Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
ELISA(Cap): | 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. |
Figure 1. Western blot analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: rat spleen tissue lysates,
Lane 3: mouse spleen lysates,
Lane 4: mouse thymus tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IFN Gamma/IFNG antigen affinity purified polyclonal antibody (A00393-3) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for IFN Gamma/IFNG at approximately 19 kDa. The expected band size for IFN Gamma/IFNG is at 19 kDa.
Figure 2. IHC analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3).
IFN Gamma/IFNG was detected in a paraffin-embedded section of mouse colon tissue. The tissue section was incubated with rabbit anti-IFN Gamma/IFNG Antibody (A00393-3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3).
IFN Gamma/IFNG was detected in a paraffin-embedded section of human melanoma tissue. The tissue section was incubated with rabbit anti-IFN Gamma/IFNG Antibody (A00393-3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 1. Western blot analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: rat spleen tissue lysates,
Lane 3: mouse spleen lysates,
Lane 4: mouse thymus tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IFN Gamma/IFNG antigen affinity purified polyclonal antibody (A00393-3) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for IFN Gamma/IFNG at approximately 19 kDa. The expected band size for IFN Gamma/IFNG is at 19 kDa.
Figure 2. IHC analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3).
IFN Gamma/IFNG was detected in a paraffin-embedded section of mouse colon tissue. The tissue section was incubated with rabbit anti-IFN Gamma/IFNG Antibody (A00393-3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (A00393-3).
IFN Gamma/IFNG was detected in a paraffin-embedded section of human melanoma tissue. The tissue section was incubated with rabbit anti-IFN Gamma/IFNG Antibody (A00393-3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.