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Anti γδ tcr

Manufactured by BD

The Anti-γδ TCR is a laboratory reagent used for the detection and analysis of γδ T cells. It binds specifically to the γδ T cell receptor, allowing for the identification and quantification of this cell population within a sample.

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2 protocols using anti γδ tcr

1

Immunofluorescence Analysis of Skin Immune Cells

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Frozen sections were fixed with 4% paraformaldehyde/phosphate-buffered saline and stained with the following antibodies conjugated with Alexa 488 or FITC or Alexa 633: anti-CD3 (BD Pharmingen, San Diego, CA, clone 17A2), anti-CD4 (eBioscience, San Diego, CA, clone RM4-5), anti-γδ TCR (BD Pharmingen, clone GL3), anti-Vγ3 TCR (BD Pharmingen, clone 536), or anti-Ly6G/Gr-1 (Beckman Coulter, Miami, FL, clone RB6-8C5). Formalin-fixed paraffin sections were treated with citrate buffer for antigen retrieval and incubated with anti-Camp (Abcam, Cambridge, UK) or anti-β3 defensin (Alpha Diagnostic, San Antonio, TX) followed by Alexa 488-conjugated donkey anti-rabbit antibody (Life Technologies). DAPI or PI was used for nuclear staining. Images were acquired using a TCS SP5 Tandem Scanner or an FV1000 confocal microscope (Olympus, Tokyo, Japan). When quantifying cells that expressed a particular marker, at least six fields were analyzed per skin section.
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2

Multicolor Immunofluorescence Staining of Skin Sections

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Frozen sections were fixed with 4% peraformaldehyde/PBS and stained with the following antibodies conjugated with Alexa 488, fluorescein isothiocyanate (FITC) or Alexa 633: anti-CD3 (BDPharmingen, clone 17.A2), anti-CD4 (eBioscience, clone RM4-5), anti-γδ TCR (BDPharmingen, clone GL3), anti-Vγ3 TCR (BDPharmingen, clone 536) or anti-Ly6G/Gr-1 (Beckman Coulter, clone RB6-8C5). Formalin-fixed paraffin sections were treated with citrate buffer for antigen retrieval and incubated with anti-Camp (Abcam) or anti-β3 defensin (Alpha Diagnostic) followed by Alexa 488-conjugated donkey anti-rabbit antibody (Life Technologies). DAPI or PI was used for nuclear staining. Images were acquired using a Leica TCS SP5 Tandem Scanner or an Olympus FV1000 confocal microscope. When quantifying cells that expressed a particular marker, at least 6 fields were analysed per skin section.
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