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  • MACS® Cell Analysis
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Cell separation reagents Cell separation reagents
  for human cells
  Stem and progenitor cells
  T cells
  NK cells
  B Cells
 
 
 
  Monocytes
  Dendritic cells
  Antigen-presenting cells
  Granulocytes and myeloid cells
  Leukocytes
  Erythroid cells
  Megakaryocytes and platelets
  Endothelial cells
  Epithelial cells
  Fibroblasts
  Neural cells
  Cytokine-producing cells
  Tumor cells
  Fc receptor blocking
  for non-human primate cells
  for mouse cells
  for rat cells
  for indirect magnetic labeling
  for apoptotic and dead cells
  for isolation of mitochondria
Manual cell separation Manual cell separation
Automated cell separation Automated cell separation
MACS® Technology MACS® Technology
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CD22 MicroBeads
Overview
CD22 MicroBeads were developed for positive selection or depletion of human B cells from PBMCs, bone marrow, or single-cell suspensions from lymphoid tissues.
Details
Background information
In peripheral blood, cell surface expression of the CD22 antigen is found on mature B cells, but is lost during terminal differentiation to plasma cells. In bone marrow, surface expression of CD22 can be detected from the pre-B cell stage on. Cytoplasmic expression of CD22 can also be found in late pro-B cells and early pre-B cells.

Downstream applications
The purified B cells may be used for cell biological studies, such as analysis of signal transduction2, mixed lymphocyte responses1, antigen presentation, or for molecular studies, e.g. PCR analysis3.
Columns
For positive selection: MS, LS, XS, or autoMACS® Columns. For depletion: LD, CS, D, or autoMACS Columns.
 
Figure 1
Separation of CD22+ cells from PBMCs using CD22 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells are stained with CD19-FITC.
Figure 2
B cells isolated from PBMCs using MACS® Technology, Giemsa stained.
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Details
Products
CD22 MicroBeads, human
- for 109 total cells
Download datasheet
130-046-401
Qty.:
 

Related products
CD19 Antibodies
CD20 Antibodies
CD45 Antibodies
References
1. Butch et al. (1999) Blood 94: 216-224.
2. Jacquot et al. (2001) Int. Immunol. 13: 871-876.
3. Borson et al. (2002) Blood 100: 4629-4639.
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