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Methylenetetrahydrofolate Reductase (NAD(P)H) (MTHFR) ELISA Kits

The protein encoded by MTHFR catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Additionally we are shipping MTHFR Antibodies (102) and MTHFR Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
MTHFR 17769 Q9WU20
MTHFR 4524 P42898
Anti-Rat MTHFR MTHFR 362657  
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Top MTHFR ELISA Kits at antibodies-online.com

Showing 8 out of 16 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 23.5 pg/mL 62.5-4000 pg/mL 96 Tests Log in to see 9 to 11 Days
$736.84
Details
Mouse 3.9 pg/mL 15.6-1000 pg/mL Typical standard curve 96 Tests Log in to see 11 to 13 Days
$910.56
Details
Pig 46.875 pg/mL 78.125-5000 pg/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Chicken 2.344 pg/mL 3.906-250 pg/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Monkey 46.875 pg/mL 78.125-5000 pg/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Rabbit 1.875 pg/mL 3.125-200 pg/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Guinea Pig 2.344 pg/mL 3.906-250 pg/mL   96 Tests Log in to see 8 to 9 Days
$715.00
Details
Cow
  96 Tests Log in to see 11 to 13 Days
$1,029.60
Details

More ELISA Kits for MTHFR Interaction Partners

Mouse (Murine) Methylenetetrahydrofolate Reductase (NAD(P)H) (MTHFR) interaction partners

  1. Study demonstrated that maternal MTHFR deficiency (i.e., in utero MTHFR deficiency) and early life exposure to vigabatrin separately and together alter the levels of proteins in the glutamatergic synapse

  2. Mildly hyperhomocysteinemic Mthfr+/- mice demonstrate reduced ganglion cell function, thinner NFL (show NEFL ELISA Kits), and mild vasculopathy by 24 weeks.

  3. DNA methylation (show HELLS ELISA Kits) patterns in undifferentiated spermatogonia are relatively stable in culture over time under conditions of altered methionine and MTHFR levels.

  4. Data from Mthfr knockout mice (in homozygous/heterozygous matings) suggest that maternal genotype contributes to sensitivity to arsenic as embryotoxin (i.e., genetic predisposition to fetal resorption/congenital malformation in arsenic poisoning).

  5. our results support an interaction between mild neonatal stress, the MTHFR genotype and sex

  6. investigation of Mthfr regulation in an in vivo mouse model revealed temporal- and tissue-specific regulation that supports important roles for MTHFR in the developing embryo, and in postnatal brain and male reproductive tissues

  7. A possible mechanism for the epigenetic involvement of Mthfr deficiency is proposed in the gender-dependent regulation of proteins associated with plasticity of the excitatory synapse.

  8. These results showed that methylenetetrahydrofolate reductase deficiency impairs endothelial progenitor cell formation and increases endothelial progenitor cell senescence by endothelial nitric oxide synthase (show NOS3 ELISA Kits) uncoupling and downregulation of SIRT1 (show SIRT1 ELISA Kits).

  9. Variable presentation of MTHFR deficiency in different genetic backgrounds; plasma homocysteine is not a predictor of severity.

  10. Newborn reflex development was slightly influenced by Mthfr +/- genotype and by the combination genotype and the neonatal vigabatrin (GVG) administration, in a sex-independent manner. Females presented attenuated anxiety due to Mthfr +/- genotype and GVG.

Human Methylenetetrahydrofolate Reductase (NAD(P)H) (MTHFR) interaction partners

  1. The prognostic index comprising XRCC1 (show XRCC1 ELISA Kits) rs25487, ERCC2 (show ERCC2 ELISA Kits) rs13181, and rs1799793 polymorphisms may be a useful predictor of clinical outcomes in MGC treated with EOF.

  2. The prevalence of factor V G1691A, prothrombin (show F2 ELISA Kits) G20210A and MTHFR C677T single nucleotide polymorphism among Syrians is 11.5%, 2.5% and 84.5%, respectively.

  3. MTHFR C677T polymorphism, qualitatively, is not a genetic factor for the pathogenesis of psoriasis but could quantitatively reflect the severity of psoriasis to some extent. Meta-analysis.

  4. the studied polymorphisms MTHFR C677T (rs1801133) and MTR (show MTR ELISA Kits) A2756G (rs1805087) do not contribute to genetic susceptibility to varicose veins in ethnical Russians.

  5. the influence of polymorphisms in methylenetetrahydrofolate reductase (MTHFR-C677T) and apolipoprotein-E (apo-E (show APOE ELISA Kits)) as risk factors for ischemic stroke patients in south Indian population

  6. Rheumatoid arthritis patients with the MTHFR 677TT genotype had the highest asymmetric dimethylarginine levels, significantly higher than either those patients carrying the MTHFR 677CT or the MTHFR 677CC genotype.

  7. There is an association between variants of the MTHFR gene and hypertension in Cameroonian patients from the South West region.

  8. There were no other associations between single -nucleotide polymorphisms and the efficacy of MTX (show MTX1 ELISA Kits) treatment. CONCLUSIONS: The MTHFR 677CC and GGH (show GGH ELISA Kits) 401TT and CT genotypes were associated with a reduction in the number of MTX (show MTX1 ELISA Kits)-related adverse events.

  9. Frequency of MTHFR risk allele (T) in patients with maternal age <25 years is marginally significant higher than those in cases with maternal age >/=25 years (p = .069) with an OR of 2.7 (95% CI = 0.90-8.07). Conclusions: MTHFR is a common susceptibility factor for gastroschisis in Indonesia.

  10. The association of colorectal adenomas with the rs6983267 variant at 8q24 was considered as 'highly credible', the 'less credible' associations were identified with a further four variants of four independent genes: MTHFR c.677C>T p.A222V(rs1801133), TP53 (show TP53 ELISA Kits) c.215C>G p.R72P (rs1042522), NQO1 (show NQO1 ELISA Kits) c.559C>T p.P187S (rs1800566), and NAT1 (show EIF4G2 ELISA Kits) alleles imputed as fast acetylator genotypes. [meta-analysis]

MTHFR Antigen Profile

Antigen Summary

The protein encoded by this gene catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Genetic variation in this gene influences susceptibility to occlusive vascular disease, neural tube defects, colon cancer and acute leukemia, and mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.

Gene names and symbols associated with MTHFR

  • methylenetetrahydrofolate reductase (NAD(P)H) (mthfr) antibody
  • methylenetetrahydrofolate reductase (NAD(P)H) (MTHFR) antibody
  • methylenetetrahydrofolate reductase (metF) antibody
  • methylenetetrahydrofolate reductase (DDB_G0279137) antibody
  • 5,10-methylenetetrahydrofolate reductase (Mthfr) antibody
  • methylenetetrahydrofolate reductase (NAD(P)H) (Mthfr) antibody
  • AI323986 antibody
  • DDBDRAFT_0204686 antibody
  • DDBDRAFT_0230137 antibody
  • DDB_0204686 antibody
  • DDB_0230137 antibody

Protein level used designations for MTHFR

5,10-methylenetetrahydrofolate reductase , 5,10-methylenetetrahydrofolate reductase (NADPH) , methylenetetrahydrofolate reductase (NAD(P)H) , methylenetetrahydrofolate reductase-like , methylenetetrahydrofolate reductase

GENE ID SPECIES
379784 Xenopus laevis
469800 Pan troglodytes
100125082 Xenopus (Silurana) tropicalis
100391000 Callithrix jacchus
1209960 Coxiella burnetii RSA 493
8621890 Dictyostelium discoideum AX4
17769 Mus musculus
4524 Homo sapiens
362657 Rattus norvegicus
478230 Canis lupus familiaris
397180 Sus scrofa
497032 Bos taurus
419489 Gallus gallus
100715703 Cavia porcellus
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