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Primary Cells

Human SLE Peripheral Blood Mononuclear Cells

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Peripheral blood mononuclear cells are isolated from Systemic Lupus Erythematosus (SLE) peripheral blood by diluting the whole blood with PBS and using gradient separation techniques. After centrifugation,the mononuclear cell layer is collected. Mononuclear Cells can be processed further to isolate subpopulations. Fresh SLE PBMCs is available upon request.
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Species

Human

Cat.No

ABC-TC4254

Quality Control

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

Product Category Primary Cells
Size/Quantity

1 vial

Cell Type

Mononuclear Cell

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

Peripheral Blood

Disease

Systemic Lupus Erythematosus

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Diseased Human Peripheral Blood Mononuclear Cells

Description

Human SLE Peripheral Blood Mononuclear Cells are derived from the peripheral blood of patients with systemic lupus erythematosus (a systemic autoimmune disease), including lymphocytes (T cells, B cells, NK cells), monocytes and dendritic cells, Typical mononuclear morphology with small to medium round cells; suspension growth[1-2].Peripheral blood from systemic lupus erythematosus (SLE) patients PBMCs play a core role in the pathogenesis of SLE. Their functional abnormalities include overactivation of B cells leading to autoantibody secretion, imbalanced T cell regulation, and release of proinflammatory factors (IFN-α, IL-6) [3-4]. These abnormalities are closely related to the typical characteristics of SLE, such as immune complex deposition and multi-organ damage (kidney, skin, joints). Increased expression of activation markers like CD69, CD86 on B and T cells; elevated type I interferon signature genes; high autoantibody (anti-dsDNA) producing B cells.Abnormal immune complex deposition triggers chronic inflammation and multi-organ damage typical of SLE.

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Application

  • Human SLE Peripheral Blood Mononuclear Cells (PBMCs) can be used to study the immunopathogenesis of systemic lupus erythematosus (SLE) and develop novel therapeutic strategies. They can also be applied to investigate disease-specific immune dysregulation, including B-cell hyperactivation, T-cell dysfunction, and aberrant cytokine production.

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