Za mu ba da kanmu don baiwa masu siyan mu masu daraja ta amfani da mafi kyawun sabis na tunani akan farashin da aka faɗi donGwajin China LhZazzage Siyar da Za a iya zubarwa Lh Ovulation Test Midstream, Muna yin iyakar ƙoƙarinmu don bayar da mafi kyawun sabis ga duk abokan ciniki da 'yan kasuwa.
Za mu ba da kanmu don ba wa masu siyan mu masu daraja ta amfani da mafi yawan hidimomin tunani donGwajin China Lh, Matakan Gwaji, Kamfaninmu zai bi "Quality farko, , kammala har abada, mutane-daidaitacce , fasahar fasaha" falsafar kasuwanci. Yin aiki tuƙuru don ci gaba da samun ci gaba, ƙirƙira a cikin masana'antu, yin kowane ƙoƙari don yin kasuwanci a matakin farko. Muna ƙoƙarin mafi kyawun mu don gina samfurin sarrafa kimiyya, don koyon ilimin ƙwararrun ƙwararrun ƙwararrun ƙwararrun ƙwararrun ƙwararrun ƙwararrun ƙwararrun ƙwararrun masana'antu, haɓaka kayan aikin samarwa da tsarin samarwa, don ƙirƙirar samfuran ƙira na farko da mafita, farashi mai ma'ana, babban ingancin sabis, bayarwa da sauri, don samarwa. ka ƙirƙiri sabon darajar .
Kit ɗin bincike don Alpha-fetoprotein(Fluorescence immunochromatographic assay)
Don bincikar in vitro amfani kawai
Da fatan za a karanta wannan fakitin a hankali kafin amfani kuma a bi umarnin sosai. Ba za a iya tabbatar da amincin sakamakon kima ba idan akwai wasu sabani daga umarnin a cikin wannan fakitin.

AMFANI DA NUFIN

Kit ɗin bincike don Alpha-fetoprotein (ƙaddamar da fluorescence immunochromatographic assay) shine gwajin immunochromatographic mai haske don gano ƙididdigar ƙima na Alpha-fetoprotein (AFP) a cikin ƙwayar ɗan adam ko plasma, wanda galibi ana amfani dashi don ƙarin ganewar asali, tasirin warkewa da tsinkayen cututtukan cututtukan hanta na farko. Duk samfuran tabbatacce dole ne a tabbatar da su ta wasu hanyoyin. Anyi nufin wannan gwajin don amfanin ƙwararrun kiwon lafiya kawai.

TAKAITACCEN

Alpha-fetoprotein (AFP) yana daya daga cikin alamomin ƙari da aka saba amfani da su. Yana da glycoprotein mai nauyin kwayoyin halitta 70,000 da sukari 4%. An fi hada shi da hanta tayi, bi da jakar gwaiduwa. Tayi ya fara hadawa don Makonni 6, kaiwa ga kololuwar makonni 12 zuwa 15, karfin jini na 1 zuwa 3 g/L, da jinin cibiya a lokacin haihuwar 10 zuwa 100 mg/L; 1 zuwa 2 shekaru bayan haihuwa zuwa matakin manya; Ciwon ciki na al'ada zai iya kaiwa. 90 zuwa 500 ng/mL a tsakiya; Abubuwan al'ada na mutum na al'ada na AFP yana tsakanin 2 da 8 ng/mL, amma yawancin cututtuka, musamman ma ciwon hanta, suna shafar darajar AFP.

KA'IDAR HANYA

An lulluɓe jikin na'urar gwajin da antibody na AFP akan yankin gwajin da goat anti-zomo IgG antibody akan yankin sarrafawa. Label pad an lullube shi ta hanyar walƙiya mai lakabin antibody na AFP da zomo IgG a gaba. Lokacin gwada ingantaccen samfurin, antigen na AFP a cikin samfurin yana haɗa tare da mai walƙiya mai lakabin antibody na AFP, kuma ya samar da cakudar rigakafi. A karkashin aikin da immunochromatography, da hadaddun ya kwarara a cikin shugabanci na absorbent takarda, a lokacin da hadaddun wuce gwajin yankin, shi a hade tare da anti AFP shafi antibody, Forms sabon hadaddun.AFP matakin ne gaskiya dangantaka da kyalli siginar, da kuma taro na AFP. a cikin samfurin za a iya gano ta hanyar fluorescence immunoassay assay.

REAgents DA KAYAN DA AKA BAYAR

Abubuwan kunshin 25T:

.Katin gwajin daidaiku da foil ɗin da aka shayar da shi tare da 25T na busa
.Sample diluents 25T
. Kunshin saka 1

KAYAN DA AKE BUKATA AMMA BA'A SAMU BA
Samfurin tarin akwati, mai ƙidayar lokaci
MISALI TATTAUNAWA DA AJIYA
1. Samfuran da aka gwada na iya zama jini, heparin anticoagulant plasma ko EDTA anticoagulant plasma.
2.According ga daidaitattun dabaru tattara samfurin. Za'a iya adana ruwan magani ko samfurin plasma a cikin firiji a 2-8 ℃ na tsawon kwanaki 7 kuma ana kiyaye cryopreservation ƙasa -15 ° C na watanni 6.
3.All samfurin guje wa daskare-narke hawan keke.

HANYAR ASSAY
Da fatan za a karanta jagorar aiki na kayan aiki da saka fakiti kafin gwaji.
1.Lay a gefe duk reagents da samfurori zuwa dakin zafin jiki.
2.Bude Portable Immune Analyzer (WIZ-A101), shigar da kalmar sirri shiga asusu bisa ga tsarin aiki na kayan aiki, da kuma shigar da ganowa dubawa.
3.Scan da lambar haƙori don tabbatar da gwajin abu.
4.Dauki katin gwaji daga jakar foil.
5.Saka katin gwaji a cikin ramin katin, duba lambar QR, kuma ƙayyade abin gwajin.
6.Add 20μL serum ko plasma samfurin zuwa samfurin diluent, da kuma Mix da kyau ..
7.Add 80μL samfurin bayani don samfurin rijiyar katin.
8. Danna maɓallin "gwajin misali", bayan minti 15, kayan aiki za su gano katin gwajin ta atomatik, zai iya karanta sakamakon daga allon nuni na kayan aiki, kuma rikodin / buga sakamakon gwajin.
9. Koma zuwa ga umarnin Portable Immune Analyzer (WIZ-A101).

DABI'UN DA AKE SARANSU

AFP: 10ng/ml
Ana ba da shawarar cewa kowane dakin gwaje-gwaje ya kafa nasa kewayon al'ada wanda ke wakiltar yawan majinyacinsa.

SAKAMAKON JARRABAWA DA FASSARA
Bayanan da ke sama sakamakon gwajin reagent na AFP ne, kuma ana ba da shawarar cewa kowane dakin gwaje-gwaje ya kafa kewayon ƙimar ganowa na AFP wanda ya dace da yawan jama'a a wannan yanki. Sakamakon da ke sama don tunani ne kawai.
.Sakamakon wannan hanyar yana aiki ne kawai ga jeri na tunani da aka kafa a cikin wannan hanyar, kuma babu kwatankwacin kai tsaye da sauran hanyoyin.
.Wasu dalilai kuma na iya haifar da kurakurai a cikin sakamakon ganowa, gami da dalilai na fasaha, kurakuran aiki da sauran abubuwan samfuri.

AJIYA DA KWANTA
1.The kit ne 18 watanni shiryayye-rai daga ranar da aka yi. Ajiye kayan da ba a yi amfani da su ba a 2-30 ° C. KAR KA DANKE. Kar a yi amfani da bayan ranar karewa.
2.Kada ku buɗe jakar da aka rufe har sai kun shirya don yin gwaji, kuma ana ba da shawarar yin amfani da gwajin amfani ɗaya a ƙarƙashin yanayin da ake buƙata (zazzabi 2-35 ℃, zafi 40-90%) a cikin 60 mins da sauri. kamar yadda zai yiwu.
3.Sample diluent ana amfani da shi nan da nan bayan an bude shi.

GARGADI DA TSIRA
.Kit ɗin yakamata a rufe shi kuma a kiyaye shi daga danshi.
.Duk samfurori masu inganci za a inganta su ta wasu hanyoyin.
.Duk samfuran za a kula da su azaman masu gurɓata yanayi.
.KADA KA yi amfani da reagent da ya ƙare.
. BA musanya reagents tsakanin kits tare da daban-daban kuri'a No..
.KADA KA sake amfani da katunan gwaji da duk wani kayan haɗi da za'a iya zubarwa.
.Misoperation, wuce kima ko kadan samfurin iya haifar da sabawa sakamakon.

LIMITATION
Kamar yadda yake tare da kowane gwajin amfani da ƙwayoyin rigakafi na linzamin kwamfuta, akwai yuwuwar kutsawa daga ƙwayoyin rigakafin linzamin kwamfuta na ɗan adam (HAMA) a cikin samfurin. Samfura daga marasa lafiya waɗanda suka karɓi shirye-shiryen rigakafin ƙwayoyin cuta na monoclonal don ganewar asali ko jiyya na iya ƙunsar HAMA. Irin waɗannan samfurori na iya haifar da sakamako mara kyau na ƙarya ko ƙarya.
.Wannan sakamakon gwajin shine kawai don tunani na asibiti, bai kamata ya zama tushen kawai don ganewar asibiti da magani ba, masu kula da marasa lafiya ya kamata a yi la'akari da su sosai tare da alamunta, tarihin likita, sauran gwaje-gwaje na dakin gwaje-gwaje, amsawar magani, cututtukan cututtuka da sauran bayanai. .
.Wannan reagent ana amfani dashi ne kawai don gwajin jini da jini. Maiyuwa baya samun ingantaccen sakamako idan aka yi amfani da shi don wasu samfura kamar yau da fitsari da sauransu.

HALAYEN YI

REFERENCES
1.Hansen JH, et al.HAMA Tsangwama tare da Murine Monoclonal Antibody-Based Immunoassays[J].J na Clin Immunoassay,1993,16:294-299.
2.Levinson SS.Yanayin Heterophilic Antibodies da Matsayin Tsangwama na Immunoassay[J].J na Clin Immunoassay,1992,15:108-114.

Maɓalli ga alamomin da aka yi amfani da su:

	In Vitro Diagnostic Medical Na'urar
	Mai ƙira
	Adana a 2-30 ℃
	Ranar Karewa
	Kada a sake amfani
	HANKALI
	Tuntuɓi Umarnin Don Amfani

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