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Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B

Inkcazelo emfutshane:

Inombolo yomzekelo: AMDH46B

Ubunzima: Ubunzima obushiyekileyo: Kg

Ubuncinci boMyinge woMyalelo: ISeti ye-1 iSeti/iSeti

Ukubonelela ngokubonelela: iiSeti ezingama-300 ngonyaka

Imigaqo yeNtlawulo: T/T,L/C,D/A,D/P,Western Union,MoneyGram,PayPal


Iinkcukacha zeMveliso

Iithegi zeMveliso

I-Lateral flow immunochromatographic assay

Inokugcinwa kwiqondo lobushushu begumbi (4-30°C)

Ukusetyenziswa kokuxilongwa kwezilwanyana kwi-in vitro

Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B

UKUSETYENZISWA OKUHLOSIWEYO

I-CPV-CDV-EHR Combo Rapid Test is a lateral flow immunochromatographic assay for the semi-quantitative monitoring of Canine Distemper, Parvo Virus Antigen and Ehrlichia in the dog's specimen.

Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B (1)
Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B (5)
Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B (4)
Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B (2)

Ixesha loVavanyo: 5-10 imizuzu

Umzekelo: CPV Ag--- ilindle okanye umgabho

CDV Ag--- ukukhutshwa kwamehlo enja, imingxuma yeempumlo, kunye nomgudu okanye kwiserum, iplasma.

EHR Ab---Serum, iplasma okanye igazi elipheleleyo

UMGAQO

I-CPV-CDV-EHR Combo Rapid Test isekelwe kwisandwich lateral flow immunochromatographic assay.

I-REAGENTS kunye nezixhobo

-Izixhobo zovavanyo, nganye inekhasethi enye, enye i-40μL eyehlayo kunye ne-desiccant (X10)

- 40μL idropha elahlayo(X10)

- 10μL i-capillary dropper(X10)

-CDV Ag Assay buffer (X10)

-I-CPV Ag Assay buffer (X10)

- EHR Ab Assay Buffer(X10)

- Umqhaphu Swab(X10)

- IiMveliso Manual(X1)

Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B (3)

Ukuchaneka okuphezulu kwe-antigen combo uvavanyo olukhawulezayo lwe-AMDH46B

ALMACENAMIENTO

Ikiti ingagcinwa kwindawo yokushisa (4-30 ° C).Ikhithi yovavanyo izinzile ngomhla wokuphelelwa kwexesha ophawulwe kwileyibhile yephakheji.MUSA UKUMKHENZA.Musa ukugcina ikiti yovavanyo kwilanga elithe ngqo.

IITOLIKO DE OF RESULTADOS

- Okuhle (+): Ubukho bazo zombini umgca "C" kunye nomgca wezowuni "T", nokuba umgca we-T ucacile okanye awucacanga.

- Engalunganga (-): Kuvela umgca C ocacileyo kuphela.Akukho mgca T.

-Ayisebenzi: Akukho mgca mbala uvelayo kwindawo C.Kungakhathaliseki ukuba umgca we-T uyavela.

IMIQATHANGO

- Zonke ii-reagents kufuneka zibe kwiqondo lobushushu legumbi ngaphambi kokuqhuba uvavanyo.

- Musa ukususa ikhasethi yovavanyo kwisingxobo sayo de kube kanye phambi kokusetyenziswa.

- Musa ukusebenzisa uvavanyo ngaphaya komhla wokuphelelwa kwayo.

- Amacandelo kule khithi avavanywe ulawulo lomgangatho njengeyunithi yebhetshi eqhelekileyo.Musa ukuxuba amacandelo ukusuka kumanani eqashiso ahlukeneyo.

- Yonke imizekelo yolosulelo olunokwenzeka.Kufuneka iphathwe ngokungqongqo ngokwemigaqo kunye nemimiselo ngamazwe asekuhlaleni.

I-LIMITACIONES

UVavanyo oluKhawulezayo lwe-CPV-CDV-EHR lolwe-in vitro lokuxilongwa kwezilwanyana kuphela.Zonke iziphumo kufuneka ziqwalaselwe kunye nolunye ulwazi lwekliniki olukhoyo kunye nogqirha wezilwanyana.Kucetyiswa ukuba kusetyenziswe enye indlela yokuqinisekisa xa kubonwa isiphumo esihle.


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    Bhala umyalezo wakho apha kwaye uwuthumele kuthi.

    Shiya uMyalezo Wakho:

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