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ECM512

Sigma-Aldrich

QCM Chemotaxis Cell Migration Assay, 96-well (5 µm), fluorimetric

The QCM 5 um 96-well Migration Assay utilizes a 5 um pore size, which is appropriate for studying monocyte/macrophage migration.

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Synonym(s):
5 μm pore migration invasion assay, monocyte macrophage migration assay
eCl@ss:
32161000
NACRES:
NA.32

Quality Level

species reactivity (predicted by homology)

all

manufacturer/tradename

Chemicon®
QCM

technique(s)

activity assay: suitable
cell based assay: suitable

detection method

fluorometric

shipped in

wet ice

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ECM509ECM508ECM555
species reactivity (predicted by homology)

all

species reactivity (predicted by homology)

all

species reactivity (predicted by homology)

all

species reactivity (predicted by homology)

-

manufacturer/tradename

Chemicon®

manufacturer/tradename

Chemicon®, QCM

manufacturer/tradename

Chemicon®, QCM

manufacturer/tradename

Chemicon®, QCM

detection method

fluorometric

detection method

fluorometric

detection method

colorimetric

detection method

fluorometric

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

Application

Research Category
Cell Structure

Packaging

96 wells

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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

CorrosionEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3


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Karen S Aboody et al.
Science translational medicine, 5(184), 184ra59-184ra59 (2013-05-10)
High-grade gliomas are extremely difficult to treat because they are invasive and therefore not curable by surgical resection; the toxicity of current chemo- and radiation therapies limits the doses that can be used. Neural stem cells (NSCs) have inherent tumor-tropic
Scott Ferguson et al.
The AAPS journal, 20(4), 67-67 (2018-05-02)
Exosomes are nano-sized vesicles composed of lipids, proteins, and nucleic acids. Their molecular landscape is diverse, and exosomes derived from different cell types have distinct biological activities. Since exosomes are now being utilized as delivery vehicles for exogenous therapeutic cargoes
Iryna A Falkenstein et al.
Current eye research, 33(7), 599-609 (2008-07-05)
To investigate the intraocular properties and toxicity of IMS2186, a small molecule developed as an anti-choroidal neovascularization (anti-CNV) drug. Cellular toxicity and mechanism of action was tested on cell lines in vitro. Intraocular studies used rabbits for drug dissolution as
Shrinidh Joshi et al.
Journal of cellular physiology, 234(11), 20420-20431 (2019-04-17)
CD34+ hematopoietic stem/progenitor cells (HSPCs) are vasculogenic and hypoxia is a strong stimulus for the vasoreparative functions of these cells. Angiotensin-converting enzyme 2 (ACE2)/angiotensin-(1-7)/Mas receptor (MasR) pathway stimulates vasoprotective functions of CD34+ cells. This study tested if ACE2 and MasR
Jing Wu et al.
Stem cells international, 2022, 4249843-4249843 (2022-08-16)
Impairment of bone marrow-derived hematopoietic stem/progenitor cells (HSPCs) contributes to the progression of vascular complications in subjects with diabetes. Very small amounts of bacterial-derived pathogen-associated molecular patterns (PAMPs) establish the bone marrow cell pool. We hypothesize that alteration of the

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