

562892 ·
BDB Bioscience · Cat: 562892
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Description
Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II. Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II. Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II. Show More Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II. Show More Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II. Multicolor flow cytometric analysis of gammadelta TCR expression on mouse peripheral T lymphocytes. C57BL/6 lymph node cells were incubated simultaneously with PE Rat anti-Mouse CD3 Molecular Complex Cat. No. 555275/561799 and with either BV421 Hamster IgG2, kappa Isotype Control Cat. No. 562612, left panel or BV421 Hamster Anti-Mouse gammadelta T-Cell Receptor Cat. No. 562892, right panel . Two-color flow cytometric dot plots showing the correlated expression of gammadelta T-Cell Receptor or Ig Isotype control staining versus CD3 were derived from gated events with the forward and light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSR II.







