Na'urar ganowa don Subtype Antibody zuwa Helicobacter Pylori
Bayanan samarwa
| Lambar Samfura | HP-ab-s | Shiryawa | 25 Gwaje-gwaje/kit, 30kits/CTN |
| Suna | Subtype Antibody zuwa Helicobacter Pylori | Rarraba kayan aiki | Darasi na I |
| Siffofin | Babban hankali, Mai sauƙin aiki | Takaddun shaida | CE/ISO13485 |
| Daidaito | > 99% | Rayuwar rayuwa | Shekaru Biyu |
| Hanya | Fluorescence Immunochromatographic Assay | OEM/ODM sabis | Akwai |
Takaitawa
Helicobacter pylori kwayoyin cuta ne na gram-negative, kuma siffar karkace ta lankwasa tana ba ta sunan helicobacterpylori. Helicobacter pylori yana rayuwa ne a wurare daban-daban na ciki da kuma duodenum, wanda zai haifar da ƙananan kumburi na mucosa na ciki, ciwon ciki da duodenal ulcers, da ciwon daji na ciki. Hukumar Bincike Kan Kansa ta Duniya ta gano kamuwa da cutar HP a matsayin nau'in carcinogen Class I a cikin 1994, kuma cutar kansar HP galibi tana ƙunshe da cytotoxins guda biyu: ɗayan furotin na CagA mai alaƙa da cytotoxin, ɗayan kuma shine vacuolating cytotoxin (VacA). Ana iya raba HP zuwa nau'i biyu bisa la'akari da CagA da VacA: nau'in I shine nau'i mai guba (tare da bayyanar CagA da VacA ko kowane ɗayansu), wanda ke da matukar damuwa da sauƙi don haifar da cututtuka na ciki; nau'in II shine atoxigenic HP (ba tare da bayyanar CagA da VacA ba), wanda ba shi da guba kuma yawanci ba shi da alamar asibiti akan kamuwa da cuta.
Siffa:
• Babban m
• karatun sakamako a cikin mintuna 15
• Sauƙi aiki
• Farashin kai tsaye na masana'anta
• buƙatar inji don karatun sakamako
Nufin Amfani
Wannan kit ɗin yana aiki ne don gano in vitro qualitative detection na Urease antibody, CagA antibody da VacA antibody zuwa helicobacter pylori a cikin jini na ɗan adam, ruwan magani ko samfurin plasma, kuma ya dace da ƙarin bincike na kamuwa da cuta na HP da kuma gano nau'in mara lafiyar helicobacter pylori. kamuwa da. Wannan kit ɗin yana ba da sakamakon gwaji ne kawai na Urease antibody, CagA antibody da VacA antibody zuwa helicobacter pylori, kuma sakamakon da aka samu za a yi amfani da shi tare da sauran bayanan asibiti don bincike. Dole ne kawai kwararrun kiwon lafiya su yi amfani da shi.
Hanyar gwaji
| 1 | I-1: Amfani da šaukuwa na rigakafi analyzer |
| 2 | Bude fakitin jakar foil na aluminium na reagent kuma fitar da na'urar gwaji. |
| 3 | Saka na'urar gwaji a tsaye a cikin ramin mai nazarin rigakafi. |
| 4 | A shafi na gida na aikin dubawar rigakafi, danna "Standard" don shigar da dubawar gwaji. |
| 5 | Danna "QC Scan" don duba lambar QR a gefen ciki na kit; Abubuwan shigar da abubuwan da ke da alaƙa cikin kayan aiki kuma zaɓi nau'in samfuri. Lura: Kowane adadin adadin kayan aikin za a duba shi na lokaci ɗaya. Idan an duba lambar batch, to tsallake wannan matakin. |
| 6 | Bincika daidaiton "Sunan samfur", "Lambar Batch" da dai sauransu akan gwajin gwaji tare da bayani akan alamar kit. |
| 7 | Fara ƙara samfurin idan akwai tabbataccen bayani:Mataki na 1: sannu a hankali pipette 80μL serum / plasma / dukan samfurin jini a lokaci daya, kuma kula kada ku kumfa pipette; Mataki na 2: samfurin pipette zuwa samfurin diluent, da kuma haɗuwa sosai tare da samfurin diluent; Mataki na 3: pipette 80µL sosai gauraye bayani a cikin rijiyar na'urar gwaji, kuma kula da kumfa pipette. a lokacin samfur |
| 8 | Bayan cikakken ƙarin samfurin, danna "Lokaci" kuma sauran lokacin gwajin za a nuna ta atomatik akan mu'amala. |
| 9 | Mai nazarin rigakafi zai kammala gwaji ta atomatik da bincike lokacin da lokacin gwaji ya kai. |
| 10 | Bayan an gama gwajin rigakafin rigakafi, za a nuna sakamakon gwajin akan gwajin gwaji ko kuma ana iya duba shi ta hanyar “Tarihi” akan shafin gida na mu’amala. |
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