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Kit ɗin Bincike don Alpha-fetoprotein(gwajin immunochromatographic na fluorescence)
Don amfani da ganewar asali kawai a cikin vitro
Da fatan za a karanta wannan fakitin da aka saka a hankali kafin amfani kuma a bi umarnin sosai. Ba za a iya tabbatar da ingancin sakamakon gwaji ba idan akwai wata matsala daga umarnin da ke cikin wannan fakitin.
AN YI NIYYA DA AMFANI
Kayan Bincike na Alpha-fetoprotein (gwajin fluorescence immunochromatographic) gwajin fluorescence immunochromatographic ne don gano adadi na Alpha-fetoprotein (AFP) a cikin jini ko plasma na ɗan adam, wanda galibi ana amfani da shi don gano cutar kansa ta hanta, tasirin warkarwa da kuma hasashen cutar kansa ta hepatocellular. Dole ne a tabbatar da duk wani samfurin da ya nuna yana da inganci ta wasu hanyoyin. Wannan gwajin an yi shi ne don amfanin ƙwararru a fannin kiwon lafiya kawai.
TAƘAITACCE
Alpha-fetoprotein (AFP) yana ɗaya daga cikin alamomin ciwon daji da ake amfani da su. Yana da sinadarin glycoprotein mai nauyin kwayoyin halitta 70,000 kuma sukari 4%. Hanta ce ke haɗa shi, sannan sai jakar yolk ta biyo baya. Tayin ya fara yin hadawa na tsawon makonni 6, inda ya kai kololuwar makonni 12 zuwa 15, yawan sinadarin a cikin jini 1 zuwa 3 g/L, da kuma jinin igiyar mahaifa a lokacin haihuwa 10 zuwa 100 mg/L; shekaru 1 zuwa 2 bayan haihuwa zuwa matakin babba; Ciki na yau da kullun na iya kaiwa 90 zuwa 500 ng/mL a tsakiya; Yawan sinadarin AFP na jini na ɗan adam yana tsakanin 2 zuwa 8 ng/mL, amma cututtuka da yawa, musamman cutar hepatitis, suna shafar ƙimar AFP.
KA'IDUN TSARIN
An shafa membrane na na'urar gwajin da maganin rigakafi na AFP a yankin gwaji da kuma maganin rigakafi na IgG na akuya a yankin sarrafawa. Ana shafa murfin label da aka yiwa lakabi da maganin rigakafi na AFP da kuma maganin rigakafi na zomo IgG a gaba. Lokacin gwada samfurin da ya dace, maganin rigakafi na AFP a cikin samfurin yana haɗuwa da maganin rigakafi na AFP mai suna fluorescence, kuma yana samar da cakuda garkuwar jiki. A ƙarƙashin aikin immunochromatography, kwararar hadaddun a cikin jagorancin takardar sha, lokacin da hadaddun ya wuce yankin gwaji, tare da maganin rigakafi na anti AFP, yana samar da sabon hadaddun. Matakin AFP yana da alaƙa mai kyau da siginar haske, kuma ana iya gano yawan AFP a cikin samfurin ta hanyar gwajin immunoassay na fluorescence.
MASU YIN REAGENTS DA KAYAN DA AKA KAWO
Kayan aikin fakitin 25T:
.Katin gwaji daban-daban an saka shi a cikin jaka mai ɗauke da ruwan zafi 25T
.Samfurin mai narkewa 25T
.Saka fakiti 1
ANA BUKATAR KAYAN AIKI AMMA BA A BA DA SU BA
Samfurin tarin akwati, mai ƙidayar lokaci
TARIN SAMFURI DA AJIYEWA
1. Samfuran da aka gwada na iya zama na jini, heparin anticoagulant plasma ko EDTA anticoagulant plasma.
2. Dangane da dabarun da aka saba amfani da su, ana iya ajiye samfurin jini ko na plasma a cikin firiji a zafin 2-8℃ na tsawon kwanaki 7, kuma ana iya ajiye shi a wuri mai sanyi a ƙasa da -15°C na tsawon watanni 6.
3. Duk samfurin da aka yi amfani da shi don guje wa daskarewa da narkewar zagayowar.
Tsarin Gwaji
Da fatan za a karanta littafin aikin kayan aiki da kuma abin da aka saka a cikin fakitin kafin a gwada.
1. A ajiye dukkan sinadaran da aka yi amfani da su da kuma samfuran da aka yi amfani da su a zafin ɗaki.
2. Buɗe Mai Nazarin Jiki Mai Ɗaukewa (WIZ-A101), shigar da kalmar sirri ta asusun bisa ga hanyar aiki ta kayan aikin, sannan ka shigar da hanyar ganowa.
3. Duba lambar haƙoran don tabbatar da abin gwajin.
4. Cire katin gwaji daga jakar foil.
5. Saka katin gwaji a cikin ramin katin, duba lambar QR, sannan ka tantance abin gwajin.
6. Ƙara samfurin serum ko plasma 20μL a cikin samfurin mai narkewa, sannan a gauraya sosai.
7. Ƙara maganin samfurin 80μL don yin samfurin rijiyar katin.
8. Danna maɓallin "gwaji na yau da kullun", bayan mintuna 15, kayan aikin zai gano katin gwaji ta atomatik, zai iya karanta sakamakon daga allon nuni na kayan aikin, kuma ya yi rikodin/buga sakamakon gwajin.
9. Duba umarnin Portable Immune Analyzer (WIZ-A101).
DARAJOJI DA AKA YI TSAMMANI
AFP<<10ng/mL
Ana ba da shawarar kowane dakin gwaje-gwaje ya kafa nasa kewayon da ya dace wanda ke wakiltar yawan marasa lafiya.
SAKAMAKON GWAJI DA FASSARAR
. Bayanan da ke sama sakamakon gwajin AFP reagent ne, kuma ana ba da shawarar cewa kowane dakin gwaje-gwaje ya kamata ya kafa kewayon ƙimar gano AFP da ta dace da yawan jama'a a wannan yanki. Sakamakon da ke sama don tunani ne kawai.
Sakamakon wannan hanyar ya shafi jeri na tunani da aka kafa a cikin wannan hanyar, kuma babu wani kwatancen kai tsaye da wasu hanyoyi.
.Wasu dalilai kuma na iya haifar da kurakurai a sakamakon ganowa, gami da dalilan fasaha, kurakuran aiki da sauran abubuwan samfurin.
Ajiya da kwanciyar hankali
1. Kayan aikin yana da tsawon watanni 18 daga ranar da aka ƙera shi. Ajiye kayan da ba a yi amfani da su ba a zafin 2-30°C. KAR A DASKARE. Kada a yi amfani da su fiye da ranar karewa.
2. Kar a buɗe jakar da aka rufe har sai kun shirya yin gwaji, kuma ana ba da shawarar a yi amfani da gwajin amfani da shi sau ɗaya a ƙarƙashin yanayin da ake buƙata (zafin jiki 2-35℃, danshi 40-90%) cikin mintuna 60 da sauri.
3. Ana amfani da samfurin maganin shafawa nan da nan bayan an buɗe shi.
GARGAƊI DA HANKALI
.Ya kamata a rufe kayan aikin kuma a kare shi daga danshi.
Duk samfuran da aka tabbatar za a tabbatar da su ta wasu hanyoyi.
.Duk samfuran za a yi musu la'akari da su a matsayin masu iya gurɓata muhalli.
.KADA a yi amfani da maganin da ya ƙare.
. BA a musanya sinadaran da ke cikin kayan aiki da sauran kayan aiki ba.
.KADA a sake amfani da katunan gwaji da duk wani kayan haɗi da za a iya yarwa.
.Rashin aiki daidai, ko wuce gona da iri ko ƙarancin samfur na iya haifar da karkacewar sakamako.
LKWAIKWAYO
Kamar yadda yake da kowace gwaji da ake amfani da maganin rigakafi na linzamin kwamfuta, akwai yiwuwar tsangwama daga ƙwayoyin rigakafi na ɗan adam (HAMA) a cikin samfurin. Samfuran marasa lafiya waɗanda aka yi musu shirye-shiryen ƙwayoyin rigakafi na monoclonal don ganewar asali ko magani na iya ƙunsar HAMA. Irin waɗannan samfuran na iya haifar da sakamako mara kyau ko mara kyau na ƙarya.
.Wannan sakamakon gwajin an yi shi ne kawai don bayanin asibiti, bai kamata ya zama tushen ganewar asali da magani na asibiti ba, ya kamata a yi la'akari da kulawar marasa lafiya sosai tare da alamominsa, tarihin likita, sauran gwajin dakin gwaje-gwaje, amsawar magani, ilimin cututtuka da sauran bayanai.
.Wannan sinadarin ana amfani da shi ne kawai don gwaje-gwajen jini da na jini. Yana iya ba zai sami sakamako mai kyau ba idan aka yi amfani da shi ga wasu samfura kamar su yau da fitsari da sauransu.
HALAYEN AYYUKA
| Layi | 1ng/mL zuwa 1000ng/mL | karkacewar dangantaka: -15% zuwa +15%. |
| Ma'aunin haɗin kai na layi:(r)≥0.9900 | ||
| Daidaito | Adadin murmurewa zai kasance tsakanin kashi 85% - 115%. | |
| Maimaitawa | CV≤15% | |
| Takamaiman Bayani (Babu wani abu da aka gwada a wurin da aka yi wa maganin da ya yi katsalandan a cikin gwajin) | Mai shiga tsakani | Yawan tsangwama |
| Acetaminophen | 1500μg/mL | |
| Acetylsalicylic acid | 10mg/mL | |
| CEA | 500μg/mL | |
| Haemoglobin | 200μg/mL | |
| transferrin | 100μg/mL | |
| Radish peroxidase | 2000μg/mL | |
| LH | 200mIU/mL | |
| FSH | 200mIU/mL | |
| HCG | 20000mIU/mL | |
| Tsarin TSH | 200μIU/mL | |
| BSA | 5mg/mL | |
| Vinblastine | 500μg/mL | |
| Cisplatin | 1000μg/mL | |
| Azathioprine | 30mg/L | |
| Bleomycin | 100μU/mL | |
RNAZARI
1. Hansen JH, da sauransu. Tsoma bakin HAMA ga gwajin rigakafi na Murine Monoclonal Antibody-based [J].J na Clin Immunoassay, 1993,16:294-299.
2. Levinson SS. Yanayin Kwayoyin Haɗaka Masu Yawa da Matsayinsu a Cikin Tsangwama Kan Tsarin Immunoassay[J].J na Clin Immunoassay, 1992,15:108-114.
Maɓallin alamomin da aka yi amfani da su:
![]() | Na'urar Lafiya ta In Vitro Diagnostic |
![]() | Mai ƙera |
![]() | Ajiye a 2-30℃ |
![]() | Ranar Karewa |
![]() | Kada a sake amfani da shi |
![]() | HANKALI |
![]() | Duba Umarnin Amfani |
Kamfanin Xiamen Wiz Biotech CO.,LTD
Adireshi: Bene na 3-4, Ginin No.16, Bita na Bio-likita, 2030 Titin West Wengjiao, Gundumar Haicang, 361026, Xiamen, China
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