PKM1 Antibody - BSA Free

Western Blot: PKM1 AntibodyBSA Free [NBP2-14833]

Western Blot: PKM1 Antibody [NBP2-14833] - Detection of PKM1 on HEK293T and U-87 cells. Lane 1: HEK293T cells (major isoform is PKM2, human). Lane 2: HEK293T cells with plasmid overexpressing mouse PKM1. Lane 3: HEK293T cells with plasmid overexpressing mouse PKM2. Lane 4: U-87 cells with control shRNA (major isoform is PKM2, human). Lane 5: U-87 cells with PTB/A1/A2 shRNAs (major isoform is PKM1, human). Photo courtesy of product review by verified customer.

Western Blot: PKM1 AntibodyBSA Free [NBP2-14833]

Western Blot: PKM1 Antibody [NBP2-14833] - Expression of PTB1, PKM1, and PKM2 proteins at 72 h after transfection of DLD-1, RD or KYM-1 cells with miR-133b (10, 20 nM). Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license.

Western Blot: PKM1 AntibodyBSA Free [NBP2-14833]

Western Blot: PKM1 Antibody [NBP2-14833] - Expression profile of PKM isoforms in various cancer cell lines, control cell lines, and cells in primary culture. PKM1 and PKM2 were detected by Western blotting under the same experimental conditions at the same time. The full-length blots are presented in Supplementary Figure S2a. Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license.

Simple Western: PKM1 AntibodyBSA Free [NBP2-14833]

Simple Western: PKM1 Antibody [NBP2-14833] - Simple Western lane view shows a specific band for PKM1 in 0.5 mg/ml of Human Brain lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.

Immunohistochemistry-Paraffin: PKM1 Antibody - BSA Free [NBP2-14833] -

Immunohistochemistry-Paraffin: PKM1 Antibody - BSA Free [NBP2-14833] - Expression of PKM1 & PKM2 in clinical colorectal cancer samples.(a) The protein expression of PKM1 & PKM2 in clinical specimens of cancer tumor (T) & the adjacent normal tissues (N) is shown. PKM1 & PKM2 were detected by Western blotting in under the same experimental conditions at the same time. The full-length blots are presented in Supplementary Figure S3b. (b–d) Immunohistochemical staining of normal colon tissue adjacent to tumor tissue of case 10. Results of H&E staining (b), staining with anti-PKM1 antibody (c), & staining with anti-PKM2 (d) are shown. The boxed regions in “c” & “d” are enlarged in the images below. (e–h) Immunohistochemical staining of clinical colorectal cancer tissue specimen of representative case 3. H&E-stained section with normal tissue (upper right corner) neighboring the tumor area in the section is shown (e), along with the same section stained with anti-PKM2 antibody (f). Enlarged views of boxed areas in “f” show normal colorectal crypt in mucosa (g) & tumor area (h) stained with anti-PKM2 antibody. Image collected & cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] -

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] - (a) Luciferase activities after co-transfection of DLD-1 cells w/ control or miR-124 (wild-type or mutant-type) pMIR vectors having predictive miR-124 binding site in 3′UTR of PTB1. Upper panel region of 3′-UTR of human PTB1 mRNA complementary to mature miR-124. Box indicates predicted binding sites for miR-124. (b) Same as “a” except miR-133b used. (c) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB9 or IMR-32 cells w/ miR-124 (10, 20 or 40 nM). (d) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, RD or KYM-1 cells w/ miR-133b (10, 20 nM). (e) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB-9 or RD cells w/ siR-PTB1 (2, 5 nM). (f) Effect of combined treatment of DLD-1 cells w/ antagomiR-124 & miR-124 or antagomiR-133b & miR-133b. DLD-1 cells transfected w/ non-specific control, miR-124/miR-133b (10 nM), miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (5 nM) or miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (10 nM). Expression level of PTB1 assessed at 48 h after transfection. The full-length blots are presented in Supplementary Figure S3a. (g) IF of PKM1 (upper panels) & PKM2 (lower panels) at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM) or miR-133b (20 nM). Left panels, treatment w/ control miRNA; middle panels, treatment w/ miR-124; right panels, treatment w/ miR-133b. PKM1 or PKM2 is stained red, & nuclei are stained blue. (h) Lactate production measured at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM), miR-133b (20 nM) or siR-PTB1 (5 nM). Results are presented as mean± SD (* P < 0.05; ** P < 0.01; *** P < 0.001; N.S., not statistically significant). Image collected & cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Immunocytochemistry/ Immunofluorescence: PKM1 Antibody - BSA Free [NBP2-14833] -

Immunocytochemistry/ Immunofluorescence: PKM1 Antibody - BSA Free [NBP2-14833] - (a) Luciferase activities after co-transfection of DLD-1 cells w/ control or miR-124 (wild-type or mutant-type) pMIR vectors having predictive miR-124 binding site in 3′UTR of PTB1. Upper panel region of 3′-UTR of human PTB1 mRNA complementary to mature miR-124. Box indicates predicted binding sites for miR-124. (b) Same as “a” except miR-133b used. (c) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB9 or IMR-32 cells w/ miR-124 (10, 20 or 40 nM). (d) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, RD or KYM-1 cells w/ miR-133b (10, 20 nM). (e) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB-9 or RD cells w/ siR-PTB1 (2, 5 nM). (f) Effect of combined treatment of DLD-1 cells w/ antagomiR-124 & miR-124 or antagomiR-133b & miR-133b. DLD-1 cells transfected w/ non-specific control, miR-124/miR-133b (10 nM), miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (5 nM) or miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (10 nM). Expression level of PTB1 assessed at 48 h after transfection. The full-length blots are presented in Supplementary Figure S3a. (g) IF of PKM1 (upper panels) & PKM2 (lower panels) at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM) or miR-133b (20 nM). Left panels, treatment w/ control miRNA; middle panels, treatment w/ miR-124; right panels, treatment w/ miR-133b. PKM1 or PKM2 is stained red, & nuclei are stained blue. (h) Lactate production measured at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM), miR-133b (20 nM) or siR-PTB1 (5 nM). Results are presented as mean± SD (* P < 0.05; ** P < 0.01; *** P < 0.001; N.S., not statistically significant). Image collected & cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] -

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] - (a) Luciferase activities after co-transfection of DLD-1 cells w/ control or miR-124 (wild-type or mutant-type) pMIR vectors having predictive miR-124 binding site in 3′UTR of PTB1. Upper panel region of 3′-UTR of human PTB1 mRNA complementary to mature miR-124. Box indicates predicted binding sites for miR-124. (b) Same as “a” except miR-133b used. (c) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB9 or IMR-32 cells w/ miR-124 (10, 20 or 40 nM). (d) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, RD or KYM-1 cells w/ miR-133b (10, 20 nM). (e) Expression of PTB1, PKM1, & PKM2 proteins at 72 h after transfection of DLD-1, NB-9 or RD cells w/ siR-PTB1 (2, 5 nM). (f) Effect of combined treatment of DLD-1 cells w/ antagomiR-124 & miR-124 or antagomiR-133b & miR-133b. DLD-1 cells transfected w/ non-specific control, miR-124/miR-133b (10 nM), miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (5 nM) or miR-124/miR-133b (10 nM) + antagomiR-124/antagomiR-133b (10 nM). Expression level of PTB1 assessed at 48 h after transfection. The full-length blots are presented in Supplementary Figure S3a. (g) IF of PKM1 (upper panels) & PKM2 (lower panels) at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM) or miR-133b (20 nM). Left panels, treatment w/ control miRNA; middle panels, treatment w/ miR-124; right panels, treatment w/ miR-133b. PKM1 or PKM2 is stained red, & nuclei are stained blue. (h) Lactate production measured at 48 h after transfection of DLD-1 cells w/ miR-124 (20 nM), miR-133b (20 nM) or siR-PTB1 (5 nM). Results are presented as mean± SD (* P < 0.05; ** P < 0.01; *** P < 0.001; N.S., not statistically significant). Image collected & cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] -

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] - Expression of PKM1 & PKM2 in clinical colorectal cancer samples.(a) The protein expression of PKM1 & PKM2 in clinical specimens of cancer tumor (T) & the adjacent normal tissues (N) is shown. PKM1 & PKM2 were detected by Western blotting in under the same experimental conditions at the same time. The full-length blots are presented in Supplementary Figure S3b. (b–d) Immunohistochemical staining of normal colon tissue adjacent to tumor tissue of case 10. Results of H&E staining (b), staining with anti-PKM1 antibody (c), & staining with anti-PKM2 (d) are shown. The boxed regions in “c” & “d” are enlarged in the images below. (e–h) Immunohistochemical staining of clinical colorectal cancer tissue specimen of representative case 3. H&E-stained section with normal tissue (upper right corner) neighboring the tumor area in the section is shown (e), along with the same section stained with anti-PKM2 antibody (f). Enlarged views of boxed areas in “f” show normal colorectal crypt in mucosa (g) & tumor area (h) stained with anti-PKM2 antibody. Image collected & cropped by CiteAb from the following publication (https://www.nature.com/articles/srep08647), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] -

Western Blot: PKM1 Antibody - BSA Free [NBP2-14833] - Characterization of NOX4 & PKM2 in human RCC tumors & adjacent tissue. a Mitochondrial fractions were prepared from human tumors (T) or uninvolved adjacent tissue (N). NOX4 expression was examined by western blot analysis. Prohibitin was probed as a mitochondrial marker & loading control. b Quantitation of NOX4 distribution in the mitochondrial fraction from a. The results are expressed as the means using one-way ANOVA with Tukey’s post hoc test where ± S.E.M. *p < 0.05 compared to normal (N). c Mitochondria fractions were prepared from RCC tumors & NADPH-dependent superoxide generation was examined in the presence (+) or absence (−) of ATP. The results are from eight tumors & are expressed as the means using one-way ANOVA with Tukey’s post hoc test where ±S.E.M. **p < 0.01 is compared to without (−) ATP. d PKM2 & PKM1 expression was examined by western blot analysis in lysates prepared from human tumors (T) or uninvolved adjacent tissue (N) from the same patient. Actin as loading control Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/29051480), licensed under a CC-BY license. Not internally tested by Novus Biologicals.