠性

通過2010年與Asuragen達(dá)成的合作伙伴關(guān)系,Theradiag展示了這一快速增長(zhǎng)領(lǐng)域的發(fā)展意愿Asuragen專注于分子生物學(xué)測(cè)試的開發(fā),包括致力于診斷脆性X染色體綜合征的AmplideX™產(chǎn)品系列,對(duì)患者的監(jiān)測(cè)用于慢性粒細(xì)胞白血病BCR / ABL1轉(zhuǎn)錄物的定量)和癌基因領(lǐng)域的其他產(chǎn)物,例如KRAS / BRAF基因分型。

Theradiag通過收購(gòu)microRNA平臺(tái)鞏固了分子生物學(xué)的這一發(fā)展戰(zhàn)略,以便在未來幾年內(nèi)將其自己的分子生物學(xué)試劑盒商業(yè)化。

AmplideX™ FMR1

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.

  •  All expansions detected
  • Detects interrupting AGG sequences
  • Great sensitivity
  • Resolves female zygosity

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

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 Norovirusfoodborne 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:

  • Detect 95% of pathogens responsible for infectious gastroenteritis
  • Provide fast and accurate answers for a better patient management and monitoring of epidemics
  • Decrease the cost of the patient management

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

xTAG® RVP – Respiratory virus detection

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

BCR/ABL1 Quant™

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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6:我們還是Santa,Advanced Biotechnologies Inc,Athens Research & Technology,bangs,BBInternational,crystalchem,dianova,FD Neurotechnologies,Inc. FormuMax Scientific,Inc, Genebridege, Glycotope Biotechnology GmbH; iduron,Innovative Research of America, Ludger, neuroprobe,omicronbio, Polysciences,prospecbi, QA-BIO,quickzyme,RESEARCH DIETS,INC,sterlitech;sysy,TriLink BioTechnologies,Inc;worthington-biochem,zyagen等幾十家國(guó)外公司授權(quán)代理。

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