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anti-Human MTR Antibodies:
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Human Polyclonal MTR Primary Antibody for ELISA, IHC - ABIN256634
Jiang, Hurt, Breen, Stabler, Allen, Orlicky, Maclean: Sex-specific dysregulation of cysteine oxidation and the methionine and folate cycles in female cystathionine gamma-lyase null mice: a serendipitous model of the methylfolate trap. in Biology open 2015
Show all 2 Pubmed References
MTHFR (show MTHFR Antibodies) A1298C and MS A2756G polymorphisms may be unrelated to male infertility.
The evaluation of genetic association showed that, MTHFR (show MTHFR Antibodies) C6877T (OR: 8.89, 95% CI: 2.01-39.40) and MTR A2756G (OR: 1.48, 95% CI: 1.09-2.00) polymorphisms associated with higher risk of CVD.
The MTR A2756G, MTRR (show MTRR Antibodies) A66G, MTHFR (show MTHFR Antibodies) C677T and MTHFR (show MTHFR Antibodies) A1298C polymorphisms were assessed. MTR A2756G, MTRR (show MTRR Antibodies) A66G, and MTHFR (show MTHFR Antibodies) C677T gene polymorphisms were associated with the risk of NSCL (show NHLH1 Antibodies)/P (all p < 0.05). Logistic regression analysis revealed that MTR A2756G, MTR RA66G, and MTHFR (show MTHFR Antibodies) C667T might increase the risk of Nonsyndromic Cleft Lip/Palate
we examined the association between methylenetetrahydrofolate reductase (MTHFR (show MTHFR Antibodies) C677T, rs1801133) and methionine synthase (MTR A2756G, rs1805087) polymorphisms and risk for thyroid and breast cancer. We found an association between MTHFR (show MTHFR Antibodies) C677T polymorphism and risks to both thyroid (OR = 2.50; 95%CI = 1.15-5.46; P = 0.02) and breast cancer (OR = 2.53; 95%CI = 1.08-5.93; P = 0.03).
the studied polymorphisms MTHFR (show MTHFR Antibodies) C677T (rs1801133) and MTR A2756G (rs1805087) do not contribute to genetic susceptibility to varicose veins in ethnical Russians.
Data suggest that the MTR-A2756G polymorphism is associated with male infertility risk.
MTR A2756G single nucleotide polymorphism is significantly associated with gastric cancer risk in Korea.
There was a significant positive correlation between serum concentrations of vitamin B12 (show NDUFB3 Antibodies) and regional GM (grey matter ) volume in APOE (show APOE Antibodies) epsilon4 carriers with AD but not in non-carriers.
According to our results, the MTR A2756G polymorphism was associated with the risk of retinoblastoma in Iranian patients.
MTR genetic polymorphisms are risk factor for predicting cardiovascular manifestations in Marfan syndrome.
These findings indicate that greater synthesis of phosphatidylcholine (show SGMS1 Antibodies) and antioxidants contribute to the better performance and immuno-metabolic status in methionine-supplemented cows.
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.
5-methyltetrahydrofolate-homocysteine methyltransferase 1
, cobalamin-dependent methionine synthase
, methionine synthase
, vitamin-B12 dependent methionine synthase
, 5-methyltetrahydrofolate--homocysteine methyltransferase