Microbeads

Code: 130-048-701

Anti-FITC MicroBeads are widely used for indirect magnetic labeling and separation of cells or other materials which are labeled with a primary antibody or ligand conjugated to fluorescein isothiocyanate (FITC).

Specifications
Availability: Low

The Anti-GLAST (ACSA-1) MicroBead Kit has been developed for the separation of astrocytes based on the expression of GLAST.

Specifications
Availability: Low
Code: 130-046-101

Anti-HLA-DR MicroBeads have been developed for positive selection or depletion of antigen-presenting cells from PBMCs, cord blood, bone marrow, and tissue.

Specifications
Availability: Low
Code: 130-047-501

Anti-IgG MicroBeads were developed for the positive selection or depletion of surface IgG-expressing B cell populations from PBMCs or single-cell suspensions from lymphoid tissues.

Specifications
Availability: Low
Code: 130-093-230

Anti-IgM MicroBeads were developed for the positive selection or depletion of cells expressing IgM on their surface from PBMCs or single-cell suspensions from lymphoid tissues. The Anti-IgM MicroBeads recognize human IgM antibodies.

Specifications
Availability: Low
Code: 130-094-842

Anti-iNKT MicroBeads have been developed for the positive selection of human invariant natural killer T cells (iNKT cells) based on the expression of the TCR α-chain Vα24-Jα18.

Specifications
Availability: Low

The Anti-Ly6B.2 (7/4) MicroBeads, mouse can be used for isolation of neutrophils, inflammatory monocytes or myeloid progenitors from bone marrow or spleen.

 

Specifications
Availability: Low

Overview

Anti-Melanoma (MCSP) MicroBeads were developed for
  • enrichment of disseminated melanoma cells from peripheral blood, bone marrow, leukapheresis harvest, and lymphoid tissue of melanoma patients – even in early disease stages,
  • isolation of melanoma cells from single-cell suspensions of primary tumor tissue or primary skin cell culture.
Anti-Melanoma MicroBeads can be used in combination with the Inside Stain Kit. This enables the in-column staining of enriched melanoma cells for intracellular antigens, e. g., Melan-A. By performing combined enrichment and staining, a sensitivity of melanoma cell detection of one melanoma cell in 2×10
7
 PBMC background cells can be achieved
. For convenient subsequent immunocytochemical detection the Melanoma Enrichment and Detection Kit can be used.

Specifications
Availability: Low