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Human Multiple Myeloma Peripheral Blood Mononuclear Cells (Relapsed/Refractory)

  • BSL

    1

  • 195
Multiple Myeloma Peripheral Blood Mononuclear Cells are isolated from Multiple Myeloma-peripheral blood by diluting the blood with phosphate-buffered salineand using gradient separation techniques. After centrifugation, the Mononuclear Cells layer is collected. Mononuclear Cells can be processed further to isolate subpopulations. Multiple Myeloma PBMCs products are available in both the newly diagnosed and the relapsed/refractory stages.
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Home | Primary Cells | Human Primary Cells | PBMCs | Human Multiple Myeloma Peripheral Blood Mononuclear Cells (Relapsed/Refractory)
Species

Human
Cat.No

ABC-TC3951
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

Multiple Myeloma
Biosafety Level

1
Storage

Liquid Nitrogen
Product Type

Diseased Human Peripheral Blood Mononuclear Cells

Description

Multiple Myeloma Peripheral Blood Mononuclear Cells are isolated from Multiple Myeloma-peripheral blood by diluting the blood with phosphate-buffered salineand using gradient separation techniques. After centrifugation, the Mononuclear Cells layer is collected. Mononuclear Cells can be processed further to isolate subpopulations. Multiple Myeloma PBMCs products are available in both the newly diagnosed and the relapsed/refractory stages.

AcceGen Frozen Cells & Cell Lines 1 vial
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Citation

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Application

  • For research use only.

  • Peripheral blood mononuclear cells (PBMCs) are widely used in experimental studies. They are isolated from peripheral blood and are often employed to assess immune responses. PBMCs have wide application in many hot topics, for example, multi-omics analysis of PBMCs based on CITE-seq data, in vitro differentiation of PBMCs into cardiomyocytes or vascular-associated cells. Our products are ideal for establishing an in vitro PBMC differentiation system that allows you to combine molecular and cytological approaches to study the differentiation mechanisms of PBMCs.

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