Modifying the Glycocalyx of Melanoma Cells via Metabolic Glycoengineering Using <i>N</i>-Acetyl-d-glucosamine Analogues.

(b) In the second group, we observed a similar reduction concerning the binding affinity of 4- O Me-Glc N Al 2 compared to Glc N Al 1 and the control for lectins such as PSA, PNA, GNA, HHA, BPA, HPA, WFA, MPA, MAA, SNA, and PHA-E; however, based on the variances, this did not reach statistical significance ( Figure 6 C).

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