Primary Cells

Human Subclavian Artery Endothelial Cells, Adult

  • For research use only

Cat No.

ABC-TC3820

Product Type

Vascular Cells

Cell Type

Endothelial

Species

Human

Growth Conditions

37 ℃, 5% CO2

Disease

Normal

Storage

Liquid Nitrogen

Human Subclavian Artery Endothelial Cells are derived from normal human subclavian arteries.

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Description

Human Subclavian Artery Endothelial Cells, Adult (HScAEC, Ad) are primary endothelial cells isolated from the intimal layer of adult human subclavian arteries. These adherent cells exhibit classic flat, elongated morphology and are cryopreserved at early passage to maintain phenotypic fidelity. HScAEC, Ad express endothelial-specific markers such as CD31 (PECAM-1), VE-cadherin, and von Willebrand factor (vWF), and demonstrate functional uptake of acetylated LDL and binding of Ulex europaeus agglutinin I. These cells actively respond to shear stress, inflammatory cytokines such as TNF-α, and vasoactive stimuli such as VEGF, endothelin-1. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.
Product Code

HScAEC

Species

Human

Cat.No

ABC-TC3820

Product Category

Primary Cells

Size/Quantity

1 vial

Cell Type

Endothelial

Growth Mode

Adherent

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Disease

Normal

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Vascular Cells

Quality Control

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

Application

  • Human Subclavian Artery Endothelial Cells, Adult (HScAEC, Ad) are ideal for studying arterial endothelial physiology, atherosclerosis, vascular inflammation, and mechanotransduction. As adult human subclavian artery endothelial cells derived from primary human subclavian endothelium, representing human adult subclavian vascular cells, they are particularly useful in artery-specific drug screening, endothelial dysfunction models, and flow-based vascular engineering. Their anatomical origin supports relevance to upper-limb and thoracic vascular pathologies. These cells enable dynamic modeling of shear-stress–responsive signaling and vascular remodeling under disease-relevant conditions.

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).

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