For research use only
| Cat No. | ABC-TC4337 |
| Product Type | Diseased Human Peripheral Blood Mononuclear Cells |
| Cell Type | Mononuclear Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Atopic Dermatitis |
| Storage | Liquid Nitrogen |
Human Atopic Dermatitis PBMCs show Th2 cytokine dominance, altered immune activation, causing skin barrier dysfunction and sustaining chronic inflammation.
Human Atopic Dermatitis Peripheral Blood Mononuclear Cells are isolated from the peripheral blood of patients with atopic dermatitis (AD), a chronic inflammatory skin disorder. These cells primarily consist of lymphocytes (T cells, B cells, and NK cells) and monocytes, which are key components in the immune response. AD-PBMCs are functionally implicated in the dysregulated immune response characteristic of AD, particularly through Th2-skewed cytokine production (e.g., IL-4, IL-5, IL-13) and IgE-mediated hypersensitivity. They also exhibit abnormal T-cell activation and altered function of monocyte-derived dendritic cells, contributing to skin barrier impairment and chronic inflammation.
| Species | Human |
| Cat.No | ABC-TC4337 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Mononuclear Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Atopic Dermatitis |
| Storage | Liquid Nitrogen |
| Product Type | Diseased Human Peripheral Blood Mononuclear Cells |
Human Atopic Dermatitis Peripheral Blood Mononuclear Cells can be used to explore the molecular mechanisms underlying Th2-biased immune responses, skin barrier dysfunction and chronic inflammation. They are also suitable for in vitro experiments, such as cell culture, cytokine detection (such as IL-4, IL-5, IL-13 and IL-31), and flow cytometry analysis of changes in immune cell subsets to reveal the immune dysregulation characteristics of AD.
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