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However, phages capable of broadly controlling the LAB populations present specifically in ethanol fermentation facilities have not been described.
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Development of vaccines capable of eliciting broadly neutralizing antibodies (bNAbs) is a key goal to controlling the global AIDS epidemic.
Alternative antigens relying on the N-terminal region of minor capsid protein L2 are intrinsically less immunogenic but capable of eliciting broadly neutralizing responses.
The identification of conserved antigen mimics may lead to novel immunogens capable of inducing broadly reactive nAbs.
Stimulating the humoral arms of the host immune response and designing immunogens capable of eliciting broadly neutralizing antibodies (BNAbs) is a paramount goal for AIDS vaccine development [1].
As far as the latter point is concerned, this result is possible if new immunogens are designed, capable of eliciting broadly reacting and neutralizing antibodies.
Whilst this demonstrates that our methodology is capable of producing broadly accurate predictions of mass properties in extant taxa with known morphology, it is again important to emphasize that this fact alone does not alter (i.e. enhance) the reliability of any single volumetric model of an extinct animal with unknown soft tissue morphology.
The identification of these MAbs, directed against epitopes in the CD4-binding region, a mannose epitope on the glycosylated surface of gp120, and the membrane-proximal region of gp41 [18] demonstrates that some patients have B cell clones capable of making broadly neutralizing Abs.
Ideally a potent T-cell vaccine would be combined with an antigen capable of generating broadly cross-reactive neutralising antibodies against HCV envelope.
However all vaccines tested to date have not been capable of stimulating a broadly neutralizing immune response, the induced protection being limited only to a minor subset of neutralization-sensitive HIV-1 isolates [6] [11].
Our efforts demonstrate FDTD to be a broadly applicable technique capable of guiding design of an optimal DSC architecture.
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CEO of Professional Science Editing for Scientists @ prosciediting.com