iris tech
iris technologies international gmbh
RECIPE products
- ClinRep© | Clinical Diagnostics |
HPLC
Complete Kits - ClinRep© | Therapeutic Drug Monitoring | HPLC
Complete Kits
- ClinTox© | Human Bio-
monitoring | HPLC
Complete Kits - ClinMass© | LC-MS/MS
- ClinCal© Matrix Calibrators
- ClinChek© Matrix Controls
- ClinTest© Solutions
- RECIPE News
BIOTICA products
MINERVA products
Clinical Diagnostics ...
Pathogenic Bacteria Detection utilizing PCR
![]() |
We would like to invite you to view our Slide-Show Download: "The application of qPCR techniques in the diagnosis of respiratory infections". |
Our clinical diagnostic products focus on pathogenic bacteria detection. The tests are based on the polymerase chain reaction (PCR) and allow in vitro tests for the qualitative and quantitative diagnosis of bacteria in various clinical materials.
In many clinical settings, accurate and rapid diagnostic is important for an efficient patient management. Diagnosis of acute infections is usually based on culture and serology, known to be difficult by means of insensitivity, delayed detection and poor specificity.
By utilising the highly-sensitive PCR technology and their unique features, all these drawbacks can be avoided and efficient testing becomes available. Direct testing with the PCR detection kits is very rapid, certain and very effective. Detailed clinical studies confirm the high specificity and sensitivity of these tests, permitting early identification of clinically significant infections. By using the supplied internal control, false-negative results (due to inhibition of the reaction by the sample matrix) can be excluded individually for each sample.
| In-vitro - diagnosis of Mycoplasma pneumoniae |
Venor®Mp - conventional PCR and Venor®Mp-QP – qPCR: The selected template is highly preserved within the Mycoplasma pneumoniae strains. Subtypes I and II are detected with equal reliability. |
||
| Venor®Mp detection of M. pneumoniae for conventional PCR | 20-1025, 20-1100, 201250 | |
| Venor®Mp Type 1 & Type 2 detection of M. pneumoniae for qPCR | 20-2025, 20-2100, 202250 (Type 1) 20-3025, 20-3100, 20-3250 (Type 2) |
|
| In-vitro - diagnosis of Legionella species/pneumophila |
Onar®Ls - conventional PCR and Onar®Ls-QP - qPCR: The supplied primer set and probe are specific for a segment of the 16S rRNA region of the Legionella genomes. Clinically relevant Legionella species are detected. |
||
| Onar®Ls detection of Legionella species for conventional PCR | 21-1025, 21-1100, 21-1250 | |
| Onar®Ls Type 1 & Type 2 detection of Legionella species for qPCR | 21-2025, 21-2100, 21-2250 (Type 1) 21-4100, 21-4100, 21-4250 (Type 2) |
|
| Onar®Lp Type 1 & Type 2 detection of L. pneumophila for qPCR | 21-3025, 21-3100, 21-3250 (Type 1) 21-5025, 21-5100, 21-5250 |
|
| In-vitro - diagnosis of Methicillin-resistant Staphylococcus aureus |
Onar®MRSA - qPCR: The supplied primer sets and probes are specific for a segment of the mecA gene of the MRSA genome and specific for the femA gene of Staphylococcus aureus. |
||
| Onar®MRSA Diagnostic Kit for qPCR | 22-2025, 22-2100, 22-2250 | |
| In-vitro - diagnosis of Treponema pallidum | Onar®Tp - qPCR: The Onar®Tp is specific for the polA gene of Treponema pallidum. |
||
| Onar®Tp Diagnostic Kit for qPCR | 23-2025, 23-2100 (Type 1) 23-3025, 23-3100 (Type 2) |
|
| In-vitro - diagnosis of Chlamydia trachomatis | Onar®Ct - qPCR: The primers used in the Onar®Ct qPCR Kit exclusively amplify the chromosomal momp gene of all sexual transmitted diseases (STDs) responsible serotypes. |
||
| 24-2025, 24-2100, 24-2250 (Type 1) 24-3025, 24-3100, 24-3250 (Type 2) |
||
| In-vitro - diagnosis of Bordetella pertussis/parapertussis |
Onar®Pertussis - qPCR: The Onar®Pertussis is designed to amplify a conserved region of the dnt gene of the genomes of Bordetella pertussis and Bordetella parapertussis. |
||
| 25-2025, 25-2100, 25-2250 (Type 1) 25-3025, 25-3100, 25-3250 (Type 2) |
||
| Additionally we offer: | ||
| Genomic DNA Extracts | ||
| PCR Quantification Standards | ||
| MB Taq DNA Polymerases | ||
Instrument Compatibility
| Document | Size |
| LightCycler® 480 | 875 kb |
| Rotor-GeneTM 6000 | 235 kb |
| Smart Cycler® | 128 kB |
| Please select your Cycler to identify the right kit version: | ||
| Instrument | Type 1 | Type 2 |
| LightCycler® 1.2 | +v | - |
| LightCycler® 1.5 | + | - |
| LightCycler® 2.0 | + | o |
| LightCycler® 480 | + | o |
| Rotor-GeneTM 3000 | + | o |
| Rotor-GeneTM 6000 | +v | o |
| ABI Prism® 7000 | - | + |
| ABI Prism® 7300 | - | + |
| ABI Prism® 7500 | - | +v |
| ABI Prism® 7700 | - | + |
| ABI Prism® 7900 | - | + |
| iCycler iQ® | o | o |
| iQ™5 | o | o |
| Opticon 2 | - | o |
| Chromo 4 | o | o |
| MX3000P® | + | o |
| MX3005P® | + | o |
| MX4000® | o | o |
| + = recommended kit version – = not compatible o = untested but presumed to be compatible V = validated |
||
