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Anti cd138 coated magnetic beads

Manufactured by Miltenyi Biotec
Sourced in Germany

Anti-CD138–coated magnetic beads are a lab equipment product designed for the isolation and purification of cells expressing the CD138 antigen. The beads are made of a magnetic core coated with antibodies specific to the CD138 molecule, allowing for the selective capture and separation of CD138-positive cells from complex samples using a magnetic field.

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4 protocols using anti cd138 coated magnetic beads

1

Plasma Cell Isolation from Bone Marrow Aspirates

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In order to select plasma cells from BMA samples of MM and SMM patients, we performed CD138-positive selection among mononuclear cells of BMA as a method of choice. CD138, officially known as Syndecan 1, is a transmembrane (type I) heparan sulfate proteoglycan encoded by the human SDC1 gene; its expression is considered to be a hallmark of MM cells and plasma cells in the bone marrow [31 (link),32 (link),33 (link)]. Therefore, 10 mL of BMA were collected in tubes containing ethylenediaminetetraacetic acid (EDTA) and BMA samples were processed, immediately after collection, for CD138 enrichment. More specifically, the Ficoll-Paque technique was used to isolate mononuclear cells from BMA. Following that, a positive selection of CD138+ plasma cells was performed using anti-CD138–coated magnetic beads (Miltenyi Biotec, Bergisch Gladbach, Germany).
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2

Isolation of Plasma Cells from Bone Marrow

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Given that the expression of the cell surface antigen syndecan‐1 (CD138) is an important marker of plasma cells in the bone marrow,
24 (link) CD138+ selection among mononuclear cells was carried out, to isolate most of the plasma cells from the BMA samples of all patients included in this study. For this purpose, 10 mL of BMA from each subject was collected in ethylenediaminetetraacetic acid (EDTA). The CD138+ enrichment procedure was immediately performed. Thus, Ficoll‐Paque separation of the BMA mononuclear cells was followed by the selection of CD138+ plasma cells using anti‐CD138‐coated magnetic beads (Miltenyi Biotech).
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3

Isolation of CD138+ Plasma Cells

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Ten (10) mL of BMA from each participant were collected in tubes containing ethylenediaminetetraacetic acid (EDTA). The BMA samples were processed immediately after collection for CD138+ selection. The BMA mononuclear cells were first isolated using the Ficoll–Paque technique. After that, anti-CD138–coated magnetic beads (Miltenyi Biotech, Bergisch Gladbach, Germany) were used to perform a positive selection of CD138+ plasma cells.
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4

Profiling Genetic Aberrations in Multiple Myeloma

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All MM cell samples were purified using Miltenyi technology (anti-CD138-coated magnetic beads; Paris, France) before FISH as reported previously [31 (link)]. Plasma cells were then analyzed using DNA probes specific for the following chromosomal aberrations: 13q14 deletion, 17p13 deletion, t(11;14), t(4;14), and t(14;16). Gains of 1q21 were assessed using a bacterial artificial chromosome probe at 1q21 (RP11-307C12) [32 (link)]. A total of 200 interphase nuclei were analyzed. According to Intergroupe Francophone du Myélome (IFM), high-risk MM was defined as the presence of any one or more of the following genetic abnormalities: deletion of 17p13, t(4;14), and t(14;16) [31 (link)].
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