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            Glycotope 10-0200 說明書

            更新時間:2017-10-13      點(diǎn)擊次數(shù):2603

            世界*實(shí)驗(yàn)材料供應(yīng)商 Glycotope正式授權(quán)上海起發(fā)為其中國代理, Glycotope在一直是行業(yè)的*,一直為廣大科研客戶提供zui為的產(chǎn)品和服務(wù),上海起發(fā)一直秉承為中國科研客戶帶來的產(chǎn)品,的服務(wù),簽約 Glycotope就是為了給廣大科研客戶帶來更加完善的產(chǎn)品和服務(wù),您的滿意將是我們zui大的收獲

            Glycotope中國代理Glycotope上海代理, Glycotope北京代理,Glycotope廣東代理, Glycotope江蘇代理Glycotope湖北代理,Glycotope天津,Glycotope黑龍江代理,Glycotope內(nèi)蒙古代理,Glycotope吉林代理,Glycotope福建代理, Glycotope江蘇代理, Glycotope浙江代理, Glycotope四川代理,

             

            GLYCOTOPE是前Nemod Biotherapeutics 安全官及Max-Delbrueck中心分子醫(yī)藥研究團(tuán)隊(duì)學(xué)術(shù)帶頭人 Dr. Steffen Goletz,以及Eckert & Ziegler Strahlen- und Medizintechnik AGCEO及創(chuàng)建人Dr. Andreas Eckert2001年創(chuàng)立。公司創(chuàng)立之初僅有員工8人,主要開發(fā)了GlycoExpress™糖基化純化技術(shù)。目前,GLYCOTOPE已經(jīng)擁有員工超過160人,在柏林及海德堡均設(shè)有公司,基于zui初的GlycoExpress™糖基化純化技術(shù),GLYCOTOPE已成長為第二代生物治療企業(yè)。除糖基化研究之外,GLYCOTOPE公司于2008年收購Orpegen Pharma的生物技術(shù)部,成立了GLYCOTOPE生物技術(shù)公司,該公司擁有GMP生產(chǎn)條件,使得GLYCOTOPE公司的所有產(chǎn)品均可實(shí)現(xiàn)GMP生產(chǎn)。

            作為糖生物學(xué)研究領(lǐng)域的,GLYCOTOPE致力于研發(fā)創(chuàng)新性的生物制藥技術(shù)用以優(yōu)化人類糖基化結(jié)構(gòu)修飾、分析以及開發(fā)高度特異的抗腫瘤細(xì)胞表面糖分子抗體。基于GlycoExpress以及GlycoBody技術(shù), Glycotope擁有一個可全面研究、生產(chǎn)糖蛋白的研究平臺,可提供多種純化糖蛋白以及高特異性的抗糖蛋白抗體。

            Glycotope的主要產(chǎn)品:

            一、臨床糖基化抗體:

            Glycotope公司目前在已處于臨床試驗(yàn)的糖基化抗體主要包括:

            1PankoMab-GEX (GT-MAB 2.5-GEX™):已處于二期臨床(Ovarian Cancer2013)的腫瘤治療糖基化抗體。

            2)新型EGFR抗體 CetuGEX (GT-MAB 5.2-GEX™), 已處于二期臨床(Head&Neck Cancer2013) (3TrasGEX (GT-MAB 7.3-GEX™) :HER2抗體,已完成一期臨床試驗(yàn)。

            4FSH-GEX (GT-GP 2.4-GEX™):糖基化修飾的Follicle-Stimulating Hormone,是Glycotope’s*臨床治療的非抗體產(chǎn)品,已于2014年進(jìn)入三期臨床試驗(yàn)。

            二、免疫診斷試劑:

            Glycotope生物技術(shù)公司的診斷試劑盒產(chǎn)品集中于細(xì)胞功能的定量評估領(lǐng)域,其免疫功能檢測試劑盒基于流式細(xì)胞術(shù)可以快速的檢測細(xì)胞在免疫反應(yīng)下的各種功能特性,其方便快速的檢測試劑系統(tǒng)使其適用于臨床檢測。

            三、科研服務(wù):

            基于*的科研平臺及訓(xùn)練有素的員工,Glycotope除了上述有形試劑外還提供多種形式的科研服務(wù),包括試驗(yàn)研究設(shè)計(jì)、實(shí)施及分析等流程。

             

            PHAGOBURST™

            貨號:10-0200 

            規(guī)格:100 analyses

            Clinical Diagnostic for the Quantitative Analysis of Leukocyte Oxidative Burst in whole blood 

            臨床診斷人體全血白細(xì)胞氧化破裂的定量檢測

            · Functional test ex vivo

            來自體內(nèi)的功能測試

            · Evaluation of single cells to detect heterogenous populations

            評價檢測單個細(xì)胞異質(zhì)種群

            · Whole blood assay: No isolation procedures and optimal culture medium

            全血檢測:沒有隔離程序和*培養(yǎng)基

            · Physiological stimulans for phagocytes: Bacteria and fMLP

            吞噬細(xì)胞生理興奮勁:細(xì)菌和fMLP

            · Dose response: Low and high stimulant

            沒有靜電工件比較乳膠珠子聚苯乙烯管內(nèi)

            · Standardized test procedure

            標(biāo)準(zhǔn)化測試程序

            · Exclusion of aggregation artifacts by DNA staining

            通過DNA染色排除聚合工件

            · Compatible with whole blood of mice and rats

            兼容的小鼠和大鼠全血

            · Fast assay: Whole assay time is 1.5 hours

            快速測定:整個試驗(yàn)時間是1.5小時

            100 analyses. Clinical Diagnostic for the Quantitative Analysis of Leukocyte Oxidative Burst in Human Whole Blood. Evaluation by flow cytometry.

            100次分析。臨床診斷人體全血白細(xì)胞氧化破裂的定量檢測。通過流式細(xì)胞術(shù)進(jìn)行評估。

            Clinical Diagnostic for the Quantitative Analysis of Leukocyte Oxidative Burst in Human Whole Bloods

            SUMMARY and EXPLANATION

            BURSTTEST (PHAGOBURST) allows the quantitative determination of leukocyte oxidative burst in heparinized whole blood. It contains unlabeled opsonized bacteria (E.coli), phorbol 12-myristate 13-acetate (PMA) and the chemotactic peptide N-formyl-Met-Leu-Phe (fMLP) as stimulants, Dihydrorhodamine (DHR) 123 as a fluorogenic substrate and necessary reagents. It determines the percentage of phagocytic cells which produce reactive oxidants (conversion of DHR 123 to R 123) and their enzymatic activity (amount of R 123 per cell).

            The evaluation of these bioactivities should be performed by flow cytometry.

            BURSTTEST(PHAGOBURST)允許定量測定白細(xì)胞氧化闖入肝素化全血。 它包含未標(biāo)記的促進(jìn)調(diào)理作用的細(xì)菌(大腸桿菌),佛波醇12十四烷酸乙酸13(PMA)和趨化作用的多肽n甲酰遇見亮氨酸板式換熱器(fMLP),二氫若丹明(DHR)123作為一個熒光襯底和必要的試劑。它決定了吞噬細(xì)胞產(chǎn)生活性氧化劑的比例(轉(zhuǎn)換DHR 123 到 R 1233)及其酶活性(每個細(xì)胞R 123的數(shù)量)。

            這些生物活性的測定應(yīng)該有流式細(xì)胞術(shù)完成。

            APPLICATIONS

            The diagnostic kit is intended to investigate the altered oxidative burst activity found in various disorders and to evaluate the effects of drugs.

            Reduced or missing burst activity is observed in inborne defects like the chronic granulomatous disease (CGD). CGD is a heterogenous group of inherited disorders that usually manifests itself during the first two years of life (3, 4). The disease is characterized clinically by repeated and life-threatening infections caused by bacterial and fungal organisms. These infections typically consist of pneumonia, lymphadenitis, or abscesses that involve lymph nodes, lungs, and liver. The NADPH oxidase is the enzyme system responsible for producing superoxide anion, which is quickly converted to hydrogen peroxide and hydroxyl radicals. Abnormalities in the constituent peptides of the NADPH oxidase enzyme system lead to the dysfunctions characteristic of CGD. Neutrophils from CGD patients fail to produce a significant oxidative burst following stimulation. Different forms of CGD are described (classical X-linked CGD and autosomal recessive patterns). BURSTTEST (PHAGOBURST?) is a rapid and sensitive method for the diagnosis of CGD and for the detection of X-linked carriers.

            The oxidative burst of granulocytes is impaired in transplant patients and patients with AIDS (6). The spontaneous and fMLP-induced neutrophil respiratory burst was shown to be increased in neonates with laboratory signs of infection (7). Various immunomodulators (e.g., cytokines (GM-CSF, G-CSF, TNF) or drugs) seem to have effects on the oxidative burst. By using fMLP as a low stimulant one can investigate additive or priming effects (8) of test substances.

            The diagnostic kit is also applicable on blood of mice, rats, rabbits, dogs, cattle and other species.

            診斷測試組旨在研究改變了的氧化破裂活動中發(fā)現(xiàn)各種障礙和評估藥物的影響。

            觀察細(xì)胞的減少或缺失的破裂活動像慢性肉芽腫性疾病(CGD)

            慢性肉芽腫性疾病是一個異構(gòu)群遺傳疾病,通常體現(xiàn)在生命的zui初兩年期間(3、4)。這種疾病的臨床特征是由于細(xì)菌和真菌重復(fù)和危機(jī)生命的感染。這些感染通常包括肺炎、淋巴腺炎或膿腫涉及到淋巴結(jié)、肺和肝。NADPH氧化酶的酶系統(tǒng)是負(fù)責(zé)生產(chǎn)超氧化物陰離子,迅速轉(zhuǎn)化為過氧化氫和羥基自由基。NADPH氧化酶系統(tǒng)在組成多肽中的畸形導(dǎo)致慢性肉芽腫性疾病功能障礙性特點(diǎn)。CGD患者的中性粒細(xì)胞刺激后無法產(chǎn)生顯著的氧化破裂。BURSTTEST (PHAGOBURST?)是一種快速有效診斷慢性肉芽腫性疾病和檢測X連鎖隱性遺傳疾病攜帶者的方法。

            氧化破裂的粒細(xì)胞在需要移植的病人和艾滋病患者中受損。無意識和誘發(fā)性fMLP嗜中性粒細(xì)胞破裂被證明會增加新生兒實(shí)驗(yàn)室感染的跡象。各種免疫調(diào)節(jié)劑(如細(xì)胞激素(GM-CSF, G-CSF, TNF)或藥品)似乎會對氧化破裂產(chǎn)生影響。通過使用fMLP可以研究添加劑或激發(fā)效應(yīng)(8)的測試物質(zhì)。

            診斷試劑盒也適用于小老鼠、大老鼠、兔子、狗、牛和其他物種的血液。


            TEST PRINCIPLES
            Phagocytosis by polymorphonuclear neutrophils and monocytes constitutes an essential arm of host defense against bacterial or fungal infections. The phagocytic process can be separated into several major stages: chemotaxis (migration of phagocytes to inflammatory sites), attachment of particles to the cell surface of phagocytes, ingestion (phagocytosis) and intracellular killing by oxygen-dependent (oxidative burst) and oxygen-independent mechanisms (1, 2).

            BURSTTEST (PHAGOBURST?) allows the quantitative determination of leukocyte oxidative burst. The BURSTEST kit contains unlabelled opsonized E.coli bacteria as particulate stimulus, the protein kinase C ligand phorbol 12-myristate 13-acetate (PMA) as high stimulus and the chemotactic peptide N-formyl-MetLeuPhe (fMLP) as low physiological stimulus, Dihydrorhodamine (DHR) 123 as a fluorogenic substrate (5) and necessary reagents. Heparinized whole blood is incubated with the various stimuli at 37°C, a sample without stimulus serves as negative background control. Upon stimulation, granulocytes and monocytes produce reactive oxygen metabolites (superoxide anion, hydrogen peroxide, hypochlorous acid) which destroy bacteria inside the phagosome. Formation of the reactive oxidants during the oxidative burst can be monitored by the addition and oxidation of DHR 123. The reaction is stopped by addition of LYSING SOLUTION, which removes erythrocytes and results in a partial fixation of leukocytes. After one washing step with WASHING SOLUTION, DNA STAINING SOLUTION is added to exclude aggregation artifacts of bacteria or cells. The percentage of cells having produced reactive oxygen radicals are then analyzed as well as their mean fluorescence intensity (enzymatic activity).

            溫馨提示:不可用于臨床治療。  

             

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