H. Pylori Antigen Rapid test kit (Lateral chromatography)

Inkcazelo emfutshane:

Umzekelo	Ilindle	Ifomathi	Ikhasethi
Uvakalelo	98.58%	Ukuchaza ngokuthe ngqo	98.16%
Trans.& Sto.Temp.	2-30℃ / 36-86℉	Ixesha lovavanyo	15 imiz
Inkcazo	Uvavanyo lwe-1 / Kit;Iimvavanyo ezingama-25/Ikhithi

Thumela i-imeyile kuthi

Iinkcukacha zeMveliso

Iithegi zeMveliso

Ukusetyenziswa okucetywayo

H. Pylori Antigen Rapid Test Kit (Lateral chromatography) iza kusetyenziselwa in vitro qualitative diagnostic of helicobacter pylori antigen kwilindle lomntu.Uvavanyo kufuneka lusetyenziswe kuphela ziingcali zonyango.

Umgaqo woVavanyo

Ikhithi i-immunochromatographic kwaye isebenzisa indlela yesandwich ephindwe kabini ye-antibody ukubona i-H. Pylori Antigen.Iqulethe i-Coloured spherical particles ebhalwe H. Pylori monoclonal antibody esongelwe kwi-conjugate pad.Enye i-antibody ye-H. Pylori ye-monoclonal elungiswe kwi-membrane ye-NC.kunye nomgangatho wolawulo lomgca C oqatywe nge-anti-mouse ye-IgG yebhokhwe, yamkele i-antigen-antibody reaction kunye ne-lateral chromatography technology, imisela ngokomgangatho amanqanaba e-H. Pylori Antigen kwilindle lomntu.

Imixholo ephambili

Amacandelo anikiweyo adweliswe kwitheyibhile.

Icandelo/REF	B012C-01	B012C-25
Ikhasethi yoVavanyo	1 uvavanyo	Iimvavanyo ezingama-25
I-Diluent yesampuli	1 ibhotile	Iibhotile ezingama-25
Imiyalelo yokusetyenziswa	Iqhekeza eli-1	iipcs ezi-1
Isiqinisekiso sokuhambelana	Iqhekeza eli-1	Iqhekeza eli-1

Operation Flow

Inyathelo 1: Iisampulu

Qokelela izikhongozeli zefecalspecimensin ezicocekileyo nezingavuziyo.

Inyathelo lesi-2: Uvavanyo

1. Susa ikhasethi yovavanyo kwisingxobo sefoil uze uyibeke kumphezulu osicaba

2. Khipha ibhotile yesampula, sebenzisa intonga ye-applicator encanyathiselwe kwi-cap ukuhambisa iqhekeza elincinci lesampuli ye-stool (3-5 mm ububanzi; malunga ne-30-50 mg) kwibhotile yesampuli equlethe i-specimen buffer yokulungiselela.

3.Buyisela intonga kwibhotile kwaye uqinise ngokukhuselekileyo.Xuba isampuli yesitulo kunye nesithinteli ngokucokisekileyo ngokushukumisa ibhotile amatyeli amaninzi kwaye ushiye ityhubhu yodwa imizuzu emi-2.

4. Khupha isampula yebhotile kwaye ubambe ibhotile kwindawo ethe nkqo phezu kwesampulu kakuhle yeCassette, uhambise i-3 yehla (malunga ne-100 -120μL) yesampuli ye-stool diluted kwisampuli kakuhle.

Inyathelo lesi-3: Ukufunda

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

Isiphumo sokutolika

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.
H. Pylori Antigen Rapid test kit (Lateral chromatography)	B012C-01	Uvavanyo olu-1/ikhithi	Ilindle	Iinyanga ezili-18	2-30℃ / 36-86℉
H. Pylori Antigen Rapid test kit (Lateral chromatography)	B012C-25	Iimvavanyo ezingama-25/ikhithi	Ilindle	Iinyanga ezili-18	2-30℃ / 36-86℉