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(COVID-19) Ikhithi yovavanyo lwe-IgM/IgG ye-Antibody Rapid (Latex Chromatography)

Inkcazelo emfutshane:

Umzekelo ISerum/Plasma/Igazi Elipheleleyo Ifomathi Ikhasethi
Trans.& Sto.Temp. 2-30℃ / 36-86℉ Ixesha lovavanyo 15 imiz
Inkcazo Uvavanyo lwe-1 / Kit;Iimvavanyo ezingama-25/Ikhithi

Iinkcukacha zeMveliso

Iithegi zeMveliso

Ukusetyenziswa okucetywayo

Yenzelwe ukufunyaniswa okukhawulezileyo, okusemgangathweni kwe-acute acute breathing syndrome 2 (SARS-CoV-2) IgG/IgM ye-antibody kwigazi lomntu lonke, i-serum okanye isampuli yeplasma.Uvavanyo kufuneka lusetyenziswe njengoncedo ekuxilongeni isifo sosulelo lwe-coronavirus, esibangelwa yi-SARS-CoV-2.Uvavanyo lubonelela ngeziphumo zovavanyo lokuqala.Iziphumo ezibi aziluthinteli usulelo lwe-SARS-CoV-2 kwaye azinakusetyenziswa njengesiseko sonyango okanye esinye isigqibo solawulo.Ukusetyenziswa kwe-in vitro diagnostic kuphela.

Umgaqo-siseko wokufunyanwa kwe-Antibody

Umgaqo woVavanyo

Isekwe kumgaqo wokubamba i-immunoassay yokumisela izilwa-buhlungu ze-COVID-19 ze-IgG/IgM kwigazi lomntu lonke, i-serum kunye neplasma.Xa isampulu yongezwa kwisixhobo sovavanyo, isampulu iya kufunxwa kwisixhobo ngesenzo se-capillary, ixutywa ne-SARS-CoV-2 recombinant antigen-color latex conjugate kwaye iqukuqela kwi-membrane eqatywe ngaphambili.

Imixholo ephambili

Amacandelo anikiweyo adweliswe kwitheyibhile.

 

Icandelo REF REF B001C-01 B001C-25
Ikhasethi yoVavanyo 1 uvavanyo Iimvavanyo ezingama-25
Iyalahlwa Iqhekeza eli-1 25 iipcs
Isampulu yeLysis Solution ityhubhu e-1 25 iityhubhu
Imiyalelo yokusetyenziswa Iqhekeza eli-1 Iqhekeza eli-1
Isatifikethi sokuThobela Iqhekeza eli-1 Iqhekeza eli-1

Operation Flow

Ukuba i-reagent igcinwe efrijini kwi-4-8 ℃, susa ikhadi le-reagent kwaye uilibrate kwiqondo lokushisa elingaphezulu kwemizuzu engama-30.

1. Vula ibhegi yefoyile ye-aluminium yekhadi lokuhlola.Susa ikhadi lovavanyo kwaye ulibeke ngokuthe tye etafileni.

2. Sebenzisa i-pipette kwi-aspirate isampuli (i-serum, i-plasma okanye igazi elipheleleyo) kwaye udibanise i-10μL kumngxuma wesampulu yekhadi lovavanyo, uze udibanise isisombululo se-dilution ye-60μL ngokukhawuleza.Qala ukubala.

3. Imizuzu eyi-15 kamva, funda iziphumo ngokubonakalayo.(Qaphela: SUKUFUNDA iziphumo emva kwemizuzu engama-20!)

Isiphumo sokutolika

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1.Isiphumo esibi

Ukuba kuphela umgca wolawulo lomgangatho C ubonakala kwaye imigca yokubona i-G kunye ne-M ayibonisi, oko kuthetha ukuba akukho noveli ye-antibody ye-coronavirus efunyenweyo kwaye isiphumo sibi.

2. Isiphumo Esilungileyo

2.1 Ukuba zombini umgca wolawulo lomgangatho C kunye nomgca wokubona u-M uyavela, oko kuthetha ukuba kubhaqwe i-antibody ye-IgM ye-novel coronavirus, kwaye isiphumo sibe sithi positive kwi-antibody ye-IgM.

2.2 Ukuba zombini umgca wolawulo lomgangatho C kunye nomgca wokubona u-G uyavela, oko kuthetha ukuba kubhaqwe i-antibody ye-IgG yenoveli kwaye isiphumo sithi si-positive kwi-antibody ye-IgG.

2.3 Ukuba zombini umgca wolawulo lomgangatho C kunye nemigca yokubona i-G kunye ne-M ibonakala, oko kuthetha ukuba i-novel coronavirus IgG kunye ne-IgM antibodies zifunyenwe, kwaye umphumo ulungile kuzo zombini ii-antibodies ze-IgG kunye ne-IgM.

3. Isiphumo esingasebenziyo

Ukuba umgca wokulawula umgangatho we-C awukwazi ukubonwa, iziphumo ziya kuba zingasebenzi kungakhathaliseki ukuba umgca wokuvavanya ubonisa, kwaye uvavanyo kufuneka luphindwe.

Ulwazi lweodolo

Igama lemveliso Ikati.Hayi Ubungakanani Umzekelo Beka ubomi kwishelufa Trans.& Sto.Temp.
(COVID-19) Ikhithi yovavanyo lwe-IgM/IgG ye-Antibody Rapid (Latex Chromatography) B001C-01 Uvavanyo olu-1/ikhithi ISerum/Plasma/Igazi Elipheleleyo Iinyanga ezili-18 2-30℃ / 36-86℉
B001C-01 Iimvavanyo ezingama-25/ikhithi

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