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PE Mouse anti-Zap70 (pY292)
PE Mouse anti-Zap70 (pY292)

LEFT: Analysis of ZAP70 (pY292) in activated human T lymphocytes.  Human whole blood was either stimulated by cross-linking of CD3 with NA/LE Mouse anti-Human CD3 mAb UCHT1 (Cat. No. 555329) on ice for 15 minutes followed by Purified Goat anti-Mouse Ig (Cat. No. 553998) on ice for 15 minutes, and then allowed to undergo phosphorylation at 37°C for 5 minutes (shaded histogram), or unstimulated (open histogram).  The cells were lysed and fixed with 1X BD Phosflow™ Lyse/Fix Buffer (Cat. No. 558049) for 10-15 minutes at 37ºC, permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for 30 minutes, blocked with normal mouse immunoglobulin, and then stained with PE Mouse anti-ZAP70 (pY292) and PerCP-Cy5.5 Mouse anti-human CD3 mAb SK7 (Cat. No. 340949).  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.  For data analysis, CD3-positive and -negative lymphocytes were selected by their scatter and staining profiles.  The figure displays the CD3-positive T lymphocytes.  Up-regulated phosphorylation of ZAP70 (pY292) was not observed in the CD3-negative lymphocytes (data not shown).

RIGHT: Analysis of ZAP70 (pY292) in activated human T leukemia cells.  Jurkat cells (ATCC TIB152) were either stimulated by cross-linking of CD3 and CD28 with NA/LE Mouse anti-Human CD3 mAb UCHT1 (Cat. No. 555329) and NA/LE Mouse anti-Human CD28 mAb CD28.2 (Cat. No. 555725) on ice for 15 minutes followed by Purified Goat anti-Mouse Ig (Cat. No. 553998) on ice for 15 minutes, and then allowed to undergo phosphorylation at 37°C for 5 minutes (shaded histogram), or unstimulated (open histogram).  The cells were fixed (BD Cytofix™ buffer, Cat. No. 554655) for 10 minutes at 37°C, permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for at least 30 minutes, blocked with normal mouse immunoglobulin, and then stained with PE Mouse anti-ZAP70 (pY292).  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.

LEFT: Analysis of ZAP70 (pY292) in activated human T lymphocytes.  Human whole blood was either stimulated by cross-linking of CD3 with NA/LE Mouse anti-Human CD3 mAb UCHT1 (Cat. No. 555329) on ice for 15 minutes followed by Purified Goat anti-Mouse Ig (Cat. No. 553998) on ice for 15 minutes, and then allowed to undergo phosphorylation at 37°C for 5 minutes (shaded histogram), or unstimulated (open histogram).  The cells were lysed and fixed with 1X BD Phosflow™ Lyse/Fix Buffer (Cat. No. 558049) for 10-15 minutes at 37ºC, permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for 30 minutes, blocked with normal mouse immunoglobulin, and then stained with PE Mouse anti-ZAP70 (pY292) and PerCP-Cy5.5 Mouse anti-human CD3 mAb SK7 (Cat. No. 340949).  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.  For data analysis, CD3-positive and -negative lymphocytes were selected by their scatter and staining profiles.  The figure displays the CD3-positive T lymphocytes.  Up-regulated phosphorylation of ZAP70 (pY292) was not observed in the CD3-negative lymphocytes (data not shown).

RIGHT: Analysis of ZAP70 (pY292) in activated human T leukemia cells.  Jurkat cells (ATCC TIB152) were either stimulated by cross-linking of CD3 and CD28 with NA/LE Mouse anti-Human CD3 mAb UCHT1 (Cat. No. 555329) and NA/LE Mouse anti-Human CD28 mAb CD28.2 (Cat. No. 555725) on ice for 15 minutes followed by Purified Goat anti-Mouse Ig (Cat. No. 553998) on ice for 15 minutes, and then allowed to undergo phosphorylation at 37°C for 5 minutes (shaded histogram), or unstimulated (open histogram).  The cells were fixed (BD Cytofix™ buffer, Cat. No. 554655) for 10 minutes at 37°C, permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for at least 30 minutes, blocked with normal mouse immunoglobulin, and then stained with PE Mouse anti-ZAP70 (pY292).  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.

Product Details
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BD Phosflow™
ZAP-70 (pY292)
Human (QC Testing)
Mouse BALB/c IgG1, κ
Phosphorylated Human ZAP70
Intracellular staining (flow cytometry) (Routinely Tested)
20 µl
AB_647236
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 R-PE under optimum conditions, and unconjugated antibody and free PE were removed.

Recommended Assay Procedures

This antibody conjugate is suitable for intracellular staining of human whole blood (using BD Phosflow™ Lyse/Fix Buffer) and peripheral blood mononuclear cells (using BD Cytofix™ Fixation Buffer).  Any of the three BD Phosflow™ permeabilization buffers may be used.

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. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  3. 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.
  4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  5. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
558510 Rev. 2
Antibody Details
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J34-602

The 70-kDa ζ chain-associated protein (ZAP70) is a Syk-family protein tyrosine kinase (PTK) that associates with the ζ subunit of the T cell antigen receptor (TCR) and undergoes tyrosine phosphorylation following TCR stimulation.  ZAP70 contains two SH2-like domains with the PTK domain located at the C-terminus.  TCR-mediated Lck activity leads to phosphorylation of ZAP70 on Tyrosine 493 in the regulatory loop of the PTK domain leading to upregulation of ZAP70 kinase activity.  Tyrosine 292 (Y292), in the linker region between the SH2 and PTK domains, is autophosphorylated by the activated PTK domain.  By binding with c-Cbl, the phosphorylated Y292 can down-regulate TCR signaling.

The J34-602 antibody recognizes ZAP70 phosphorylated at Y292.

558510 Rev. 2
Format Details
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PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE 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 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
altImg
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
558510 Rev.2
Citations & References
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Development References (3)

  1. Kong G, Dalton M, Wardenburg JB, Straus D, Kurosaki T, Chan AC. Distinct tyrosine phosphorylation sites in ZAP-70 mediate activation and negative regulation of antigen receptor function. Mol Cell Biol. 1996; 16:5026-5035. (Biology). View Reference
  2. Magnan A, Di Bartolo V, Mura AM, et al. T cell development and T cell responses in mice with mutations affecting tyrosines 292 or 315 of the ZAP-70 protein tyrosine kinase. J Exp Med. 2001; 194:491-505. (Biology). View Reference
  3. Rao N, Lupher ML Jr, Ota S, Reedquist KA, Druker BJ, Band H. The linker phosphorylation site Tyr292 mediates the negative regulatory effect of Cbl on ZAP-70 in T cells. J Immunol. 2000; 164:4616-4626. (Biology). View Reference
558510 Rev. 2

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.