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Improve data resolution with PE-CF594 alternative with reduced spillover and enhanced brightness! Try BD RealBlue™ 613 SKU# 758405 today! More Info on RB613 #
562383Image1.png

Multicolor flow cytometric analysis of CD34 expressed by human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were incubated in the presence of Human BD Fc Block™(Cat. No. 564219/564220) and were stained with PE Mouse Anti-Human CD14 antibody (Cat. No. 555398/561707), FITC Mouse Anti-Human CD45 (Cat. No. 555482/560976/561865) and either a BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat No. 562292, Left Panel) or the BD Horizon™ PE-CF594 Mouse Anti-Human CD34 antibody (Cat. No. 562383, Right Panel). Flow cytometric dot plots showing side-scattered light signals versus CD34 fluorescence (or Ig isotype control staining) were derived from gated events based on the light scattering characteristics for viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.

PECF594CD34Contour.png

Multicolor flow cytometric analysis of CD34 expressed by human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were incubated in the presence of Human BD Fc Block™(Cat. No. 564219/564220) and were stained with PE Mouse Anti-Human CD14 antibody (Cat. No. 555398/561707), FITC Mouse Anti-Human CD45 (Cat. No. 555482/560976/561865) and either a BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat No. 562292, Left Panel) or the BD Horizon™ PE-CF594 Mouse Anti-Human CD34 antibody (Cat. No. 562383, Right Panel). Flow cytometric dot plots showing side-scattered light signals versus CD34 fluorescence (or Ig isotype control staining) were derived from gated events based on the light scattering characteristics for viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.

562383Image1.png PECF594CD34Contour.png Orange-Cap-Blue-Label.jpg

Multicolor flow cytometric analysis of CD34 expressed by human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were incubated in the presence of Human BD Fc Block™(Cat. No. 564219/564220) and were stained with PE Mouse Anti-Human CD14 antibody (Cat. No. 555398/561707), FITC Mouse Anti-Human CD45 (Cat. No. 555482/560976/561865) and either a BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat No. 562292, Left Panel) or the BD Horizon™ PE-CF594 Mouse Anti-Human CD34 antibody (Cat. No. 562383, Right Panel). Flow cytometric dot plots showing side-scattered light signals versus CD34 fluorescence (or Ig isotype control staining) were derived from gated events based on the light scattering characteristics for viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.

Multicolor flow cytometric analysis of CD34 expressed by human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were incubated in the presence of Human BD Fc Block™(Cat. No. 564219/564220) and were stained with PE Mouse Anti-Human CD14 antibody (Cat. No. 555398/561707), FITC Mouse Anti-Human CD45 (Cat. No. 555482/560976/561865) and either a BD Horizon™ PE-CF594 Mouse IgG1, κ Isotype Control (Cat No. 562292, Left Panel) or the BD Horizon™ PE-CF594 Mouse Anti-Human CD34 antibody (Cat. No. 562383, Right Panel). Flow cytometric dot plots showing side-scattered light signals versus CD34 fluorescence (or Ig isotype control staining) were derived from gated events based on the light scattering characteristics for viable CD14-negative cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.

Product Details
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BD Horizon™
gp105-120; My10; Hematopoietic progenitor cell antigen CD34
Human (QC Testing)
Mouse IgG1, κ
Flow cytometry (Routinely Tested)
5 µl
V MA27, VI E004
AB_11154586
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 with BD Horizon™ PE-CF594 under optimum conditions, and unconjugated antibody and free PE-CF594 were removed.
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Recommended Assay Procedures

BD™ CompBeads can be used as surrogates to assess fluorescence spillover (Compensation).  When fluorochrome conjugated antibodies are bound to CompBeads, they have spectral properties very similar to cells.   However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls.  It is strongly recommended that when using a reagent for the first time, users compare the spillover on cells and CompBead to ensure that BD Comp beads are appropriate for your specific cellular application.

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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. Please observe the following precautions: Absorption of visible light can significantly alter the energy transfer occurring in any tandem fluorochrome conjugate; therefore, we recommend that special precautions be taken (such as wrapping vials, tubes, or racks in aluminum foil) to prevent exposure of conjugated reagents, including cells stained with those reagents, to room illumination.
  6. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  7. CF™ is a trademark of Biotium, Inc.
  8. When excited by the yellow-green (561-nm) laser, the fluorescence may be brighter than when excited by the blue (488-nm) laser.
  9. This product is provided under an Agreement between BIOTIUM and BD Biosciences. The manufacture, use, sale, offer for sale, or import of this product is subject to one or more patents or pending applications owned or licensed by Biotium, Inc. This product, and only in the amount purchased by buyer, may be used solely for buyer’s own internal research, in a manner consistent with the accompanying product literature. No other right to use, sell or otherwise transfer (a) this product, or (b) its components is hereby granted expressly, by implication or by estoppel. This product is for research use only. Diagnostic uses require a separate license from Biotium, Inc. For information on purchasing a license to this product including for purposes other than research, contact Biotium, Inc., 3159 Corporate Place, Hayward, CA 94545, Tel: (510) 265-1027. Fax: (510) 265-1352. Email: btinfo@biotium.com.
  10. Because of the broad absorption spectrum of the tandem fluorochrome, extra care must be taken when using multi-laser cytometers, which may directly excite both PE and CF™594.
  11. Texas Red is a registered trademark of Molecular Probes, Inc., Eugene, OR.
  12. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  13. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
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562383 Rev. 3
Antibody Details
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581

The 581 monoclonal antibody specifically binds to CD34, a sialomucin-like type I transmembrane glycoprotein. This single-chain, 105-120 kDa, heavily O-glycosylated protein is expressed on hematopoietic progenitor cells, vascular endothelium, bone marrow stromal cells and embryonic fibroblasts. The cytoplasmic region of the CD34 antigen is a target for phosphorylation by activated protein kinase C suggesting CD34 may play a role in signal transduction. CD34 may also play a role as an adhesion molecule since it binds to CD62E and CD62L. Clone 581 binds to the class III CD34 epitope. It is resistant to neuraminidase, chymopapain and glycoprotease. The 581 antibody blocks reactivity of another anti-CD34 monoclonal antibody, 8G12.

This antibody is conjugated to BD Horizon PE-CF594, which has been developed exclusively by BD Biosciences as a better alternative to PE-Texas Red®. PE-CF594 excites and emits at similar wavelengths to PE-Texas Red® yet exhibits improved brightness and spectral characteristics. Due to PE having maximal absorption peaks at 496 nm and 564 nm, PE-CF594 can be excited by the blue (488-nm), green (532-nm) and yellow-green (561-nm) lasers and can be detected with the same filter set as PE-Texas Red® (eg, 610/20-nm filter).

562383 Rev. 3
Format Details
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PE-CF594
BD Horizon™ PE-CF594 dye is a part of the BD PE family of dyes. This tandem fluorochrome is comprised of a R-Phycoerythrin (PE) donor that has excitation maxima (Ex Max) of 496-nm and 566-nm and an acceptor dye with an emission maximum (Em Max) at 615-nm. PE-CF594, driven by BD innovation, is designed to be excited by the blue (488-nm), Green (532-nm) and Yellow-Green (561-nm) lasers and detected using an optical filter centered near 615 nm (e.g., a 610/20-nm bandpass filter). The donor dye can be excited by the Blue (488-nm), Green (532-nm) and Yellow-Green (561-nm) lasers and the acceptor dye can be excited by the Green (532-nm) laser resulting in cross-laser excitation and fluorescence spillover. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
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PE-CF594
496 nm, 566 nm
615 nm
562383 Rev.3
Citations & References
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View product citations for antibody "562383" on CiteAb

Development References (5)

  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. 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.
  5. Zola H. Leukocyte and stromal cell molecules : the CD markers. Hoboken, N.J.: Wiley-Liss; 2007.
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562383 Rev. 3

Please refer to Support Documents for Quality Certificates

 

Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

 

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.