Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
(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 NRG1 using anti-NRG1 antibody (BA3235). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human Hacat whole cell lysates,
Lane 3: rat brain tissue lysates,
Lane 4: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NRG1 antigen affinity purified polyclonal antibody (BA3235) 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 NRG1 at approximately 100,65,40 kDa. The expected band size for NRG1 is at 70,65,40,25 kDa.
IHC analysis of NRG1 using anti-NRG1 antibody (BA3235).
NRG1 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-NRG1 Antibody (BA3235) 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 of NRG1 using anti-NRG1 antibody (BA3235) and anti-Beta Tubulin antibody (M01857-3).
NRG1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-NRG1 Antibody (BA3235) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) and Dylight550-conjugated Anti- mouse IgG Secondary Antibody (red)(Catalog#BA1133) were used as secondary antibody.
Western blot analysis of NRG1 using anti-NRG1 antibody (BA3235). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human Hacat whole cell lysates,
Lane 3: rat brain tissue lysates,
Lane 4: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NRG1 antigen affinity purified polyclonal antibody (BA3235) 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 NRG1 at approximately 100,65,40 kDa. The expected band size for NRG1 is at 70,65,40,25 kDa.
IHC analysis of NRG1 using anti-NRG1 antibody (BA3235).
NRG1 was detected in a paraffin-embedded section of human tonsil tissue. The tissue section was incubated with rabbit anti-NRG1 Antibody (BA3235) 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 of NRG1 using anti-NRG1 antibody (BA3235) and anti-Beta Tubulin antibody (M01857-3).
NRG1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-NRG1 Antibody (BA3235) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) and Dylight550-conjugated Anti- mouse IgG Secondary Antibody (red)(Catalog#BA1133) were used as secondary antibody.