epitope mapping within an internal region of HEMK2 of human origin
recommended for detection of HEMK2 of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
HEMK2 Background Information HEMK2 (HemK methyltransferase family member 2), also known as N6AMT1 (N-6 adenine-specific DNA methyltransferase 1), MTQ2 or N6AMT, is a 214 amino acid protein that belongs to the methyltransferase superfamily and exists as multiple alternatively spliced isoforms. The gene encoding HEMK2 maps to human chromosome 21, which houses approximately 300 genes and comprises nearly 1.5% of the human genome. Chromosome 21-associated disorders include Alzheimer's disease, amyotrophic lateral sclerosis and, most notably, Down syndrome (also known as trisomy 21).
HEMK2 (S-17)
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HEMK2 (S-17): sc-83305. Western blot analysis of HEMK2 expression in mouse brain tissue extract.
