Freeze-dried Chlamydia trachomatis Detection Kit (Isothermal Amplification)

For qualitative detection of Chlamydia trachomatis nucleic acid in male urine, male urethral swab, and female cervical swab specimens. Aids in the diagnosis of urogenital chlamydial infections.

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

For qualitative detection of Chlamydia trachomatis nucleic acid in male urine, male urethral swab, and female cervical swab specimens. Aids in the diagnosis of urogenital chlamydial infections.

Product typeAssay / Kit
Technology platformIsothermal Amplification
Application areaSexually Transmitted Disease

Epidemiology

Chlamydia trachomatis (CT) is a prokaryotic organism that lives exclusively as an intracellular parasite within eukaryotic hosts[1]. Based on serotyping, it is classified into serotypes A through K. Urogenital infections predominantly arise from the trachoma biovar serotypes D–K. In males, the primary presentation is urethritis, which may resolve spontaneously but often evolves into a chronic state with episodic exacerbations, and can be associated with epididymitis, proctitis, and related conditions[2]. In females, possible manifestations include urethritis and cervicitis, with the more severe complication being salpingitis[3].

Work Flow

Option 1

Using Sample Release Reagent, extraction must follow the manufacturer's instructions precisely. Combine the DNA obtained via sample release reagent with the reaction buffer and immediately analyze on the instrument; alternatively, hold extracted samples at 2–8°C for up to 24 hours.

Option 2

With a General DNA/RNA Kit and an Automatic Nucleic Acid Extractor, adhere strictly to the IFU during extraction; the suggested elution volume is 80 µL. DNA recovered by the magnetic bead method should be heated at 95°C for 3 minutes, then promptly chilled on an ice bath for 2 minutes. Add the treated DNA to the reaction buffer and proceed with testing, or keep processed samples below -18°C for no longer than 4 months, with a maximum of 4 freeze–thaw cycles.

SKU codeOn request
Storage≤30℃
Shelf-life12 months
Specimen TypeFemale cervical swab Male urethral swab Male urine
Tt≤28
CV≤10.0%
LoD400 Copies/mL
Specificitythere is no cross-reactivity between this kit and other genitourinary tract infection pathogens such as high-risk Human papillomavirus type 16, Human papillomavirus type 18, Herpes simplex virus type Ⅱ, Treponema pallidum, Ureaplasma urealyticum, Mycoplasma hominis, Mycoplasma genitalium, Staphylococcus epidermidis, Escherichia coli, Gardnerella vaginalis, Candida albicans, Trichomonas vaginalis, Lactobacillus crispatus, Adenovirus, Cytomegalovirus, Beta Streptococcus, Human immunodeficiency virus, Lactobacillus casei and human genomic DNA, etc.
Applicable InstrumentsApplied Biosystems 7500 Real-Time PCR System Applied Biosystems 7500 Fast Real-Time PCR Systems QuantStudio ® 5 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems(Hongshi Medical Technology Co. Ltd.) LightCycler ® 480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection System (FQD-96A, Hangzhou Bioer technology) MA-6000 Real-Time Quantitative Thermal Cycler BioRad CFX96 Real-Time PCR System and BioRad CFX Opus 96 Real-Time PCR System Easy Amp Real-time Fluorescence Isothermal Detection 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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