Monkeypox Virus Antigen Detection Kit (Colloidal Gold)

Intended for the qualitative detection of monkeypox virus antigen in human rash fluid and throat swab specimens.

SKU Code
AENE-OT079
Approval
On request
Product Type
Assay / Kit
Status
Available

Intended for the qualitative detection of monkeypox virus antigen in human rash fluid and throat swab specimens.

Product typeAssay / Kit
Technology platformColloidal Gold
Application areaOthers

Certificate

CE

Epidemiology

Monkeypox (MP) is an acute zoonotic infectious disease caused by the Monkeypox Virus (MPV). The virus is a double-stranded DNA virus, approximately 197Kb in length, with a round-brick or oval shape. Transmission primarily occurs from animals to humans through bites or direct contact with infected animal blood, body fluids, or rash lesions. Human-to-human transmission can occur via respiratory droplets during prolonged face-to-face contact, or by direct contact with a patient's body fluids or contaminated materials. Clinically, human monkeypox resembles smallpox: after an incubation period of about 12 days, symptoms such as fever, headache, muscle and back pain, lymph node enlargement, and fatigue appear. A rash typically develops 1–3 days after the onset of fever, often starting on the face and spreading to other body parts. The illness usually lasts 2–4 weeks, with a case fatality rate ranging from 1% to 10%. Lymphadenopathy is a key distinguishing feature from smallpox.

Work Flow

  • Rash fluid
  • Throat swab
  • Read the results (15-20 minutes)
SKU codeAENE-OT079
Target regionMonkeypox virus
Storage temperature4℃-30℃
Sample typeRash fluid,throat swab
Shelf life24 months
Auxiliary instrumentsNot required
Extra ConsumablesNot required
Detection time15-20 mins
SpecificityUse the kit to test other viruses like smallpox virus (pseudovirus), varicella-zoster virus, rubella virus, herpes simplex virus, and there is no cross-reactivity.
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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