Kit ɗin bincike don D-Dimer(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 Diagnostic don D-Dimer (ƙaddamarwar fluorescence immunochromatographic assay) shine ƙirar immunochromatographic fluorescence don gano ƙimar D-Dimer (DD) a cikin plasma na ɗan adam, ana amfani dashi don gano cututtukan thrombosis na jijiyoyi, watsa coagulation na intravascular, da saka idanu na thrombolytic. far .Duk samfurin tabbatacce dole ne a tabbatar da shi ta wasu hanyoyin. Anyi nufin wannan gwajin don amfanin ƙwararrun kiwon lafiya kawai.

TAKAITACCEN
DD yana nuna aikin fibrinolytic.Dalili na karuwa na DD: 1. Hyperfibrinolysis na biyu, irin su hypercoagulation, watsawa na intravascular coagulation, cututtuka na koda, watsi da kwayoyin halitta, maganin thrombolytic, da dai sauransu. ; 3.Myocardial infarction, cerebral infarction, huhu embolism, venous thrombosis, tiyata, ƙari, yada intravascular coagulation, kamuwa da cuta da kuma nama necrosis, da dai sauransu

KA'IDAR HANYA
An lulluɓe jikin na'urar gwajin da anti-DD antibody akan yankin gwajin da goat anti-zomo IgG antibody akan yankin sarrafawa. Label pad an lullube shi ta hanyar walƙiya mai lakabin anti DD antibody da zomo IgG a gaba. Lokacin gwada ingantaccen samfuri, DD antigen a cikin samfurin yana haɗuwa tare da mai walƙiya mai lakabin anti DD antibody, kuma ya samar da cakudawar rigakafi. A karkashin aikin immunochromatography, da hadaddun ya kwarara a cikin shugabanci na absorbent takarda, a lokacin da hadaddun wuce gwajin yankin, shi hade da anti DD shafi antibody, Forms sabon hadaddun. Matsayin DD yana da alaƙa da alaƙa da siginar kyalli, kuma ana iya gano yawan DD a cikin samfur ta hanyar gwajin immunoassay fluorescence.

REAgents DA KAYAN DA AKA BAYAR

Abubuwan kunshin 25T:
Katin gwajin ɗai-ɗai wanda aka sanye da jakar 25T
Samfurin diluents 25T
Kunshin saka 1

KAYAN DA AKE BUKATA AMMA BA'A SAMU BA
Samfurin tarin akwati, mai ƙidayar lokaci

MISALI TATTAUNAWA DA AJIYA
.Samfurin da aka gwada na iya zama heparin anticoagulant plasma ko EDTA anticoagulant plasma.
.Bisa ga daidaitattun dabarun 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.
.Duk 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 40μL 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
DD <0.5mg/L
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 DD reagent gwajin ne, kuma ana ba da shawarar cewa kowane dakin gwaje-gwaje ya kafa kewayon ƙimar gano DD 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
1.Kit ɗin ya kamata a rufe shi kuma a kare shi daga danshi.
2.Dukan samfurori masu kyau za a inganta su ta wasu hanyoyin.
3.Duk samfuran za a ɗauke su azaman masu gurɓatacce.
4.KADA kayi amfani da reagent da ya ƙare.
5.KADA KA musanya reagents tsakanin kits tare da kuri'a daban-daban No..
6.KADA KA sake amfani da katunan gwaji da duk wani kayan haɗi da za'a iya zubarwa.
7.Misoperation, wuce kima ko ƙananan samfurin zai 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

Kudin hannun jari Xiamen Wiz Biotech Co.,Ltd
Adireshi: 3-4 Floor, NO.16 Gina, Bio-Likita Bitar, 2030 Wengjiao West Road, Haicang District, 361026, Xiamen, China
Lambar waya: + 86-592-6808278
Fax: + 86-592-6808279