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Western blot analysis of various lysates using CD3 Rabbit mAb (A26443)at 1:1000 dilutionincubated overnight at 4°C. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Negative control (NC): PC-3 Exposure time: 10s. |
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Confocal imaging of paraffin-embedded Human spleen tissue using CD3 Rabbit mAb (A26443, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x. |
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Confocal imaging of paraffin-embedded Human tonsil tissue using CD3 Rabbit mAb (A26443, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x. |
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Flow cytometry: 1X10 6 Raji cells (negative control,left) and Human PBMC (right) were surface-stained with CD3 Rabbit mAb (A26443,2 µg/mL,orange line) or Rabbit IgG isotype control (AC042,2 µg/mL,blue line), followed by Alexa Fluor 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line). |
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Flow cytometry: 1X10 6 Human PBMC were surface-stained with Rabbit IgG isotype control (AC042,2 µg/mL,left) or CD3 Rabbit mAb (A26443,2 µg/mL,right), followed by Alexa Fluor 647 conjugated goat anti-rabbit pAb staining. |
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Confocal imaging of paraffin-embedded Human tonsil tissue using CD3 Rabbit mAb (A26443, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IF staining. Objective: 40x. |
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Flow cytometry: 1X10 6 Raji cells (negative control,left) and Human PBMC (right) were surface-stained with CD3 Rabbit mAb (A26443,2 µg/mL,orange line) or Rabbit IgG isotype control (AC042,2 µg/mL,blue line), followed by Alexa Fluor 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line). |
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Flow cytometry: 1X10 6 Human PBMC were surface-stained with Rabbit IgG isotype control (AC042,2 µg/mL,left) or CD3 Rabbit mAb (A26443,2 µg/mL,right), followed by Alexa Fluor 647 conjugated goat anti-rabbit pAb staining. |