Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 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. |
Figure 1. Western blot analysis of Anti-CTNNA1 antibody (BA0425). The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: MCF-7 whole cell lysates,Use rabbit Anti-CTNNA1 1:1000, probed with a goat Anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002). A specific band was detected for CTNNA1 at approximately 100KD. The expected band size for CTNNA1 is at 100KD.
Figure 2. IHC analysis using Anti-CTNNA1 antibody (BA0425) detected in paraffin-embedded section of mammary cancer tissue. Biotinylated goat Anti-rabbit IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.
Figure 1. Western blot analysis of Anti-CTNNA1 antibody (BA0425). The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: MCF-7 whole cell lysates,Use rabbit Anti-CTNNA1 1:1000, probed with a goat Anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002). A specific band was detected for CTNNA1 at approximately 100KD. The expected band size for CTNNA1 is at 100KD.
Figure 2. IHC analysis using Anti-CTNNA1 antibody (BA0425) detected in paraffin-embedded section of mammary cancer tissue. Biotinylated goat Anti-rabbit IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.