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Solarbio Inc rabbit polyclonal antibody against pkm2
Primers used in this study.
Rabbit Polyclonal Antibody Against Pkm2, supplied by Solarbio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "CCL4 participates in the reprogramming of glucose metabolism induced by ALV-J infection in chicken macrophages"

Article Title: CCL4 participates in the reprogramming of glucose metabolism induced by ALV-J infection in chicken macrophages

Journal: Frontiers in Microbiology

doi: 10.3389/fmicb.2023.1205143

Primers used in this study.
Figure Legend Snippet: Primers used in this study.

Techniques Used: Sequencing

CCL4 regulates the expression of glucose metabolism genes. (A) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (B) Western blotting analysis of HK1, HK2, PKM2, MYC, and LDHA gene expression in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (C) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. (D) Western blotting analysis of HK1, MYC, and LDHA gene expression in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. Error bars represent the s.d., n = 3. ** p < 0.01 (two-tailed Student’s t -test).
Figure Legend Snippet: CCL4 regulates the expression of glucose metabolism genes. (A) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (B) Western blotting analysis of HK1, HK2, PKM2, MYC, and LDHA gene expression in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (C) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. (D) Western blotting analysis of HK1, MYC, and LDHA gene expression in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. Error bars represent the s.d., n = 3. ** p < 0.01 (two-tailed Student’s t -test).

Techniques Used: Expressing, Transfection, Control, Plasmid Preparation, Western Blot, Two Tailed Test

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Expressing:

Article Title: CCL4 participates in the reprogramming of glucose metabolism induced by ALV-J infection in chicken macrophages
Article Snippet: .. The following antibodies were used to determine protein expression: rabbit polyclonal antibody against HK1 (A1054, Abclonal), rabbit polyclonal antibody against HK2 (A0994, Abclonal), rabbit polyclonal antibody against PKM2 (K001645P, Solarbio), rabbit monoclonal antibody against actin (ab179467, Abcam), mouse monoclonal antibody against c-Myc (ab56, Abcam), rabbit polyclonal antibody against LDHA (K002251P, Solarbio) and mouse monoclonal antibody against JE9, which is specific to the envelope protein of ALV-J. ..



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Proteintech rabbit polyclonal antibodies against pkm2
Figure 1. <t>PKM2</t> is inversely correlated with CD8+ T-cell infiltration in ESCC, as demonstrated by in silico analysis of data from the TCGA database Pearson correlation analysis was used to evaluate the relationship between PKM2 mRNA expression and the expression of immune checkpoint molecules, as well as that of tumor-associated lymphocyte markers. Tpm stands for transcripts per million.
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Figure 1. <t>PKM2</t> is inversely correlated with CD8+ T-cell infiltration in ESCC, as demonstrated by in silico analysis of data from the TCGA database Pearson correlation analysis was used to evaluate the relationship between PKM2 mRNA expression and the expression of immune checkpoint molecules, as well as that of tumor-associated lymphocyte markers. Tpm stands for transcripts per million.
Rabbit Polyclonal Antibody Against Pkm2 K001645p, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Primers used in this study.
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Primers used in this study.
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Primers used in this study.
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Image Search Results


Figure 1. PKM2 is inversely correlated with CD8+ T-cell infiltration in ESCC, as demonstrated by in silico analysis of data from the TCGA database Pearson correlation analysis was used to evaluate the relationship between PKM2 mRNA expression and the expression of immune checkpoint molecules, as well as that of tumor-associated lymphocyte markers. Tpm stands for transcripts per million.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 1. PKM2 is inversely correlated with CD8+ T-cell infiltration in ESCC, as demonstrated by in silico analysis of data from the TCGA database Pearson correlation analysis was used to evaluate the relationship between PKM2 mRNA expression and the expression of immune checkpoint molecules, as well as that of tumor-associated lymphocyte markers. Tpm stands for transcripts per million.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: In Silico, Expressing

Figure 2. PKM2 regulates PD-L1 and PD-L2 expression in tumor cells (A) In HeLa cells, compared with controls, PKM2 knockout significantly reduced PD-L1 expression while increasing PD-L2 expression. A similar pattern was observed in the A549 lung cancer cell line, where PKM2 knockout notably increased PD-L2 expression and decreased PD-L1 expression. (B) Additionally, PKM2 down- regulates GATA3 expression in tumor cells. β-Actin served as the internal control. The images shown are representative samples, with band intensity variations quantified via ImageJ software.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 2. PKM2 regulates PD-L1 and PD-L2 expression in tumor cells (A) In HeLa cells, compared with controls, PKM2 knockout significantly reduced PD-L1 expression while increasing PD-L2 expression. A similar pattern was observed in the A549 lung cancer cell line, where PKM2 knockout notably increased PD-L2 expression and decreased PD-L1 expression. (B) Additionally, PKM2 down- regulates GATA3 expression in tumor cells. β-Actin served as the internal control. The images shown are representative samples, with band intensity variations quantified via ImageJ software.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: Expressing, Knock-Out, Control, Software

Figure 3. PKM2 knockout (KO) significantly suppressed tumor cell proliferation and metastasis in a HeLa cell xenograft mouse model (A) PKM2 knockout drastically inhibited the proliferation of HeLa cells in nude mice xenografted with both HeLa cells and PKM2-knockout HeLa cells (n = 5 per group, **P < 0.01). (B) Similarly, PKM2 knockout markedly reduced lung and liver metastases in nude mice after tail vein injection of PKM2- knockout HeLa cells (n = 5 per group). Representative hematoxylin‒eosin (H&E)-stained sections are shown. Scale bar: 25 μm. (C) Immunohistochemical analysis of PKM2, GATA3, PD-L1, PD-L2, and Ki-67 expression in tumor lesions from xenografted mice with HeLa and PKM2-knockout HeLa cells. Scale bar: 25 μm. Average optical density (AOD) scores were calculated for each section via ImageJ software. Statistical significance was determined via a two-tailed independent sample t test. *P < 0.05, **P < 0.01, ***P < 0.001 relative to the control. (D) Clonogenic assays were performed on A549 and HeLa cells with PKM2 knockout. Statistical analysis was conducted via a two-tailed independent sample t test. ***P < 0.001, ****P < 0.0001 compared with the control.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 3. PKM2 knockout (KO) significantly suppressed tumor cell proliferation and metastasis in a HeLa cell xenograft mouse model (A) PKM2 knockout drastically inhibited the proliferation of HeLa cells in nude mice xenografted with both HeLa cells and PKM2-knockout HeLa cells (n = 5 per group, **P < 0.01). (B) Similarly, PKM2 knockout markedly reduced lung and liver metastases in nude mice after tail vein injection of PKM2- knockout HeLa cells (n = 5 per group). Representative hematoxylin‒eosin (H&E)-stained sections are shown. Scale bar: 25 μm. (C) Immunohistochemical analysis of PKM2, GATA3, PD-L1, PD-L2, and Ki-67 expression in tumor lesions from xenografted mice with HeLa and PKM2-knockout HeLa cells. Scale bar: 25 μm. Average optical density (AOD) scores were calculated for each section via ImageJ software. Statistical significance was determined via a two-tailed independent sample t test. *P < 0.05, **P < 0.01, ***P < 0.001 relative to the control. (D) Clonogenic assays were performed on A549 and HeLa cells with PKM2 knockout. Statistical analysis was conducted via a two-tailed independent sample t test. ***P < 0.001, ****P < 0.0001 compared with the control.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: Knock-Out, Injection, Staining, Immunohistochemical staining, Expressing, Software, Two Tailed Test, Control

Figure 5. GATA3 overexpression (OE) in PKM2-knockout A549 and HeLa cells restores effects similar to those observed with PKM2, enhancing PD-L1 and reducing PD-L2 expression (A) Overexpression of GATA3 in PKM2-knockout A549 and HeLa cells reinstates the original PKM2- induced regulation, where PD-L1 expression is increased and PD-L2 expression is decreased. (B) GATA3 overexpression also restored the migratory capacity of A549 and HeLa cells following PKM2 knockout. (C) Similarly, GATA3 overexpression re-established the invasive properties of A549 and HeLa cells after PKM2 knockout. Statistical analysis was performed via a two-tailed independent sample t test. *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001 compared with the control.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 5. GATA3 overexpression (OE) in PKM2-knockout A549 and HeLa cells restores effects similar to those observed with PKM2, enhancing PD-L1 and reducing PD-L2 expression (A) Overexpression of GATA3 in PKM2-knockout A549 and HeLa cells reinstates the original PKM2- induced regulation, where PD-L1 expression is increased and PD-L2 expression is decreased. (B) GATA3 overexpression also restored the migratory capacity of A549 and HeLa cells following PKM2 knockout. (C) Similarly, GATA3 overexpression re-established the invasive properties of A549 and HeLa cells after PKM2 knockout. Statistical analysis was performed via a two-tailed independent sample t test. *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001 compared with the control.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: Over Expression, Knock-Out, Expressing, Two Tailed Test, Control

Figure 6. PKM2 is inversely correlated with CD8+ T-cell infiltration in a xenograft model in C57BL/6N mice (A) Evaluation of lentiviral shRNA- mediated PKM2 knockdown efficiency at the mRNA level via qRT-PCR. (B) Confirmation of the knockdown efficiency via western blot analysis. (C) Detection of variations in PD-L1 and PD-L2 expression in AKR cells following PKM2 knockdown, as demonstrated by western blot analysis. (D) Development of a xenograft mouse model using the C57BL/6N strain. (E) Macroscopic examination of subcutaneous tumor growth in the PKM2-shRNA2 (n = 5) and control (n = 5) groups. (F) Quantitative analysis of tumor weight. (G) Representative immunohistochemistry images and corresponding quantifications showing differences in the expressions of GATA3, PKM2, PD-L1, PD-L2, CD206, and CD8+ T cells in tumor tissues from xenograft C57BL/6 N mice. Scale bar: 25 μm, magnification, 200×. Average optical density (AOD) scores were calculated for each section via ImageJ software. Differences between groups were analyzed via an independent sample t test. *P < 0.05, **P < 0.01, and ***P < 0.001 compared with the control group.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 6. PKM2 is inversely correlated with CD8+ T-cell infiltration in a xenograft model in C57BL/6N mice (A) Evaluation of lentiviral shRNA- mediated PKM2 knockdown efficiency at the mRNA level via qRT-PCR. (B) Confirmation of the knockdown efficiency via western blot analysis. (C) Detection of variations in PD-L1 and PD-L2 expression in AKR cells following PKM2 knockdown, as demonstrated by western blot analysis. (D) Development of a xenograft mouse model using the C57BL/6N strain. (E) Macroscopic examination of subcutaneous tumor growth in the PKM2-shRNA2 (n = 5) and control (n = 5) groups. (F) Quantitative analysis of tumor weight. (G) Representative immunohistochemistry images and corresponding quantifications showing differences in the expressions of GATA3, PKM2, PD-L1, PD-L2, CD206, and CD8+ T cells in tumor tissues from xenograft C57BL/6 N mice. Scale bar: 25 μm, magnification, 200×. Average optical density (AOD) scores were calculated for each section via ImageJ software. Differences between groups were analyzed via an independent sample t test. *P < 0.05, **P < 0.01, and ***P < 0.001 compared with the control group.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: shRNA, Knockdown, Quantitative RT-PCR, Western Blot, Expressing, Control, Immunohistochemistry, Software

Figure 7. Schematic diagram highlighting the species-dependent regulation of PKM2 In a human model, PKM2 enhances PD-L1 expression while suppressing PD-L2 expression, facilitating immune evasion through PD-L1 upregulation. Conversely, in a mouse model, PKM2 suppresses both PD-L1 and PD-L2 expression, leading to increased CD8+ T-cell infiltration upon PKM2 knockdown. KO, knockout; KD, knockdown; OE, overexpression. The blue arrow indicates downregulation; the red arrow indicates upregulation.

Journal: Acta biochimica et biophysica Sinica

Article Title: Divergent roles of PKM2 in regulating PD-L1 and PD-L2 expression and their implications in human and mouse cancer models.

doi: 10.3724/abbs.2025019

Figure Lengend Snippet: Figure 7. Schematic diagram highlighting the species-dependent regulation of PKM2 In a human model, PKM2 enhances PD-L1 expression while suppressing PD-L2 expression, facilitating immune evasion through PD-L1 upregulation. Conversely, in a mouse model, PKM2 suppresses both PD-L1 and PD-L2 expression, leading to increased CD8+ T-cell infiltration upon PKM2 knockdown. KO, knockout; KD, knockdown; OE, overexpression. The blue arrow indicates downregulation; the red arrow indicates upregulation.

Article Snippet: The membranes were incubated with rabbit polyclonal antibodies against PKM2 (15822-1-AP; Proteintech, Wuhan, China), PD-L1 (28076-1-AP), PD-L2 (18251-1-AP), GATA3 (66400-1-Ig), and βactin (66009-1-Ig).

Techniques: Expressing, Knockdown, Knock-Out, Over Expression

Primers used in this study.

Journal: Frontiers in Microbiology

Article Title: CCL4 participates in the reprogramming of glucose metabolism induced by ALV-J infection in chicken macrophages

doi: 10.3389/fmicb.2023.1205143

Figure Lengend Snippet: Primers used in this study.

Article Snippet: The following antibodies were used to determine protein expression: rabbit polyclonal antibody against HK1 (A1054, Abclonal), rabbit polyclonal antibody against HK2 (A0994, Abclonal), rabbit polyclonal antibody against PKM2 (K001645P, Solarbio), rabbit monoclonal antibody against actin (ab179467, Abcam), mouse monoclonal antibody against c-Myc (ab56, Abcam), rabbit polyclonal antibody against LDHA (K002251P, Solarbio) and mouse monoclonal antibody against JE9, which is specific to the envelope protein of ALV-J.

Techniques: Sequencing

CCL4 regulates the expression of glucose metabolism genes. (A) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (B) Western blotting analysis of HK1, HK2, PKM2, MYC, and LDHA gene expression in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (C) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. (D) Western blotting analysis of HK1, MYC, and LDHA gene expression in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. Error bars represent the s.d., n = 3. ** p < 0.01 (two-tailed Student’s t -test).

Journal: Frontiers in Microbiology

Article Title: CCL4 participates in the reprogramming of glucose metabolism induced by ALV-J infection in chicken macrophages

doi: 10.3389/fmicb.2023.1205143

Figure Lengend Snippet: CCL4 regulates the expression of glucose metabolism genes. (A) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (B) Western blotting analysis of HK1, HK2, PKM2, MYC, and LDHA gene expression in HD11 cells transfected with pcDNA3.1-CCL4 or the control plasmid for 48 h. (C) Relative expression analysis of the chicken CCL4, GLUT1, GLUT3, HK1, HK2, PFKM, PFKL, PKM2, LDHA, and c-myc genes in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. (D) Western blotting analysis of HK1, MYC, and LDHA gene expression in HD11 cells transfected with the control or chicken CCL4 siRNA for 48 h. Error bars represent the s.d., n = 3. ** p < 0.01 (two-tailed Student’s t -test).

Article Snippet: The following antibodies were used to determine protein expression: rabbit polyclonal antibody against HK1 (A1054, Abclonal), rabbit polyclonal antibody against HK2 (A0994, Abclonal), rabbit polyclonal antibody against PKM2 (K001645P, Solarbio), rabbit monoclonal antibody against actin (ab179467, Abcam), mouse monoclonal antibody against c-Myc (ab56, Abcam), rabbit polyclonal antibody against LDHA (K002251P, Solarbio) and mouse monoclonal antibody against JE9, which is specific to the envelope protein of ALV-J.

Techniques: Expressing, Transfection, Control, Plasmid Preparation, Western Blot, Two Tailed Test