Contacts and Location
Contact 1 | Linda Piekuse |
---|---|
Contact 2 | Linda Gabrusenoka |
Enquire about this service | |
Organisational Unit |
Rīga Stradiņš University Scientific Laboratory of Molecular Genetics - Latvia, Rīga |
Description
dF508 mutation (alternative names: rs113993960, NM_000492.3:c.1521 1523delCTT (p.Phe508del, F508del)), is found in 1:30 Caucasians and in homozygous state or in compound heterozygous state with other CF causing allele is causing Cystic fibrosis. Worldwide, the ∆F508 mutation is responsible for approximately two thirds (66%) of all CF chromosomes (Bobadilla JL, 2002).
Specification
Sample DNA or material for DNA isolation. dF508 mution in patients DNA is detected by heteroduplex PCR and PAGE.
Accreditation
Delivery time
Negotiable. Depends on many factors: for example, number of samples.