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Typical Testing Data/Standard Curve (for reference only)

Human Methionine synthase ELISA Kit | MTR elisa kit

Human Methionine synthase ELISA Kit

Gene Names
MTR; MS; HMAG; cblG
Reactivity
Human
Synonyms
Methionine synthase; Human Methionine synthase ELISA Kit; 5-methyltetrahydrofolate--homocysteine methyltransferase; Vitamin-B12 dependent methionine synthase; MS; MTR; 2.1.1.13; MTR elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Specificity
This assay recognizes recombinant and natural HumanEcto-NOX disulfide-thiol exchanger 2. No significant cross-reactivity or interference was observed.
Samples
Serum, Plasma, Tissue Homogenates, Cell Culture Supernates, And Other Biological Fluids
Assay Type
Quantitative Competitive
Detection Range
0.31-20.0ng/mL.
Preparation and Storage
Store at 4 degree C

Typical Testing Data/Standard Curve (for reference only)

Typical Testing Data/Standard Curve (for reference only)
Related Product Information for MTR elisa kit
Intended Uses: This immunoassay kit allows for the in vitro quantitative determination of humanEcto-NOX disulfide-thiol exchanger 2concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.

Principle of the Assay: The ELISA is based on the competitive binding enzyme immunoassaytechnique. The microtiter plate provided in this kit has been pre-coated with an antibody specific toEcto-NOX disulfide-thiol exchanger 2, During the reaction,Ecto-NOX disulfide-thiol exchanger 2in the sample or standard competes with a fixed amount of biotin-labeledEcto-NOX disulfide-thiol exchanger 2 for sites on a pre-coated Monoclonal antibody specific to Ecto-NOX disulfide-thiol exchanger 2. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Thena TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of Ecto-NOX disulfide-thiol exchanger 2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
134,793 Da
NCBI Official Full Name
methionine synthase isoform 1
NCBI Official Synonym Full Names
5-methyltetrahydrofolate-homocysteine methyltransferase
NCBI Official Symbol
MTR
NCBI Official Synonym Symbols
MS; HMAG; cblG
NCBI Protein Information
methionine synthase
UniProt Protein Name
Methionine synthase
Protein Family
UniProt Gene Name
MTR
UniProt Synonym Gene Names
MS

NCBI Description

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. [provided by RefSeq, May 2014]

Uniprot Description

MTR: Catalyzes the transfer of a methyl group from methyl- cobalamin to homocysteine, yielding enzyme-bound cob(I)alamin and methionine. Subsequently, remethylates the cofactor using methyltetrahydrofolate. Defects in MTR are the cause of methylcobalamin deficiency type G (cblG); also known as homocystinuria-megaloblastic anemia complementation type G. It is an autosomal recessive inherited disease that causes mental retardation, macrocytic anemia, and homocystinuria. Mild deficiency in MS activity could be associated with mild hyperhomocysteinemia, a risk factor for cardiovascular disease and possibly neural tube defects. MS mutations could also be involved in tumorigenesis. Defects in MTR may be a cause of susceptibility to folate-sensitive neural tube defects (FS-NTD). The most common NTDs are open spina bifida (myelomeningocele) and anencephaly. Genetic defects in MTR may affect the risk of spina bifida via the maternal rather than the embryonic genotype. Belongs to the vitamin-B12 dependent methionine synthase family.

Protein type: Amino Acid Metabolism - cysteine and methionine; Cofactor and Vitamin Metabolism - one carbon pool by folate; EC 2.1.1.13; Methyltransferase

Chromosomal Location of Human Ortholog: 1q43

Cellular Component: cytosol

Molecular Function: methionine synthase activity; protein binding

Biological Process: axon regeneration; cobalamin metabolic process; methionine biosynthetic process; methylation; nervous system development; response to axon injury; sulfur amino acid metabolic process

Disease: Homocystinuria-megaloblastic Anemia, Cblg Complementation Type; Neural Tube Defects, Folate-sensitive

Research Articles on MTR

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Product Notes

The Human MTR mtr (Catalog #AAA9427377) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9427377 ELISA Kit recognizes Human MTR. It is sometimes possible for the material contained within the vial of "Methionine synthase, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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