| Hematology: |
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Faktor V/II + HR2
(Cat.no.: RDB2005, 12 Tests/ RDB2005X, 60 Tests) |
Reverse hybridization kit for the determination of the mutation FV:Q506 in the Factor V gene and the mutation 20210A in the Factor ll gene and the HR2 allele
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Faktor V/II + MTHFR New!
(Cat.no.: RDB2020, 12 Tests/ RDB2020X, 60 Tests) |
Reverse hybridization kit for the determination of the mutation FV:Q506 in the Factor V gene, the mutation 20210A in the Factor II gene and the MTHFR polymorphism C667T and A1298C
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| Methylentetrahydrofolate Reduktase (MTHFR) New!
(Cat.no.: RDB2060, 12 Tests/ RDB2060X, 60 Tests) |
Reverse hybridization kit for the determination of the C677T and A1298C polymorphism in the coronary artery disease Marker gene MTHFR
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| Hereditary Hemochromatosis :
Gene mutations C282Y and H63D
(Cat.no.: RDB2045, 12 Tests/ RDB2045X, 60 Tests) |
Determination of the mutation C282Y and the predisposing allel H63D in the hemochromatosis (Hfe) gene
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| Immunology: |
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| HLA-B Haplotype B*27
(Cat.no.: RDB2015, 12 Tests/ RDB2015X, 60 Tests) |
Reverse hybridization kit for the determination
of the HLA-B allele B*27
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| HLA-DRB1 Shared epitope QKRAA/QRRAA/RRRAA
(Cat.no.: RDB2035, 12 Tests/ RDB2035X, 60 Tests) |
Reverse hybridization kit for the detection of the shared epitope QKRAA/QRRAA/RRRAA of rheumatoid arthritis in all known HLA-DRB1 alleles; differentiation between homozygot and heterozygot
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Celiac disease:
HLA-DQ and DR4
(Cat.no.: RDB2065, 12 Tests/ RDB2065X, 60 Tests) |
Detection of the celiac disease heterodimer DQ(a 1*0501, b 1*0201) and the DR4 allele.
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Celiac disease:
HLA-DQ2, DQ8 and DR4
(Cat.no.: RDB2105, 12 Tests/ RDB2015X, 60 Tests) |
Detection of the celiac disease heterodimer DQ(a 1*0501, b 1*0201), HLA-DQ8(a 1*0301, b 1*0302) and the DR4 allele.
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IDDM
(Cat.no.: RDB2100, 12 Tests/ RDB2100X, 60 Tests)
Available on Request! |
Detection of the HLA-alleles DQA1*0301, DQA1*05, DQB1*0201, DQB1*0302, DR3 and DR4
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| Metabolism and Regulation: |
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Apolipoprotein E and B (ApoE and ApoB)
Risk alleles for familiar hyperlipoproteinaemie and ateriosclerosis
(Cat.no.: RDB2050, 12 Tests/ RDB2050X, 60 Tests) |
Determination of the ApoE risk-alleles e2, e3 and e4 in the gene for familial hyperlipoproteinaemie, detection of the Arg3500GIn-mutation for arteriosclerosis in the ApoB gene
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Osteoporosis riskfactors:
Vitamin D receptor B/b- and collagen I a 1 S/s-Alleles
(Cat.no.: RDB2055, 12 Tests/ RDB2055X, 60 Tests) |
Reverse hybridization kit for the simultaneous detection of the major osteoporosis risk factors Collagen Type I a 1 S/s and Vitamin D receptor B/b
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Cytochrom P450:
poor metabolizer allele CYP2C19*2
(Cat.no.: RDB2070, 12 Tests/ RDB2070X, 60 Tests)
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Determination of the "poor metabolizer" allele CYP2C19*2
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Cytochrom P450:
CYP2C9 alleles *2 and *3
(Cat.no.: RDB2075, 12 Tests/ RDB2075X, 60 Tests)
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Determination of the predisposing alleles for warfarin hypersensitivity R144C and I359L
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Glutathion-S-Transferase New!
Polymorphismus M1, T1 and P1
(Cat.no.: RDB2090, 12 Tests/ RDB2090X, 60 Tests) |
Detection of the alleles M1, T1 and P1 in the Glutathion- S-Transferase (GST) gene
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| Alpha-1-Antitrypsin
(Cat.no.: RDB2010, 12 Tests/ RDB2010X, 60 Tests)
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Reverse hybridisation assay for the determination of the point mutations PiZ and PiS in the human gene for alpha-1-antitrypsin
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| Lactose intolerance
(Best.nr.: RDB2120,12 Tests/ RDB2120X, 60 Tests)
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Reverse hybridization kit to verify the polymorphisms G/A-22018 and C/T-13910 in patients suffering probably on lactose intolerance
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Hereditary Fructose Intolerance (HFI):
New!
 product overview
Predisposing alleles within the Aldolase B Gene
(Best.nr.: RDB2175,12 Tests/ RDB2175X, 60 Tests)
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Determination of the mutation for A149P, A174D, N334K and Δ4E4 in Aldolase B gene
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