DIVERSITY NAVIGATOR

Reagents for use in genetic, medical and scientific analysis and research, namely analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases; assays and kits comprised primarily of reagents, with or without reagent carriers, for use in genetic, medical and scientific analysis and research for analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases; reagents for use in medical research, namely analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases; assays and kits comprised primarily of reagents, with or without reagent carriers, for use in medical research for analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases

Reagents consisting of fluorescent labeled polynucleotide sequences for detection of genetic materials, for clinical or medical laboratory use; reagents for use in medical analysis, namely analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases; assays and kits comprised primarily of reagents, with or without reagent carriers, for use in medical analysis for analyzing, detecting, quantifying and sequencing polypeptides and polynucleotides, including polypeptide variants, polynucleotide variants, genetic mutations, single nucleotide polymorphisms, haplotypes and heterozygosity and for use in identifying diseases