Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry: | 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- LMNA antibody (BA1227).The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: Human placenta tissue lysates,Lane 2: Human PC-3 whole cell lysates,Lane 3: Human HELA whole cell lysates,Lane 4: Human HepG2 whole cell lysates,Lane 5: Human CACO-2 whole cell lysates,Lane 6: rat spleen tissue lysates,Lane 7: mouse liver tissue lysates.Use rabbit anti- LMNA 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 LMNA at approximately 70-74KD. The expected band size for LMNA is at 74KD.
Figure 1. Western blot analysis of anti- LMNA antibody (BA1227).The sample well of each lane was loaded with 50ug of sample under reducing conditions.Lane 1: Human placenta tissue lysates,Lane 2: Human PC-3 whole cell lysates,Lane 3: Human HELA whole cell lysates,Lane 4: Human HepG2 whole cell lysates,Lane 5: Human CACO-2 whole cell lysates,Lane 6: rat spleen tissue lysates,Lane 7: mouse liver tissue lysates.Use rabbit anti- LMNA 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 LMNA at approximately 70-74KD. The expected band size for LMNA is at 74KD.