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While previous B12 analytical methods commonly employed cyanidation conversion to reduce analyte complexity, increase analyte concentrations, and improve analyte stability, the present study revealed limitations associated with this approach

HETEROLOGOUS EXPRESSION OF AsGGT1, AsGGT2, AND AsGGT3 IN YEAST The coding regions of AsGGT1 , AsGGT2 , and AsGGT3 were amplified by PCR using the cloned cDNA fragments described above, KOD plus DNA polymerase (Toyobo), and the following gene-specific primers: AsGGT1-FKpn3A (5- GGTACC AAAATGAACCAAATGGCGCCGGCTTC-3) and AsGGT1-stop-RXh (5- CTCGAG CTATACACAAGCAGGACTTC CATC-3) for AsGGT1

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The histological analysis of naive mouse models treated with 300 mg/kg of green tea extract consistently demonstrated a gradual restoration of the Purkinje layer and cells

Erratum in: JMIR Mhealth Uhealth