Plasmodium Falciparum Antigen Detection Kit (Colloidal Gold)

Qualitative detection of Plasmodium falciparum antigens in human peripheral and venous blood. For auxiliary diagnosis of suspected P. falciparum infection and malaria screening.

SKU Code
AENE-OT056
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative detection of Plasmodium falciparum antigens in human peripheral and venous blood. For auxiliary diagnosis of suspected P. falciparum infection and malaria screening.

Product typeAssay / Kit
Technology platformColloidal Gold
Application areaArbovirus

Certificate

CE

Epidemiology

Malaria (Mal) arises from infection with Plasmodium, a unicellular eukaryotic parasite. The causative species include Plasmodium falciparum, P. vivax, P. malariae, and P. ovale. Transmitted by mosquitoes and through blood contact, this parasitic disease poses a severe threat to human health. Among the human malaria parasites, Plasmodium falciparum is the most fatal. The disease is found worldwide, predominantly in tropical and subtropical regions like Africa, Central America, and South America.

Work Flow

1. Sampling

  • Clean the fingertip with an alcohol pad.
  • Squeeze the fingertip end and pierce it using the provided lancet.

2. Add sample and solution

  • Add one drop of sample to the "S" well of the cassette.
  • Hold the buffer bottle vertically and dispense 3 drops (about 100 µL) into the "A" well.

3. Interpret the result (15-20 minutes)

SKU codeAENE-OT056
Target regionPlasmodium falciparum
Storage temperature4-30 ℃ sealed dry storage
Sample typehuman peripheral blood and venous blood
Shelf life24 months
Auxiliary instrumentsNot required
Extra ConsumablesNot required
Detection time15-20 mins
SpecificityThere is no cross-reactivity with influenza A H1N1 virus, H3N2 influenza virus, influenza B virus, dengue fever virus, Japanese encephalitis virus, respiratory syncytial virus, meningococcus, parainfluenza virus, rhinovirus, toxic bacillary dysentery, There was no crossover between Staphylococcus aureus, Escherichia coli, Streptococcus pneumoniae or Klebsiella pneumoniae, Salmonella typhi, and Rickettsia tsutsugamushi.
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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