nerobrowser.blogg.se - Massarray agena

#Massarray agena manual#
#Massarray agena pro#
#Massarray agena plus#

#Massarray agena pro#

iPLEX Pro Sample ID Panel (44 SNPs and 3 gender markers generate unique genetic fingerprint).42 antigens in 12 blood group systems and 3 beta globin markers.Ready-to-use genotyping assays for extended antigen typing of erythrocytes, platelets, and neutrophils.49 variants with known CFTR relevance and allele frequency >0.1%.23 mutations recommended by ACMG and ACOG.Cost-Effective Solution to detect 74 of the most common variants of the CFTR gene.CFTR Panel - targeted Cystic Fibrosis Mutation Analysis.Designed to be tolerant to low quality DNA, suitable for challenging samples.

#Massarray agena plus#

Interrogates 68 SNPs/INDELs across 20 genes, plus 5 CNVs targets in CYP2D6.Targets the most relevant variants in 20 principal genes implicated in drug metabolism pathways.This panel can be combined with genotyping panels using the same workflow.Interrogates 22 points in 7 regions of across the CYP2D6 gene.Provides accurate detection of CYP2D6 hybrid alleles.96- and 384-well formats offer the flexibility to generate results from 10s to 1000s of samples a day.Simultaneous testing of key pharmacogenetic SNPs, INDELs, and CNVs in a single reaction.OncoFOCUS Panel (detection of over 200 variants across BRAF, EGFR, KIT, KRAS and NRAS).LungFUSION Panel (fusion detection of NSCLC across ALK, RET, and ROS1).From samples including formalin-fixed tissue, fine needle aspirates, core needle biopsies, smears.Highly sensitive detection of somatic mutations as low as 1% allele frequency.iPLEX HS Melanoma Panel (over 90 variants from BRAF, KIT, NRAS, TERT genes).iPLEX HS Lung Panel (70 variants across BRAF, EGFR, ERBB2, KRAS, and PIK3CA genes).iPLEX HS Colon Panel (80 variants across BRAF, EGFR, KRAS, NRAS and PIK3CA genes).Ultrasensitive - Indentify variants at as low as 0.1% variant allele frequency.UltraSEEK EGFR Panel (detection of 6 variants, incl.UltraSEEK Melanoma Panel (more than 55 variants across 13 genes including BRAF, KIT and NRAS).UltraSEEK Lung Panel (over 70 variants across BRAF, EGFR, ERBB2, KRAS and PIK3CA genes).UltraSEEK Colon Panel (over 100 variants across BRAF, EGFR, KRAS, NRAS and PIK3CA genes).Beginning with extracted DNA, multiplexed PCR reactions are followed by extension reactions analyte is then dispensed onto a SpectroCHIP Array for detection on the MassARRAY Analyzer 4. The MassARRAY process enables sample-to-answer testing with minimal hands-on time in a single eight-hour work shift. Online design tools enable you to design custom assays.Provides interactive visualization of the data for results management and reporting.Flexible and robust tools for the creation and analysis of new test methods.MassARRAY Dx provides clinically actionable mutation reports.MassARRAY Dx - CE-IVD marked genetic analysis system.Mature and well-proven MALDI-TOF technology provides high-quality data.Maximizes laboratory resources with rapid turnaround time.Powered by sensitive and accurate mass-based detection.Multiplexed analysis of up to hundreds of clinically relevant mutations in a single workflow.MassARRAY Analyzer 4 / MassARRAY Dx Analyzer 4

#Massarray agena manual#

Reduces the risk of contamination associated with manual handling.

Chip prep module minimizes hands on time.

Ability to automatically process up to two multiplexed 96-, or 384-pad per run.

MassCLEAVE chemistries are for quantification of methylation changes with limit of detection 5%.

Suitable for degraded or low quality samples from FFPE, FNA, or plasma.

Efficiently multiplex variants, including SNPs, indels, somatic mutations and CNV’s in the same reaction.

Suitable for standard germline genotypes to rare somatic variants.

Compatible with a broad range of nucleic acid biomarkers.

Simple PCR-based iPLEX, UltraSEEK or MassCLEAVE chemistries.

Ideal for targeted genetic analysis including.

Direct detection of short amplicons enables compatibility with all nucleic acid sample types.

A new Chip prep module provides post-PCR automation.

Efficient Workflow Obtain results in a single day with limited hands-on time.

A system set up for 96- and/or 384-well format of samples and assay throughput.

Highly accurate alternative to fluorescent-based methods.

Nucleic acid detection by mass spectrometry enables readout by molecular mass.

Testing Rare Blood Donor Identification.

Sample Identification and Qualification.

System is a complete genomic solution for molecular laboratories. With throughput capacity to meet the needs of any testing volume, rapid results, and the ability to cost-effectively target hundreds of genetic mutations. The MassARRAY System is a benchtop MALDI-TOF mass spectrometer that provides sensitive, accurate, and rapid analysis of nucleic acid samples.