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Merck
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MMMP3MAG-79K

MILLIPLEX® Mouse MMP Panel

Configurable Mouse MMP 5-Plex Panel 3 for cell culture samples

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About This Item

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

MILLIPLEX® Mouse MMP Panel, Configurable Mouse MMP 5-Plex Panel 3 for cell culture samples

species reactivity

mouse

manufacturer/tradename

Milliplex®

Quality Level

packaging

1 ea of

assay range

standard curve range: 12-50,000 pg/mL
(MMP-8)

standard curve range: 12-50,000 pg/mL
(proMMP-9)

standard curve range: 2-10,000 pg/mL
(MMP-3)

standard curve range: 49-200,000 pg/mL
(MMP-2)

standard curve range: 5-20,000 pg/mL
(MMP-12)

technique(s)

multiplexing: suitable

input

cell culture supernatant(s)

detection method

fluorometric (Luminex® xMAP® technology)

shipped in

wet ice

storage temp.

2-8°C

Legal Information

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

Application

MILLIPLEX® Qualified assays undergo rigorous assay development, verification, and Quality Control testing to achieve optimal performance. Simultaneously analyze up to 5 analytes in mouse cell culture supernatants.

Analytes included: MMP-2, MMP-3, MMP-8, proMMP-9, MMP-12

Assay Characteristics: Refer to kit protocol for assay cross-reactivity, sensitivity, precision, and accuracy.

Disclaimer

For research use only. Not for use in diagnostic procedures.

Label License/Sticker for Assay Product:

By opening the packaging containing this Assay Product (which contains fluorescently labeled microsphere beads authorized by Luminex Corporation) or using this Assay Product in any manner, you are consenting and agreeing to be bound by the End User Terms and Conditions and the End User License Agreement available at http://support.diasorin.com/end-user-terms-and-conditions/. If you do not agree to all of the terms and conditions, you must promptly return this Assay Product for a full refund prior to using it in any manner.

Features and Benefits

5-Plex Multiplex Assay: Simultaneous detection of MMP-2, MMP-3, MMP-8, proMMP-9, and MMP-12 in a single sample. Enables comprehensive profiling of matrix metalloproteinase activity.

Optimized for Tissue Culture Samples: Validated for use with cell/tissue culture supernatants and extracts, ideal for in vitro studies.

Comprehensive ECM Remodeling Insight: MMPs play a central role in tissue morphogenesis, wound healing, angiogenesis, and immune regulation. This panel enables researchers to monitor key enzymes involved in these processes.

Supports Disease Research: Ideal for investigating autoimmune diseases, arthritis, cardiovascular conditions, and tumor progression, where MMP dysregulation is implicated.

Efficient Sample Use: Multiplexing reduces sample volume and reagent consumption, saving time and resources.

High Sensitivity & Specificity: Detects both active and pro-forms of MMPs, providing deeper insight into enzyme activation dynamics.

General description

The MMPs (matrix metalloproteinases), a family of zinc proteases responsible for the breakdown of extracellular matrix (ECM), play a key role in normal physiological processes, such as embryonic development and tissue morphogenesis, tissue and bone remodeling, wound healing, and angiogenesis. These processes rely on MMPs′ role in the cleavage of cell surface receptors, the release of apoptotic ligands, cell proliferation and differentiation, and chemokine activity modulation. Similar in structure, MMPs are synthesized and secreted as inactive pro-enzymes that require proteolytic cleavage for activation. This process can be mediated by serine proteases or other MMPs. An increase in MMP expression occurs in response to a wide range of stimuli, including adhesion molecules, growth factors, cytokines, and hormones. Regulation of MMP activity is controlled primarily by TIMPs (tissue inhibitors of metalloproteinases). Therefore, disruption of the MMP/TIMP balance can result in autoimmune disease, arthritis, cardiovascular disease, and tumor growth and metastasis.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2

target_organs

Respiratory Tract

Storage Class

10 - Combustible liquids

wgk

WGK 3

Regulatory Information

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Lucy M Hinder et al.
Experimental neurology, 305, 33-43 (2018-03-20)
Diabetic peripheral neuropathy is the most common complication of diabetes and a source of considerable morbidity. Numerous molecular pathways are linked to neuropathic progression, but it is unclear whether these pathways are altered throughout the course of disease. Moreover, the
Taotao Lao et al.
Proceedings of the National Academy of Sciences of the United States of America, 113(32), E4681-E4687 (2016-07-23)
Genetic variants in Hedgehog interacting protein (HHIP) have consistently been associated with the susceptibility to develop chronic obstructive pulmonary disease and pulmonary function levels, including the forced expiratory volume in 1 s (FEV1), in general population samples by genome-wide association
Phillipe D O'Brien et al.
Neurobiology of disease, 73, 348-355 (2014-12-03)
Given the lack of treatments for diabetic neuropathy (DN), a common diabetic complication, accurate disease models are necessary. Characterization of the leptin-deficient BTBR ob/ob mouse, a type 2 diabetes model, demonstrated that the mice develop robust diabetes coincident with severe
Delphine Le Guennec et al.
Cancers, 14(1) (2022-01-12)
Our goal was to evaluate the effect of spontaneous physical activity on tumour immunity during aging. Elderly (n = 10/group, 33 weeks) ovariectomized C57BL/6J mice fed a hyperlipidic diet were housed in standard (SE) or enriched (EE) environments. After 4
Ludovic Boytard et al.
Nature communications, 11(1), 4311-4311 (2020-08-29)
Pulmonary disease increases the risk of developing abdominal aortic aneurysms (AAA). However, the mechanism underlying the pathological dialogue between the lungs and aorta is undefined. Here, we find that inflicting acute lung injury (ALI) to mice doubles their incidence of

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