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Primary Cells

Human Atopic Dermatitis Peripheral Blood Mononuclear Cells

  • 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.

Product Image

Description

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

Application

  • 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.

Citation

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