Background:

This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme| also known as cobalamin-dependent methionine synthase| catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Classification:

Primary antibody

Alternative names:

METH

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human METH

Concentration:

1 mg/ml

Molecular weight:

139150

Applications:

WB

Storage:

-20°C for 1 year

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