Diagnostic Kit quia isoenzyme Mb de Creatine Kinase(Fluorizing Immunochromatographic Asay)
Nam in vitro diagnostic usu modo
Please legit hoc sarcina insert diligenter prior ad uti et stricte sequi instructiones. Reliability Assay praecessi non potest praestati si sunt aliqua deviationes ex instructiones in hoc sarcina inserta.

Intendebat usum
Diagnostic Kit quia ISOENZYME MB de Creatine Kinase (Fluorzening Immunochromatographic Asay) est a Fluorzence Immunochromatographic Assay pro quantitatis Deprehensio isoenzyme MB Creatine Kinase (CK-MB) in Humanum Serum aut Plasma, quod est usus ad Auxiliaribus Disputatio de AMI (Acutus Myocardial Infarctione). Omnes positivum sample debet confirmari ab aliis methodologies. Hoc test est in animo pro curis professional usum tantum.

Summary
CK-MB campester augeri 4-6 horis post myocardial infarctione occurrit, bakeed ad 18-24 horas et rediit ad normalis 2-3 dies post. CK-MB release in circulationem postea hemoglobin.ck-MB est traditional titulum acuti myocardial infarction

Principle procedendi
Membrana in test fabrica est iactaret cum anti ck-MB, in test regionem et caprae anti lepus IGG antibody in imperium regione. Lable PAD sunt iactaret fluorescence intitulatum anti CK-MB, et lepus, et CK-MB. Cum probatio positivum sample, in CK-MB antigen in sample miscere cum fluorescence intitulatum anti CK-MB, et forma immune mixtisque. Sub actione immunochromatography, in universa fluxus in directionem absorbent charta, cum complexu transierunt in test regionem, cum anti CK-MB coating antibody, formas novum complexu. CK-MB gradu est positive connectuntur cum fluorescence signum, et concentration CK-MB in sample potest deprehendi a fluoronia immunoassay asay.

Reagentia et materiae suppleverunt

25T sarcina components:
Test card singulos ffoyle pouched cum a desiccant 25t
Sample diluents 25t
Package Insert I

Materials requiritur sed non provisum
Sample Collection Container, Timer

Sample Collection et Storage
1.The exempla probata potest esse serum, Heparin Anticoagult Pure Pureza et EDTA Anticoagulant Pure.
2.AcCording ad Latin Techniques Oratio Sample. Serum vel Plasma Sample potest tenentur refrigerated 2-8 ℃ ad 7days et cryopreservation infra -15 ° C ad VI mensibus.
3.All sample vitare Congelo-CALLUM CYCLII.

Procedure
Placere legit instrumentum operationem manual et sarcina inserta ante tentat.
1.Lay intrahunt omnes reagentia et exempla ad locus temperatus.
2.Open in portable immune analyzer (wiz-a101), Intra rationem password login secundum operationem modum instrumenti, et intrare deprehendatur interface.
3.Scan dentification codice confirmare test item.
4.Take de test card de ffoyle peram.
5.Insert in test card in card socors, scan in QR code, determinare test item.
5.Add 40μl Serum vel Pure Sample to sample Diluent, et misce bene ..
6.Add 80μl sample solutio ad sample bene de card.
7.Click in "Latin test" puga pyga, post XV minuta, instrumentum et automatice deprehendere in test card, quod potest lego eventus ex ostentationem screen of instrumenta et record / print in test results.
8.Refer ad disciplinam Portable immune analyzer (wiz-a101).

Expectata values
CK-MB <5ng / ml
Commendatur quod quisque laboratorium statuam suam normalem range representing sua patientes estote population.

Test eventus et interpretatione
.The supra notitia est effectus CK-MB Reagent test, et quod sit suggesserant ut quisque laboratorium debet constituere a range of CK-MB deprehensio values ​​idoneam ad population in hac regione. Et super praecessi sunt enim reference tantum.
.The results of hunc modum sunt tantum applicentur ad reference Ranges statutum in hoc modum, et non est recta comparability cum aliis modi.
Umbra EtOthe factors potest etiam causa errores in deprehendendo results, comprehendo technica rationes, operational errores et alia sample factors.

Repono et stabilitatem
1.The ornamentum est XVIII menses PLUTEUM-vita a date de fabricantibus. Store ad insolita rhoncus ad 2-30 ° c. Nolite rigabant. Noli ultra expirata.
2.Do non aperire signatum massa usque ad vos es parati ad praestare a test et una-usu test suggesserant utendum sub requiritur environment (temperatus 2-35 ℃, humiditas 40-90%) in LX min ut cito quam maxime.
3.Sample diluent adhibetur statim postquam aperuit.

Monitus et cautiones
.The ornamentum sit signari et protected contra humorem.
.All positivum specimina erit convalescere ab aliis methodologies.
.All specimens et tractata est potentiale pollutant.
.Do non utor exspiravit Reagent.
.Do non intercedit Reagents inter Kits cum diversis sorte non ..
.Do non reuse test cards et nihil PROMPTIOCCULA.
.Misoperation, nimia aut parum specimen potest ad eventum deviationibus.

LImitatio
.As cum aliquo assau usus mus elibodarum, facultatem existit pro intercessiones ab humana anti-mus elencodies (Hama) in specimine. Specimens aegris qui accepit apparatu of Monoclonal antibodies ad diagnosi vel illic ut quae Hama. Tales specimina potest causare falsum positivum vel falsum negative praecessi.
.This test result is only for clinical reference, should not serve as the only basis for clinical diagnosis and treatment, the patients clinical management should be comprehensive consideration combined with its symptoms, medical history, other laboratory examination, treatment response, epidemiology and other information .
.This Reagent est solum usus est Serum et Plasma probat. Non potest obtinere accurate consequuntur, cum usus ad alia exempla ut saliva et urina etc.

Perficientur characteres

RE
1.hansen JH et al.hama intercessiones cum murine Monoclonal Antibody, secundum immunoassays [J] .j de Clin Immunoassay, 1993,16: 294-299.
2.Levinson ss.The natura heterophilic antibodies et partes in immunoassay intercessiones [J] .j de Clin Immunoassay, 1992,15, 108-114.

Key ad symbola usus:

	In Vitro Diagnostic Medical fabrica
	Manufacturer
	Store ad 2-30 ℃
	Expiration Date
	Non reuse
	Cautio
	Consule instructiones ad usum

Xiamen Vivamus Biotech Co., Ltd
Oratio: 3-4 area, no.16 aedificationem, bio-medical officia, MMXXXX Wengjiao Occidentem Road, Haicang regio, (XXXVI) CXXVI, Xiamen, Sina
Tel: + 86-592-6808278
Fax: + 86-592-6808279