Diagnostic Kit ad luteinizing hormone (Fluorescence immunochromatographic Asay)
Diagnostic ornamentum estLuteinizing hormoneFluorescence 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 ad luteinizing hormone (fluorescence immunochromatographic assa) est fluorescence immunochromatographic pro quantitatis deprehensio luteinizing hormone (LH) in humanis Serum aut Pure.All.All positivum sample est confirmatus alii methodologies. Hoc test est in animo pro curis professional usum tantum.
Summary
Luteinizing hormone (LH) est a glycoprotein cum molecular pondus de 30,000 Dalton, quod producitur per anteriorem pituitam. Et concentration LH propinqua ad ovulation ovariorum, et apicem LH praedicatur esse XXIV ad XXXVI horas de ovulation. Ideo ad apicem valorem de LH potest monitored per mensis exolvuntur determinare meliorem conceptionem tempore. Abnormes endocrinarum munus in pituitam glandulae potest facere LH secretio irregularity.The concentration de LH potest esse ad aestimandas pituitam endocrinarum munus. In diagnostic ornamentum fundatur in immunochromatography et potest dare effectus in XV minutes.
Principle procedendi
Membrana in test fabrica est iactaret cum anti LH antibody in test regionem et caprae anti lepus IGG antibody in imperium regionem. Lable codex tunicata fluorescen intitulatum anti LH antibody et lepus IGG pre. Cum probatio positivum specimen, in LH antigen in sample miscere cum fluorescence intitulatum anti LH, et forma immune mixtisque. Sub actione immunochromatography, in universa fluxus in directionem absorbent charta, cum complexu transierunt in test regionem, cum anti LH coating antibody, formas novum complexu. LH gradu est positive connectuntur fluorescence signo et concentratio LH in sample potest deprehendi a fluorescit immunoassaysy asay.
Reagentia et materiae suppleverunt
25T sarcina components:
.Test card singulos ffoyle pouched cum a desiccant 25t
.Sample Diluents
.Package Insert
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
In test procedure instrumenti animadverto the immunoanalyzer manual. In reagent test procedure est ut sequitur
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.
6.Add 20μl Serum vel Pure Sample to Diluent Sample, et misce ..
7.Add 80μl sample solutio ad sample bene de card.
8.Click in "Latin Test" puga pyga, post XV minutes, instrumentum erit automatice deprehendere test card, quod potest legi eventus ex ostentationem screen in instrumenti, et record / print in test results.
9.Refer ad disciplinam Portable immune analyzer (wiz-a101).
Test eventus et interpretatione
Scaena | Range (Miu / ml) | |
Masculus | 1.50-9.25 | |
Femina | folliclicularis phase | 1.25-11.80 |
| Ovulatory tempus | 13.15-94.75 |
| Luteal phase | 1.05-14.50 |
| Menopause | 7.70-64.20 |
.The supra notitia est reference intervallum statutum pro deprehendatur notitia huius ornamentum, et hoc est suggesserant ut quisque laboratorium debet constituere a refertione intervallo ad relevant orci significationem de populatio in hac regione.
.The concentration of LH altior quam referat range et physiologica mutationes vel accentus responsio debet esse excluded.indeed abnormes, si non miscere orci indicium diagnosi.
.The results of hunc modum sunt tantum applicabiles ad referat range statutum per modum, et eventus non directe comparari cum aliis modis.
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.
. NOVAE NOTA NOTA NUMBER NOTIC
.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
Lineamentum | 10miu / ml ad 10000miu / ml | Relativum deviation: -15% ad + XV%. |
Linear Correlation coefficiente (R) ≥0,9900 | ||
Accuratio | Et recuperatio rate erit in LXXXV% - CXV%. | |
Repeatability | CV≤15% | |
Specifica (nemo substantiae ad interpensed temptavit impedire in asay) | Interpensatus | Intercessio |
Hemoglobin | 200μg / ml | |
transferret | 100μg / ml | |
Equus radicula peroxidase | 2000μg / ml | |
Fsh | 200miu / ml | |
HCG | 20000miu / ml | |
Tsh | 200μiu / ml |
References
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 |
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![]() | Store ad 2-30 ℃ |
![]() | Expiration Date |
![]() | Non reuse |
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![]() | 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