SET Antibody - BSA Free

Immunoprecipitation: SET Antibody [NBP1-33713]

Immunoprecipitation: SET Antibody [NBP1-33713] - SET antibody immunoprecipitates SET protein in IP experiments. IP samples: HeLa whole cell extract. A. Control with 4 ug of preimmune Rabbit IgG. B. Immunoprecipitation of SET protein by 4 ug SET antibody. 10 % SDS-PAGE. The immunoprecipitated SET protein was detected by SET antibody diluted at 1:500.

Western Blot: SET Antibody [NBP1-33713] -

Western Blot: SET Antibody [NBP1-33713] - Various whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with SET antibody (NBP1-33713) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.

Western Blot: SET Antibody [NBP1-33713] -

Western Blot: SET Antibody [NBP1-33713] - Non-transfected (–) and transfected (+) C2C12 whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with SET antibody diluted at 1:1000.

Immunocytochemistry/ Immunofluorescence: SET Antibody [NBP1-33713] -

SET antibody detects SET protein at cytoplasm and nucleus by immunofluorescent analysis.
Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: SET protein stained by SET antibody (NBP1-33713) diluted at 1:500.
Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] diluted at 1:1000.
Blue: Hoechst 33342 staining.

Western Blot: SET Antibody - BSA Free [NBP1-33713] -

Raddeanin A‐treated NK cells enhance apoptosis in FaDu cells. (A, B) Mitochondrial membrane potential assay and (C, D) annexin V/PI stain assay of FaDu cells were measured after Raddeanin A treatment by Muse Cell Analyser. Quantitative data were analysed by Muse Cell Software V1.4.0.0. (E) Fas protein levels of Raddeanin A‐induced apoptosis. FaDu cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 And then treated with Raddeanin A for 24 h. (F) FaDu cells were treated with Raddeanin A for 24 h. Cell viability was assessed using WST‐8 assays. (G, H) Protein levels of Raddeanin A‐induced apoptosis. FaDu cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 and then treated with Raddeanin A for 24 h. ImageJ was used for protein quantification; the levels of all proteins were normalized to that of beta ‐Actin. Data were presented as the mean +/- standard deviation (n = 3) of three independent experiments. *p < 0.05 compare with control; # p < 0.05 compare with cotreatment control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39175122), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: SET Antibody - BSA Free [NBP1-33713] -

Raddeanin A‐treated NK cells enhance apoptosis in K562 cells. Raddeanin A induced apoptosis in cocultured K562 cells. KHYG‐1 cells were pretreated with Raddeanin A for 24 h before being transferred to a co‐culture system. (A and B) Mitochondrial membrane potential assay and (C and D) annexin V/PI stain assay of K562 cells were measured after Raddeanin A treatment by Muse Cell Analyser. Quantitative data were analysed by Muse Cell Software V1.4.0.0. (E) Fas protein levels of Raddeanin A‐induced apoptosis. K562 cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 And then treated with Raddeanin A for 24 h. (F) K562 cells were treated with Raddeanin A for 24 h. Cell viability was assessed using WST‐8 assays. (G, H) Protein levels of Raddeanin A‐induced apoptosis. K562 cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 And then treated with Raddeanin A for 24 h. ImageJ was used for protein quantification; the levels of all proteins were normalized to that of beta ‐Actin. Data were presented as the mean +/- standard deviation (n = 3) of three independent experiments. *p < 0.05 compare with control; # p < 0.05 compare with cotreatment control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39175122), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: SET Antibody - BSA Free [NBP1-33713] -

Raddeanin A‐treated NK cells enhance apoptosis in NPC‐039 cells. (A, B) Mitochondrial membrane potential assay and (C, D) annexin V/PI stain assay of NPC‐039 cells were measured after Raddeanin A treatment by Muse Cell Analyser. Quantitative data were analysed by Muse Cell Software V1.4.0.0. (E) Fas protein levels of Raddeanin A‐induced apoptosis. NPC‐039 cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 And then treated with Raddeanin A for 24 h. (F) NPC‐039 cells were treated with Raddeanin A for 24 h. Cell viability was assessed using WST‐8 assays. (G, H) Protein levels of Raddeanin A‐induced apoptosis. NPC‐039 cells were cocultured with KHYG‐1 cells at an effector: Target ratio of 6:1 And then treated with Raddeanin A for 24 h. ImageJ was used for protein quantification; the levels of all proteins were normalized to that of beta ‐Actin. Data were presented as the mean +/- standard deviation (n = 3) of three independent experiments. *p < 0.05 compare with control; # p < 0.05 compare with cotreatment control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39175122), licensed under a CC-BY license. Not internally tested by Novus Biologicals.