Primary Cells

Human Amyotrophic Lateral Sclerosis (ALS) Peripheral Blood Mononuclear Cells

  • For research use only

Cat No.

ABC-TC4344

Product Type

Diseased Human Peripheral Blood Mononuclear Cells

Cell Type

Mononuclear Cell

Species

Human

Growth Conditions

37 ℃, 5% CO2

Source Organ

Peripheral Blood

Disease

Amyotrophic Lateral Sclerosis

Storage

Liquid Nitrogen

Explore Human Amyotrophic Lateral Sclerosis Peripheral Blood Mononuclear Cells for immune profiling, neuroinflammation, and ALS-related biomarker studies.

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Description

Human Amyotrophic Lateral Sclerosis (ALS) Peripheral Blood Mononuclear Cells (PBMCs) are isolated from patients with clinically confirmed amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease affecting motor neurons. These human-derived PBMCs contain lymphocytes (T cells, B cells, NK cells) and monocytes that exhibit neuroinflammatory characteristics, including elevated pro-inflammatory cytokine production (IL-6, TNF-α) and increased CD4⁺ T cell activation. The cells demonstrate typical mononuclear morphology with intact surface markers and retain functional immune responses. ALS PBMCs are particularly valuable for studying neuroimmune interactions, as emerging evidence suggests peripheral inflammation contributes to disease progression.

Species

Human

Cat.No

ABC-TC4344

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

Amyotrophic Lateral Sclerosis

Storage

Liquid Nitrogen

Product Type

Diseased Human Peripheral Blood Mononuclear Cells

Quality Control

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

Application

  • Human Amyotrophic Lateral Sclerosis (ALS) Peripheral Blood Mononuclear Cells can be used to study the immunopathological mechanism of ALS progression, biomarker screening and drug efficacy evaluation. In addition, the distinct immune phenotype of PBMCs may offer a potential basis for the early diagnosis of the disease.

Citation

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