Dengue NS1 Antigen Detection Kit (Colloidal Gold)

Qualitative detection of dengue NS1 antigen in human serum, plasma, peripheral blood, and whole blood using colloidal gold immunochromatography. For auxiliary diagnosis of suspected dengue infection and screening in affected areas.

SKU Code
AENE-FE029
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative detection of dengue NS1 antigen in human serum, plasma, peripheral blood, and whole blood using colloidal gold immunochromatography. For auxiliary diagnosis of suspected dengue infection and screening in affected areas.

Product typeAssay / Kit
Technology platformColloidal Gold
Application areaArbovirus

Certificate

CE

Epidemiology

Dengue fever, an acute infection caused by the dengue virus, is among the most widespread mosquito-borne diseases globally. The virus is classified into four serotypes: DENV-1, DENV-2, DENV-3, and DENV-4[1]. In many regions, these serotypes alternate in prevalence, raising the risk of severe forms like dengue hemorrhagic fever and dengue shock syndrome. Global warming is expanding the geographic range of dengue, leading to higher incidence and greater epidemic severity. Consequently, dengue fever poses a serious worldwide public health challenge.

The Dengue NS1 Antigen Detection Kit (Immunochromatography) provides swift, point-of-care, and precise detection of the Dengue NS1 antigen. Within the first five days of dengue virus infection, the detection rates for nucleic acid and antigen exceed those for antibody detection[2]. Moreover, the antigen can be detected in blood for an extended period.

SKU codeAENE-FE029
Target regionDengue virus NS1
Storage temperature4℃-30℃
Sample typeserum, plasma, peripheral blood and venous whole blood
Shelf life24 months
Auxiliary instrumentsNot required
Extra ConsumablesNot required
Detection time15-20 mins
ApprovalOn request
DocumentsDatasheet, IFU, SDS, COA / conformance, origin, and export documents where available

FAQ

What should be confirmed before quotation?

Sample context, collection method, and extraction workflow should be confirmed before final kit selection.

Which documents can be requested?

Datasheet, IFU, SDS, COA / conformance, origin, insurance, and export documents can be checked where available.

Can the format be adjusted for different workflows?

Liquid or lyophilized format options should be confirmed together with instrument compatibility and shipment requirements.

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