Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (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 anti- KRT18 antibody (BM0032). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: A431 whole cell lysates,
Lane 3: Caco-2 whole cell lysates,
Lane 4: HepG2 whole cell lysates.
Use mouse anti- KRT18 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for KRT18 at approximately 48KD. The expected band size for KRT18 is at 48KD.
Western blot analysis of anti- KRT18 antibody (BM0032). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: A431 whole cell lysates,
Lane 3: Caco-2 whole cell lysates,
Lane 4: HepG2 whole cell lysates.
Use mouse anti- KRT18 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for KRT18 at approximately 48KD. The expected band size for KRT18 is at 48KD.