WB
Western blot analysis of various lysates using CD326/EpCAM Rabbit mAb at 1:3000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit .
Negative control (NC): C2C12.
IHC
Immunohistochemistry analysis of paraffin-embedded Human small intestine tissue using CD326/EpCAM Rabbit mAb at a dilution of 1:1000 (40x lens). High pressure antigen retrieval was performed with 0.01 M citrate buffer (pH 6.0) prior to IHC staining.
Exposure time: 20s.
IF-P
Confocal imaging of paraffin-embedded Mouse small intestine tissue using CD326/EpCAM Rabbit mAb (dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Perform high pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining. objective: 40x.
FC
Flow cytometry: 1X10^6 293T cells (negative control,left) and 293T (Transfection,right) cells were surface-stained with CD326/EpCAM Rabbit mAb (2ug/mL,orange line) or ABflo® 647 Rabbit IgG isotype control (5ul/Test,blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).