

Fluorescence PCR · Others
Candida albicans/Candida tropicalis/Candida glabrata Nucleic Acid Combined Detection Kit (Fluorescence PCR)
Qualitative detection of Candida albicans, Candida tropicalis, and Candida glabrata nucleic acids in urogenital tract or sputum samples. Aids in the diagnosis of candidiasis in urogenital and respiratory tracts.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Candida albicans, Candida tropicalis, and Candida glabrata nucleic acids in urogenital tract or sputum samples. Aids in the diagnosis of candidiasis in urogenital and respiratory tracts.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Others |
Epidemiology
As the most abundant normal fungal flora in humans, Candida species inhabit the respiratory, digestive, and urogenital tracts, as well as other sites exposed to the external environment. These organisms are typically non-pathogenic and act as opportunistic pathogens. Factors such as widespread use of immunosuppressive drugs, extensive broad-spectrum antibiotics, tumor radiation and chemotherapy, invasive procedures, and organ transplantation can disrupt the normal microbial balance, leading to Candida infections in the genitourinary and respiratory tracts. Among Candida species, C. albicans is the most frequently encountered clinically, while over 16 non-albicans species can cause disease; notably C. tropicalis, C. glabrata, C. parapsilosis, and C. krusei are common. C. albicans is an opportunistic fungus that ordinarily colonizes mucosal surfaces and skin, such as the intestines, oral cavity, and vagina. When host defenses weaken or the microecology becomes disturbed, it can overgrow and trigger infection. C. tropicalis is also an opportunistic pathogen ubiquitous in nature and the human body; with diminished immunity, it may produce skin, vaginal, urinary tract, and even systemic infections.
In recent years, among Candida isolates from candidiasis patients, C. tropicalis has often ranked first or second among non-albicans species. It predominantly affects individuals with leukemia, immunodeficiency, long-term indwelling catheters, or broad-spectrum antibiotic therapy. The epidemiology of C. tropicalis infection shows significant geographic variation; in certain regions, its incidence may exceed that of C. albicans. Key pathogenic determinants include hyphae formation, cell surface hydrophobicity, and biofilm production. C. glabrata is a frequent cause of vulvovaginal candidiasis (VVC). Its colonization and infection rates correlate with age—extremely rare in infants and children but increasing substantially in older populations. The prevalence of C. glabrata is influenced by geographic location, age, population demographics, and fluconazole usage.
Reagent required but not provided
The following reagents are required but not provided:
- Sample Release Reagent
- Viral DNA/RNA Kit and Automatic Nucleic Acid Extractor
- Nucleic Acid Extraction or Purification Kit (YDP302)
- 4% sodium hydroxide or sputasol (mucolytic agent)
- Normal saline, Lysozyme Diluent (20 mM Tris, pH 8.0; 2 mM Na2-EDTA; 1.2% Triton), and Lysozyme (RT401)
| SKU code | On request |
|---|---|
| Storage | -18℃ |
| Shelf-life | 12 months |
| Specimen Type | urogenital tract,sputum |
| Ct | ≤38 |
| CV | ≤5.0% |
| LoD | 1000 Copies/μL |
| Applicable Instruments | Applicable to type I detection reagent: Applied Biosystems 7500 Real-Time PCR Systems, QuantStudio ® 5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.), LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, Hangzhou Bioer technology), MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co. Ltd.), 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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