Since N-terminal sequences of AsGGT1, AsGGT2, and AsGGT3 are long and may contain the signal sequence for secretion or targeting to cellular organelles, three types of fusion proteins, GFP C-terminally fused to the N-terminal 100-amino acid residues of GGT (AsGGT1 N100 -GFP, AsGGT2 N100 -GFP, and AsGGT3 N100 -GFP), GFP C-terminally fused to the N-terminal 300-amino acid residues of GGT (AsGGT1 N300 -GFP, AsGGT2 N300 -GFP, and AsGGT3 N300 -GFP), and GFP C-terminally fused to the full-length GGT protein (AsGGT1 Full -GFP, AsGGT2 Full -GFP, and AsGGT3 Full -GFP), were analyzed
doi:10.1038/aja.2010.183
Thus, in a nutshell, it is possible that the initial DNA damage that predisposes melanocytes to malignant transformation and cytogenetic alterations that later promote actual malignant transformation of the initially transformed melanocytes may be driven by dysregulation in melanin biosynthesis and by the increased cellular content of melanin [10]
Yes, in the practical sense: you enter your reconstitution volume so the calculator can work out concentration (mcg/mL)