Colloidal Gold · Arbovirus
Dengue Virus IgM/IgG Antibody Detection Kit (Colloidal Gold)
Qualitative detection of dengue virus IgM and IgG antibodies in human serum, plasma, and whole blood samples.
- SKU Code
AENE-FE030- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of dengue virus IgM and IgG antibodies in human serum, plasma, and whole blood samples.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Arbovirus |
Certificate
CE
Epidemiology
This kit is designed for the qualitative detection of dengue virus IgM and IgG antibodies in human serum, plasma, or whole blood specimens.
Dengue is an acute mosquito-borne infectious disease caused by dengue virus, among the most widespread globally. It comprises four serotypes: DENV-1, DENV-2, DENV-3, and DENV-4[1]. Clinical manifestations include sudden high fever, severe muscle and joint pain, profound fatigue, widespread bleeding, and often rash, lymph node enlargement, and leukopenia[2]. Due to global warming, the geographic range of dengue is expanding, with rising incidence and severity, making it a major global public health threat.
This kit provides rapid, on-site, and accurate detection of dengue IgM and IgG antibodies. A positive IgM result suggests a recent infection, while a positive IgG result indicates a longer-standing or past infection. In primary dengue, IgM antibodies appear 3–5 days after symptom onset, peak around 2 weeks, and persist for 2–3 months; IgG antibodies are detectable about 1 week after onset and remain for years or a lifetime. Detection of high IgG levels within the first week of illness points to a secondary infection, and the IgM/IgG ratio from capture methods can aid interpretation. This test serves as a supplement to viral nucleic acid detection.
| SKU code | AENE-FE030 |
|---|---|
| Target region | Dengue IgM and IgG |
| Storage temperature | 4℃-30℃ |
| Sample type | human serum, plasma, venous blood and peripheral blood, including blood samples containing clinical anticoagulants (EDTA, heparin, citrate). |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 15-20 mins |
| Approval | On request |
|---|---|
| Documents | Datasheet, 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.
Inquiry
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