Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (IF): | 1:50-400 |
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. |
Western blot analysis of NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NeuN/RBFOX3 antigen affinity purified polyclonal antibody (A11954-1) 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 NeuN/RBFOX3 at approximately 46-55 kDa. The expected band size for NeuN/RBFOX3 is at 41 kDa.
IHC analysis of NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1).
NeuN/RBFOX3 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-NeuN/RBFOX3 Antibody (A11954-1) 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 NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1).
NeuN/RBFOX3 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NeuN/RBFOX3 Antibody (A11954-1) 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.
IF analysis using anti- NEUN antibody (A11954-1). detected in paraffin-embedded section of rat brain tissue. The tissue section were stained using the cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog # BA1032).
Western blot analysis of NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NeuN/RBFOX3 antigen affinity purified polyclonal antibody (A11954-1) 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 NeuN/RBFOX3 at approximately 46-55 kDa. The expected band size for NeuN/RBFOX3 is at 41 kDa.
IHC analysis of NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1).
NeuN/RBFOX3 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-NeuN/RBFOX3 Antibody (A11954-1) 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 NeuN/RBFOX3 using anti-NeuN/RBFOX3 antibody (A11954-1).
NeuN/RBFOX3 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NeuN/RBFOX3 Antibody (A11954-1) 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.
IF analysis using anti- NEUN antibody (A11954-1). detected in paraffin-embedded section of rat brain tissue. The tissue section were stained using the cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog # BA1032).