The phrase "assembly assay" is correct and usable in written English.
It can be used in scientific or technical contexts, particularly in biology or chemistry, to refer to a test or analysis that evaluates the assembly of components, such as proteins or nucleic acids.
Example: "The researchers conducted an assembly assay to determine the efficiency of the protein complex formation."
Alternatives: "assembly test" or "assembly analysis".
DOI: http://dx.doi.org/10.7554/eLife.04234.003 Initially we tested whether EspP(46+β) would assemble in vitro using a previously described OM protein assembly assay (Hagan et al., 2010).
In particular, tubulin assembly assay and immunofluorescence analysis results are reported.
Here we describe how to use the pyrene actin assembly assay to determine the effect of a protein on the kinetics of actin assembly, either directly or as mediated by proteins such as nucleation or capping factors.
The pyrene actin assembly assay is a powerful tool for determining the effect of a protein on the kinetics of actin assembly, either directly or as mediated by proteins such as nucleators or capping factors.
This series was identified using a previously described capsid (CA) assembly assay, employing a recombinant HIV-1 CA-NC protein and immobilized TG-rich deoxyoligonucleotides.
Our in vitro assembly assay provides an easy and efficient means of screening for assembly inhibitors, and we have identified several inhibitory peptides that could represent a starting point for drug design.
Using in vitro Sm core assembly assays, we found that lowering the intracellular amounts of Gemin3 by either poliovirus infection or small interfering RNA (siRNA -mediated knockdown of Gemin3 resiRNA -mediateded assembly of U snRNPs.
Similar in vitro assembly assays showed that CCMV CP subunits also packaged BMV RNAs lacking 3′ TLS as well as two other non-bromoviral RNAs although with lesser efficiency.
Actin assembly assays using 5% pyrene actin were performed as previously reported [48].
Clones expressing FLNa, FLNaΔ3, or vector control (FLNa-) were examined in matrix assembly assays as previously described [15], [28].
In vitro assembly assays also have shown that concentrations of αB crystallin exceeding that of tubulin inhibited microtubule assembly [15], [27].
