Candida tropicalis Nucleic Acid Detection Kit (EPIA)

Qualitative in vitro detection of Candida tropicalis nucleic acid in genitourinary tract and sputum samples.

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

Qualitative in vitro detection of Candida tropicalis nucleic acid in genitourinary tract and sputum samples.

Product typeAssay / Kit
Technology platformIsothermal Amplification
Application areaOthers

Certificate

CE

Epidemiology

Candida species represent the predominant normal fungal flora in humans, commonly inhabiting the respiratory, digestive, and genitourinary tracts, as well as other environmentally exposed sites. They are typically non-pathogenic and are classified as opportunistic pathogens. Disruption of the normal microbial balance—often due to extensive use of immunosuppressive agents, tumor radiotherapy and chemotherapy, invasive procedures, organ transplantation, and broad-spectrum antibiotics—can result in Candida infections of the genital and respiratory tracts.

Genitourinary Candida infections can lead to vulvovaginitis in women and balanitis, posthitis, and prostatitis in men, severely impacting patients' lives and daily activities. The incidence of genital tract candidiasis continues to rise each year. Women account for approximately 36% of cases, men about 9%, and Candida albicans (CA) is responsible for roughly 80% of these infections.

Candida albicans infection is a major cause of mortality from nosocomial infections. Among ICU patients, C. albicans accounts for about 40% of cases. Pulmonary fungal infections are the most frequent among all deep fungal infections, with rates increasing annually. Early diagnosis and identification of pulmonary fungal infections hold critical clinical value.

Clinically reported genotypes of Candida albicans primarily include types A, B, and C, which together account for more than 90% of cases. Accurate diagnosis of Candida albicans infection informs the management of vulvovaginal candidiasis, male balanitis, posthitis, prostatitis, and respiratory tract infections caused by this organism.

SKU codeOn request
StorageLiquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark
Shelf-lifeLiquid: 9 months; Lyophilized: 12 months
Specimen TypeGenitourinary Tract Swab, Sputum
Tt≤28
CV≤10.0%
LoD5Copies/µL, 102 bacteria/mL
SpecificityNo cross-reactivity with other pathogens of genitourinary tract infections, such as Candida tropicalis, Candida glabrata, Trichomonas vaginalis, Chlamydia trachomatis, Ureaplasma urealyticum, Neisseria gonorrhoeae, Group B streptococcus, Herpes simplex virus type 2, etc; there is no cross-reactivity between this kit and other pathogens of respiratory infections, such as Adenovirus, Mycobacterium tuberculosis, Klebsiella pneumoniae, Measles, Candida tropicalis, Candida glabrata and normal human sputum samples, etc.
Applicable InstrumentsEasy Amp Real-time Fluorescence Isothermal Detection System 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
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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