Sentence examples for fundamental assay from inspiring English sources

Assays were run on an automated Luminex MAP™ platform at the Myriad RBM CLIA certified lab and validated for the fundamental assay parameters of least detectable dose (LDD), lower limit of quantitation (LLO Q, spike recovery, linearity, precision and sample stability.

The technique described herein provides a robust tool developed from coupling two fundamental assays for investigating the effects of various metabolites, reagents, ligands, and substrates on the mechanisms of Ca2+ sequestration within the ER.

High purity isolations are also significant in -omic analyses (e.g., genomics and proteomics), and fundamental biological assays as nontarget cells result in unwanted background noise or interference.

This inherent limitation is also true of other fundamental biological assays based on lysed cells, where the binding chemistries cause interference in the analyses.

The preferred devices for most fundamental biological assays, including proteomics and genomics, are label-free to minimize labeling interference, but in -omic analysis, because cells can be lysed after purification, magnetic bead labels can be easily separated from the lysate.

This process is fundamental to various assays of DNA breaks that are described in this review.

The demonstrated fidelity of the system opens the doors to the use of this recombinantly produced protein in a wide variety of fundamental and applied assays, offering tunable control over molecular parameters not accessible in tissue-derived samples.

The ability to perform these highly parallel genomic assays depends on two fundamental characteristics of the assays: a highly parallel array based read-out and an intrinsically scalable multiplexing sample preparation.

It is therefore fundamental to develop an assay that is faster and more sensitive than the traditional bacterial culturing method for the detection of the pathogen in the food matrix.

Regardless of the target, the robustness of the HTS assay is fundamental for success.

The fundamental principle of this assay is that DNA damage will impede the progression of the DNA polymerase used in the PCR reactions [ 38, 39].