Kit ɗin bincike don Procalcitonin
Na'urar ganowa don ƙwayar zuciya Troponin I ∕Isoenzyme MB na Creatine Kinase ∕Myoglobin
Hanyar: Fluorescence Immunochromatographic Assay
Bayanan samarwa
| Lambar Samfura | cTnI/CK-MB/MYO | Shiryawa | 25 Gwaje-gwaje/kit, 30kits/CTN |
| Suna | Na'urar ganowa don ƙwayar zuciya Troponin I ∕Isoenzyme MB na Creatine Kinase ∕Myoglobin | Rarraba kayan aiki | Darasi na II |
| Siffofin | Babban hankali, Mai sauƙin aiki | Takaddun shaida | CE/ISO13485 |
| Daidaito | > 99% | Rayuwar rayuwa | Shekaru Biyu |
| Hanya | Fluorescence Immunochromatographic Assay | OEM/ODM sabis | Akwai |
AMFANI DA NUFIN
Wannan kit ɗin yana aiki ne don gano ƙididdige ƙididdige in vitro na yawan adadin alamun raunin zuciya na zuciya.
troponin I, isoenzyme MB na creatine kinasein da myoglobin a cikin jinin mutum/plasma/dukan samfurin jini, da
ya dace da karin bincike na ciwon zuciya.Wannan kit ɗin yana ba da sakamakon gwajin cardiac troponin I kawai,
isoenzyme MB na creatine kinasein da myoglobin, kuma sakamakon da aka samu za a yi amfani da shi tare da wasu.
bayanan asibiti don bincike.Dole ne kawai kwararrun kiwon lafiya su yi amfani da shi.
Hanyar gwaji
| 1 | Kafin amfani da reagents, karanta abin da aka saka a hankali kuma ka saba da hanyoyin aiki. |
| 2 | Zaɓi daidaitaccen yanayin gwaji na WIZ-A101 mai nazarin rigakafi mai ɗaukar nauyi |
| 3 | Bude fakitin jakar foil na aluminium na reagent kuma fitar da na'urar gwaji. |
| 4 | Saka na'urar gwaji a tsaye a cikin ramin mai nazarin rigakafi. |
| 5 | A shafi na gida na aikin dubawar rigakafi, danna "Standard" don shigar da dubawar gwaji. |
| 6 | Danna "QC Scan" don duba lambar QR a gefen ciki na kit;shigar da kit masu alaƙa da sigogi cikin kayan aiki kuma zaɓi nau'in samfurin. Lura: Kowace adadin adadin kayan aikin za a duba shi na lokaci ɗaya.Idan an duba lambar batch, to ku tsallake wannan matakin. |
| 7 | Bincika daidaiton "Sunan samfur", "Lambar Batch" da dai sauransu akan gwajin gwaji tare da bayani akan alamar kit. |
| 8 | Ɗauki samfurin diluent akan daidaitattun bayanai, ƙara 80μL serum/plasma/dukan samfurin jini, sannan a haɗa su sosai; |
| 9 | Ƙara 80µL da aka ambata sosai gauraye bayani a cikin rijiyar na'urar gwaji; |
| 10 | Bayan cikakken samfurin ƙari, danna "Lokaci" kuma sauran lokacin gwajin za a nuna ta atomatik akan ƙirar. |
| 11 | Mai nazarin rigakafi zai kammala gwaji ta atomatik da bincike lokacin da lokacin gwaji ya kai. |
| 12 | Bayan an gama gwajin rigakafin rigakafi, za a nuna sakamakon gwajin akan gwajin gwaji ko kuma ana iya duba shi ta hanyar “Tarihi” a shafin gida na mu’amala. |
Lura: kowane samfurin za a yi bututu ta hanyar pipette mai tsaftataccen zubarwa don guje wa gurɓacewar giciye.
fifiko
Lokacin gwaji:10-15mins
Adana:2-30℃/36-86℉
Hanyar: Fluorescence Immunochromatographic Assay
Siffa:
• Babban m
• karatun sakamako a cikin mintuna 15
• Sauƙi aiki
Gwaje-gwaje 3 a cikin lokaci ɗaya, lokutan adanawa.
• Babban Daidaito
Ayyukan Clinical
An tantance aikin asibiti na wannan samfurin ta hanyar tarin lokuta 150 na samfuran asibiti.
a) Idan akwai wani abu na cTnI, kayan aikin siyar da aka yi daidai da kit ɗin chemiluminescence assay da aka yi amfani da shi azaman reagent,
An kwatanta sakamakon ganowa kuma an yi nazarin kwatankwacinsu ta hanyar koma baya na layi, da
Ƙididdigar daidaituwa na ƙididdiga biyu sune Y=0.975X+0.074 da R=0.9854 bi da bi;
b) Idan akwai abu na CK-MB, kit ɗin da aka yi daidai da siyar da kit ɗin gwaje-gwajen electrochemiluminescence da aka yi amfani da shi azaman tunani.
reagent, an kwatanta sakamakon ganowa kuma an yi nazarin kwatancensu ta hanyar layi
regression, da haɗin kai na ƙididdiga biyu sune Y=0.915X+0.242 da R=0.9885 bi da bi.
c) Game da abu na MYO, kit ɗin tallan da ya dace na gwajin immunoassays na lokaci-lokaci wanda aka yi amfani da shi azaman tunani.
reagent, an kwatanta sakamakon ganowa kuma an yi nazarin kwatancensu ta hanyar layi
regression, da haɗin kai na ƙididdiga guda biyu sune y=0.989x+2.759 da R=0.9897 bi da bi.
Kuna iya kuma son:
