Vumela isivivinyo, i-specimen kanye / noma izilawuli ukufinyelela amazinga okushisa egumbi (15 - 30 ° C) Ukuhlolwa kwePriorto.
1. Letha isikhwama sokushisa segumbi ngaphambi kokukuvula. Susa idivaysi yokuhlola esikhwameni esivalekile bese uyisebenzisa ngokushesha ngangokunokwenzeka.Best imiphumela izotholakala uma ukuhlolwa kwenziwa ngokushesha ngemuva kokuvula isikhwama se-foil.
2. Beka idivaysi yokuhlola endaweni ehlanzekile neleveli.
Okwe-serum noma ama-plasma acembu:Bamba i-dropper mpo futhi udlulise amaconsi ama-2 we-ofserum noma i-plasma (cishe ama-50 ul) ku-specimen kahle (bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
Ukuze uthole ukubonakala okuphelele kwegazi:Bamba i-dropper mpo futhi udlulise amaconsi e-thonipuncture igazi lonke (cishe i-100 ul) ku-specimen kahle (ikhasi) le-specimen 1 yedivayisi yokuhlola, bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
Okwe-Finastick yonke igazi legazi:
Ukuze usebenzise ishubhu le-capillary:Gcwalisa ishubhu le-capillary bese udlulisela cishe i-100 ul of Fingerstick yonke i-Fingerimen Specimen ku-specimen kahle (bese uqala isibali sikhathi.Bona umfanekiso ongezansi.
Ukuze usebenzise amaconsi we-Hanging:Vumela amaconsi ama-4 wokulengiswa we-Fingerstick yonke igazi eliphelele (cishe i-100 ul) ukuwela enkabeni ye-specimen (s) kahle kudivayisi yokuhlola, bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
3. Lindela umugqa onemibala ukuze uvele. Funda imiphumela ngemizuzu eyi-10. Ungahumushi imiphumela ngemuva kwemizuzu engama-20.