Skip to Content
MilliporeSigma
All Photos(2)

Documents

MCVD1MAG-77K

Millipore

MILLIPLEX® Mouse Cardiovascular Disease (CVD) Magnetic Bead Panel 1 - Cardiovascular Disease Multiplex Assay

This MILLIPLEX MAP Mouse Cardiovascular Disease Magnetic Bead Panel 1 includes the following analytes: sE-Selectin, sICAM-1, Pecam-1, sP-Selectin, PAI-1 (total), proMMP-9 & Thrombomodulin.

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
12161503
eCl@ss:
32161000
NACRES:
NA.84

Quality Level

species reactivity

mouse

manufacturer/tradename

Milliplex®

assay range

accuracy: 88-99%
sensitivity: 0.008 ng/mL
(proMMP-9)

sensitivity: 0.012 ng/mL
(PAI-1 (total))

sensitivity: 0.012 ng/mL
(Pecam-1)

sensitivity: 0.013 ng/mL
(sICAM-1)

sensitivity: 0.033 ng/mL
(sE-Selectin)

sensitivity: 0.039 ng/mL
(Thrombomodulin)

sensitivity: 0.429 ng/mL
(sP-Selectin)

standard curve range: 0.007-30 ng/mL
(sICAM-1)

standard curve range: 0.012-50 ng/mL
(proMMP-9)

standard curve range: 0.018-75 ng/mL
(PAI-1 (total))

standard curve range: 0.024-100 ng/mL
(Pecam-1)

standard curve range: 0.024-100 ng/mL
(Thrombomodulin)

standard curve range: 0.049-200 ng/mL
(sE-Selectin)

standard curve range: 0.439-1800 ng/mL
(sP-Selectin)

inter-assay cv: <15%
intra-assay cv: <10%

technique(s)

multiplexing: suitable

detection method

fluorometric (Luminex xMAP)

shipped in

wet ice

General description

Cardiovascular disease, particularly atherosclerotic vascular disease, is a leading cause of global mortality, accounting for 30% of all global deaths (WHO, 2010). Inflammatory mechanisms play a vital role in the initiation, maintenance, and progression of vascular disease with a strong correlation between inflammatory markers and prognosis in acute and chronic coronary artery disease. Numerous studies have demonstrated an association of obesity and diabetes with cardiovascular risk factors.

MILLIPLEX® Mouse CVD Panel 1 is a 7-plex kit to be used for the simultaneous quantification of any or all of the following analytes in serum and plasma samples: sE-Selectin, sICAM-1, Pecam-1, sP-Selectin, PAI-1 Total, proMMP-9, and Thrombomodulin. This kit uses a 96-well format, contains a lyophilized standard cocktail, two internal assay quality controls and can measure up to 38 samples in duplicate.

The Luminex® xMAP® platform uses a magnetic bead immunoassay format for ideal speed and sensitivity to quantitate multiple analytes simultaneously, dramatically improving productivity while conserving valuable sample volume.

Panel Type: Cardiovascular

Specificity

Cross Reactivty
Non-detectable within the panel

Application

  • Analytes: CD31 (sPecam-1), sE-Selectin, sICAM-1, PAI-1 (Total), ProMMP-9, sP-Selectin,
  • Thrombomodulin, s Recommended Sample Type: Mouse serum, plasma or cell/tissue culture supernatants or lysates
  • Recommended Sample Dilution: 25 μL per well of 1:20 diluted serum or plasma; cell/tissue culture samples may require dilution in appropriate control mediumAssay Run Time: Overnight (16-18 hours) at 2-8°C
  • Research Category: Cardiovascular Disease
  • Research Subcategory: Metabolism

Features and Benefits

Design your multiplex kit by choosing available analytes within this panel.

Other Notes

Please contact Technical Service for linearity of dilution.

Legal Information

Luminex is a registered trademark of Luminex Corp
MILLIPLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
xMAP is a registered trademark of Luminex Corp

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

pictograms

Skull and crossbonesEnvironment

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ulrike Kogel et al.
Journal of applied toxicology : JAT, 41(10), 1598-1619 (2021-04-08)
Cigarette smoking is one major modifiable risk factor in the development and progression of chronic obstructive pulmonary disease and cardiovascular disease. To characterize and compare cigarette smoke (CS)-induced disease endpoints after exposure in either whole-body (WB) or nose-only (NO) exposure
K Monica Lee et al.
Inhalation toxicology, 30(13-14), 553-567 (2019-03-09)
We compared early biological changes in mice after inhalation exposures to cigarette smoke or e-vapor aerosols (MarkTen® cartridge with Carrier, Test-1, or Test-2 formulations; 4% nicotine). Female C57BL/6 mice were exposed to 3R4F cigarette smoke or e-vapor aerosols by nose-only
Lucie Aumailley et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 32(7), 3623-3640 (2018-02-18)
Werner syndrome (WS) is a premature aging disorder caused by mutations in a RecQ-family DNA helicase (WRN). Mice lacking part of the helicase domain of the WRN ortholog exhibit several phenotypic features of WS. In this study, we generated a
Lucie Aumailley et al.
Aging, 8(3), 458-483 (2016-02-29)
Suboptimal intake of dietary vitamin C (ascorbate) increases the risk of several chronic diseases but the exact metabolic pathways affected are still unknown. In this study, we examined the metabolic profile of mice lacking the enzyme gulonolactone oxidase (Gulo) required
Lucie Aumailley et al.
PloS one, 10(10), e0140292-e0140292 (2015-10-09)
Werner syndrome (WS) is a premature aging disorder caused by mutations in a RecQ-family DNA helicase, WRN. Mice lacking part of the helicase domain of the WRN orthologue exhibit many phenotypic features of WS, including metabolic abnormalities and a shorter

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service