

Fluorescence PCR · Respiratory Infections
Human Cytomegalovirus (HCMV) Detection Kit (Fluorescence PCR)
Qualitative determination of human cytomegalovirus (HCMV) nucleic acids in serum or plasma samples from patients with suspected HCMV infection, aiding in the diagnosis of HCMV infection.
- SKU Code
AENE-UR008A- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative determination of human cytomegalovirus (HCMV) nucleic acids in serum or plasma samples from patients with suspected HCMV infection, aiding in the diagnosis of HCMV infection.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Respiratory Infections |
Epidemiology
Human cytomegalovirus (HCMV) possesses the largest genome among herpesviruses, encoding over 200 proteins. Its host range is strictly limited to humans, and no animal model for infection currently exists. The virus replicates slowly over an extended cycle, forming intranuclear inclusion bodies and inducing perinuclear and cytoplasmic inclusions accompanied by cellular swelling (cytomegaly), which gives the virus its name. Genomic and phenotypic diversity allows classification into multiple strains, but antigenic differences between them lack clinical significance.
HCMV causes systemic infections that can involve many organs. Clinical manifestations are often silent yet diverse and complex; in some individuals, infection leads to conditions such as retinitis, hepatitis, pneumonitis, encephalitis, colitis, monocytosis, and thrombocytopenic purpura. The virus is distributed globally, with seroprevalence rates of 45–50% in industrialized nations and over 90% in developing regions. HCMV can persist in a latent state and reactivate during immunosuppression, particularly in leukemia and transplant recipients, potentially resulting in graft necrosis and life-threatening disease. Congenital infection, transmitted in utero, may cause stillbirth, miscarriage, preterm delivery, and developmental anomalies, thereby impacting perinatal health and population quality.
Work Flow
For sample preparation, nucleic acid extraction can be carried out with an automatic extractor or by hand. The procedure should be performed according to the selected extraction kit’s instructions. Using 200 µL of patient material, the recommended elution volume is 80 µL for certain protocols.
An appropriate commercial extraction kit, such as a silica spin-column or magnetic bead-based system, may be employed. With these reagents, a sample input of 200 µL and an elution volume of 100 µL is generally advised. Always consult the manufacturer’s protocol for exact details.
| SKU code | AENE-UR008A |
|---|---|
| Storage | Liquid: ≤-18℃ In dark |
| Shelf-life | 12 months |
| Specimen Type | Serum Sample, Plasma Sample |
| Ct | ≤38 |
| CV | ≤5.0% |
| LoD | 50 Copies/reaction |
| Specificity | There is no cross-reactivity with hepatitis B virus, hepatitis C virus, human papilloma virus, herpes simplex virus type 1, herpes simplex virus type 2, normal human serum samples, etc. |
| Applicable Instruments | : It can match the mainstream fluorescent PCR instruments on the market. Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR Systems QuantStudio®5 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems LightCycler®480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection System MA-6000 Real-Time Quantitative Thermal Cycler BioRad CFX96 Real-Time PCR System BioRad CFX Opus 96 Real-Time PCR System |
| 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.
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