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AAT Bioquest

Anti-Myeloperoxidase (MPO) antibody *Mouse anti-human, monoclonal IgG2a*

Myeloperoxidase (MPO) is a 150 kDa cationic hemoprotein that consists of two covalently bound subunits each containing a heavy chain (60 kDa) and a light chain (15 kDa). MPO is abundantly expressed in neutrophils and is released during degranulation. It plays a vital role in inflammatory responses by catalyzing chloride ion oxidation to produce hypochlorous acid which is used by neutrophils to kill bacteria and other pathogens. MPO is also known to cause oxidative modification of low density lipoproteins to a high uptake form. This is considered to be a key event in the promotion of atherogenesis and is linked to the progression of cardiovascular diseases. As such, MPO is considered to be a promising cardiovascular biomarker as elevated MPO levels indicates a high risk for atherosclerosis and coronary heart disease (CHD). Anti-MPO monoclonal antibodies are highly sensitive for the detection of human MPO. They can be used for a broad range of immunoassays such as latex enhanced turbidimetric immunoassays (LETIA), chemiluminescent immunoassays (CLIA) and ELISA.

Conjugation

We provide custom conjugation services for this antibody (eg. labeling of Anti-Myeloperoxidase (MPO) antibody *Mouse anti-human, monoclonal IgG2a* with HRP). A list of available labels can be found in the table below:

AFAF350, AF488, AF555, AF594, AF647, AF680, AF700, AF750
ProteinsHRP, Alkaline Phosphatase, Streptavidin
TandemsAPC, APC/Cy7, APC/AF750, APC/iFluor™ 700, APC/iFluor™ 750, PE, PE/Cy5, PE/Cy7, PE/AF610, PE/AF700, PE/iFluor™ 594, PE/iFluor™ 647, PE/iFluor™ 700, PE/iFluor™ 750, PE/Texas Red®, PerCP, PerCP/Cy5.5
Small MoleculesBiotin
Traditional DyesFITC (fluorescein), TRITC, PacBlue, PacOrange, Cy3, Cy5
iFluor350, 405, 430, 450, 488, 514, 532, 546, 555, 560, 568, 594, 610, 633, 647, 660, 670, 680, 700, 710, 750, 790, 800, 810, 820, 840, 860, A7
mFluorUV375, UV460, Violet 450, Violet 500, Violet 510, Violet 540, Blue 570, Green 620, Red 700, Red 780

For additional information about custom conjugations, please consult our services page here.
Page updated on November 19, 2024

Ordering information

Price
Unit size
50 ug
1 mg
Catalog Number
V100100V100101
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
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Emailsales@aatbio.com
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Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
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Antibody properties

Other names
Hostmouse
Reactivityhuman
ApplicationLETIA; ELISA; CLIA; LFIA

Physical properties

Solvent

Water

Storage, safety and handling

Intended useResearch Use Only (RUO)

Storage

Freeze (< -15 °C)
Samples from healthy donors and patients with myocardial&nbsp;injury were detected using the chemiluminescence immunoassay (CLIA) MPO assays, A and B. Results show good correlation between CLIA MPO assays and comparison kits.
Samples from healthy donors and patients with myocardial&nbsp;injury were detected using the chemiluminescence immunoassay (CLIA) MPO assays, A and B. Results show good correlation between CLIA MPO assays and comparison kits.
Samples from healthy donors and patients with myocardial&nbsp;injury were detected using the chemiluminescence immunoassay (CLIA) MPO assays, A and B. Results show good correlation between CLIA MPO assays and comparison kits.
Calibration curve for MPO in latex enhanced turbidimetric immunoassay (LETIA): human MPO proteins were reacted with anti-human MPO antibodies coated onto latex microspheres, resulting in agglutination and an increase in turbidity. Changes in absorbance were monitored using a spectrometer to quantitatively measure the MPO concentration in the samples.
Calibration curve for MPO in chemiluminescent immunoassay (CLIA) using the best two-site MAb combination for&nbsp;the&nbsp;quantitative&nbsp;detection of MPO. A double monoclonal antibody sandwich method was used using Cat# V100095 (Clone 1) as capture antibodies and Cat# V100095 (Clone 2) labeled with horseradish peroxidase (HRP) as detection antibodies. The calibration curve between MPO concentration and relative light units&nbsp;was analyzed by four-parameter logistic (4PL) regression model (R<sup>2</sup>=0.9996).
Shows the comparison of MPO concentrations determined using AAT Bioquest&rsquo;s anti-MPO monoclonal antibodies and two high-quality kits (A and B). Anti-MPO monoclonal antibodies were evaluated by immunoturbidimetric assay in medium-scale clinical trials with random&nbsp;blood samples from donors (n=72). Results reveal good agreement between AAT Bioquest&rsquo;s immunoassay and comparison assays.