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Human Type II Diabetes Peripheral Blood Mononuclear Cells

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Human Peripheral Blood Mononuclear Cells are available as positive and negative controls for T-cell monitoring in ELISPOT, ELISA, cytokine bead array, tetramer/pentamer, and flow cytometry assays. A peripheral blood mononuclear cell is defined as any blood cell with a round nucleus. These blood cells are a critical component in the immune system to fight infection […]
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Species

Human

Cat.No

ABC-TC4265

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

Type II Diabete

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Diseased Human Peripheral Blood Mononuclear Cells

Description

Human Type II Diabetes Peripheral Blood Mononuclear CellsHuman Type II Diabetes Peripheral Blood Mononuclear Cells (PBMCs) are immune cells isolated from the peripheral blood of patients with Type II Diabetes Mellitus (T2DM) using density gradient centrifugation. These cells consist mainly of monocytes (20%) and lymphocytes (T and B cells). PBMCs from T2DM patients exhibit elevated CD68 expression and reduced CD11b and CD163 expression, with corresponding decreases in the mRNA levels of CD11b, CD11c, CD169, and CD163. In culture, PBMCs are grown in RPMI-1640 medium supplemented with 10% fetal bovine serum and are known to have limited in vitro proliferation. These cells do not exhibit tumorigenic or metastatic behavior. They serve as an important model for studying immune system alterations in T2DM. PBMCs from T2DM patients also show a higher prevalence of Epstein-Barr virus (EBV) infection, which may contribute to immune dysfunction.

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Citation

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Application

  • Human Type II Diabetes Peripheral Blood Mononuclear Cells (PBMCs) have important application value in diabetes-related research. In terms of disease mechanism research, by analyzing the gene expression profiles and signal pathway changes of these cells, it is helpful to deeply explore the pathogenesis of type II diabetes and clarify which genes or pathway abnormalities lead to insulin resistance, impaired pancreatic β-cell function, and other problems.

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