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PhenoVue Fluor - Rat anti-Mouse IgG Isotype Specific Antibody Conjugates
This is a product information sheet for PhenoVue Fluor - Rat anti-mouse IgG isotype specific antibody conjugates. View validation data, product information, protocols, and more.
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PhenoVue anti-MAP2 Antibody
This is a product information sheet for PhenoVue anti-MAP2 antibody. View validation data, product information, protocols, and more.
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PhenoVue anti-Tubulin Antibody Product Information Sheet
This is a product information sheet for PhenoVue anti-tubulin antibody. View validation data, product information, protocols, and more.
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Liquid Scintillation Counting with Confidence
Liquid scintillation cocktails with trusted NEN® Radiochemicals, high-quality counting vials, consumables and market-leading radiometric detection instrumentation offering your complete single-source solution for your radiometric application needs.
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PhenoVue Fluo-4 AM, Calcium Indicator Product Sheet
Product Information Sheet for PhenoVue Fluo-4 AM, Calcium Indicator
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Whole genome sequencing is a powerful “one-stop shop” screening assay for uncovering undiagnosed conditions in apparently healthy pediatric cohort
This abstract indicates that WGS screening can serve as a “one-stop shop” for uncovering a wide range of looming genetic conditions in apparently healthy children, this way enabling the family and treating clinicians to take timely appropriate actions to maximize their healthcare outcomes and inform future reproductive decisions.
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Cellometer Ascend automated cell counter brochure
Brochure describing the Cellometer Ascend automated cell counter.
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Development of a Hemolysis Index for Vanadis® cfDNA NIPT Sample Acceptance
Investigating samples that are below 1% hemolysis does not affect the accuracy of Vanadis® cfDNA NIPT results. Either spectrophotometry or a color comparison chart can be used to preferentially remove those samples that are highly hemolyzed from the workflow.
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Importance of parental segregation studies and its role in variant classification
This poster highlights importance of parental segregation. Analysis helps to verify the phasing of the causative variants, to verify the de novo occurrences thereby aiding reclassification of the reported variants. Parental analysis post proband testing to better understand complex genetic variations.
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Genetic Screening of a Reportedly Healthy Population for Familial Hypercholesterolemia, Hereditary Breast and Ovarian cancer syndrome, and Lynch syndrome
This poster highlights the benefits of healthy population screening for the conditions like Familial Hypercholesterolemia, Hereditary Breast and Ovarian cancer syndrome, and Lynch syndrome
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Unparalleled power of genome sequencing in screening ostensibly healthy newborns and children: findings from the first real-world dataset
This poster concludes that ostensibly healthy babies are at-risk for pediatric onset mendelian condition. Majority of the GS findings are likely to influence healthcare management of babies at risk, and provide valuable information for other family members.
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SampleSheet Generation for PGSeq Rapid v2_12NT Instructions
These instructions describe the process to prepare Illumina sample sheets for sequencing with the 12NT PG-seq primers.
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