Immunohistochemistry (IHC): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of mouse lymphaden tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of rat lymphaden tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of mouse PBMC cells using anti-TNFRSF7/CD27 antibody (A01148-2).
Overlay histogram showing mouse PBMC cells stained with A01148-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of mouse lymphaden tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of rat lymphaden tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of TNFRSF7/CD27 using anti-TNFRSF7/CD27 antibody (A01148-2).
TNFRSF7/CD27 was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of mouse PBMC cells using anti-TNFRSF7/CD27 antibody (A01148-2).
Overlay histogram showing mouse PBMC cells stained with A01148-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TNFRSF7/CD27 Antibody (A01148-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.