PRODUCTS
Inverted Microscope for Assisted Reproduction
As the demand for the use of intracytoplasmic sperm injection (ICSI) in assisted reproductive technology (ART) applications has increased, so has the burden of the microscopy work it involves. Olympus’ IX73SC assisted reproduction microscope solution helps facilitate the ICSI workflow, improving the speed and efficiency of each procedure. Easy Oocyte Condition Checks through Spindle Visualization: Olympus’ observation method enables you to easily view the metaphase II (MII) spindle through the microscope oculars
CarrierScan – Expanded Carrier Screening
CarrierScan Assay is an innovative, comprehensive, and high-throughput microarray-based tool for the reliable and robust detection of sequence and structural variation for preconception expanded carrier screening research across a wide range of ethnicities. The unique feature of this tool is the ability to consolidate multiple copy number and genotyping tests into a single molecular assay. With simple data analysis and reporting software included in the complete solution, high-throughput molecular labs can generate all relevant carrier screening research data quickly. The complete CarrierScan Assay solution offers flexibility and scalability to meet the changing needs of high-throughput molecular research labs.
StemExpress
StemExpress is the leading Biospecimen Provider of human bone marrow, cord blood, peripheral blood, Leukopaks, Mobilized Leukopaks, maternal blood, disease state products, and primary cells.
Omega
Omega Bio-tek provide simple, rapid, and cost-effective DNA and RNA extraction kits compared to the most popular sources of nucleic acid purification methods.
CytoScan 750
CytoScan 750K Suite enables cytogenetic researchers to detect and analyze relevant chromosomal aberrations with confidence. CytoScan 750K Suite provides high-resolution coverage of cancer and constitutional genes of interest, along with high-density SNP coverage for loss of heterozygosity (LOH) detection.
Cytoscan HD
CytoScan HD Suite provides the broadest coverage and highest performance for detecting chromosomal aberrations. CytoScan HD Suite has greater than 99% sensitivity and can reliably detect 25-50kb copy number changes across the genome at high specificity with single-nucleotide polymorphism (SNP) allelic corroboration. With more than 2.6 million copy number markers, CytoScan HD Suite covers all OMIM™ and RefSeq genes.Our proprietary manufacturing technology produces arrays that are highly reproducible between each batch with no risk of probe dropout inherent in bead manufacturing techniques. Surpassing the limitations of current database curations, the whole-genome array ensures that novel findings can be catalogued for future discoveries and annotations, which are often missed by targeted designs
CarrierMax™ FMR1
The CarrierMax FMR1 Reagent Kit is used to detect the number of CGG repeats in the Fragile X Mental Retardation (FMR1) gene. This kit uses a dual PCR system combining full length and triplet primed PCR amplification (TP-PCR), followed by fragment analysis on the Applied Biosystems 3500/3500xL Genetic Analyzer or SeqStudio Genetic Analyzer, to accurately determine up to 200 CGG repeats and detect alleles that are >200 CGG repeats.
Cytoscan HT-CMA
The CytoScan HT-CMA assay enables cytogenetic researchers to detect and analyze relevant chromosomal aberrations with confidence. The assay provides high-resolution coverage of OMIM and DECIPHER genes, along with high-density SNP coverage for loss of heterozygosity (LOH) and UPD detection. The CytoScan HT-CMA assay also includes up to 178 relevant single nucleotide variants (SNV) and content for analysis of SMN1, which allows for consolidation of testing.
Sample storage, identification and handling
2D barcoded tubes, barcode readers, de-capping, capping and liquid handling equipment