Primary Cells

C57BL/6 Mouse Cardiac Microvascular Endothelial Cells

  • For research use only

Cat No.

ABC-TC3179

Product Type

Mouse Primary Cells

Cell Type

Endothelial

Species

C57BL/6 Mouse

Growth Conditions

37 ℃, 5% CO2

Source Organ

Heart

Disease

Normal

Storage

Liquid Nitrogen

C57BL/6 Mouse Cardiac Microvascular Endothelial Cells support cardiac microvascular biology, angiogenesis, and barrier assays in pathogen-free mice.

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Description

C57BL/6 Mouse Cardiac Microvascular Endothelial Cells (CMECs) are primary cells isolated from the myocardial microvasculature of pathogen-free laboratory mice. They reside in the capillary network of the cardiac microvasculature, embedded within the myocardium between cardiomyocyte bundles. Following primary culture, these cells are cryopreserved. These cardiac endothelial cells govern myocardial perfusion by regulating capillary tone via vasoactive molecules, maintain microvascular barrier integrity through junctional proteins (e.g., claudin-5), and mediate cardiomyocyte-endothelial crosstalk for metabolic exchange. CMECs express VE-cadherin, vWF, and CD31/PECAM-1. Repeated freezing and thawing should be avoided during culture. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from Mycoplasma, Fungi, Yeast, and Bacteria.

Product Code

C57BL/6 Mouse Cardiac Microvascular Endothelial Cells,Mouse Cardiac Microvascular Endothelial Cells,Microvascular Endothelial Cells,ECs,C57BL/6 CMVECs

Species

C57BL/6 Mouse

Cat.No

ABC-TC3179

Product Category

Primary Cells

Size/Quantity

1 vial

Cell Type

Endothelial

Growth Mode

Adherent

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

Heart

Disease

Normal

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Mouse Primary Cells

Quality Control

All cells test negative for mycoplasma, bacteria, yeast, and fungi.

Application

  • C57BL/6 Mouse Cardiac Microvascular Endothelial Cells can be used as an in vitro model to study the pathogenesis of microvascular dysfunction in disease conditions such as diabetic cardiomyopathy and myocardial ischemia. For example, by investigating molecular pathways like hyperglycemia-induced mitochondrial fission (DRP1 activation) or ROS-mediated degradation of claudin-5 tight junctions, these cells help elucidate mechanisms of impaired perfusion, capillary leakage, and cardiomyocyte injury, aiding the development of endothelial-protective therapies to rescue cardiac microcirculation.

Citation

When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).

Frequently Asked Questions

  • How viable are the cells after long-term culture?

    These cells are recommended for culture up to 3 weeks. After 1 month in culture, cell viability is expected to be around 60%.

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
Customization Options
Tailed to your research

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