Elucigene CF-HT

Elucigene™ CF-HT v.3 is a CFTR genotyping assay for cystic fibrosis that incorporates the latest fluorescent ARMS technology enabling rapid, cost efficient high-throughput genetic testing.

Why choose Elucigene™ CF-HT v.3?

Detects 28 of the most common CFTR mutations found in Caucasian populations plus the intron 8 polymorphism 5T/7T/9T (poly T)
Poly T reporting can be easily switched on or off as required
Includes all mutations approved by ACOG/ACMG for US cystic fibrosis screening
Detects wildtype and mutant alleles at all loci (i.e. full genotyping)
Validated for use on Applied Biosystems’3100/3130 Genetic Analyzers using POP 6 or 7
Results can be analysed using GeneMapper® or GeneScan®/Genotyper® software

CE Marked

Elucigene CF-HT v.3 complies with the EC Directive 98/79/CE, carries the CE mark and is manufactured within quality systems accredited to ISO9001:2000 and ISO13485. Full technical support is provided to purchasers of kits to ensure acceptable performance and customer satisfaction.

Mutations & Polymorphisms detected

Mutations detected

E60X

G85E

R117H

621+1 G>T

711+1 G>T

1078delT

R334W

R347P

A455E

dI507

dF508

1717-1 G>A

G542X

G551D

R553X

R560T

1898+1 G>A

2183 AA>G

2184delA

2789+5 G>A

3120+1 G>A

D1152H

R1162X

3659delC

3849+10kb C>T

S1251N

W1282X

N1303K

Polymorphisms detected

IVS8-5T

IVS8-7T

IVS8-9T

• How to Order • Cat. No. CF0HTB2

For more details on Elucigene CF-HT v3 please go to the downloads section.