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This enzyme catalyzes the final step in methionine biosynthesis. MTR mutations have been identified as an underlying cause of methylcobalamin deficiency complementation group G. Principle Names - MTR; 5-methyltetrahydrofolate-homocysteine methyltransferase methionine synthase
Our Abpromise guarantee covers the use of ab9209 in the following tested applications.
|WB||Use a concentration of 1 - 3 µg/ml. Detects a band of approximately 150 kDa (predicted molecular weight: 150 kDa).Can be blocked with Human MTR peptide (ab23154).|
|IHC-P||Use a concentration of 3 - 5 µg/ml. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.|
9209 (3.8µg/ml) staining of paraffin embedded Human Adrenal Gland following Steamed antigen retrieval with citrate buffer pH 6 and AP-staining shows cytoplasm staining in the cortex.
Goat polyclonal to MTR (2