Diagnostic Kit foriprotheni ye-hypersensitive C-reactive

(uvavanyo lwe-fluorescence immunochromatographic)

Ukusetyenziswa kwe-in vitro diagnostic kuphela

Nceda ufunde le phakheji ifake ngononophelo phambi kokuba uyisebenzise kwaye ulandele ngokungqongqo imiyalelo.Ukuthembeka kweziphumo zovavanyo akunakuqinisekiswa ukuba kukho nakuphi na ukutenxa kwimiyalelo kolu fakelo lwephakheji.

UKUSETYENZISWA OKUHLOSIWEYO

I-Diagnostic Kit ye-hypersensitive C-reactive protein (i-fluorescence immunochromatographic assay) luvavanyo lwe-fluorescence immunochromatographic yokufumanisa ubuninzi beprotheyini ye-C-reactive (CRP) kwi-serum yabantu / plasma/ Igazi elipheleleyo.Luphawu olungachanekanga lokudumba.Zonke iisampuli ezilungileyo kufuneka ziqinisekiswe ngezinye iindlela.Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.

USHWANKATHELO

Iprotheyini ye-C-reactive yiprotheni yesigaba esibukhali eveliswa yi-lymphokine yokuvuselela isibindi kunye neeseli ze-epithelial.Ikhona kwi-serum yomntu, kwi-cerebrospinal fluid, pleural and abdominal fluid, njl.6-8h emva kokuvela kosulelo lwebhaktiriya, i-CRP yaqala ukwanda, i-24-48h yafikelela kwincopho, kwaye ixabiso lencopho linokufikelela kumakhulu amaxesha aqhelekileyo.Emva kokupheliswa kosulelo, i-CRP yehla ngokukhawuleza kwaye yabuyela kwimeko yesiqhelo kwiveki enye.Nangona kunjalo, i-CRP ayinyuki kakhulu kwimeko yosulelo lwentsholongwane, olubonelela ngesiseko sokuchongwa kweentlobo zosulelo lokuqala lwezifo, kwaye sisixhobo sokuchonga usulelo lwentsholongwane okanye ibhaktheriya.

UMGAQO WENKQUBO

I-membrane yesixhobo sovavanyo igqunywe nge-anti-CRP ye-antibody kwindawo yovavanyo kunye ne-antibody ye-IgG yebhokhwe kwindawo yolawulo.Iphedi elayibhile iqatywe nge-fluorescence ebhalwe i-anti-CRP ye-antibody kunye nomvundla we-IgG kwangaphambili.Xa uvavanyo lwesampulu eqinisekileyo, i-antigen ye-CRP kwisampulu idibanisa ne-fluorescence ebhalwe i-anti-CRP ye-antibody, kwaye yenze umxube wokuzivikela komzimba.Phantsi kwesenzo se-immunochromatography, ukuhamba okuntsonkothileyo kwicala lephepha lokufunxa, xa i-complex iphumelele ummandla wovavanyo, idityaniswe ne-anti-CRP yokwambathisa i-antibody, yenza into entsha.Inqanaba le-CRP lihambelana ngokufanelekileyo kunye nomqondiso we-fluorescence, kwaye ukuxinwa kwe-CRP kwisampulu kunokubonwa nge-fluorescence immunoassay assay.

IIREGENTS KUNYE NEZINTO EZIBONISWAYO

Amacandelo ephakheji ye-25T:

Ikhadi lokuvavanya ifoyile nganye efakwe kwi-desiccant 25T

Isampulu yediluyinti 25T

Faka ipakethi 1

IZINTO EZIFUNEKAYO KODWA AKUNIKEZWA

Isampulu yokuqokelela isitya,ixesha

UKUQOKELELWA KWEsampuli NOKUGCINWA

1. Iisampulu ezivavanyiweyo zinokuba yi-serum, i-heparin anticoagulant plasma okanye i-EDTA anticoagulant plasma.
2. Ngokweendlela eziqhelekileyo zokuqokelela isampuli.I-Serum okanye isampuli ye-plasma inokugcinwa efrijini kwi-2-8 ℃ ye-7days kunye ne-cryopreservation engaphantsi kwe-15 ° C kwiinyanga ezi-6.Isampulu yegazi lonke inokugcinwa efrijini kwi-2-8℃ iintsuku ezi-3
3. Zonke iisampulu zinqanda imijikelo yokunyibilika komkhenkce.