Plasmodium falciparum/Plasmodium vivax Antigen Detection Kit (Colloidal Gold)

Qualitative in-vitro detection of Plasmodium falciparum and Plasmodium vivax antigens in human peripheral or venous blood. Intended for auxiliary diagnosis of suspected P. falciparum infection and malaria case screening.

SKU Code
AENE-OT055
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative in-vitro detection of Plasmodium falciparum and Plasmodium vivax antigens in human peripheral or venous blood. Intended for auxiliary diagnosis of suspected P. falciparum infection and malaria case screening.

Product typeAssay / Kit
Technology platformColloidal Gold
Application areaArbovirus

Certificate

CE

Epidemiology

Malaria (often shortened to Mal) is a parasitic disease caused by Plasmodium, a group of single-celled eukaryotic organisms. The main species infecting humans include Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae Laveran, and Plasmodium ovale Stephens. This mosquito- and blood-borne illness poses a serious risk to human health. Among these parasites, Plasmodium falciparum is the most deadly and is primarily found in sub-Saharan Africa, where it causes the majority of malaria deaths worldwide. Plasmodium vivax, on the other hand, is the most common malaria parasite in most countries outside sub-Saharan Africa.

Work Flow

1. Sampling

  • Disinfect the fingertip with an alcohol pad.
  • Gently squeeze the fingertip end and prick it with the supplied lancet.

2. Add the sample and solution

  • Dispense one drop of the sample into the "S" well of the test cassette.
  • Holding the buffer bottle upright, add 3 drops (approximately 100 μL) to the "A" well.

3. Read the result (15–20 minutes)

*Pf: Plasmodium falciparum Pv: Plasmodium vivax

SKU codeAENE-OT055
Target regionPlasmodium falciparum and Plasmodium vivax
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, encephalitis B virus, respiratory syncytial virus, meningococcus, parainfluenza virus, rhinovirus, toxic bacillary dysentery, staphylococcus aureus, escherichia coli, streptococcus pneumoniae or klebsiella pneumoniae, salmonella typhi, and rickettsia tsutsugamushi, and the test results are all negative.
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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