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SKU:SEB477Mu

ELISA Kit for Matrix Gla Protein (MGP)

ELISA Kit for Matrix Gla Protein (MGP)

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UOM
Sensitivity
Detection range

Enzyme-linked immunosorbent assay for Antigen Detection.

Product No.

SEB477Mu

Organism Species

Mus musculus (Mouse).

Sample Type

Serum, plasma, tissue homogenates and other biological fluids

Test Method

Double-antibody Sandwich

Assay Length

3h

Detection Range

0.47-30ng/mL

Sensitivity

The minimum detectable dose of this kit is typically less than 0.19ng/mL.

UOM

48T 96T 96T*5 96T*10 96T*100

Specificity

This assay has high sensitivity and excellent specificity for detection of Matrix Gla Protein (MGP).
No significant cross-reactivity or interference between Matrix Gla Protein (MGP) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Matrix Gla Protein (MGP) and the recovery rates were calculated by comparing the measured value to the expected amount of Matrix Gla Protein (MGP) in samples.

Matrix

Recovery range (%)

Average(%)

serum(n=5)

95-103

99

EDTA plasma(n=5)

83-103

98

heparin plasma(n=5)

99-105

102

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Matrix Gla Protein (MGP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Matrix Gla Protein (MGP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Matrix Gla Protein (MGP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample

1:2

1:4

1:8

1:16

serum(n=5)

94-101%

80-91%

84-93%

91-105%

EDTA plasma(n=5)

87-97%

80-90%

78-103%

78-95%

heparin plasma(n=5)

83-101%

78-98%

78-101%

87-95%

Stability

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Reagents and materials provided

Reagents

Quantity

Reagents

Quantity

Pre-coated, ready to use 96-well strip plate

1

Plate sealer for 96 wells

4

Standard

2

Standard Diluent

1×20mL

Detection Reagent A

1×120µL

Assay Diluent A

1×12mL

Detection Reagent B

1×120µL

Assay Diluent B

1×12mL

TMB Substrate

1×9mL

Stop Solution

1×6mL

Wash Buffer (30 × concentrate)

1×20mL

Instruction manual

1

Assay procedure summary

  1. Prepare all reagents, samples and standards;
    2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
    3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
    4. Aspirate and wash 3 times;
    5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
    6. Aspirate and wash 5 times;
    7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
    8. Add 50µL Stop Solution. Read at 450nm immediately.

Magazine

Citations

Nephrology Dialysis Transplantation

Magnesium prevents phosphate-induced calcification in human aortic vascular smooth muscle cells PubMed: PMC3611891

Maturitas.

Bone metabolism regulators and arterial stiffness in postmenopausal women Pubmed: 23916080

The Egyptian Rheumatologist

Osteoprotegerin (OPG) and Matrix Gla protein (MGP) in rheumatoid arthritis patients: Relation to disease activity ScienceDirect: S1110116414000076

Toxicology Reports

Canola and hydrogenated soybean oils accelerate ectopic bone formation induced by implantation of bone morphogenetic protein in mice Researchgate:Source

Lipids in Health and Disease

Markers of increased cardiovascular risk in patients with chronic kidney disease Biomedcentral:Source

Human &amp; Veterinary Medicine

The behavior of circulating matrix Gla protein, matrix metalloproteinase-9 and nitrotyrosine in patients with varicose veins Hvm:Source

Pol Arch Med Wewn

Effect of Vitamin K2 on progression of atherosclerosis and vascular calcification in nondialyzed patients with chronic kidney disease stages 3-5 PubMed: 26176325

Lipids Health Dis.

Markers of increased atherosclerotic risk in patients with chronic kidney disease: a preliminary study pmc:PMC4739105

Kidney Blood Press Res.

Plasma Desphospho-Uncarboxylated Matrix Gla Protein as a Marker of Kidney Damage and Cardiovascular Risk in Advanced Stage of Chronic Kidney Disease Pubmed:27100101

Archives of Oral Biology

Matrix-Gla Protein rs4236 [A/G] gene polymorphism and serum and GCF levels of MGP in patients with subgingival dental calculus pubmed:27348051

Cell Death & Disease

Mesenchymal stromal cells-derived matrix Gla protein contribute to the alleviation of experimental colitis Pubmed:29880866

Urology

High concentration of calcium promotes mineralization in NRK52E cells via inhibiting the expression of matrix Gla protein Pubmed:29935264

Clinica Chimica Acta

Serum total matrix Gla protein: Reference interval in healthy adults and variations in patients with vascular and osteoarticular diseases Pubmed: 30597137

Biological Trace Element Research

Altered Mineral Metabolism and Disequilibrium Between Calcification Promoters and Inhibitors in Chronic Hemodialysis Patients Pubmed: 30847765

Renal Failure

Relationship of matrix Gla protein and vitamin K with vascular calcification in hemodialysis patients Pubmed: 31538831

Heliyon

Matrix Gla protein maintains normal and malignant hematopoietic progenitor cells by interacting with bone morphogenetic protein-4 Pubmed: 32322728


Catalog No.

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