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Diagnostic Agents - Supply Of Kits, Reagents And Consumables For Activities Under Ordinance No. 26/2007, To Provide Obstetric Care To Women Without Health Insurance And To Carry Out Tests Outside The Scope Of Compulsory Health Insurance For Children And Pregnant Women, Part Iii, Including 42 Independently Identified Positions.. Kit For Rapid (Up To 30 Minutes) Extraction Of Dna From Whole Blood, Serum, Plasma, Body Fluids, Amniocytes, Chorion, Buccal Mucosa And Viral Dna - For Samples Up To 200 Ul, Column-Operated. Complete With All Reagents And Consumables.,Kit For Enzymatic Purification Of Pcr Product For Sequencing Containing Exonuclease I And Shrimp Alkaline Phosphatase,Kit For Dna Sequencing Of Pcr Products (Including 5050 Heterozygous), Single-Stranded Dna, Bacterial Genomic Dna, Plasmid Dna (≤15Kb) And Others Based On Dideoxynucleotides Labeled With Fluorescent Dyes.,5 X Seq Buffer For Abi 3130/3130 Xl Compatible With Position 3 Kit For Dna Sequencing Of Pcr Products (Including 5050 Heterozygous), Single-Stranded Dna, Bacterial Genomic Dna, Plasmid Dna (≤15Kb) And Others Based On Fluorescent Dye-Labeled Dideoxynucleotides,Kit For The Determination Of Deletions And Duplications In The Atp7b Gene Of Patients With Wilsons Disease By The Mlpa Method,Kit For Determination Of Deletions And Duplications In Pmp22, Gjb1 And Mpz Genes By Mlpa Method,Kit For Detection Of Large Deletions In Cyp21a2. Additional Determination Of Mutations In Cyp21a2p, Tnxb And Atf6b Genes By Mlpa Method,Kit For Detection Of Deletions And Duplications In Chromosomal Regions 1P36, 3P22/3P21.3 And 11Q23a By Mlpa Method,Kit For Detection Of Deletions And Duplications In Chromosomal Regions 2P24.1/Mycn, 2Q33 And 17P13/Tp53 And 17Q By Mlpa Method,Kit For Detection Of Deletions And Duplications In Chromosomes 4, 7, 9, 12 And 14 By Mlpa Method,Kit To Diagnose Expansion Of Cgg Repeats Within The Fmr1 Gene. Pcr Based With Triple Primer Repeat Reaction (Tp-Pcr) And Determination Of Fragment Sizes By Capillary Electrophoresis.,Set Of Reagents For Isolation Of Nucleic Acids From Blood With Magnetic Particles.,Dna Microarray Kit For The Detection Of Copy Number Changes And Single Nucleotide Polymorphisms (Snps) With High Resolution - Up To 2.5 Mb In Autosomal Chromosomes For The Study Of Loss Of Heterozygosity (Loh) And Compatible Products,Human Exome Sequencing Kit, Including A Panel Of Primers For Whole Human Exome Sequencing, Containing Oligo Probes For Library Enrichment, With No Less Than 99.1% Coverage Against Reference Human Genomic Databases – Refseq, Ccds, Clinvar And Acmg Pathogenic/Likely Pathogenic Variants, Cosmic Cancer Gene Census, Omim At No Less Than 37Mb Maximum Genomic Content.,A Complete Set Of Reagents And Consumables For Library Preparation And Whole Human Genome Sequencing, By Pcr-Free Protocol For Library Preparation, Using The Principle Of Tagging By Transpososomes Linked To Microparticles And Ensuring Unification Of The Obtained Fragments, Uniform Coverage, Reduction Of The Probability Of Errors Regardless Of The Concentration Of The Starting Dna.,Molecular Marker Of Dna Fragments With A Size Of 50 To 1000 Bases (From 50 To 300 Bases Via 50 Bases And From 300 To 1000 Via 100 Bases) Concentration (0.1 Μg/Μl),Nucleotides 100 Mm Each (Datp, Dctp, Dgtp, Dttp) Pack 250 Microliters For Each Nucleotide,Optimized Polymer (Pop7), Suitable For 24-Capillary Genetic Analyzer Model 3500 Xl Applied Biosystems, 384 Reactions/Op.,Anode Buffer Container Ready To Use, Suitable For 24-Capillary Genetic Analyzer Model 3500 Xl Applied Biosystems, 4 Pieces/Pack.,Ready-To-Use Cathode Buffer Container Suitable For Applied Biosystems 24-Capillary Genetic Analyzer Model 3500Xl, 4 Pcs/Pack.,Primers 2
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