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Merck

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.

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About This Item

UNSPSCコード:
12161503
eCl@ss:
32161000
NACRES:
NA.84

品質水準

化学種の反応性

mouse

メーカー/製品名

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%

テクニック

multiplexing: suitable

検出方法

fluorometric (Luminex xMAP)

輸送温度

wet ice

詳細

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

特異性

Cross Reactivty
Non-detectable within the panel

アプリケーション

  • 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

特徴および利点

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

その他情報

Please contact Technical Service for linearity of dilution.

法的情報

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

免責事項

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.

ピクトグラム

Skull and crossbonesEnvironment

シグナルワード

Danger

危険有害性情報

危険有害性の分類

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

保管分類コード

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


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

MCVD1MAG-77K-07:
MCVD1MAG-77K-04:
MCVD1MAG-77K-06:
MCVD1MAG-77K-02:
MCVD1MAG-77K-05:
MCVD1MAG-77K:
MCVD1MAG-77K-03:
MCVD1MAG-77K-01:


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

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

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