Real-Time PCR Kits
STDs
Sexually transmitted diseases (STDs) can lead to infertility, ectopic pregnancy, miscarriage and cancer. Though all genders are prone to risks related to STDs, in majority of the cases, women are affected far more severely. Globally, over 1 billion people were shown to have contracted STDs caused by bacteria, parasites, fungi or viruses.
Features
Workflow
Technical Specifications
Thermal Protocol | Single thermal protocol for all parameters |
Sample Typing | Urine, tissue/biopsy specimen, swabs |
Shelf Life | 18 Months |
Channels | FAM, HEX/VIC, Texas Red/ROX, Cy5 |
Shipping / Storage | -80°C / -20°C |
STDs Kits
Chlamydia trachomatis, Neisseria gonorrhoeae, and Mycoplasma genitalium are bacterial pathogens that cause the most common sexually transmitted infections worldwide. These infections are major causes of infertility, ectopic pregnancy, and pelvic inflammatory disease (PID).
Bosphore CT/NG/MG Panel Kit v1 identifies C. trachomatis, N. gonorrhoeae, and M. genitalium DNA in human biological samples. The presence of C. trachomatis DNA is detected through FAM, N. gonorrhoeae DNA through HEX, and M. genitalium DNA is detected through Texas Red filters. An internal control has been integrated into the kit to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter.
*For research use only.
Bosphore HPV Detection Kit v1, is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore HPV Detection Kit v1 is a qualitative test used to detect human papilloma virus encompassing the most predominant HPV genotypes found in human biological samples (6, 7, 11, 13, 16, 18, 31, 33, 45). Fluorescence detection is accomplished using the FAM filter. Detection Mix contains the specific primers required to detect HPV DNA. The amplification data of the human papilloma virus (HPV) is detected qualitatively with the SYBR Green filter.
Bosphore HPV Detection Kit v4, is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore HPV Detection Kit v4 is a qualitative test used to detect human papilloma virus encompassing the 32 most predominant HPV genotypes found in human biological samples (19 high risk HPV genotypes of 16,18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 67, 68, 69, 73 and 13 low risk HPV genotypes of 6, 7, 11, 13, 40, 43, 44, 62, 72, 74, 81, 83, 89).
Fluorescence detection is accomplished using the FAM filter in two separate tubes, with PCR Master Mix 1 and PCR Master Mix 2 respectively. In the first tube, HPV genotypes 6, 11, 16, 18, 26, 31, 33, 35, 40, 43, 44, 53, 56, 58, 62, 66, 67, 68, 69, 72, 73, 81, 83, 89 are detected and in the second tube, HPV genotypes 6,7, 11, 13, 16,18, 26, 31, 33, 35, 39, 45, 51, 52, 59, 68 are detected. The amplification data of the human papilloma virus (HPV) is detected qualitatively with the SYBR Green filter.
Bosphore HPV Genotyping High Risk Basic Kit v1, is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore HPV Genotyping High Risk Basic Kit v1 detects and characterizes the genotype of human papilloma virus in human biological samples, encompassing the basic high risk group of HPV genotypes; 16, 18 and 31. Fluorescence detection is accomplished using the FAM, HEX, Texas Red and Cy5 filters. The genotypes 16, 18, 31 and internal control are detected with PCR Master Mix including labelled probes in the same well/reaction.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control is added into the sample at the PCR step.
Bosphore HPV Genotyping High Risk Kit v1, is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore HPV Genotyping High Risk Kit v1 detects and characterizes the genotype of human papilloma virus in human biological samples, encompassing high risk group of HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68). Fluorescence detection is accomplished using the FAM, HEX, Texas Red and Cy5 filters.
Genotypes 16, 18, 31 and internal control are detected in Detection Mix 1; the genotypes 51, 56, 58 and internal control are detected in Detection Mix 2, the genotypes 33, 35, 52, 59 and internal control are detected in Detection Mix 3 and the genotypes, 39, 45, 66, 68 and internal control are detected in Detection Mix 4 with using labelled probes. The four PCR master mixes function in four separate wells/reactions.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control is added into the sample at the PCR step.
Bosphore HPV Genotyping High Risk Kit v4 (Fast Extraction) is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore HPV Genotyping High Risk Kit v4 detects and characterizes the genotype of human papilloma virus in human biological samples, encompassing high risk group of HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68). Fluorescence detection is accomplished using the FAM, HEX, Texas RED and Cy5 filters.
The genotypes 16, 18, 31 and internal control are detected in PCR Master Mix 1;
The genotypes 51, 56, 58 and internal control are detected in PCR Master Mix 2,
The genotypes 45, 35, 59 and internal control are detected in PCR Master Mix 3,
The genotypes, 39, 66, 68 and internal control are detected in PCR Master Mix 4 and
The genotypes 33, 52 and internal control are detected in PCR Master Mix 5 with using labelled probes. The five PCR master mixes function in five separate wells/reactions.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control is added into the sample at the PCR step. Only a single incubation with the EX-Tract DNA solution is enough to prepare the samples for qPCR. There is no need to apply an external DNA isolation.
Bosphore HPV HR-LR Genotyping Kit v1 detects and characterizes the genotype of human papilloma virus in human biological samples (swab, tissues, biopsy specimen, serum, plasma), encompassing high risk (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68) and low risk (6, 11, 42, 61, 70) groups of HPV genotypes. Fluorescence detection is accomplished using the FAM, HEX, Texas Red and Cy5 filters.
The genotypes 16, 18, 31 and internal control are detected in PCR Master Mix 1; the genotypes 51, 56, 58 and internal control are detected in PCR Master Mix 2, the genotypes 35, 45, 59 and internal control are detected in PCR Master Mix 3, the genotypes, 39, 66, 68 and internal control are detected in PCR Master Mix 4 and the genotypes 33, 52 and internal control are detected in PCR Master Mix 5, the genotypes 6, 11, 42 and internal control are detected in PCR Master Mix 6, the genotypes 61, 70 and internal control are detected in PCR Master Mix 7 with using labeled probes. Seven PCR master mixes are used in seven separate wells/reactions.
An internal control has been integrated into the kit in order to check DNA extraction and PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Genital Ulcer Panel Kit detects and characterizes HSV-1, HSV-2 and Treponema pallidum in human biological samples including urine, tissue/biopsy specimen, swabs (flocking swabs and liquid amies, UTM, VCM, Sigma Transwab, Copan ESwab, Sigma VCM, vaginal swab, endocervical swab, urethral swab) and semen sample. Fluorescence detection is accomplished using the FAM, HEX, Texas Red and Cy5 filters.
An internal control has been integrated into the kit in order to check DNA extraction, PCR inhibition and application mistakes. The internal control can be added either during DNA extraction or PCR step.
FAM | HEX | Texas Red | Cy5 |
HSV-1 | Treponema pallidum | Internal Control | HSV-2 |
Bosphore C. trachomatis Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore C. trachomatis Detection Kit v1 detects C. trachomatis DNA in human biological samples. A region of C. trachomatis omp A gene is amplified and fluorescence detection is accomplished using the FAM filter.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the HEX filter. The internal control is added during PCR step.
Bosphore Gardnerella vaginalis Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Gardnerella vaginalis Detection Kit v1 detects Gardnerella vaginalis DNA in human biological samples. A specific region in Gardnerella vaginalis genome is amplified and fluorescence detection is accomplished using the Cy5 filter.
An internal control has been integrated into the kit in order to check DNA extraction and PCR inhibition. The amplification data of the internal control is detected with the Texas Red filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Mycoplasma genitalium Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Mycoplasma genitalium Detection Kit v1 detects Mycoplasma genitalium DNA in human biological samples. Mycoplasma genitalium genome is amplified and fluorescence detection is accomplished using the Texas RED filter.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Mycoplasma hominis Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Mycoplasma genitalium Detection Kit v1 detects Mycoplasma hominis DNA in human biological samples. Mycoplasma genitalium genome is amplified and fluorescence detection is accomplished using the Texas Red filter.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Neisseria gonorrhoeae Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Neisseria gonorrhoeae Detection Kit v1 detects Neisseria gonorrhoeae DNA in human biological samples. Neisseria gonorrhoeae genome is amplified and fluorescence detection is accomplished using the FAM filter.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the HEX filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Treponema pallidum Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Treponema pallidum Detection Kit v1 detects Treponema pallidum DNA in human biological samples, encompassing all the subtypes. A specific region of polA gene in Treponema pallidum genome is amplified and fluorescence detection is accomplished using the Cy5 filter.
An internal control has been integrated into the kit in order to check DNA extraction and PCR inhibition. The amplification data of the internal control is detected with the HEX filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Trichomonas vaginalis Detection Kit v1 is, a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Trichomonas vaginalis Detection Kit v1 detects Trichomonas vaginalis DNA in human biological samples. A specific region in Trichomonas vaginalis beta-tubulin gene is amplified and fluorescence detection is accomplished using the HEX filter.
An internal control has been integrated into the kit in order to check DNA extraction and PCR inhibition. The amplification data of the internal control is detected with the Cy5 filter. The internal control can be added either during DNA extraction or PCR step.
Bosphore Ureaplasma parvum Detection Kit v1 detects and characterizes Ureaplasma parvum in human biological samples including urine, tissue/biopsy specimen, swabs (flocking swabs and liquid amies, UTM, VCM, Sigma Transwab, Copan ESwab, Sigma VCM, vaginal swab, endocervical swab, urethral swab) and semen. Ureaplasma parvum is amplified and fluorescence detection is accomplished using the HEX filter.
An internal control has been integrated into the kit in order to check DNA/RNA extraction, PCR inhibition and application failures. The amplification data of the internal control is detected with Cy5 filter. The internal control can be added either during DNA extraction or PCR step.
HEX | Cy5 |
Ureaplasma parvum | Internal Control |
Bosphore Ureaplasma urealyticum Detection Kit v1, is a Real-Time PCR based in-vitro diagnostic medical device, IVD CE marked according to 98/79/EC Directive. Bosphore Ureaplasma urealyticum Detection Kit v1 detects U. urealyticum DNA in human biological samples, encompassing all U. urealyticum subtypes. A region within the urease gene is amplified and fluorescence detection is accomplished using the FAM filter.
An internal control has been integrated into the kit in order to check PCR inhibition. The amplification data of the internal control is detected with the Cy5/HEX/JOE filter. The internal control is added during PCR step.