INNO-LiPA® CFTR Italian Regional
For an increased detection rate in populations with Italian ancestry
INNO-LiPA CFTR Italian Regional is a multiparameter line probe assay, based on the reverse hybridization principle, for the simultaneous detection and identification of 21 Italian Cystic Fibrosis-related mutations and their wild-type sequences in human whole blood, dried blood spots and buccal brush samples.
This product is in addition to the INNO-LiPA CFTR 19 and INNO-LiPA CFTR 17+Tn Update kits that test for the most common mutations worldwide.
Product number 80710
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Details
Features & Benefits
- One amplification and one strip.
- INNO-LiPA CFTR Italian Regional provides probes for 21 additional CFTR-related mutations, giving an increased detection rate for populations of (or related to) Italian descent.
- Analysis of both the mutant and the wild-type sequences demonstrates homo- or heterozygosity for each tested mutation, allowing the discrimination between carrier status and patients.
- The test is fast and easy to perform, offers quick visual interpretation, and full results are obtained within one working day.
- Fully automated processing of the strips is possible using Auto-LiPA™ 48 and AutoBlot 3000H.
- Objective, automated reading and interpretation of the strips is possible
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Conditions of sale
To read the end user conditions of sale for this product please visit our Resource center.
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Documentation
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Other documents
FileFAQ - LIPA General (pdf, 137.77 kb)FileFAQ - INNO-LIPA CFTR (pdf, 157.08 kb)FileList_of_recommended_reading_publications_for_INNO-LiPA_CFTR.pdf (pdf, 183.12 kb)Get access to this section and more
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Insights
Early, easy, efficient and cost-effective diagnosis of Cystic Fibrosis
Cystic Fibrosis is one of the most frequent life threatening inherited diseases. If detected early, effective treatment can be started improving...
Nov 28, 2019
Cystic Fibrosis, diagnosis and molecular testing
Cystic fibrosis (CF) is one of the most frequent human genetic disorders, predominantly affecting individuals of Caucasian descent in North America...
May 22, 2019
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FAQ
How does the coronavirus disease Covid-19 impact Fujirebio's operations?
Please see the following statement on the impact of coronavirus disease Covid-19 on the operations of Fujirebio Europe (updated January 19, 2021).
Can the strips of the different CFTR products be tested together in the same trough?
The following strips can be tested in the same trough:
- INNO-LiPA CFTR17+Tn Update + INNO-LiPA CFTR19
- INNO-LiPA CFTR Italian Regional + INNO-LiPA CFTR Deletions + 6
Other strip combinations have not been validated.
What kind of Taq DNA polymerase needs to be used?
The use of a Hot Start Taq DNA polymerase is required, but not provided. Validation studies were performed with Hot Start Taq (Qiagen®), but other Hot Start enzymes can be used.
Initial denaturation temperature (95°C) and time (15 minutes) of the amplification profile included in the package insert should be verified with the Hot Start Taq DNA polymerase manufacturer instructions and potentially adjusted.
What sample types can be used in combination with the CFTR product portfolio?
Internal and external validation studies proved compatibility with whole blood, dried blood spots and buccal brushes for the complete CFTR product portfolio.
What controls are included in the INNO-LiPA CFTR kits?
Conjugate control line:
- Monitors the color development step meaning the addition and incubation of conjugate and substrate.
Wild type probes:
- For every mutant probe a corresponding wild type probe is coated on the strip. The presence of the wild type probes on the strip verifies a successful amplification.
What is the clinical relevance of R117H?
When R117H is detected, the Tn status should also be established:
- R117H-T5 is considered a mild CF-causing complex allele
- R117H-T7 is more likely a CFTR-related disorder mutation
When found in compound heterozygosity with a CF-causing mutation, or possibly even in homozygosity, R117H-T5 generally results in pancreatic sufficient CF, while R117H-T7 may result in a mild form of CF, obstructive azoospermia, or no disease at all.
* Castellani C, Cuppens H, Macek JR M et al. J Cyst Fibros 2008; 7:179-196
Dequeker E, Stuhrmann M, Morris MA et al. Eur j Hum Genet 2008; 1-15 -
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