The phrase "assay speed" is correct and usable in written English.
It can be used in contexts related to scientific testing or analysis, particularly in laboratories where the speed of conducting assays is relevant.
Example: "The researchers were pleased to report a significant increase in assay speed, allowing for quicker results in their experiments."
Alternatives: "testing speed" or "analysis speed".
This is because current assays, such as TaqMan®, are limited, in terms of assay speed, by the 5′ 3′ exonuclease activity of Taq DNA polymerase.
Compared with those methods mentioned above, the chemiluminescence CL) method has been growing in popularity and acceptance because of its advantages such as high sensitivity, rapid assay speed and simple instrumentation.
Assay speed, simplicity, sensitivity, and cost significantly impacts the effectiveness of biomarker validation.
We measured pFR and speed at the earliest time point of the assay (speed at 0.18 sec) of these NILs.
In order to compare the assay speed and robustness, the Tt value is converted to minutes by 1 Tt = 2 minutes.
Through continued future development with more hydrophilic and cleavable cross-linkers such as DHEBA, with the effective separation and probing initially demonstrated here, we plan to further push the bounds of sample molecular weight, sensitivity, and assay speed.
A new DNA line probe assay (Speed-oligo Mycobacteria, Vircell) has been launched for rapid differentiation of Mycobacterium spp. from cultures.
Compared to other line-probe assays, Speed-oligo Mycobacteria covers a relatively limited spectrum of species but uses a simpler and faster dip-stick technique.
Compared to other line-probe assays, Speed-oligo Mycobacteria differentiates most of the species only to a level of complexes or groups.
The advantage of this type of assay is speed and ease of quantitative determination.
The BD GeneOhm™ MRSA assay's speed (amplification time of 2 h versus 36 48 h for the culture method) gives it a critical advantage.
