Review





Similar Products

95
ABclonal Biotechnology ampk
Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/AMPK%CE%B11+Rabbit+pAb/pm42892631-69-74-75
Average 95 stars, based on 1 article reviews
ampk - by Bioz Stars, 2026-10
95/100 stars
  Buy from Supplier

96
Cell Signaling Technology Inc anti p ampk thr172
Anti P Ampk Thr172, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/Phospho-AMPKalpha+(Thr172)+Rabbit+mAb/pm42854287-45-49-52
Average 96 stars, based on 1 article reviews
anti p ampk thr172 - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier

94
ABclonal Biotechnology phospho ampk
Phospho Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/Phospho-AMPK%CE%B11-S485+Rabbit+pAb/pm42842576-61-5-19
Average 94 stars, based on 1 article reviews
phospho ampk - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

95
ABclonal Biotechnology protein kinase alpha 1 ampk
Protein Kinase Alpha 1 Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/AMPK%CE%B11+Rabbit+pAb/pm41962267-76-21-58
Average 95 stars, based on 1 article reviews
protein kinase alpha 1 ampk - by Bioz Stars, 2026-10
95/100 stars
  Buy from Supplier

94
ABclonal Biotechnology p ampk s496
P Ampk S496, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/Phospho-AMPK%CE%B11-S496+Rabbit+mAb/pm41634533-71-11-16
Average 94 stars, based on 1 article reviews
p ampk s496 - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

94
ABclonal Biotechnology p ampk
RNA-Seq analysis and validation of mouse liver following FSP intervention. (A) Heatmap of hepatic gene expression profiles in vehicle group and FSP-2X group, with red and green indicating up- and down-regulated genes respectively ( n = 3); (B) Volcano plot displaying overall distribution of DEGs in FSP-treated liver tissues ( n = 3); (C) Bubble chart of KEGG pathway enrichment analysis for DEGs ( n = 3); (D) Heatmap visualization of differentially expressed genes ( n = 3); (E) mRNA expression analysis of target genes ( n = 6); (F, G) Expression levels and semi-quantitative analysis of key proteins in <t>AdipoRs-AMPK</t> signaling pathway ( n = 3); (H, I) Regulatory effects of FSP on proteins related to inflammation, oxidative stress, mitochondrial function and lactate metabolism ( n = 3); (J) mRNA levels of mitochondrial biogenesis genes Nrf1 (NRF1) and Tfam (TFAM) ( n = 6); (K) Mitochondrial DNA copy number in mouse liver tissues ( n = 6); (L–Q) Immunohistochemical staining and statistical analysis of PGC1α, TFAM and COXIV proteins (Scale bar: 20 μm, Total magnification: 200x, n = 5); (R) Hepatic ATP content ( n = 5); (S) ROS levels in liver tissues ( n = 4). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.
P Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/ADIPOR2+Rabbit+pAb/pmc13312815-159-13-14
Average 94 stars, based on 1 article reviews
p ampk - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

94
ABclonal Biotechnology anti p ampk
RNA-Seq analysis and validation of mouse liver following FSP intervention. (A) Heatmap of hepatic gene expression profiles in vehicle group and FSP-2X group, with red and green indicating up- and down-regulated genes respectively ( n = 3); (B) Volcano plot displaying overall distribution of DEGs in FSP-treated liver tissues ( n = 3); (C) Bubble chart of KEGG pathway enrichment analysis for DEGs ( n = 3); (D) Heatmap visualization of differentially expressed genes ( n = 3); (E) mRNA expression analysis of target genes ( n = 6); (F, G) Expression levels and semi-quantitative analysis of key proteins in <t>AdipoRs-AMPK</t> signaling pathway ( n = 3); (H, I) Regulatory effects of FSP on proteins related to inflammation, oxidative stress, mitochondrial function and lactate metabolism ( n = 3); (J) mRNA levels of mitochondrial biogenesis genes Nrf1 (NRF1) and Tfam (TFAM) ( n = 6); (K) Mitochondrial DNA copy number in mouse liver tissues ( n = 6); (L–Q) Immunohistochemical staining and statistical analysis of PGC1α, TFAM and COXIV proteins (Scale bar: 20 μm, Total magnification: 200x, n = 5); (R) Hepatic ATP content ( n = 5); (S) ROS levels in liver tissues ( n = 4). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.
Anti P Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/Phospho-AMPK%CE%B11-S496+Rabbit+mAb/pm42191057-88-36-37
Average 94 stars, based on 1 article reviews
anti p ampk - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

94
ABclonal Biotechnology anti ampk
RNA-Seq analysis and validation of mouse liver following FSP intervention. (A) Heatmap of hepatic gene expression profiles in vehicle group and FSP-2X group, with red and green indicating up- and down-regulated genes respectively ( n = 3); (B) Volcano plot displaying overall distribution of DEGs in FSP-treated liver tissues ( n = 3); (C) Bubble chart of KEGG pathway enrichment analysis for DEGs ( n = 3); (D) Heatmap visualization of differentially expressed genes ( n = 3); (E) mRNA expression analysis of target genes ( n = 6); (F, G) Expression levels and semi-quantitative analysis of key proteins in <t>AdipoRs-AMPK</t> signaling pathway ( n = 3); (H, I) Regulatory effects of FSP on proteins related to inflammation, oxidative stress, mitochondrial function and lactate metabolism ( n = 3); (J) mRNA levels of mitochondrial biogenesis genes Nrf1 (NRF1) and Tfam (TFAM) ( n = 6); (K) Mitochondrial DNA copy number in mouse liver tissues ( n = 6); (L–Q) Immunohistochemical staining and statistical analysis of PGC1α, TFAM and COXIV proteins (Scale bar: 20 μm, Total magnification: 200x, n = 5); (R) Hepatic ATP content ( n = 5); (S) ROS levels in liver tissues ( n = 4). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.
Anti Ampk, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+ampk/Phospho-AMPK%CE%B11-S496+Rabbit+mAb/pmc13179142-86-12-13
Average 94 stars, based on 1 article reviews
anti ampk - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

Image Search Results


RNA-Seq analysis and validation of mouse liver following FSP intervention. (A) Heatmap of hepatic gene expression profiles in vehicle group and FSP-2X group, with red and green indicating up- and down-regulated genes respectively ( n = 3); (B) Volcano plot displaying overall distribution of DEGs in FSP-treated liver tissues ( n = 3); (C) Bubble chart of KEGG pathway enrichment analysis for DEGs ( n = 3); (D) Heatmap visualization of differentially expressed genes ( n = 3); (E) mRNA expression analysis of target genes ( n = 6); (F, G) Expression levels and semi-quantitative analysis of key proteins in AdipoRs-AMPK signaling pathway ( n = 3); (H, I) Regulatory effects of FSP on proteins related to inflammation, oxidative stress, mitochondrial function and lactate metabolism ( n = 3); (J) mRNA levels of mitochondrial biogenesis genes Nrf1 (NRF1) and Tfam (TFAM) ( n = 6); (K) Mitochondrial DNA copy number in mouse liver tissues ( n = 6); (L–Q) Immunohistochemical staining and statistical analysis of PGC1α, TFAM and COXIV proteins (Scale bar: 20 μm, Total magnification: 200x, n = 5); (R) Hepatic ATP content ( n = 5); (S) ROS levels in liver tissues ( n = 4). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Journal: Frontiers in Nutrition

Article Title: The herbal pair of Smilax glabra Roxb. and Ficus hirta Vahl. improves exercise performance by regulating mitochondrial function via the adiponection receptors-mediated AMPK signaling pathway

doi: 10.3389/fnut.2026.1782001

Figure Lengend Snippet: RNA-Seq analysis and validation of mouse liver following FSP intervention. (A) Heatmap of hepatic gene expression profiles in vehicle group and FSP-2X group, with red and green indicating up- and down-regulated genes respectively ( n = 3); (B) Volcano plot displaying overall distribution of DEGs in FSP-treated liver tissues ( n = 3); (C) Bubble chart of KEGG pathway enrichment analysis for DEGs ( n = 3); (D) Heatmap visualization of differentially expressed genes ( n = 3); (E) mRNA expression analysis of target genes ( n = 6); (F, G) Expression levels and semi-quantitative analysis of key proteins in AdipoRs-AMPK signaling pathway ( n = 3); (H, I) Regulatory effects of FSP on proteins related to inflammation, oxidative stress, mitochondrial function and lactate metabolism ( n = 3); (J) mRNA levels of mitochondrial biogenesis genes Nrf1 (NRF1) and Tfam (TFAM) ( n = 6); (K) Mitochondrial DNA copy number in mouse liver tissues ( n = 6); (L–Q) Immunohistochemical staining and statistical analysis of PGC1α, TFAM and COXIV proteins (Scale bar: 20 μm, Total magnification: 200x, n = 5); (R) Hepatic ATP content ( n = 5); (S) ROS levels in liver tissues ( n = 4). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Article Snippet: The specific antibodies used were as follows: AdipoR1 (Abclonal, A1509), AdipoR2 (Abclonal, A12777), p-AMPK (Abclonal, AP1441), AMPK (Abclonal, A1229), p-LKB1 (Abclonal, AP0601), LKB1 (Abclonal, A22636), PGC1α (Proteintech, 66369-1-Ig), SIRT1 (Proteintech, 13161-1-AP), LDHB (Proteintech, 14824-1-AP), COXIV (Cell Signaling Technology, 3E11), TFAM (Abclonal, A3173), NRF2 (Proteintech, 16396-1-AP), HO-1 (Abclonal, A19062), TNFα (Proteintech, 80258-6-RR), COX2 (Abclonal, A3560), and β-actin (Proteintech, 20536-1-AP).

Techniques: RNA Sequencing, Biomarker Discovery, Gene Expression, Expressing, Immunohistochemical staining, Staining

Effects of FSP serum treatment on gene expression in HepG2 cells. (A) Experimental design of FSP serum treatment in HepG2 cells (Created in https://BioRender.com ); (B, C) Impact of FSP serum on HepG2 cell proliferation capacity and quantitative analysis ( n = 6); (D) Transcript levels of differentially expressed genes and mitochondrial biogenesis-related genes (Nrf1/NRF1, Tfam/TFAM) in HepG2 cells ( n = 6); (E, F) Protein expression and semi-quantification of key AdipoRs-AMPK pathway components in HepG2 cells ( n = 3); (G, H) Effects of FSP serum on inflammation, oxidative stress, mitochondrial function and lactate metabolism-related proteins with semi-quantitative analysis ( n = 3); (I) Immunofluorescence co-localization of SIRT1 and PGC-1α proteins in HepG2 cells (Scale bar: 20 μm, Total magnification: 200x); (J, K) Immunofluorescence detection of mitochondrial function proteins COXIV and TFAM (Scale bar: 20 μm, Total magnification: 200x); (L, M) Mitochondrial membrane potential assay (JC-1) and analysis (Scale bar: 20 μm, Total magnification: 200x, n = 5). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Journal: Frontiers in Nutrition

Article Title: The herbal pair of Smilax glabra Roxb. and Ficus hirta Vahl. improves exercise performance by regulating mitochondrial function via the adiponection receptors-mediated AMPK signaling pathway

doi: 10.3389/fnut.2026.1782001

Figure Lengend Snippet: Effects of FSP serum treatment on gene expression in HepG2 cells. (A) Experimental design of FSP serum treatment in HepG2 cells (Created in https://BioRender.com ); (B, C) Impact of FSP serum on HepG2 cell proliferation capacity and quantitative analysis ( n = 6); (D) Transcript levels of differentially expressed genes and mitochondrial biogenesis-related genes (Nrf1/NRF1, Tfam/TFAM) in HepG2 cells ( n = 6); (E, F) Protein expression and semi-quantification of key AdipoRs-AMPK pathway components in HepG2 cells ( n = 3); (G, H) Effects of FSP serum on inflammation, oxidative stress, mitochondrial function and lactate metabolism-related proteins with semi-quantitative analysis ( n = 3); (I) Immunofluorescence co-localization of SIRT1 and PGC-1α proteins in HepG2 cells (Scale bar: 20 μm, Total magnification: 200x); (J, K) Immunofluorescence detection of mitochondrial function proteins COXIV and TFAM (Scale bar: 20 μm, Total magnification: 200x); (L, M) Mitochondrial membrane potential assay (JC-1) and analysis (Scale bar: 20 μm, Total magnification: 200x, n = 5). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Article Snippet: The specific antibodies used were as follows: AdipoR1 (Abclonal, A1509), AdipoR2 (Abclonal, A12777), p-AMPK (Abclonal, AP1441), AMPK (Abclonal, A1229), p-LKB1 (Abclonal, AP0601), LKB1 (Abclonal, A22636), PGC1α (Proteintech, 66369-1-Ig), SIRT1 (Proteintech, 13161-1-AP), LDHB (Proteintech, 14824-1-AP), COXIV (Cell Signaling Technology, 3E11), TFAM (Abclonal, A3173), NRF2 (Proteintech, 16396-1-AP), HO-1 (Abclonal, A19062), TNFα (Proteintech, 80258-6-RR), COX2 (Abclonal, A3560), and β-actin (Proteintech, 20536-1-AP).

Techniques: Gene Expression, Expressing, Immunofluorescence, Membrane

AMPK inhibition reverses biological effects of FSP serum intervention. (A) AMPK inhibition experiment in HepG2 cells under FSP serum intervention (Created in https://BioRender.com ); (B) Transcript levels of AMPK downstream effectors (SIRT1, PGC-1α) and mitochondrial genes (Nrf1/NRF1, Tfam/TFAM) ( n = 6); (C, D) Protein expression and semi-quantitative analysis of AMPK pathway molecules after AMPK inhibitor intervention ( n = 3); (E, F) Mitochondrial DNA copy number analysis ( n = 4); (G) Measurement of cellular ATP content ( n = 3); (H) Detection of cellular reactive oxygen species (ROS) levels ( n = 3); (I) SIRT1 and PGC-1α immunofluorescence co-localization (Scale bar: 20 μm, Total magnification: 200x); (J, K) Mitochondrial membrane potential (JC-1) staining and analysis (Scale bar: 20 μm, Total magnification: 200x, n = 5); (L–N) TEM analysis of mitochondrial ultrastructure with mitochondrial number ( n = 5) and area quantification ( n = 100) (Scale bar: 1/0.2 μm, Total magnification: 20,000/80,000x). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001compared to the vehicle gro,Q22up.

Journal: Frontiers in Nutrition

Article Title: The herbal pair of Smilax glabra Roxb. and Ficus hirta Vahl. improves exercise performance by regulating mitochondrial function via the adiponection receptors-mediated AMPK signaling pathway

doi: 10.3389/fnut.2026.1782001

Figure Lengend Snippet: AMPK inhibition reverses biological effects of FSP serum intervention. (A) AMPK inhibition experiment in HepG2 cells under FSP serum intervention (Created in https://BioRender.com ); (B) Transcript levels of AMPK downstream effectors (SIRT1, PGC-1α) and mitochondrial genes (Nrf1/NRF1, Tfam/TFAM) ( n = 6); (C, D) Protein expression and semi-quantitative analysis of AMPK pathway molecules after AMPK inhibitor intervention ( n = 3); (E, F) Mitochondrial DNA copy number analysis ( n = 4); (G) Measurement of cellular ATP content ( n = 3); (H) Detection of cellular reactive oxygen species (ROS) levels ( n = 3); (I) SIRT1 and PGC-1α immunofluorescence co-localization (Scale bar: 20 μm, Total magnification: 200x); (J, K) Mitochondrial membrane potential (JC-1) staining and analysis (Scale bar: 20 μm, Total magnification: 200x, n = 5); (L–N) TEM analysis of mitochondrial ultrastructure with mitochondrial number ( n = 5) and area quantification ( n = 100) (Scale bar: 1/0.2 μm, Total magnification: 20,000/80,000x). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001compared to the vehicle gro,Q22up.

Article Snippet: The specific antibodies used were as follows: AdipoR1 (Abclonal, A1509), AdipoR2 (Abclonal, A12777), p-AMPK (Abclonal, AP1441), AMPK (Abclonal, A1229), p-LKB1 (Abclonal, AP0601), LKB1 (Abclonal, A22636), PGC1α (Proteintech, 66369-1-Ig), SIRT1 (Proteintech, 13161-1-AP), LDHB (Proteintech, 14824-1-AP), COXIV (Cell Signaling Technology, 3E11), TFAM (Abclonal, A3173), NRF2 (Proteintech, 16396-1-AP), HO-1 (Abclonal, A19062), TNFα (Proteintech, 80258-6-RR), COX2 (Abclonal, A3560), and β-actin (Proteintech, 20536-1-AP).

Techniques: Inhibition, Expressing, Immunofluorescence, Membrane, Staining

Synergistic activation of the AdipoRs-AMPK pathway by taxifolin and apigenin combination (A) Schematic design of monomer compound cell experiments (Created in https://BioRender.com ); (B) mRNA expression levels of STRT1, Ppargc1a, Nrf1 (NRF1), and Tfam (TFAM) ( n = 6); (C, D) Protein expression in AdipoRs-AMPK pathway and mitochondrial function ( n = 3); (E, F) Mitochondrial DNA copy number detection ( n = 6); (G) Intracellular ATP content measurement ( n = 3); (H) Detection of reactive oxygen species (ROS) levels ( n = 5); (I, J) Measurement of mitochondrial membrane potential (JC-1) (Scale bar: 20 μm, Total magnification: 200x, n = 5); (K–M) Transmission electron microscopy (TEM) observation of mitochondrial ultrastructure (Scale bar: 1/0.2 μm, Total magnification: 20,000/80,000x), statistical analysis of mitochondrial quantity ( n = 5) and mitochondrial area ( n = 100). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Journal: Frontiers in Nutrition

Article Title: The herbal pair of Smilax glabra Roxb. and Ficus hirta Vahl. improves exercise performance by regulating mitochondrial function via the adiponection receptors-mediated AMPK signaling pathway

doi: 10.3389/fnut.2026.1782001

Figure Lengend Snippet: Synergistic activation of the AdipoRs-AMPK pathway by taxifolin and apigenin combination (A) Schematic design of monomer compound cell experiments (Created in https://BioRender.com ); (B) mRNA expression levels of STRT1, Ppargc1a, Nrf1 (NRF1), and Tfam (TFAM) ( n = 6); (C, D) Protein expression in AdipoRs-AMPK pathway and mitochondrial function ( n = 3); (E, F) Mitochondrial DNA copy number detection ( n = 6); (G) Intracellular ATP content measurement ( n = 3); (H) Detection of reactive oxygen species (ROS) levels ( n = 5); (I, J) Measurement of mitochondrial membrane potential (JC-1) (Scale bar: 20 μm, Total magnification: 200x, n = 5); (K–M) Transmission electron microscopy (TEM) observation of mitochondrial ultrastructure (Scale bar: 1/0.2 μm, Total magnification: 20,000/80,000x), statistical analysis of mitochondrial quantity ( n = 5) and mitochondrial area ( n = 100). Results are expressed as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 compared to the vehicle group.

Article Snippet: The specific antibodies used were as follows: AdipoR1 (Abclonal, A1509), AdipoR2 (Abclonal, A12777), p-AMPK (Abclonal, AP1441), AMPK (Abclonal, A1229), p-LKB1 (Abclonal, AP0601), LKB1 (Abclonal, A22636), PGC1α (Proteintech, 66369-1-Ig), SIRT1 (Proteintech, 13161-1-AP), LDHB (Proteintech, 14824-1-AP), COXIV (Cell Signaling Technology, 3E11), TFAM (Abclonal, A3173), NRF2 (Proteintech, 16396-1-AP), HO-1 (Abclonal, A19062), TNFα (Proteintech, 80258-6-RR), COX2 (Abclonal, A3560), and β-actin (Proteintech, 20536-1-AP).

Techniques: Activation Assay, Expressing, Membrane, Transmission Assay, Electron Microscopy