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Description
This compound was originally isolated from meat
This process is essential for the regulation of gene expression, particularly in the context of pain signaling pathways
Faber, 2010)
Tissues were sliced using a rotary microtome and stained with hematoxylin and eosin (H&E)
Standard assays containing 0.2 M MSA-DH or MDH in 300 L buffer 1 containing 20 mM NAD(P) + were performed in the presence of 0.512 or 20 mM of the respective substrate MSA or D-malate
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