Molecular Genetics
Filtrar los productos
Marcas
Ver todas las marcas
Tecnologías
Ver todas las tecnologías
Molecular Genetics
Marcas
Ver todas las marcas
Tecnologías
Ver todas las tecnologías
Productos de Molecular Genetics
Adellgene® Fragile X
Kit for the determination of healthy, premutation and mutant alleles in the FMR1 gene by fluorescent fragment analysis
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® Fragile X Screening
Kit for the determination of healthy and premutation alleles in the FMR1 gene by fluorescent fragment analysis
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® Friedreich’s Ataxia
NGS assay to study 28 genes commonly associated with solid tumor type cancers from circulating cell-free tumor DNA (ccfDNA/cfDNA/ctDNA).
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® Huntington Disease
Kit for the determination of the CAG triplet repeats number of the HTT gene by fluorescent fragment analysis
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® Myotonic Dystrophy Confirmatory
Kit for the determination of the CTG triplet repeats number of the DMPK gene by fluorescent fragment analysis
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® Myotonic Dystrophy Screening
Kit for the determination of the CTG triplet repeats number of the DMPK gene by fluorescent fragment analysis
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Adellgene® SCAs
NGS assays associated with solid tumors
Blackhills Diagnostic Resources
Molecular Genetics
Fragment Analysis
Aneuploidy Kits – QST*R
Analyses STR markers to diagnose aneuploidy
Cardio Solution (CAS and CAS extended)
Study of genes associated with heart diseases.
Clinical Exome Solution (CES v3)
Analysis of 4,728 genes related to rare and hereditary disorders.
Cystic Fibrosis – CF-EU2
Qualitative in vitro detection of the 50 most common human CFTR gene mutations in the European population.
Cystic Fibrosis – Iberian Panel
Qualtative detection and idenetification of 12 aditional mutations within the CFTR gene in a single reaction.
DUPLICA REAL TIME Trombofilias
Detección de mutaciones relacionadas con trombofilias a partir de ADN obtenido de muestras clínicas de sangre periférica recogidas en EDTA
ERT (Endometrial Receptivity Test)
Endometrial Receptivity Test to improve the clinical pregnancy of IVF-ET (In vitro Fertilization & Embryo Transfer).
Yikon Genomics
Molecular Genetics
Next Generation Sequencing (NGS)
Fibrosis Quística – CF-EU2
Detección cualitativa in vitro de las 50 mutaciones del gen humano CFTR más comunes en población europea
Fibrosis Quística – Panel Ibérico
Detección cualitativa e identificación de 12 mutaciones adicionales en el gen CFTR en una sola reacción de PCR.
Free DNA Fetal Kit® RhD
Genotyping fetal RhD maternal blood samples.
Institute of Biotechnologies Jacques Boy
Fetal RhD
RT-PCR
Genvinset® Diabetes Mellitus T1
Kit for detecting HLA-DRB1*03, DRB1*04, DQB1*02:01 and DQB1*03:02 alleles by Real Time PCR using TaqMan® probes technology
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® Factor II G20210A
Kit for detecting the G20210A mutation of the prothrombin gene by Real Time PCR using TaqMan® probes technology Information about the product Prothrombin (Factor II) is a glycoprotein generated in liver. It is an essential component of the blood-clotting mechanism. The regulation of the prothrombin expression is crucial for the homeostasis maintenance. The G20210A mutation of Factor…
Blackhills Diagnostic Resources
Hematology and blood bank
RT-PCR
Genvinset® Factor V G1691A
Kit for detecting the G1691A mutation of the Factor V (FV) gene by Real Time PCR using TaqMan® probes technology Information about the product The Factor V Leiden is a variant of the Factor V of human coagulation. It has an important role in the coagulation cascade. The mutation G1691A is the most common hereditary…
Blackhills Diagnostic Resources
Hematology and blood bank
RT-PCR
Genvinset® HFE C282Y
Kit for detecting the C282Y mutation of HFE gene by Real Time PCR using TaqMan® probes technology Information about the product Hereditary hemochromatosis (HH) is an autosomal recessive inherited disorder of iron metabolism. Due to excessive intestinal absorption, iron accumulates in the parenchymal cells of the liver, pancreas, heart and other organs resulting in damage to its…
Blackhills Diagnostic Resources
Hematology and blood bank
RT-PCR
Genvinset® HFE H63D
Kit for detecting the H63D mutation of HFE gene by Real Time PCR using TaqMan® probes technology Information about the product Hereditary hemochromatosis (HH) is an autosomal recessive inherited disorder of iron metabolism. Due to excessive intestinal absorption, iron accumulates in the parenchymal cells of the liver, pancreas, heart and other organs resulting in damage to its…
Thrombophilias and hemochromatosis
Genvinset® HFE S65C
Kit for detecting the S65C mutation of HFE gene by Real Time PCR using TaqMan® probes technology Information about the product Hereditary hemochromatosis (HH) is an autosomal recessive inherited disorder of iron metabolism. Due to excessive intestinal absorption, iron accumulates in the parenchymal cells of the liver, pancreas, heart and other organs resulting in damage to its…
Blackhills Diagnostic Resources
Hematology and blood bank
RT-PCR
Genvinset® HLA A29
GENVINSET HLA-A29 detects HLA-A29 group of allelesby real time PCR
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® HLA B27v5
Kit for detecting HLA-B*27 alleles by Real time PCR using TaqMan® probes technology Information about the product The major histocompatibility complex (MHC) is the genetic region that contains the most polymorphic loci of the human genome. It is involved in the mechanism of antigen presentation and, as such, defines the general immunological response. Within the MHC,…
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® HLA B57v5
Kit for detecting the HLA-B*57:01 alleles by Real-Time PCR using TaqMan® probes technology Information about the product Abacavir sulfate is a synthetic carboxylic nucleoside drug, which works as a reverse transcriptase inhibitor and is used to treat HIV (Human Immunodeficiency Virus). This drug has been associated with the occurrence of fatal hypersensitivity reaction with symptoms…
Blackhills Diagnostic Resources
Immunology and transplantation
RT-PCR
Genvinset® HLA Behçet v5
Kit for detecting the HLA-B*51 and B*52 alleles by Real-Time PCR using TaqMan® probes technology
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® HLA C*06
Kit for detecting the HLA-C*06 alleles by Real Time PCR using TaqMan® probes technology Information about the product Psoriasis vulgaris is a chronic inflammatory disease of skin, which affects 2% of world population. The cutaneous manifestations of psoriasis are obvious and have a negative impact on quality of life of patients. Family studies have demonstrated…
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® HLA Celiac
Kit for detecting the HLA-DQB1*02, DQB1*03:02 and DQA1*05 alleles by Real Time PCR using TaqMan® probes technology
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR
Genvinset® HLA Celiac Plus
Kit para la detección de los alelos HLA-DQB1*02, DQB1*03:02, DQA1*05 y DQA1*03 mediante PCR en tiempo real, Kit for detecting the HLA-DQB1*02, DQB1*03:02, DQA1*05 and DQA1*03 alleles by Real Time PCR using TaqMan® probes technology Information about the product Susceptibility to gluten sensitivity is, in part, genetically determined. The strong predisposition is associated with HLA-DQ…
Blackhills Diagnostic Resources
HLA associated diseases
RT-PCR