Ikhithi yokuxilonga ye-C-reactive protein/serum amyloid Umzi-mveliso weprotheyini kunye nabavelisi

I-Diagnostic Kit ye-C-reactive protein/serum amyloid A protein

inkcazelo emfutshane:

I-Diagnostic Kit ye-C-reactive protein/serum amyloid A protein

Ixesha lovavanyo:Imizuzu eyi-10-15

Ixesha elisebenzayo:Iinyanga ezingama-24

Ukuchaneka:Ngaphezulu kwe-99%

Inkcazo:1/25 uvavanyo / ibhokisi

Ubushushu bokugcina :2℃-30℃

Indlela yokusebenza:Fluorescence Immunochromatographic assay

Thumela i-imeyile kuthi Khuphela njengePDF

Iinkcukacha zeMveliso

Iithegi zeMveliso

https://www.baysenrapidtest.com/contact-us/

INGCACISO YEMVELISO

Inombolo yoMfanekiso	CRP/SAA	Ukupakisha	Iimvavanyo ezingama-25/ ikhithi, 30kits/CTN
Igama	I-Diagnostic Kit ye-C-reactive protein/serum amyloid A protein	Ukuhlelwa kwesixhobo	Iklasi I
Iimbonakalo	Uvakalelo oluphezulu, ukusebenza ngokulula	Isatifikethi	CE/ ISO13485
Ukuchaneka	> 99%	Beka ubomi kwishelufa	Iminyaka emibini
Indlela yokusebenza	(Fluorescence Uvavanyo lwe-Immunochromatographic	Inkonzo ye-OEM/ODM	Iyafumaneka

Ukongama

Ikhithi ichanekile kakhulu, iyakhawuleza kwaye inokuhanjiswa kwiqondo lobushushu begumbi.Kulula ukuyisebenzisa.

Uhlobo lomzekelo :i-serum/plasma/igazi elipheleleyo

Ixesha lokuvavanya: imizuzu eyi-15

Ugcino:2-30℃/36-86℉

Indlela yokusebenza:I-Fluorescence Immunochroma

-Uvavanyo lwetographic

Uphawu:

• Uvakalelo oluphezulu

• iziphumo zokufunda kwimizuzu eli-15

• Ukusebenza ngokulula

• Ukuchaneka okuphezulu

UKUSETYENZISWA OKUHLOSIWEYO

Ikiti iyasebenza kwi-in vitro quantitative ubhaqa wokugxilwa kweprotheyini ye-C-reactive (CRP) kunye ne-Serum Amyloid A (SAA) kwi-serum yabantu / i-plasma / iisampulu zegazi elipheleleyo, ukuxilongwa kwe-acute and chronic inflammation okanye usulelo. Ikiti inikezela kuphela isiphumo sovavanyo lweprotheyini ye-C-reactive kunye ne-serum amyloid A. Isiphumo esifunyenweyo siya kuhlalutywa kunye nolunye ulwazi lwekliniki.