SALL4 Antibody (A9G9-R)

Immunocytochemistry/ Immunofluorescence: SALL4 Antibody (A9G9-R) [NBP3-32926]

Immunocytochemistry/ Immunofluorescence: SALL4 Antibody (A9G9-R) [NBP3-32926] - Immunocytochemistry analysis of NCCIT cells labeling SALL4 with Mouse anti-SALL4 antibody (NBP3-32926) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-SALL4 antibody (NBP3-32926) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.

Flow Cytometry: SALL4 Antibody (A9G9-R) [NBP3-32926]

Flow Cytometry: SALL4 Antibody (A9G9-R) [NBP3-32926] - Flow cytometric analysis of NCCIT cells labeling SALL4.

Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32926, 1ug/ml) (red) compared with Mouse IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).