Request For Quotation Laboratory Reagents in Kazakhstan

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Dna Probes For Chromosomes (13,18, 21, X, Y) For 50 Studies. To Detect Aneuploidy Of Chromosomes 13,18,21,X,Y By Fluorescent In Situ Hybridization Fish Cep 18,X,Y Probe For The Alpha Satellite Sequence Of The Centromeric Regions Of Chromosomes 18,X And Y Probe Lsi 13,21-13Q14 Region, As Well As Regions 21Q22.13 To 21Q22.2. For Carrying Out On Interphase Nuclei Of Cells Obtained From Uncultured Or Cultured Amniocytes Of Women. Lsi Test 13 - Green Color For The Long Arm Of Region 14 Of Chromosome 13. Cep Test 18 - Blue Color For The Alpha Satellite Sequence Of Chromosome 18 In The Area From The Short Arm Of Region 11.1 To The Long Arm Of Region 11.1. Sample Lsi 21 Is Orange In Color For The Section Of The Long Arm Of Chromosome 21 From Region 22.13 To 22.2. The Cep X Test Is Green For The Alpha Satellite Sequence Of The Henna Chromosome In The Area From Region 11.1 To The Long Arm Of Region 11.1. The Cep Y Test Is Red For The Alpha Satellite Sequence Of Chromosome Y From The Short Arm Of Region 11.1 To The Long Arm Of 11.1. Cep Test 18\X\Y Is A Mixture Of Fluorescently Labeled Dna Probes Spectrum Aqva, Spectrum Orange And Spectrum Green, Specific To The Alphasatellite Regions (D18z1, Dxzi And Dyz3) Of Chromosomes 18, X And Y. Dna Probe Lsi 13\21 - Spectrum Green And Spectrum Oranqe Is A Fluorescent Probe Containing Unique Dna Sequences That Hybridize In The 13Q14 Region Of Chromosome 13 And Contain Unique Dna Sequences Corresponding To The D21s259, D21s341 And D21s342 Loci Of Regions From 21Q22.13 To 21Q22.2 On Chromosome 21. Sample Cep 18\X\Y (Acva, Green, Orange) - A Three-Color Mixture, Sample Lsi 13\21 - A Two-Color Mixture (Green, Orange). Mixtures Of Both Samples Must Be Pre-Denatured In Hybridization Buffer., Fluorescence Hybridization Is The Main Method For Confirming The Diagnosis Of Digeorge Syndrome. It Detects Methylation Abnormalities In The 22Q11 Region Characteristic Of Digeorge Syndrome., Fluorescence Hybridization Genetic Analysis To Detect Abnormalities In The 15Q11-13 Methylation Pattern Characteristic Of Identifying Prader-Willi Syndrome.

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