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• 2406N英文說明書

  由深圳市朗普電子科技有限公司代理深圳市深南中路南光捷佳大廈1402室TEL:0755-88851600（直線）0755-839801580755-830474150755-83986300FAX:0755-888505150755-83047419網址：綜合推廣網www.17lp.com衡器烘箱網www.1718sz.com郵箱：lp@df17.comQQ:　374542908MSN：dafusz@hotmail.com[詳細]

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• （離心機）英文說明書

  BriefintroductionandapplicationscopeAscentrifugalseparator,thiselectriccentrifugalmachinemakesuseofthecentrifugalforcetoseparateeverycompositioninsolution,adoptsteplessspeedvariationandautomaticbalancedevices,sothismachineownsvariousadvantages,suchasstableperformance,smallvolume,beautifulappearance,lowertemperaturerising,highworkingefficiencyandwiderapplication,speciallyforitsaluminumalloycentrifugalrotary-disc,itcanguaranteetoprotectthecentrifugaltubesfromdamageeffectively.Thus,thiscentrifugalseparatorhasbeenwidelyusedinhospitalandchemicalorbiologylabtocarryoutqualitativeanalysisforbloodserum,bloodplasma,etc.Technicalparameters:Model800800D80-2TDL-50XYJ-3XYJ-4TDL-5Max.rev4000rpm5000rpmRCFMac1430（xg）1790（xg）5000（xg）Max.capacity20mlx6（Angietype）20mlx1220mlx810mlx16；50mlx8100mlx4Motorpower25W40W280WTimingrangeNo0-60min0-120minAutobalanceNoYesYesSelf-lockerNoNoNoNoNoYesWeight67121035ImportantNotice：●Foryoursafety,areliablegroundingisstronglyrecommendedtobedonebeforeoperation,●Beforethefirsttimeuse,pleasereadthisOperationManualcarefully.●Workingconditions:0-40℃ambienttemperatureand80%belowrelativehumidity.●Itissuggestedtocutoffpowerwhenlongtermnonuse.OperationProcedure:●Inserttheplugintosocketandturnonthepowerswitch.●Putthemedicineintocentrifugetubeandtheninsertthetubeintothecorrespondingsleeve,closethecoverplateandselectpropercentrifugalspeedaccordingtotestrequirements,thenselectrunningtimeorcloseON.Soitiseasytooperatethisinstrumentwithbettereffect.Dailymaintenance1.Correctoperationandmaintenancecanextendtheservicelife,itissuggestedtoplacethisinstrumentunderreasonableworkingconditionssothattheinstrumentcanworknormally.2.Iftheliquidissplashedorsprayedintoinstrumentbyaccident,cutoffthepowersupplyandremovetheresidualliquidincaseshortentheservicelife.Oneyearwarrantyandlifelongmaintenanceareofferedtoourproduct（reasonablelaborandmaterialcostwillbetriggeredbyman-madedamageormisoperation）[詳細]

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• 7725I英文說明書

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• SLPe使用說明書（英文）

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• XK3190-A12E儀表英文說明書

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• 孔雀石綠英文說明書.pdf

  malachitegreen（MG）ELISA1UsepurposeThiskitforFeed,aquaticsamples,watersamplesintheMGremainingquantitativedetection.2ExperimentalprincipleThiskitadoptsmethodsincompetitionELISAInmicroplatescoatedwithantigenconjugatedMG,addMGstandardorsamples,FreeMGandpre-coatedonstripsofMGconjugatedantigencompeteagainstMGantibodyconjugates,WithTMBchromogenicsubstrate,thecolorischangedfrombluetoyellowafteraddingstopsolution,enzymestandardinstrument450nmwavelengthsintesting,absorblightvalueandinthesamplewasMGcontentisinverselyproportionaltothestandardcurve,throughcalculationsampleswasMGconcentrations.3Materialsprovidedwiththekit3.1Microelisastripplate:1block（12well×8strips）.3.2MGstandard:sixvialsof（1ml/vial）,contentisrespectively:0PPB,0.1PPB,0.3PPBand0.9PPB,2.7PPB,8.1PPB.3.3Anti-MGantibodyconjugate:1vial（6ml）.3.4ChromogenSolutionA:1vial（6ml）.3.5ChromogenSolutionB:1vial（6ml）.3.6StopSolution:1vial（6ml）,2Msulphuricacid.3.7sampledilution:1vial（10x,6ml）,usedforsampledilutedwith.3.8washsolution:1vial（20x,20ml）,usedforwashingboard.3.9Instruction.4Neednotprovidematerials4.1equipment4.4.1wavelength450nmmicroplate.4.1.2shredder.4.1.3LiangTong.4.1.4oscillators.4.1.5funnel.4.1.6WhatmanNo1orequivalentfilterpaper.4.1.7traceremoveliquiddevice.4.2reagent4.2.1thedeionizedwaterordistilledwater.4.2.2methanol.5Storage5.1kitstoredin2~8℃,Don’tfrozen5.2Don’tuseuptheMicroelisastripplate首ldbesealeddryingpreserve6.Precautions6.1pleasereadtheinstructionscarefully,beforeuseingthekit.6.2don'tuseexpiredkit.6.3beforeusingthekit,pleaseletthereagentrecovertoroomtemperature（25+2℃）,theproposalforatleast2hourstotemperature.6.4thestandardcontainMG,payspecialattentionto,theoperation,we首ldbringgloves.6.5stopsolutioniscontainingsulfate,whenusing,preventburnsskinandcorrosionclothing.6.6differentstandardandsamplesuctionheadusedcannotbemixeduse,otherwise,itwillaffecttestresults.6.7differentbatchesofreagentkitnotmix,Differentstandardandsamplesuctionheadshallnotbeusedincombination,otherwise,itwillaffecttheexperimentalresult.6.8dilutedsamplemustusethiskitofsamplediluent,otherwise,itwillaffecttheexperimentalresult6.9mixedreagents首ldavoidblistering.7Workingliquidpreparation7.1Carbendazimstandards:0ppb,0.1PPB,0.3PPBand0.9PPB,2.7PPB,8.1PPB7.2washsolution:1:20withdistilledwater（1+19）diluted.preparation7.3sampledilutions:1:10withdistilledwater（1+9）diluted.preparation7.3ChromogenSolutionreagent:alreadystandby,avoidlightstraightas7.4stopsolution:alreadyterminationaside8Sampleprocessingprogram（sampleinextractionprocess,muststrictlyaccordingtotheoperationoftheextractionprocess首ldbeaccuratedilution,canappearotherwiseresultsareinaccurate,samples首ldbekeptinacoolplacetoavoidlightandfrozenkeep）8.1Smashthesamplestaken10g,add20ml70%methanolsolution8.2powerfuloscillation3minutes8.3WhatmanNo1filterwith8.4Takethe25μltreatmentofthesamplebyadding25μlsampledilutioninthewells（sampledilutionfactorof2）9Enzyme2lindedanalysissteps9.1experimentalguidelines9.1.1experimentbeginspriortoallreagentinboxesoutsidetheroomtemperature（25fullyrecoveredto+2℃）,timeabout2hours.Returntoroomtemperature（25+2℃）againafterremoveStrips,excessporebartosealimmediatelytothe2~8℃dryingpreserveNote:besuretotemperature,otherwisefullyguaranteetheaccuracyandprecisionoftheaffectingdetection.9.1.2afterusepleaseimmediatelyreagentputback2~8℃preservation9.1.3pleasedon'tchangeanalysisprogram9.1.4pleaseuseaccuratetraceremoveliquiddevice9.1.5operationoncestarted,pleasedonotinterruptanyprogram9.1.6ELISAresultsofrepeatabilityofseveredependsonoperatingprocedures,pleasestrictlyaccordingtorequirementsoperation9.1.7toavoidcross-contamination,eachstandardandsamples首ldusedifferentsuctionheadaddsamples9.1.8plussampledomakesuckaheadcontactmicroporousthesolutionorinsidesurface9.2analysissteps9.2.1beforehandnumbered,markB0,standardandthesamplepositionrecommendeddoubleorificedetection9.2.2taketherequiredamountoftheStrips（Stripsdetachable）,willspareattribwattleandsealedimmediatelyputbackagain2~8℃preservation9.2.3sampledilutions（10）,washsolutionx（20x）dilutionintoworkingliquid（distilledwaterordeionizedwaterdilute）In9.2.4B0welljoining50μl0.0ng/mlstandard9.2.5ineachstandardwelljoining50μlstandard9.2.6ineachsamplewelljoining50μlsamplesolution9.2.7Inallwelljoining50μlAnti-MGantibodyconjugate9.2.8gentlysloshingresponseboardforafewseconds.9.337℃warmbath30min（warmbathprocesssometimespatreactionplate,canreducedoubleorificeerror）9.3.1UncoverClosureplatemembrane,discardLiquid,drybyswing,addwashingbuffertoeverywell,stillfor30sthendrain,repeat5times,drybypat..9.4reaction9.4.1washingprocedurecompleted,immediatelywithliquidapparatusineverytracemovemicroporousfirstjoin50μlChromogenSolutionA,add50μlChromogenSolutionB,Slightsloshingresponseboardmakethoroughlyincorporated379.4.2℃warmbath10min9.4.3eachwelljoining50μlStopSolution,blending9.4.4in450nmtestingabsorbency,resultin5mininsideread.10Theresultscalculated10.1quantitativeanalysis10.1.1obtainedbyeachconcentrationstandardsolutionandtheaveragevalueofasamplespectrophotometry（B）dividedbythefirststandard（0standardabsorbencyvalue（B0）multiplyingby1**%,namelypercentageabsorbencyvalues.B-standardsolutionorsamplesolutionofaverageabsorbanceofthevaluesB0-0μg/Lstandardsolutionofaverageabsorbanceofthevalues10.1.2withMGconcentrationsofvaluesfortheXaxis,100centabsorbanceofthevalueoftheYaxis,drawstandardcurve.Accordingtothesamplepercentageabsorbencyvalues,whichgetcorrespondingpointsfromcurve,namelytheabscissadenotesthemulti-goalMGconcentrationonthenumericalcurvature.theagainstseveralnamelytodetermineMGconcentrationC（ppb）10.1.3becausethesampleafterdilutedinadvance,soaccordingtothestandardcurvegainsfromdifferentconcentrationsamplesmustagainmultiplythedilutedtimes.10.2halfquantitatively10.1.1visualhalfquantitativedetermination:first,chooseanappropriatestandardfluidandsampleswithoperation,accordingtothesamplesandstandardsubstanceabsorbencyvaluethediscretionofthejudgeiscompared,samplechromavalueislessthanorgreaterthanstandardvalues.10.1.2instrumenthalfquantitativedetermination:first,chooseanappropriatestandardfluidandsampleswithoperation,accordingtothesampleandstandardcolordepthcomparison,judgesamplechromavalueislessthanorgreaterthanstandardvalues.11SpecificityPhysicalcrossreactionMG1**%CrystalViolet:95%Recessivemalachitegreen:0.1%HiddenCrystalViolet:<0.1%12KitparametersThiskitdetectionlimitis0.05PPBB0absorbanceoftheoptimalvalue首ldbegreaterthan1.0Kitabsorbencyboardinsideerrorislessthan8%,boardbetweenerrorislessthan15%.Withthismanualprovidedatissuesampleextractionmethodrecoveryisgreaterthan80%.13AnalysisrestrictionThiskittestingpositiveforsamples首lduseanothermethodsuchasHPLCorGC/MStobeverified.上海恒遠生物科技有限公司，專業(yè)銷售“孔雀石綠試劑盒”品質保證，值得信賴！如果你想了解該產品的詳細信息，歡迎來電來函！[詳細]

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• XK3190-C8控制儀表英文說明書

  XK3190-C8控制儀表英文說明書XK3190-C8儀表采用高速的Σ-△模數轉換技術。適用于電子配料秤、定值秤、分選秤等控制場合，同時具有上下限報警、峰值保持功能。3路光隔離開關量輸入，3路開關量（內置3路繼電器）輸出控制高精度A/D轉換，可讀性達1/300005點非線性修正換表無需重新標定，只需輸入原儀表的參數即可使用集加/減法秤/分選秤/上下限報警/峰值保持等功能于一體定量值、提前量、上下限、節(jié)點延時等參數可根據應用自由設置加/減法秤模式下可選1-2種配料，分選秤模式下可選外控/自檢/自由上下限模式準確度等級：3級，nind=3000AD轉換方式：Σ-△轉換方式AD轉換碼：24bit轉換速度：80次/秒輸入信號范圍：-19mV～+19mV輸入靈敏度：≥1uV/e非線性：≤0.01%F.S滿量程溫度系數：≤8PPM/℃?zhèn)鞲衅鞴螂娫矗篋C：5V；350mA傳感器連接個數：1~8[詳細]

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• 便攜式地磅（汽車衡）英文說明書

  概述行駛道路的車輛超限超載是造成道路加速損壞以及引發(fā)交通事故的潛在重要原因，隨著《道路交通安全法》的實施，我國交通和JJ等相關部門對超限超載的執(zhí)法力度不斷加強，同時相關執(zhí)法部門更需要一種能夠在其執(zhí)法過程中極ng確檢測車輛動態(tài)重量的高質量設備。為了給相關執(zhí)法管理部門提供一個便捷、GX的執(zhí)法工具，提供有力的執(zhí)法依據，根據交通部及有關部委對車輛軸類型和軸載質量的相關規(guī)定標準，我公司于1999年初自主研發(fā)生產出符合我國車輛行駛公路管理規(guī)范要求的便攜式稱重儀（軸重儀），為交通管理部門實施有效的超限超載治理提供了強有力的執(zhí)法工具。您所使用的便攜式稱重儀是我公司基于自身多年的實際動態(tài)稱重經驗以及客戶的實際需要，而Zxin研發(fā)生產的JJ系列新一代全數字便攜式稱重儀（軸重儀），旨在改善提高目前市場上同類產品不能滿足用戶的實際使用需求而研發(fā)生產，具有多項創(chuàng)新功能，主要體現在：1、采用7寸全彩觸摸式大屏顯示，完全滿足用戶在夜間操作的方便性2、國內SJ將電腦技術應用于便攜式動態(tài)稱重儀領域，即采用用戶熟悉的鼠標操作方式，使得產品實用性更強，操作更簡單明了，大大提高操作人員的工作效率。3、國內SJ推出JJ和路政聯(lián)合執(zhí)法模式功能4、國內SJ推出功能性更強的后臺軟件管理功能，只要把我們的儀表與安裝有后臺管理軟件的計算機連接，就可以實時的控制儀表操作，為更高功能的擴展打下基礎產品設計定位高、精度高、性能穩(wěn)定、使用可靠、環(huán)保節(jié)能、故障率低、維修簡捷等特點?？煞奖愕膶C動車進行軸載質量、車貨總質量的動、靜態(tài)測量。適用于公路執(zhí)法部門超限檢查、JJ進行車載質量檢查、高速公路收費站進行車載質量計量等，也適用于低值車載貨物計量，如交通運輸車載質量計量、建筑施工工地配料計量等場合。一、主要功能特點:（1）、傳感器采用一體化整體式結構整體式傳感器（2）、數據傳輸方式：有線式、無線式、有線無線兩用式（具體傳輸方式根據用戶的實際需要在采購是選擇而定）（3）、采用7寸彩色觸摸式屏幕顯示，實用（4）、可以使用觸摸方式輸入操作和無線鼠標方式操作，簡單快捷（5）、多種工作（JJ、路政、綜合）模式可供選擇（6）、動、靜兩用、性能穩(wěn)定、具有高性能防水、防振、防腐等特點（7）、雙通道式設計、使用高精度整體式傳感器，檢測精度高，故障率低（8）、統(tǒng)計分析軟件，便于記錄、統(tǒng)計、查詢；數據庫提供車型資料、政策法規(guī)、技術支持（9）、即時電腦連接操作，可以通過電腦和儀表連接直接操作，并可實現視頻和車牌自動識別功能擴展功能強大（此功能為選配）二、主要技術參數:1、名稱型號：便攜式稱重儀（JJB30BW型）2、靜態(tài)精度：靜態(tài)稱重（III）；±0.1～0.3%FS蠕變：0.3%.F.S，遲滯：0.5%.F.S3、動態(tài)精度：OIML國際建議級1%-3%F.s非線性：0.5%.F.S，重復性：0.3%.F.S4、分度值：5、10、20kg等可調節(jié)5、Zda稱重量：40000kg（單軸）6、Z小秤量：20e（e為檢定分度值）7、Zda安全載荷：安全超載能力：120%F.SZda超載能力：150%F.s8、使用環(huán)境：-20~80℃9、電源：DC12V、AC220V、車載供電三種供電方式10、引板：橡膠引板11、限制車速：≤5km/h勻速12、打印內容：牌照、車貨總質量、軸胎形式、限載值、超限值、時間等（具體打印內容依據客戶的要求而定）13、軟件：具有3種稱重軟件（路政、JJ、綜合模式）且可以自由切換14、數據輸出：RS232、USB兩種數據接口15、傳感器結構：采用整體數字傳感器，溫度補償，可以在秤臺溫度變化較大時對溫度產生的誤差進行補償，同時傳感器采用雙信號電路設計，在一個電路出現故障的同時，系統(tǒng)會自動切換到另外一個電路，提高現場設備的實用性，減少設備的故障率16、軸型表模式：軸型表采用內部電子顯示方式設定，徹底解決長期野外使用貼表式軸型表模糊不清以及操作不便的問題17、視頻：支持即時視頻聯(lián)接、支持車牌自動識別系統(tǒng)、支持后臺軟件擴展（此功能為選配）18、打印機:采用針式節(jié)能高速打印機，可保存打印內容，徹底解決熱敏打印機高耗電、而且打印內容容易自然消退的問題電子秤（上海電子秤）地磅秤（小地磅秤）大臺面地磅秤（電子磅秤）吊秤（上海吊秤）[詳細]

  2024-09-30 17:41

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• NDJ-8S數顯旋轉粘度計英文說明書

  NDJ-8S數顯旋轉粘度計英文說明書[詳細]

  2009-10-13 00:00

  報價單

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• 人L-精氨酸（L-ARG）英文說明書

  HumanL-Arginine（L-ARG）FORRESEARCHUSEONLYAssayrange：2nmol/L-48nmol/L96determinationsPurposeThiskitallowsforthedeterminationofL-ARGconcentrationsinHumanserum,cellculturesupernatesandotherbiologicalfluidsPrincipleoftheassayThekitassayHumanL-ARGlevelinthesample,usePurifiedHumanL-ARGantibodytocoatmicrotiterplatewells,makesolid-phaseantibody,thenaddL-ARGtowells,CombinedL-ARGantibodywhichWithHRPlabeled,becomeantibody-antigen-enzyme-antibodycomplex,afterwashingCompletely,AddTMBsubstratesolution,TMBsubstratebecomesbluecolorAtHRPenzyme-catalyzed,reactionisterminatedbytheadditionofasulphuricacidsolutionandthecolorchangeismeasuredspectrophotometricallyatawavelengthof450nm.TheconcentrationofHumanL-ARGinthesamplesisthendeterminedbycomparingtheO.D.ofthesamplestothestandardcurve.Materialsprovidedwiththekit1washsolution20ml×1bottle7StopSolution6ml×1bottle2HRP-Conjugatereagent6ml×1bottle8Standard（96nmol/L）0.5ml×1bottle3Microelisastripplate12well×8strips9Standarddiluent1.5ml×1bottle4Samplediluent6ml×1bottle10Instruction15ChromogenSolutionA6ml×1bottle11Closureplatemembrane26ChromogenSolutionB6ml×1bottle12Sealedbags1Specimenrequirements1.extractassoonaspossibleafterSpecimencollection,andaccordingtotherelevantliterature,and首ldbeexperimentassoonaspossibleaftertheextraction.Ifitcan’t,specimencanbekeptin-20℃topreserve,Avoidrepeatedfreeze-thawcycles.2.Can’tdetectthesamplewhichcontainNaN3,becauseNaN3inhibitsHRPactive.Assayprocedure1.Diluteandaddsample:DiluteOriginaldensityStandardasfollowtable:48nmol/L5Standard150μlOriginaldensityStandard+150μlStandarddiluent24nmol/L4Standard150μl5Standard+150μlStandarddiluent12nmol/L3Standard150μl4Standard+150μlStandarddiluent6nmol/L2Standard150μl3Standard+150μlStandarddiluent3nmol/L1Standard150μl2Standard+150μlStandarddiluent2.Addsample:Setblankwellsseparately(blankcomparisonwellsdon’taddsampleandHRP-Conjugatereagent,othereachstepoperationissame).testingsamplewell.addSampledilution40μltotestingsamplewell,thenaddtestingsample10μl(samplefinaldilutionis5-fold),addsampletowells,don’ttouchthewellwallasfaraspossible,andGentlymix.3.Incubate:AfterclosingplatewithClosureplatemembrane,incubatefor30minat37℃.4.Configurateliquid:30-fold(or20-fold)washsolutiondiluted30-fold(or20-fold)withdistilledwaterandreserve.5.Washing:UncoverClosureplatemembrane,discardLiquid,drybyswing,addwashingbuffertoeverywell,stillfor30sthendrain,repeat5times,drybypat.6.Addenzyme:AddHRP-Conjugatereagent50μltoeachwell,exceptblankwell.7.Incubate:Operationwith3.8.Washing:Operationwith5.9.Color:AddChromogenSolutionA50ulandChromogenSolutionBtoeachwell,evadethelightpreservationfor15minat37℃10.Stopthereaction:AddStopSolution50μltoeachwell,Stopthereaction(thebluecolorchangetoyellowcolor).11.Assay:takeblankwellaszero,Readabsorbanceat450nmafterAddingStopSolutionandwithin15min.StepsdescriptionStandard,SamplediluentAddStandard,Samplediluent,incubatefor30minat37℃.Wash5time,AddHRP-Conjugatereagent,incubatefor30minat37℃.Wash5times,AddChromogenSolutionAandB,incubatefor30minat37℃.AddStoppSolutionReadabsorbanceat450nmwithin15mincalculateCalculateTakethestandarddensityasthehorizontal,theODvalueforthevertical,drawthestandardcurveongraphpaper,FindoutthecorrespondingdensityaccordingtothesampleODvaluebytheSamplecurve,multipliedbythedilutionmultiple,orcalculatethestraightlineregressionequationofthestandardcurvewiththestandarddensityandtheODvalue,withthesampleODvalueintheequation,calculatethesampledensity,multipliedbythedilutionfactor,theresultisthesampleactualdensity.Importantnotes1.Thekittakesoutfromtherefrigerationenvironment首ldbebalanced15-30minutesintheroomtemperature,ELISAplatescoatedifhasnotuseupafteropened,theplate首ldbestoredinSealedbag.2.washingbufferwillCrystallizationseparation,itcanbeheatedthewaterhelpsdissolvewhendilute.Washingdoesnotaffecttheresult.3.addSamplewithsamplerEachstep,Andproofreaditsaccuracyfrequently,avoidstheexperimentalerror.addsamplewithin5min,ifthenumberofsampleismuch,recommendtouseVolley.4.ifthetestingmaterialcontentisexcessivelyhigher(ThesampleODisbiggerthanthefirststandardwell),pleasediluteSample(n-fold),Pleasediluenteandmultipliedbythedilutionfactor.（×n×5）.5.Closureplatemembraneonlylimitsthedisposableuse,toavoidcross-contamination.6.Thesubstrateevadethelightpreservation.7.Pleaseaccordingtouseinstructionstrictly,Thetestresultdeterminationmusttakethemicrotiterplatereaderasastandard.8.Allsamples,washingbufferandeachkindofreject首ldaccordingtoinfectivematerialprocess.9.Donotmixreagentswiththosefromotherlots.Storageandvalidity1．Storage：2-8℃.2．validity：sixmonths[詳細]

  2018-09-19 10:00

  產品樣冊

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• 豬DC細胞（DC）英文說明書

  PorcineDCFORRESEARCHUSEONLYAssayrange：1.0ng/L-60ng/L96determinationsPurposeThiskitallowsforthedeterminationofDCconcentrationsinPorcineserum,cellculturesupernatesandotherbiologicalfluidsPrincipleoftheassayThekitassayPorcineDClevelinthesample，usePurifiedPorcineDCantibodytocoatmicrotiterplatewells,makesolid-phaseantibody,thenaddDCtowells,CombinedDCantibodywhichWithHRPlabeled,becomeantibody-antigen-enzyme-antibodycomplex,afterwashingCompletely,AddTMBsubstratesolution,TMBsubstratebecomesbluecolorAtHRPenzyme-catalyzed,reactionisterminatedbytheadditionofasulphuricacidsolutionandthecolorchangeismeasuredspectrophotometricallyatawavelengthof450nm.TheconcentrationofPorcineDCinthesamplesisthendeterminedbycomparingtheO.D.ofthesamplestothestandardcurve.Materialsprovidedwiththekit1washsolution20ml×1bottle7StopSolution6ml×1bottle2HRP-Conjugatereagent6ml×1bottle8Standard（120ng/L）0.5ml×1bottle3Microelisastripplate12well×8strips9Standarddiluent1.5ml×1bottle4Samplediluent6ml×1bottle10Instruction15ChromogenSolutionA6ml×1bottle11Closureplatemembrane26ChromogenSolutionB6ml×1bottle12Sealedbags1Specimenrequirements1.extractassoonaspossibleafterSpecimencollection,andaccordingtotherelevantliterature,and首ldbeexperimentassoonaspossibleaftertheextraction.Ifitcan’t,specimencanbekeptin-20℃topreserve,Avoidrepeatedfreeze-thawcycles.2.Can’tdetectthesamplewhichcontainNaN3,becauseNaN3inhibitsHRPactive.Assayprocedure1.Diluteandaddsample:DiluteOriginaldensityStandardasfollowtable:60ng/L5Standard150μlOriginaldensityStandard+150μlStandarddiluent30ng/L4Standard150μl5Standard+150μlStandarddiluent15ng/L3Standard150μl4Standard+150μlStandarddiluent7.5ng/L2Standard150μl3Standard+150μlStandarddiluent3.75ng/L1Standard150μl2Standard+150μlStandarddiluent2.addsample：Setblankwellsseparately(blankcomparisonwellsdon’taddsampleandHRP-Conjugatereagent,othereachstepoperationissame).testingsamplewell.addSampledilution40μltotestingsamplewell,thenaddtestingsample10μl(samplefinaldilutionis5-fold),addsampletowells,don’ttouchthewellwallasfaraspossible,andGentlymix.3.Incubate:AfterclosingplatewithClosureplatemembrane,incubatefor30minat37℃.4.Configurateliquid:30-fold(or20-fold)washsolutiondiluted30-fold(or20-fold)withdistilledwaterandreserve.5.washing：UncoverClosureplatemembrane,discardLiquid,drybyswing,addwashingbuffertoeverywell,stillfor30sthendrain,repeat5times,drybypat.6.addenzyme：AddHRP-Conjugatereagent50μltoeachwell,exceptblankwell.7.incubate：Operationwith3.8.washing：Operationwith5.9.color：AddChromogenSolutionA50ulandChromogenSolutionB50ultoeachwell,evadethelightpreservationfor10minat37℃10.Stopthereaction：AddStopSolution50μltoeachwell,Stopthereaction(thebluecolorchangetoyellowcolor).11.assay：takeblankwellaszero,Readabsorbanceat450nmafterAddingStopSolutionandwithin15min.StepsdescriptionStandard,SamplediluentAddStandard,Samplediluent,incubatefor30minat37℃.Wash5time,AddHRP-Conjugatereagent,incubatefor30minat37℃.Wash5times,AddChromogenSolutionAandB,incubatefor10minat37℃.AddStopSolutionReadabsorbanceat450nmwithin15mincalculateCalculateTakethestandarddensityasthehorizontal,theODvalueforthevertical,drawthestandardcurveongraphpaper,FindoutthecorrespondingdensityaccordingtothesampleODvaluebytheSamplecurve,multipliedbythedilutionmultiple,orcalculatethestraightlineregressionequationofthestandardcurvewiththestandarddensityandtheODvalue,withthesampleODvalueintheequation,calculatethesampledensity,multipliedbythedilutionfactor,theresultisthesampleactualdensity.Importantnotes1.Thekittakesoutfromtherefrigerationenvironment首ldbebalanced15-30minutesintheroomtemperature,ELISAplatescoatedifhasnotuseupafteropened,theplate首ldbestoredinSealedbag.2.washingbufferwillCrystallizationseparation,itcanbeheatedthewaterhelpsdissolvewhendilute.Washingdoesnotaffecttheresult.3.addSamplewithsamplerEachstep,Andproofreaditsaccuracyfrequently,avoidstheexperimentalerror.addsamplewithin5min,ifthenumberofsampleismuch,recommendtouseVolley.4.ifthetestingmaterialcontentisexcessivelyhigher(ThesampleODisbiggerthanthefirststandardwell),pleasediluteSample(n-fold),Pleasediluenteandmultipliedbythedilutionfactor.（×n×5）.5.Closureplatemembraneonlylimitsthedisposableuse,toavoidcross-contamination.6.Thesubstrateevadethelightpreservation.7.Pleaseaccordingtouseinstructionstrictly,Thetestresultdeterminationmusttakethemicrotiterplatereaderasastandard.8.Allsamples,washingbufferandeachkindofreject首ldaccordingtoinfectivematerialprocess.9.Donotmixreagentswiththosefromotherlots.Storageandvalidity1．Storage：2-8℃.2．validity：sixmonths[詳細]

  2018-09-19 10:00

  產品樣冊

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• 人活化凝血因子Ⅻ（FⅫa）英文說明書

  HumanActivatedcoagulationfactorⅫ(FⅫa)FORRESEARCHUSEONLYAssayrange：2.2U/L-80U/L96determinationsPurposeThiskitallowsforthedeterminationofFⅫaconcentrationsinHumanserum,cellculturesupernatesandotherbiologicalfluidsPrincipleoftheassayThekitassayHumanFⅫalevelinthesample,usePurifiedHumanFⅫaantibodytocoatmicrotiterplatewells,makesolid-phaseantibody,thenaddFⅫatowells,CombinedFⅫaantibodywhichWithHRPlabeled,becomeantibody-antigen-enzyme-antibodycomplex,afterwashingCompletely,AddTMBsubstratesolution,TMBsubstratebecomesbluecolorAtHRPenzyme-catalyzed,reactionisterminatedbytheadditionofasulphuricacidsolutionandthecolorchangeismeasuredspectrophotometricallyatawavelengthof450nm.TheconcentrationofHumanFⅫainthesamplesisthendeterminedbycomparingtheO.D.ofthesamplestothestandardcurve.Materialsprovidedwiththekit1washsolution20ml×1bottle7StopSolution6ml×1bottle2HRP-Conjugatereagent6ml×1bottle8Standard（160U/L）0.5ml×1bottle3Microelisastripplate12well×8strips9Standarddiluent1.5ml×1bottle4Samplediluent6ml×1bottle10Instruction15ChromogenSolutionA6ml×1bottle11Closureplatemembrane26ChromogenSolutionB6ml×1bottle12Sealedbags1Specimenrequirements1.extractassoonaspossibleafterSpecimencollection,andaccordingtotherelevantliterature,and首ldbeexperimentassoonaspossibleaftertheextraction.Ifitcan’t,specimencanbekeptin-20℃topreserve,Avoidrepeatedfreeze-thawcycles.2.Can’tdetectthesamplewhichcontainNaN3,becauseNaN3inhibitsHRPactive.Assayprocedure1.Diluteandaddsample:DiluteOriginaldensityStandardasfollowtable:80U/L5Standard150μlOriginaldensityStandard+150μlStandarddiluent40U/L4Standard150μl5Standard+150μlStandarddiluent20U/L3Standard150μl4Standard+150μlStandarddiluent10U/L2Standard150μl3Standard+150μlStandarddiluent5U/L1Standard150μl2Standard+150μlStandarddiluent2.Addsample:Setblankwellsseparately(blankcomparisonwellsdon’taddsampleandHRP-Conjugatereagent,othereachstepoperationissame).testingsamplewell.addSampledilution40μltotestingsamplewell,thenaddtestingsample10μl(samplefinaldilutionis5-fold),addsampletowells,don’ttouchthewellwallasfaraspossible,andGentlymix.3.Incubate:AfterclosingplatewithClosureplatemembrane,incubatefor30minat37℃.4.Configurateliquid:30-fold(or20-fold)washsolutiondiluted30-fold(or20-fold)withdistilledwaterandreserve.5.Washing:UncoverClosureplatemembrane,discardLiquid,drybyswing,addwashingbuffertoeverywell,stillfor30sthendrain,repeat5times,drybypat.6.Addenzyme:AddHRP-Conjugatereagent50μltoeachwell,exceptblankwell.7.Incubate:Operationwith3.8.Washing:Operationwith5.9.Color:AddChromogenSolutionA50ulandChromogenSolutionB50ultoeachwell,evadethelightpreservationfor10minat37℃10.Stopthereaction:AddStopSolution50μltoeachwell,Stopthereaction(thebluecolorchangetoyellowcolor).11.Assay:takeblankwellaszero,Readabsorbanceat450nmafterAddingStopSolutionandwithin15min.StepsdescriptionStandard,SamplediluentAddStandard,Samplediluent,incubatefor30minat37℃.Wash5time,AddHRP-Conjugatereagent,incubatefor30minat37℃.Wash5times,AddChromogenSolutionAandB,incubatefor10minat37℃.AddStopSolutionReadabsorbanceat450nmwithin15mincalculateCalculateTakethestandarddensityasthehorizontal,theODvalueforthevertical,drawthestandardcurveongraphpaper,FindoutthecorrespondingdensityaccordingtothesampleODvaluebytheSamplecurve,multipliedbythedilutionmultiple,orcalculatethestraightlineregressionequationofthestandardcurvewiththestandarddensityandtheODvalue,withthesampleODvalueintheequation,calculatethesampledensity,multipliedbythedilutionfactor,theresultisthesampleactualdensity.Importantnotes1.Thekittakesoutfromtherefrigerationenvironment首ldbebalanced15-30minutesintheroomtemperature,ELISAplatescoatedifhasnotuseupafteropened,theplate首ldbestoredinSealedbag.2.washingbufferwillCrystallizationseparation,itcanbeheatedthewaterhelpsdissolvewhendilute.Washingdoesnotaffecttheresult.3.addSamplewithsamplerEachstep,Andproofreaditsaccuracyfrequently,avoidstheexperimentalerror.addsamplewithin5min,ifthenumberofsampleismuch,recommendtouseVolley.4.ifthetestingmaterialcontentisexcessivelyhigher(ThesampleODisbiggerthanthefirststandardwell),pleasediluteSample(n-fold),Pleasediluenteandmultipliedbythedilutionfactor.（×n×5）.5.Closureplatemembraneonlylimitsthedisposableuse,toavoidcross-contamination.6.Thesubstrateevadethelightpreservation.7.Pleaseaccordingtouseinstructionstrictly,Thetestresultdeterminationmusttakethemicrotiterplatereaderasastandard.8.Allsamples,washingbufferandeachkindofreject首ldaccordingtoinfectivematerialprocess.9.Donotmixreagentswiththosefromotherlots.Storageandvalidity1．Storage：2-8℃.2．validity：sixmonths[詳細]

  2018-09-19 10:00

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• 出口式電子地磅安裝說明書（英文）

  出口式電子地磅采用當今世界先進的稱重傳感器和稱重顯示儀及各種外配設備而設計的全電子模塊化汽車稱重系統(tǒng)。稱重傳感器采用先進技術，能對溫度系數、非線性、滯后和蠕變等進行自動數字化補償；儀表功能豐富，存儲功能強；秤臺采用U形冷彎型鋼組焊而成，整體剛度、抗扭性能及臺面的局部剛度都有很大的改進；秤臺設計模塊化、標準化、系列化，可以自由組合成多種規(guī)格。整臺汽車衡系統(tǒng)環(huán)境適應性強，加強配置后可實現全智能化及無人值守,并且計量性能優(yōu)越，準確度高，長期穩(wěn)定性好，安裝調試維護方便。廣泛用于國外冶金、礦山、機械、化工、港口及公路貨站等行業(yè)。充分考慮了海運集裝箱運輸對汽車衡秤體尺寸的限制，同時又必須兼顧秤體的剛度要求和終端客戶現場的安裝便捷要求。據此雄衡科技公司自主開發(fā)了兩款出口結構汽車衡，結構合理，安裝快捷，風靡海外市場。同時也可用于對超寬運輸有限制的國內市場。附件為出口式電子地磅英文版安裝說明書。[詳細]

  2018-10-30 10:00

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• 人白細胞介素6（IL-6）英文說明書

  HumanInterleukin6（IL-6）FORRESEARCHUSEONLYAssayrange：0.8ng/L-20ng/L96determinationsPurposeThiskitallowsforthedeterminationofIL-6concentrationsinHumanserum,cellculturesupernatesandotherbiologicalfluidsPrincipleoftheassayThekitassayHumanIL-6levelinthesample,usePurifiedHumanIL-6antibodytocoatmicrotiterplatewells,makesolid-phaseantibody,thenaddIL-6towells,CombinedIL-6antibodywhichWithHRPlabeled,becomeantibody-antigen-enzyme-antibodycomplex,afterwashingCompletely,AddTMBsubstratesolution,TMBsubstratebecomesbluecolorAtHRPenzyme-catalyzed,reactionisterminatedbytheadditionofasulphuricacidsolutionandthecolorchangeismeasuredspectrophotometricallyatawavelengthof450nm.TheconcentrationofHumanIL-6inthesamplesisthendeterminedbycomparingtheO.D.ofthesamplestothestandardcurve.Materialsprovidedwiththekit1washsolution20ml×1bottle7StopSolution6ml×1bottle2HRP-Conjugatereagent6ml×1bottle8Standard（40ng/L）0.5ml×1bottle3Microelisastripplate12well×8strips9Standarddiluent1.5ml×1bottle4Samplediluent6ml×1bottle10Instruction15ChromogenSolutionA6ml×1bottle11Closureplatemembrane26ChromogenSolutionB6ml×1bottle12Sealedbags1Specimenrequirements1.extractassoonaspossibleafterSpecimencollection,andaccordingtotherelevantliterature,and首ldbeexperimentassoonaspossibleaftertheextraction.Ifitcan’t,specimencanbekeptin-20℃topreserve,Avoidrepeatedfreeze-thawcycles.2.Can’tdetectthesamplewhichcontainNaN3,becauseNaN3inhibitsHRPactive.Assayprocedure1.Diluteandaddsample:DiluteOriginaldensityStandardasfollowtable:20ng/L5Standard150lOriginaldensityStandard+150lStandarddiluent10ng/L4Standard150l5Standard+150lStandarddiluent5ng/L3Standard150l4Standard+150lStandarddiluent2.5ng/L2Standard150l3Standard+150lStandarddiluent1.25ng/L1Standard150l2Standard+150lStandarddiluent2.Addsample:Setblankwellsseparately（blankcomparisonwellsdon’taddsampleandHRP-Conjugatereagent,othereachstepoperationissame）.testingsamplewell.addSampledilution40ltotestingsamplewell,thenaddtestingsample10l（samplefinaldilutionis5-fold）,addsampletowells,don’ttouchthewellwallasfaraspossible,andGentlymix.3.Incubate:AfterclosingplatewithClosureplatemembrane,incubatefor30minat37℃.4.Configurateliquid:30-fold（or20-fold）washsolutiondiluted30-fold（or20-fold）withdistilledwaterandreserve.5.Washing:UncoverClosureplatemembrane,discardLiquid,drybyswing,addwashingbuffertoeverywell,stillfor30sthendrain,repeat5times,drybypat.6.Addenzyme:AddHRP-Conjugatereagent50ltoeachwell,exceptblankwell.7.Incubate:Operationwith3.8.Washing:Operationwith5.9.Color:AddChromogenSolutionA50ulandChromogenSolutionBtoeachwell,evadethelightpreservationfor15minat37℃10.Stopthereaction:AddStopSolution50ltoeachwell,Stopthereaction（thebluecolorchangetoyellowcolor）.11.Assay:takeblankwellaszero,Readabsorbanceat450nmafterAddingStopSolutionandwithin15min.StepsdescriptionStandard,SamplediluentAddStandard,Samplediluent,incubatefor30minat37℃.Wash5time,AddHRP-Conjugatereagent,incubatefor30minat37℃.Wash5times,AddChromogenSolutionAandB,incubatefor30minat37℃.AddStoppSolutionReadabsorbanceat450nmwithin15mincalculateCalculateTakethestandarddensityasthehorizontal,theODvalueforthevertical,drawthestandardcurveongraphpaper,FindoutthecorrespondingdensityaccordingtothesampleODvaluebytheSamplecurve,multipliedbythedilutionmultiple,orcalculatethestraightlineregressionequationofthestandardcurvewiththestandarddensityandtheODvalue,withthesampleODvalueintheequation,calculatethesampledensity,multipliedbythedilutionfactor,theresultisthesampleactualdensity.Importantnotes1.Thekittakesoutfromtherefrigerationenvironment首ldbebalanced15-30minutesintheroomtemperature,ELISAplatescoatedifhasnotuseupafteropened,theplate首ldbestoredinSealedbag.2.washingbufferwillCrystallizationseparation,itcanbeheatedthewaterhelpsdissolvewhendilute.Washingdoesnotaffecttheresult.3.addSamplewithsamplerEachstep,Andproofreaditsaccuracyfrequently,avoidstheexperimentalerror.addsamplewithin5min,ifthenumberofsampleismuch,recommendtouseVolley.4.ifthetestingmaterialcontentisexcessivelyhigher（ThesampleODisbiggerthanthefirststandardwell）,pleasediluteSample（n-fold）,Pleasediluenteandmultipliedbythedilutionfactor.（×n×5）.5.Closureplatemembraneonlylimitsthedisposableuse,toavoidcross-contamination.6.Thesubstrateevadethelightpreservation.7.Pleaseaccordingtouseinstructionstrictly,Thetestresultdeterminationmusttakethemicrotiterplatereaderasastandard.8.Allsamples,washingbufferandeachkindofreject首ldaccordingtoinfectivematerialprocess.9.Donotmixreagentswiththosefromotherlots.Storageandvalidity1．Storage：2-8℃.2．validity：sixmonths[詳細]

  2018-11-15 10:03

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