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Basic Info.
Model NO.
P121H
HS Code
3822009000
Production Capacity
5000000 Test/Year
Product Description
Product Name:
Mycobacterium Tuberculosis Complex Nucleic Acid Detection Kit (Fluorescence PCR method)
Intended Use:
The kit is used for qualitative detection of ureaplasma urealyticum nucleic acid in male urethral swab samples or female cervical swab samples. Ureaplasma urealyticum has the closest relationship with reproductive health. It can cause urogenital infections and is considered to be an important pathogen in nongonococcal urethritis after Chlamydia (50%).
The laboratory tests of ureaplasma urealyticum include:
1) Ureaplasma urealyticum culture method;
2) Immunological methods;
3) Fluorescence quantitative polymerase chain reaction.
The kit developed by our company is suitable for the auxiliary diagnosis of ureaplasma urealyticum. The test results of this kit are for clinical reference only and cannot be used as the basis for diagnosis or exclusion of cases.
The laboratory tests of ureaplasma urealyticum include:
1) Ureaplasma urealyticum culture method;
2) Immunological methods;
3) Fluorescence quantitative polymerase chain reaction.
The kit developed by our company is suitable for the auxiliary diagnosis of ureaplasma urealyticum. The test results of this kit are for clinical reference only and cannot be used as the basis for diagnosis or exclusion of cases.
Product Name | Mycobacterium Tuberculosis Complex Nucleic Acid Detection Kit (Fluorescence PCR method) |
Cat.No | P121H |
Specification | 25T/Kit |
Specimen | human sputum sample |
Storage & Validity | All reagents should be stored at -20ºC±5 ºC. The validity period of the reagents is 12 months. |
Applicable Equipment | Amplification detection instruments with FAM and HEX/VIC fluorescence channels: ABI7500 real time PCR systems, Gentier 96E/R and Gentier48E real-time PCR system from Xi'an Tianlong Science and Technology Co. Ltd. |