The phrase "assay circle" is not a commonly recognized expression in written English, and its meaning may not be clear without context.
It could potentially be used in a scientific or technical context related to assays, but clarity would depend on the surrounding text.
Example: "The researchers gathered around the assay circle to discuss the results of their experiments."
Alternatives: "testing group" or "analysis circle".
To determine if ceob2 mutant worms exhibited increased levels of C-circles, we modified the existing C-circle assay protocol for the use with C. elegans telomeric DNA and examined the levels of C-circles in wild-type (wt) N2 strains and ceob2 mutant strains.
Enzyme solutions were incubated at 60°C for indicated time periods and residual activities were determined under the standard assay conditions (green circle).
Newborn screening for SCID using the T-cell receptor excision circle assay has revolutionized early identification of infants with SCID or severe T-cell lymphopenia.
Henson, J. D. et al. The C-Circle Assay for alternative-lengthening-of-telomeres activity.
C-circle assay was used to determine the prevalence of ALT in patient samples as previously described [ 11].
The B-cell kappa chain excision circle (KREC) assay, which is analogous to the TREC assay but for B-cells, has shown promise as an assay to detect infants with congenital agammaglobulinemia.
C-circles can be rapidly and quantitatively detected by an assay based on rolling circle amplification using Φ29 DNA polymerase (Henson et al, 2009).
After purification via two-step column chromatography, the in vitro activity of the wild-type and RifR mutant MTB RNAPs was assessed via rolling circle transcription assay.
We present this case to illustrate that patients with cDGS are at risk for nontuberculous mycobacterial infections and to discuss further antimicrobial prophylaxis prior to thymic transplantation.A 13-month old male was identified as T cell deficient by the T cell receptor excision circle (TREC) assay on newborn screening, and was subsequently confirmed to have cDGS.
For HTS, DNA was amplified by using a bacteriophage ϕ29 polymerase-based rolling circle amplification assay and random primers.
