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APC Mouse Anti-Human CD34
APC Mouse Anti-Human CD34

Flow cytometric analysis of CD34 expression on CD14-negative Rhesus macaque peripheral blood mononuclear cells. Rhesus macaque peripheral blood mononuclear cells were stained with Alexa Fluor® 488 Mouse Anti-Human CD14 antibody (Cat. No. 557700) in conjunction with either APC Mouse IgG1, κ Isotype Control (Cat. No. 554681; Left Panel) or APC Mouse Anti-Human CD34 antibody (Cat. No. 561209, Right Panel). Two-parameter flow cytometric dot plots showing the correlated expression of CD34 (or Ig Isotype control staining) versus side scattered light were derived from gated events based on the forward and side light-scattering characteristics of viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometry System.

Flow cytometric analysis of CD34 expression on CD14-negative Rhesus macaque peripheral blood mononuclear cells. Rhesus macaque peripheral blood mononuclear cells were stained with Alexa Fluor® 488 Mouse Anti-Human CD14 antibody (Cat. No. 557700) in conjunction with either APC Mouse IgG1, κ Isotype Control (Cat. No. 554681; Left Panel) or APC Mouse Anti-Human CD34 antibody (Cat. No. 561209, Right Panel). Two-parameter flow cytometric dot plots showing the correlated expression of CD34 (or Ig Isotype control staining) versus side scattered light were derived from gated events based on the forward and side light-scattering characteristics of viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometry System.

Product Details
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BD Pharmingen™
gp 105-120
Rhesus, Cynomolgus (QC Testing), Human (Tested in Development)
Mouse IgG1, κ
Flow cytometry (Routinely Tested)
5 µl
V MA030
947
AB_10683161
Aqueous buffered solution containing BSA and ≤0.09% sodium azide.
RUO


Preparation And Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to APC under optimum conditions, and unconjugated antibody and free APC were removed.

Product Notices

  1. This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
  2. An isotype control should be used at the same concentration as the antibody of interest.
  3. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  4. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
  5. This APC-conjugated reagent can be used in any flow cytometer equipped with a dye, HeNe, or red diode laser.
  6. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  7. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  8. Species cross-reactivity detected in product development may not have been confirmed on every format and/or application.
  9. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
561209 Rev. 2
Antibody Details
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563

The 563 monoclonal antibody specifically binds to CD34. CD34 is a single-chain 105-120 kDa heavily O-glycosylated transmembrane glycoprotein expressed on hematopoietic progenitor cells, vascular endothelium and some tissue fibroblasts. The intracellular chain of the CD34 antigen is a target for phosphorylation by activated protein kinase C suggesting that CD34 may play a role in signal transduction. CD34 may play a role in adhesion of specific antigens to endothelium. Clone 563 belongs to the class III epitope; it is resistant to neuraminidase, chymopapain and glycoprotease. This antibody is able to block the binding of other CD34 mAbs like 581.

Clone 563 reacts with the human form of the 105-120 kDa heavily O-glycosylated and N-glycosylated transmembrane glycoprotein, CD34, expressed on stem/progenitor hematopoietic cells, endothelial cells and some tissue. Clone 563 also cross reacts with a subset of peripheral blood mononuclear cells of both rhesus and cynomolgus macaque monkeys, but not baboon. The distribution of stem-like cells is similar to that observed with peripheral blood mononuclear cells from normal human donors.

561209 Rev. 2
Format Details
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APC
Allophycocyanin (APC), is part of the BD family of phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 651 nm and an emission maximum (Em Max) at 660 nm. APC is designed to be excited by the Red (627-640 nm) laser and detected using an optical filter centered near 660 nm (e.g., a 660/20 nm bandpass filter). Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
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APC
Red 627-640 nm
651 nm
660 nm
561209 Rev.2
Citations & References
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Development References (6)

  1. Egeland T, Tjonnfjord G, Steen R, Gaudernack G, Thorsby E. Positive selection of bone marrow-derived CD34 positive cells for possible stem cell transplantation. Transplant Proc. 1993; 25(1):1261-1263. (Biology). View Reference
  2. Kishimoto T. Tadamitsu Kishimoto .. et al., ed. Leucocyte typing VI : white cell differentiation antigens : proceedings of the sixth international workshop and conference held in Kobe, Japan, 10-14 November 1996. New York: Garland Pub.; 1997.
  3. Knapp W. W. Knapp .. et al., ed. Leucocyte typing IV : white cell differentiation antigens. Oxford New York: Oxford University Press; 1989:1-1182.
  4. Nishio H, Tada J, Hashiyama N, Hirn J, Ingles-Esteven J, Suda T. CD34. 1999. Available: http://mpr.nci.nih.gov/prow/guide/968267813_g.htm 2006, February 8.
  5. Owens MA, Loken MR. Peripheral blood stem cell quantitation. In: Owens MA, Loken MR. Flow Cytometry Principles for Clinical Laboratory Practice. New York: John Wiley & Sons; 1995:128.
  6. Schlossman SF. Stuart F. Schlossman .. et al., ed. Leucocyte typing V : white cell differentiation antigens : proceedings of the fifth international workshop and conference held in Boston, USA, 3-7 November, 1993. Oxford: Oxford University Press; 1995.
View All (6) View Less
561209 Rev. 2

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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.