Product Name
5, 10-methylenetetrahydrofolate reductase (NADPH) (MTHFR), ELISA Kit
Full Product Name
Human Methylenetetrahydrofolate reductase, MTHFR ELISA Kit
Product Synonym Names
Human Methylenetetrahydrofolate reductase (MTHFR) ELISA kit; 5; 10-methylenetetrahydrofolate reductase; OTTHUMP00000002367; 5; 10-methylenetetrahydrofolate reductase (NADPH)
Product Gene Name
MTHFR elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sample Manual Insert
Download Sample PDF Manual View Sample PDF Manual
Request for Current Manual Insert
Request Current Manual
MBS923196 Testing Data
Testing Data PDF
3D Structure
ModBase 3D Structure for P42898
Specificity
This assay has high sensitivity and excellent specificity for detection of human MTHFR. No significant cross-reactivity or interference between human MTHFR and analogues was observed.
Samples
Serum, plasma, tissue homogenates, Cell lysates
Detection Range
46.88 pg/ml -3000 pg/ml.
Sensitivity
The minimum detectable dose of human MTHFR is typically less than 11.7 pg/ml.The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the mean O.D value of 20 replicates of the zero standard added by their three standard deviations.
Intra-assay Precision
Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.
Inter-assay Precision
Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Preparation and Storage
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of MTHFR elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for MTHFR purchase
MBS923196 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the 5, 10-methylenetetrahydrofolate reductase (NADPH) (MTHFR) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing MTHFR. The ELISA analytical biochemical technique of the MBS923196 kit is based on MTHFR antibody-MTHFR antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect MTHFR antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, MTHFR. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
Related Product Information for
MTHFR elisa kit
Principle of the assay: This assay employs the quantitative sandwich enzyme immunoassay technique.
Antibody specific for MTHFR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any MTHFR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MTHFR is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MTHFR bound in the initial step. The color development is stopped and the intensity of the color is measured.
Typical Testing Data/Standard Curve (for reference only) of MTHFR elisa kit
NCBI/Uniprot data below describe general gene information for MTHFR. It may not necessarily be applicable to this product.
NCBI Accession #
NP_005948.3
[Other Products]
NCBI GenBank Nucleotide #
NM_005957.4
[Other Products]
UniProt Primary Accession #
P42898
[Other Products]
UniProt Secondary Accession #
Q5SNW6; Q5SNW9; Q7Z6M6; Q8IU73; Q9UQR2; B2R7A6[Other Products]
UniProt Related Accession #
P42898[Other Products]
Molecular Weight
74,597 Da
NCBI Official Full Name
methylenetetrahydrofolate reductase
NCBI Official Synonym Full Names
methylenetetrahydrofolate reductase (NAD(P)H)
NCBI Official Symbol
MTHFR [Similar Products]
NCBI Protein Information
methylenetetrahydrofolate reductase; 5,10-methylenetetrahydrofolate reductase (NADPH)
UniProt Protein Name
Methylenetetrahydrofolate reductase
Protein Family
Methylenetetrahydrofolate reductase
UniProt Gene Name
MTHFR [Similar Products]
UniProt Entry Name
MTHR_HUMAN
NCBI Summary for MTHFR
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.[provided by RefSeq, Oct 2009]
UniProt Comments for MTHFR
MTHFR: Catalyzes the conversion of 5,10- methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co- substrate for homocysteine remethylation to methionine. Defects in MTHFR are the cause of methylenetetrahydrofolate reductase deficiency (MTHFRD). MTHFRD is autosomal recessive disorder with a wide range of features including homocysteinuria, homocysteinemia, developmental delay, severe mental retardation, perinatal death, psychiatric disturbances, and later-onset neurodegenerative disorders. Defects in MTHFR may be a cause of susceptibility to ischemic stroke (ISCHSTR); also known as cerebrovascular accident or cerebral infarction. A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors. Defects in MTHFR 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. Belongs to the methylenetetrahydrofolate reductase family.
Protein type: Cofactor and Vitamin Metabolism - one carbon pool by folate; Energy Metabolism - methane; Oxidoreductase; EC 1.5.1.20
Chromosomal Location of Human Ortholog: 1p36.3
Cellular Component: neuron projection; cytosol
Molecular Function: FAD binding; NADP binding; methylenetetrahydrofolate reductase (NADPH) activity
Biological Process: response to drug; amino acid metabolic process; vitamin metabolic process; methionine biosynthetic process; blood circulation; response to folic acid; response to vitamin B2; response to hypoxia; S-adenosylmethionine metabolic process; homocysteine metabolic process; one-carbon compound metabolic process; folic acid metabolic process; water-soluble vitamin metabolic process
Disease: Schizophrenia; Thrombophilia Due To Thrombin Defect; Neural Tube Defects, Folate-sensitive; Homocystinuria Due To Deficiency Of N(5,10)-methylenetetrahydrofolate Reductase Activity
Research Articles on MTHFR
1. Significant association between methylenetetrahydrofolate reductase genotype and groups with venous thrombosis, peripheral arterial thrombosis and myocardial infarction. [Meta-analysis]
Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
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