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I-antibody ye-IgM ukuya kwikhithi yovavanyo ye-mycoplasma pneumoniae colloidal gold
Ikhithi yokuxilonga ye-IgM ye-Antibody ukuya kwi-Mycoplasma Pneumoniae luvavanyo lwe-colloidal yegolide ye-immunochromatographic yomiselo lomgangatho we-IgM Antibody ukuya kwi-Mycoplasma Pneumoniae kwigazi elipheleleyo lomntu, i-serum okanye i-plasma, isebenza njengosulelo lwe-Mycoplasma pneumonia encedisayo ekuxilongweni kwe-reagent ekuxilongweni kweklinikhi. Okwangoku yi-reagent yokuhlola.
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cpn igm test kit chlamydia pneumoniae test kit collodial gold
I-Diagnostic Kit (i-Colloidal Gold) ye-antibody ye-IgM ukuya kwi-Chlamydia Pneumoniae luvavanyo lwe-colloidal lwegolide lwe-immunochromatographic lokumiselwa komgangatho we-IgM Antibody ukuya kwi-Chlamydia Pneumoniae (Cpn-IgM) kwigazi elipheleleyo lomntu, i-serum okanye i-plasma ye-pneumonia i-auxilidia yokuxilongwa. i-reagent ekuxilongweni kweklinikhi. Okwangoku yi-reagent yokuhlola. Zonke iisampuli ezilungileyo kufuneka ziqinisekiswe ngezinye iindlela. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.
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Uvavanyo lwe-FOB Ikhithi ye-fecal yovavanyo lwegazi olufihlakeleyo lwe-Rapid Test Strips FOB iphepha elingasikwanga
Le khithi ilungele ukuchongwa ngokomgangatho we-antibody ukuya kwi-anti-gastric Helicobacter pylori (HP) enokubakho kwigazi elipheleleyo lomntu, i-serum okanye iisampulu zeplasma kwi-vitro. Ukuvavanya kumaziko ezonyango kunye nempilo, isetyenziswe njenge-reagent encedisayo yokuxilongwa kwi-gastric helicobacter pylori usulelo kwi-clinical diagnosis.
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colloidal igolide adenovirus inyathelo elinye av test kit AV ngokukhawuleza uvavanyo Kid
I-Diagnostic Kit (i-LATEX) ye-Rotavirus yeQela A kunye ne-adenovirus ifanelekile ukubhaqwa kwekhwalithi ye-Rotavirus yeQela A kunye ne-adenovirus antigen kwiisampuli ze-fecal yabantu. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela. Okwangoku, olu vavanyo lusetyenziselwa ukuxilongwa kweklinikhi yohudo lwabantwana kwizigulane ezine-Rotavirus Group A rotavirus kunye nosulelo lwe-adenovirus.
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Inyathelo elinye ngokukhawuleza kit rotavirus Group kunye Adenovirus latex
I-Diagnostic Kit (i-LATEX) ye-Rotavirus yeQela A kunye ne-adenovirus ifanelekile ukubhaqwa kwekhwalithi ye-Rotavirus yeQela A kunye ne-adenovirus antigen kwiisampuli ze-fecal yabantu. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela. Okwangoku, olu vavanyo lusetyenziselwa ukuxilongwa kweklinikhi yohudo lwabantwana kwizigulane ezine-Rotavirus Group A rotavirus kunye nosulelo lwe-adenovirus.
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Ikhithi yokuxilonga yeCardiac Troponin I (Fluorescence Immuno Assay)
I-Diagnostic Kit for Cardiac Troponin I(fluorescence immunochromatographic assay) luvavanyo lwe-fluorescence immunochromatographic yokufumanisa ubungakanani beCardiac Troponin I (cTnI) kwiserum yomntu okanye kwiplasma, isetyenziselwa ukuxilongwa kwe-AMI (Acute Myocardial Infar).
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I-antibody ye-IgM Enterovirus 71 EV71 ikhithi yovavanyo olukhawulezayo EV 71 antibody
I-Diagnostic Kit (i-Colloidal Gold) ye-IgM Antibody to Human Enterovirus 71 luvavanyo lwe-colloidal yegolide ye-immunochromatographic yokumisela umgangatho we-IgM Antibody to Human Enterovirus 71 (EV71-IgM) kwigazi elipheleleyo lomntu, i-serum okanye iplasma. Olu vavanyo luyi-reagent yokuhlola. Zonke iisampuli ezilungileyo kufuneka ziqinisekiswe ngezinye iindlela. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.
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colloidal gold transferrin tf quick test home use selftest kit POCT reagent
I-Diagnostic Kit (i-Colloidal Gold) ye-Transferrin (Tf) luvavanyo lwegolide lwe-colloidal immunochromatographic yokumisela umgangatho we-Tf ukusuka kwilindle lomntu. Ilungele ukuxilongwa kokuncedisa ukopha kwesisu.I-teti yi-reagent yokuhlola, yonke isampuli efanelekileyo kufuneka iqinisekiswe ngezinye iindlela. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.
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Ikhithi yovavanyo olukhawulezayo lwe-CAL
UKUSETYENZISWA OKUHLOSIWEYO I-Diagnostic Kit ye-Calprotectin(cal) luvavanyo lwe-colloidal yegolide ye-immunochromatographic yomiselo lwe-semiquantitative ye-cal esuka kwilindle lomntu, enexabiso elibalulekileyo lokuxilonga isifo se-inflammation. Olu vavanyo luyi-reagent yokuhlola. Zonke iisampuli ezilungileyo kufuneka ziqinisekiswe ngezinye iindlela. Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela. Okwangoku, olu vavanyo lusetyenziselwa i-IVD, izixhobo ezongezelelweyo azidingeki. -
Ikhithi yokuxilonga (igolide yeColloidal) yeGonadotrophin yeChorionic yoMntu
I-Diagnostic Kit (Colloidal Gold) ye-Human Chorionic Gonadotrophin Ukusetyenziswa kwi-in vitro diagnostic kuphela Nceda ufunde le phakheji yofakelo ngononophelo phambi kokuba uyisebenzise kwaye ulandele ngokungqongqo imiyalelo. Ukuthembeka kweziphumo zovavanyo akunakuqinisekiswa ukuba kukho nakuphi na ukutenxa kwimiyalelo ekweli phakheji. UKUSETYENZISWA OKUJONGISIWEYO IKhiti yokuxilonga (i-Colloidal Gold) yeGonadotrophin yeChorionic yoMntu luvavanyo lwegolide lwe-colloidal lwe-immunochromatographic yokufunyaniswa komgangatho we-chorionic gonani yomntu... -
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Ikhithi yovavanyo olukhawulezayo lwe-Helicobacter antibody
Izigulane ezineempawu kufuneka ziqokelelwe. Iisampulu kufuneka ziqokelelwe kwisikhongozeli esicocekileyo, esomileyo, nesingenamanzi nesingenazo izinto zokucoca kunye nezithinteli. Kwizigulane ezingatyibilikiyo, iisampuli zelindle eziqokelelweyo akufunekanga zibe ngaphantsi kwe-1-2 grams. Kwizigulane ezinorhudo, ukuba ilindle limanzi, nceda uqokelele ubuncinane i-1-2 ml yolwelo lwelindle. Ukuba ilindle linegazi elininzi kunye namafinyila, nceda uqokelele isampuli kwakhona. Kucetyiswa ukuba uvavanye iisampulu kwangoko emva ...