MTR is the enzyme 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.
MTR encodes the enzyme 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.
Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene.
The extent of this transcript is supported by transcript alignments.
Applications:Suitable for use in Western Blot.
Other applications not tested.
Recommended Dilution:Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：100ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by affinity chromatography.
Form：Supplied as a liquid in PBS, 2% sucrose, 0.09% sodium azide.
Specificity：Recognizes human MTR.
Isotype：IgG
Calc Applications Abbrev：WB
Calc Crossreactivity：Hu
Immunogen：Synthetic peptide corresponding to the C-terminal region of human MTR
