Sentence examples for binding we produced a from inspiring English sources

To investigate the involvement of the SOCS box of Rab40C in Varp binding, we produced a SOCS box deletion mutant, named Rab40C-ΔSOCS, and evaluated its Varp binding ability by co-immunoprecipitation assays as described above.

Taking advantage of this laminin-binding domain of NtA, we produced a tripartite fusion protein to obtain laminin binding NGF-β which contains (i) the primary sequence of the mature NGF-β, (ii) NtA as a laminin-binding domain, and (iii) a 6×histidine (His) purification tag.

From these, and using binding proteins from literature, we produced a Meq interactome model.

Here we produced a collagen-binding VEGF by fusing a collagen-binding domain to the N-terminal of native VEGF.

To confirm the role of piRNAs in the binding of Aub to maternal mRNAs, we produced a mutant form of Aub unable to load piRNAs.

To evaluate whether Che-1 phosphorylation is required for its binding to p53, we produced an anti-phospho-specific peptide antiserum directed against the phosphorylated Ser474 of Che-1, a Chk2 phosphorylation site.

To test whether the C-terminal U4/U6 di-snRNA-binding region is conserved in yPrp3, we produced a protein comprising the 177 C-terminal residues of yPrp3 (residue 296 469; yPrp3CTF).

Inclusion of SMAD1 binding along with TAL1 and GATA1 binding produced a success rate of 71% in our transfection assays.

In contrast, for fhlA53 binding to Hfq, only one of the binding interactions produced a KD comparable to that observed with fhlA220.

In addition to being a Fn-binding protein, we produced evidence (cell surface location and blocking of bacterial binding to Fn by an antiserum to PM1665) that PM1665 is likely to function as a bacterial adhesin.

When probed with a HRP-labeled secondary antibody (against primary antibody), unoccupied binding sites produced an insoluble film, leading to high RCT observed with EIS.