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This library does not have an accompanying peer-reviewed publication.
While this library does not include as many features as more full-featured applications such as Jmol, this library is relatively small (≈ 75 kb) and can easily be extended to provide a range of capabilities.
In the original CXCR3-B publication, the authors describe that they identified a clone in a leukocyte cDNA library that showed complete homology with CXCR3-B, but this library does not seem to be available on-line anymore.
This library does not contain any migrastatin-family compounds.
A focus on known MDR substrates in this library does not indicate a consistent pattern of relative resistance based on the presence of oncogenic β-catenin.
Note that this library does not contain the native antigen ADP3 nor compounds in which the critical Npip and Nlys side chains are spaced in the same way as ADP3.
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About 19.5% of the ESTs resulting from this library did not have any significant homology to any of the proteins existing in the database.
Screening this library did not identify any two-fragment IFP that retained fluorescence, suggesting that the IFP structure is easily disrupted by fragmentation.
The top protein matches range between 50 to over 500 amino acids in length and would thus indicate that the predicted open reading frame generated from this library did not have any bias towards long or short protein sequences (Table 1).
Still, the library does attract visitors to its quarters.
Although the library does not plan to bid at Doyle, he added, "It's good to know about this stuff".
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com