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Typical Testing Data/Standard Curve (for reference only)

Human Mannose Phosphate Isomerase ELISA Kit | MPI elisa kit

Human Mannose Phosphate Isomerase ELISA Kit

Gene Names
MPI; PMI; PMI1; CDG1B
Reactivity
Human
Synonyms
Mannose Phosphate Isomerase; Human Mannose Phosphate Isomerase ELISA Kit; MPI elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Samples
Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Assay Type
Competitive
Detection Range
5.0-100ng/mL
Sensitivity
0.1ng/mL
Preparation and Storage
Store all reagents at 2-8 degree C.

Typical Testing Data/Standard Curve (for reference only)

Typical Testing Data/Standard Curve (for reference only)
Related Product Information for MPI elisa kit
For Samples: Cell culture fluid & body fluid & tissue homogenate Serum or blood plasma

Intended Uses: This MKP-1 ELISA kit is intended for laboratory research use only. The stop solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of MKP-1 in the sample, this MKP-1 ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus MKP-1 concentration. The concentration of in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Principle of the Assay: The coated well immunoenzymatic assay for the quantitative measurement of MKP-1 utilizes a multiclonal anti-MKP-1 antibody and an MKP-1-HRP conjugate. The assay sample and buffer are incubated together with MKP-1-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the MKP-1 concentration since MKP-1 from samples and MKP-1-HRP conjugate compete for the anti-MKP-1 antibody binding site. Since the number of sites is limited, as more sites are occupied by MKP-1 from the sample, fewer sites are left to bind MKP-1-HRP conjugate. Standards of known MKP-1 concentrations are run concurrently with the samples being assayed and a standard curve is plotted relating the intensity of the color (Optical Density) to the concentration of MKP-1. The MKP-1 concentration in each sample is interpolated from this standard curve.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
Molecular Weight
39,834 Da
NCBI Official Full Name
mannose phosphate isomerase
NCBI Official Synonym Full Names
mannose phosphate isomerase
NCBI Official Symbol
MPI
NCBI Official Synonym Symbols
PMI; PMI1; CDG1B
NCBI Protein Information
mannose-6-phosphate isomerase; phosphohexomutase; phosphomannose isomerase 1
UniProt Protein Name
Mannose-6-phosphate isomerase
UniProt Gene Name
MPI
UniProt Synonym Gene Names
PMI1; PMI
UniProt Entry Name
MPI_HUMAN

NCBI Description

Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

Uniprot Description

MPI: Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions. Defects in MPI are the cause of congenital disorder of glycosylation type 1B (CDG1B); also known as carbohydrate-deficient glycoprotein syndrome type Ib (CDGS1B). Congenital disorders of glycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. They are characterized by under- glycosylated serum glycoproteins. CDG1B is clinically characterized by protein-losing enteropathy. Belongs to the mannose-6-phosphate isomerase type 1 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Isomerase; Carbohydrate Metabolism - fructose and mannose; Carbohydrate Metabolism - amino sugar and nucleotide sugar; EC 5.3.1.8

Chromosomal Location of Human Ortholog: 15q24.1

Cellular Component: cytosol

Molecular Function: mannose-6-phosphate isomerase activity; zinc ion binding

Biological Process: cellular protein metabolic process; dolichol-linked oligosaccharide biosynthetic process; GDP-mannose biosynthetic process; protein amino acid N-linked glycosylation via asparagine; post-translational protein modification

Disease: Congenital Disorder Of Glycosylation, Type Ib

Research Articles on MPI

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Product Notes

The Human MPI mpi (Catalog #AAA725792) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA725792 ELISA Kit recognizes Human MPI. It is sometimes possible for the material contained within the vial of "Mannose Phosphate Isomerase, 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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