Diagnostic Kit yeLuteinizing Hormonefluorescence immunochromatographic assay)
Yekushandisa in vitro diagnostic chete
Ndokumbira uverenge iyi pasuru isa nekungwarira usati washandisa uye kunyatsotevera mirairo. Kuvimbika kwemhedzisiro yeassay hakugone kuvimbiswa kana paine chero kutsauka kubva kune mirairo mune ino pasuru yekuisa.

ZVIRI KUSHANDISA
Diagnostic Kit yeLuteinizing Hormone (fluorescence immunochromatographic assay) ndeye fluorescence immunochromatographic assay yehuwandu hwekuonekwa kweLuteinizing Hormone (LH) muserum yevanhu kana plasma, iyo inonyanya kushandiswa mukuongororwa kwepituitary endocrine basa. dzimwe nzira. Muedzo uyu wakaitirwa kushandiswa nenyanzvi dzezvehutano chete.

SUMMARY

Luteinizing hormone (LH) inonzi glycoprotein ine molecular huremu hunosvika makumi matatu ezviuru zveDalton, iyo inogadzirwa neanterior pituitary. Kuwanda kweLH kwakabatana zvakanyanya nekuvharwa kwemaovari, uye nhamba yepamusoro yeLH inofungidzirwa kuva maawa 24 kusvika ku36 evhavha. Nokudaro, kukosha kwepamusoro kweLH kunogona kuongororwa panguva yekuenda kumwedzi kuti uone nguva yakakwana yekubata pamuviri. Abnormal endocrine function in the pituitary gland inogona kukonzera LH secretion irregularity.Kusangana kweLH kunogona kushandiswa kuongorora pituitary endocrine basa. Iyo Diagnostic Kit yakavakirwa pa immunochromatography uye inogona kupa mhedzisiro mukati memaminitsi gumi nemashanu.

ZVINOTAURWA ZVINOITA

Iyo membrane yechishandiso chekuyedza yakavharwa neanti LH antibody padunhu rekuyedza uye mbudzi anti tsuro IgG antibody panzvimbo yekutonga. Lable pad yakaputirwa nefluorescence yakanyorwa anti LH antibody uye tsuro IgG pamberi. Paunenge uchiyedza sampuli yakanaka, iyo LH antigen mumuenzaniso inosanganisa nefluorescence yakanyorwa anti LH antibody, uye gadzira immune system. Pasi pechiito che immunochromatography, iyo yakaoma kuyerera ikananga kune inonwisa bepa, apo yakaoma yakapfuura dunhu rekuyedzwa, yakasanganiswa neAnti LH coating antibody, inoumba nyowani yakaoma. LH nhanho yakanyatsoenderana neiyo fluorescence chiratidzo, uye kuwanda kweLH mumuenzaniso kunogona kuonekwa nefluorescence immunoassay assay.

REAGENTS NEZVINHU ZVINOPIWA

25T package zvikamu:

.Kuedza kadhi rimwe nerimwe foil yakaiswa muhomwe ine desiccant 25T
.Sample diluents
.Package isa

ZVINHU ZVINODIWA ASI ZVISINA KUPIWA
Sample yekuunganidza mudziyo, timer

SAMPLE KUCHENGA UYE KUCHENGA
1.Mienzaniso yakaedzwa inogona kuva serum, heparin anticoagulant plasma kana EDTA anticoagulant plasma.
2.According to standard techniques unganidza sampuli. Serum kana plasma sampuli inogona kuchengetwa firiji pa 2-8 ℃ kwemazuva 7 uye cryopreservation pazasi -15 ° C kwemwedzi mitanhatu.
3.Yese sampuli inodzivirira kutonhora-kunyungudika kutenderera.

ASAY PROCEDURE

Maitiro ekuyedza echiridzwa ona iyo immunoanalyzer bhuku. Iyo reagent test maitiro ndeaya anotevera
1.Kuisa parutivi zvose reagents uye samples kune tembiricha yekamuri.
2.Vhura iyo Portable Immune Analyzer (WIZ-A101), isa iyo password password login maererano nenzira yekushanda yechiridzwa, uye pinda iyo yekuona interface.
3.Scan dentification code kuti usimbise chinhu chekuedza.
4.Bvisa kadhi rekuedza kubva mubhegi refoil.
5.Isai kadhi rekuedza mukadhi yekadhi, tarisai QR code, uye sarudza chinhu chekuedza.
6.Wedzera 20μL serum kana plasma sampuli kuti sampuli diluent, uye sanganisa zvakanaka.
7.Wedzera 80μL sampuli mhinduro kuti uenzanise zvakanaka wekadhi.
8.Click "standard test" bhatani, mushure memaminitsi e15, chiridzwa chichangoona kadhi rekuedza, rinogona kuverenga migumisiro kubva pachiratidziro chechiratidzo chechiridzwa, uye nyora / kudhinda mhinduro dzekuedza.
9.Rejera kune rairo yePortable Immune Analyzer(WIZ-A101).

TEST RESULTS UYE DUDZIRIRO

.Iyo data iri pamusoro apa inguva yereferensi yakagadzwa ye data yekuona yekiti iyi, uye zvinokurudzirwa kuti laboratori yega yega inofanira kumisa nguva yereferensi yezvakakoshesesa zvekiriniki zvehuwandu hwevanhu munharaunda ino.
.Kusangana kweLH kwakakwirira kudarika chiyero chetauro, uye kuchinja kwehupenyu kana kushushikana kwepfungwa kunofanira kubviswa.Ichokwadi chisina kujairika, chinofanira kusanganisa kuongororwa kwechiratidzo chekliniki.
.Migumisiro yeiyi nzira inongoshanda kune mutsara wekutsvaga wakagadzwa nenzira iyi, uye zvigumisiro hazvifananidzi zvakananga nedzimwe nzira.
.Zvimwe zvikonzero zvinogonawo kukonzera kukanganisa mumigumisiro yekuona, kusanganisira zvikonzero zvehutano, zvikanganiso zvekushanda uye zvimwe zvinhu zvemuenzaniso.

KUCHENGA UYE KUTSIGIRA
1.Ikiti ndeye 18 mwedzi pasherufu-hupenyu kubva pazuva rekugadzirwa. Chengetedza makiti asina kushandiswa pa2-30°C. MUSAIZE. Usashandise kupfuura zuva rekupera.
2.Usavhura homwe yakavharwa kusvika wagadzirira kuita bvunzo, uye bvunzo-yekushandisa imwe chete inokurudzirwa kushandiswa pasi penzvimbo inodiwa (tembiricha 2-35 ℃, humidity 40-90%) mukati me60 mins nekukurumidza. sezvinobvira.
3.Sample diluent inoshandiswa pakarepo mushure mekuvhurwa.

YAMBIRO UYE CHENJERERO
.Ikiti inofanira kuvharwa uye kuchengetedzwa kubva pakunyorova.
.Yese mienzaniso yakanaka ichasimbiswa nedzimwe nzira.
.Mienzaniso yese ichabatwa sezvingango svibisa.
.USA shandisa expired reagent.
. HASI kuchinjana mareagents pakati pekiti ane akasiyana lot Nha.
.USAshandise zvakare makadhi ebvunzo uye chero zvinhu zvinoraswa.
.Misoperation, yakawandisa kana sampuli shoma inogona kutungamirira kumhedzisiro yekutsauka.

LIMITATION
.Sezvinoita chero muyedzo unoshandisa masoja ekudzivirira embeva, mukana uripo wekukanganiswa nemasoja ekudzivirira mbeva (HAMA) mumuenzaniso. Mienzaniso kubva kuvarwere vakagamuchira gadziriro dzemonoclonal antibodies yekuongorora kana kurapwa inogona kunge iine HAMA. Mienzaniso yakadaro inogona kukonzera nhema dzakanaka kana nhema dzisina kunaka.
.Iyi mhedzisiro yebvunzo ndeyekuongororwa kwekiriniki chete, haifanire kushanda seyo chete hwaro hwekuongororwa kwekiriniki uye kurapwa, varwere vekiriniki manejimendi vanofanirwa kutarisisa kwakadzama kusanganiswa nezviratidzo zvayo, nhoroondo yekurapa, imwe ongororo yerabhoritari, mhinduro yekurapa, epidemiology uye mamwe mashoko. .
.Iri reagent rinoshandiswa chete serum uye plasma tests. Iyo inogona kusawana mhedzisiro chaiyo kana ichishandiswa kune mamwe masampuli senge mate uye weti uye nezvimwe.

PERFORMANCE CHARACTERISTICS

REFERENCES
1.Hansen JH, et al.HAMA Kupindira neMurine Monoclonal Antibody-Based Immunoassays[J].J yeClin Immunoassay,1993,16:294-299.
2.Levinson SS.Mamiriro eHeterophilic Antibodies uye Basa muImmunoassay Interference[J].J yeClin Immunoassay,1992,15:108-114.

Kiyi yezviratidzo zvakashandiswa:

	In Vitro Diagnostic Medical Device
	Mugadziri
	Chengetedza pa2-30 ℃
	Zuva rekupera
	Usashandisezve
	KUCHENJERA
	Bvunza Mirayiridzo Yekushandisa

Xiamen Wiz Biotech CO., LTD
Kero:3-4 Floor,NO.16 Building,Bio-medical Workshop,2030 Wengjiao West Road,Haicang District,361026,Xiamen,China
Tel:+86-592-6808278
Fax:+86-592-6808279