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Devyser CFTR 68

Fragment analysis-based kit that enables fast and reliable detection of cystic fibrosis-causing mutations, using a multi-ethnic panel of 68 CFTR mutations that achieves high detection rates while keeping the workload and costs to a minimum.

68

Detects 68 CFTR mutations, the polyT tract and associated number of TG repeats

Allele-specific detection

CE-IVD

Single end-to-end CE-IVD solution

The next generation is here!

Multi-ethnic panel

For laboratories looking to improve detection rate while keeping a simple and fast workflow, Devyser CFTR 68 is a streamlined, two-tube solution that maximizes the detection rate by including a multi-ethnic panel of 68 mutations frequently found in the European population. It does not require the use of additional population-specific kits.

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Instructions for use

Enter access code found in the lower right corner of the label on the kit box.

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Certificates

Download a specific Batch Release Certificate (BRC) below.

Guidelines and handbooks (4)

CFTR - Best Practice Guidelines (EU) (English)

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Accessory Pack Devyser CFTR Core version 2018-08-20 (English)

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Data Analysis Using GeneMapper 2018-12-10 (English)

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Handbook Devyser CFTR 68 EN v2022-06-29 (English)

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Product information (1)

Flyer: Devyser CFTR 68 (English) (English)

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Software settings (5)

Fragment Analysis Using ABI PRISM 310_2020-06-15 (English)

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Fragment Analysis Using ABI 3730 & 3730xL 2020-06-15 (English)

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Fragment Analysis Using ABI 3130 & 3130xL 2020-06-15 (English)

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Fragment Analysis Using ABI 3500 & 3500xL 2020-06-15, c2021-01-19 (English)

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Devyser CFTR 68 (Sep)_POP7_GM4-5_2020-10-12 ()

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Safety data sheets (5)

Devyser SDS 2 RUO EN (English)

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Devyser SDS 1 CE-IVD EN (English)

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Devyser SDS 2 RUO DE (German)

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Devyser SDS 1 CE-IVD IT (Italian)

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Devyser SDS 2 RUO IT (Italian)

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Data tables (1)

Table: Reported insertions and deletions Devyser CFTR 68_2020-06-11 (English) (English)

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Enter access code found in the lower right corner of the label on the kit box.

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Product details

CE-IVD

Devyser CFTR 68

Detection of the following CFTR mutations: 711+ 1G>T, 2043delG, 1677delTA, W1282X, R1283M, K710X, 3849+10kbC>T, 2789+5G>A, M1101K, G85E, 3905insT, 1525-1G>A, 2184delA, 3659delC, N1303K, 2184insA, 1812-1G->A, CFTRdele2,3, 2143delT, Y569D, R1162X, A561E, S1251N, P67L, R1158X, 1609delCA, Q493X, E60X, 1898+1G>A, 1898+5G>T, I507del, F508del, V520F, 394delTT, D1152H, V232D, L218X, 621+2T>C, 1717-1G>A, L206W, E92X, 3120+1G>A, G542X, S549N, G551D, 712-1G>T, R553X, 3272-26A>G, R560T, 2183AA>G, R117H, R117C, 1811+1.6kbA>G, 2869insG, Y122X, Q890X, R1066C, R347H, R347P, 1161delC, 1154ins TC, E92K, I336K, R334W, Y1092X (C>A), 621+1G>T, 1078delT, A455E and corresponding wildtype alleles. IVS8: 5T (including identification of TG9-13), 7T, 9T. Calibrated with G5.

8-A045-8

8-A045-24

8-A045-

Pack size: 8

Pack size: 24

Pack size: 48

RUO

Devyser CFTR 68

Detection of the following CFTR mutations: 711+ 1G>T, 2043delG, 1677delTA, W1282X, R1283M, K710X, 3849+10kbC>T, 2789+5G>A, M1101K, G85E, 3905insT, 1525-1G>A, 2184delA, 3659delC, N1303K, 2184insA, 1812-1G->A, CFTRdele2,3, 2143delT, Y569D, R1162X, A561E, S1251N, P67L, R1158X, 1609delCA, Q493X, E60X, 1898+1G>A, 1898+5G>T, I507del, F508del, V520F, 394delTT, D1152H, V232D, L218X, 621+2T>C, 1717-1G>A, L206W, E92X, 3120+1G>A, G542X, S549N, G551D, 712-1G>T, R553X, 3272-26A>G, R560T, 2183AA>G, R117H, R117C, 1811+1.6kbA>G, 2869insG, Y122X, Q890X, R1066C, R347H, R347P, 1161delC, 1154ins TC, E92K, I336K, R334W, Y1092X (C>A), 621+1G>T, 1078delT, A455E and corresponding wildtype alleles. IVS8: 5T (including identification of TG9-13), 7T, 9T. Calibrated with G5.

8-A403-8

8-A403-24

8-A403-

Pack size: 8

Pack size: 24

Pack size: 48

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