Browse Equipment & Services

Different tasks of AOI in industry and research

• Organisational Unit: Faculty of Civil Engineering - Latvia, Rīga
• Price: Contract price

Orcad PCB Designer, Altium Designer and KiCAD software is used by experienced researchers to design both schematics and printed circuit boards which are ready for production. Board design specialization is in the field of power electronics and general electronics.

• Organisational Unit: Department of Industrial Electronics and Electrical Technologies - Latvia, Rīga
• Price: 20.50 €
• * All prices are specified without VAT

Custom ultrasonic devices and transducers for NDT and research

• Organisational Unit: Faculty of Civil Engineering - Latvia, Rīga
• Price: Contract price

Cystic fibrosis (CF) is caused by mutations in the CFTR gene. dF508 mutation, is found in 1:30 Caucasians and is most common mutation that is found in 60% of all CF causing alleles. Test includes 50 most common CF causing mutation in Europeans, including IVS8-5T.

• Organisational Unit: Scientific Laboratory of Molecular Genetics - Latvia, Rīga
• Price: Contract price

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).

• Organisational Unit: Scientific Laboratory of Molecular Genetics - Latvia, Rīga
• Price: Contract price

Gilbert or benign hyperbilirubinemia (nonhemolytic hyperbilirubinemia, unconjugated hyperbilirubinemia) is caused by changed number of the (TA) repeats in the promoter reagion of the UGT1A1 gene. Given mutation should be detected before treatment with irinotecan is started.

• Organisational Unit: Scientific Laboratory of Molecular Genetics - Latvia, Rīga
• Price: Contract price

Iron overload in humans is associated with a variety of genetic and acquired conditions. Of these, HFE hemochromatosis (HFE-HC) is by far the most frequent and most well-defined inherited cause when considering epidemiological aspects and risks for iron-related morbidity and mortality. The most common mutations are C282Y and H63D (EASL best practice guidelines, 2010).

• Organisational Unit: Scientific Laboratory of Molecular Genetics - Latvia, Rīga
• Price: Contract price

Equipment associated with this service:

Detection of specific resistance genes ( rust ) flax genetic resources

• Organisational Unit: Institute of Biology - Latvia, Rīga
• Price: Contract price

Wilson’s disease is an inherited disorder in which defective biliary excretion of copper leads to its accumulation, particularly in liver and brain. Wilson’s disease is due to mutations of the ATP7B gene on chromosome 13 which encodes a copper-transporting P-type ATPase (ATP7B) residing in the trans-Golgi network of hepatocytes. Wilson’s disease is a genetic disorder that is found worldwide. Wilson’s disease is recognized to be more common than previously thought, with a gene frequency of 1 in 90–150 and an incidence (based on adults presenting with neurologic symptoms) that may be as high as 1 in 30,000. More than 500 distinct mutations have been described in the Wilson gene, from which 380 have a confirmed role in the pathogenesis of the disease, most common in the Central Europe is H1069Q (EASL guidelines, 2012) .

• Organisational Unit: Scientific Laboratory of Molecular Genetics - Latvia, Rīga
• Price: Contract price

Work on site

• Organisational Unit: Construction materials laboratory - Latvia, Rīga
• Price: Contract price