Sentence examples for mab it from inspiring English sources

Exact(11)

Hence, for an objective assessment of the number of dyes on e.g. a monoclonal antibody (mAb) it is key that authors, in addition to the above features, provide an absorbance spectrum of their compound in the formulation that is applied to patients.

Furthermore, by using a blocking mAb it was possible to directly compare the relative avidities of the two TCRs [21].

Regarding glycan microheterogeneity, which is known to contribute to the correct folding and stability of a mAb, it was analyzed by CZE and HILI-UPLC.

As the clonogenic growth of XG11 was inhibited, although only partially, by the anti-IGF1R mAb, it is possible that IGF1R signaling occurred despite the expression of CD45.

Because belimumab is a fully human mAb, it is expected that patients are less likely to develop immune responses and hypersensitivity reactions.

Thus, based on our data with the 123C3 mAb, it is conceivable that the specific inhibition of the NCAM/FGFR interaction contributes to counteract EOC dissemination and recurrence.

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Similar(49)

Although conjugation of this ICG dye to proteins appeared facile, a serious loss of fluorescence was observed upon binding to a protein [22]; albeit with internalizing mAbs, it might still be applicable [23].

Since mAb 1EB12 has a much stronger reactivity to endogenous EBNA1 compared to the rest of the mAbs while the reactivity to E. coli-expressed EBNA1 is similar to the rest of the mAbs, it is possible that the modification of these arginine residues increases the affinity of mAb 1EB12 for its epitope.

Since we are studying MAbs, it is important to realize that particular antibodies are often selected for further study based on characteristics such as strength of binding, isotype or epitope, and thus the data set is not random with respect to these parameters.

In contrast, with Bi-labelled anti-CD33-mAb it was possible to induce a reduction of bone marrow blasts with tolerable haematological toxicity [ 27].

Although 2D7 and PA14/PRO 140 are both potent HIV-inhibitory mAbs, it is interesting that there is a lack of synergy between PA14 and 2D7 in inhibiting HIV-1 viral fusion to the host cells.

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