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pgc1α antibodies  (Novus Biologicals)


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    Structured Review

    Novus Biologicals pgc1α antibodies
    Pgc1α Antibodies, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+pgc1%CE%B1/PGC1+alpha+Antibody+%5BDyLight+405%5D/us12571805-519-11-21
    Average 94 stars, based on 2 article reviews
    pgc1α antibodies - by Bioz Stars, 2026-10
    94/100 stars

    Images

    Related Articles

    Western Blot:

    Article Title: Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress.
    Article Snippet: After separating equal amounts of total protein by SDSPAGE gels, the proteins were transferred to a PVDF membrane (Millipore) and blocked with 5% milk (fatty-acid free) for 1 h at room temperature. .. Followed primary antibodies: Anti-UCP1 (Abcam,ab10983, 1:1000), anti-Hsc70 (Abcam, ab51052, 1:1000), total OXPHOS Rodent WB Antibody Cocktail (Abcam, ab110413, 1:250), anti-PPARα/NR1C1 (novus, NB300-537, 1:1000), anti-PPARγ (CST, 2435, 1:1000), anti-LAMP-2A (Invitrogen, 51-2200, 1:1000), anti-PGC1α (novus, NBP1-04676, 1:1000), anti-CPT-1α (novus, NB100-53791, 1:1000), anti-CPT1β (ABclonal, A6796, 1:1000), anti-Flag (ABclonal, AE005, 1:2000), anti-DJ-1/PARK7 (ABclonal, A19097, 1:1000), anti-βtubulin (Cowin Biotech, CW0098M, 1:2000), anti-HA (Proteintech, 51064-2-AP, 1:2000), anti-V5(CST, 13202, 1:2000), anti-LAMP2a (Abmart, T55518, 1:1000) were incubated with the membranes, which were then washed three times in TBST (Tris-buffered saline containing 0.1% Tween 20) before visualization using the ECL. .. Western blot images were analyzed for densitometry using ImageJ (National Institutes of Health)58.

    Article Title: Skeletal muscle endothelial dysfunction through the activin A–PGC1α axis drives progression of cancer cachexia
    Article Snippet: .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1–04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    Article Title: Skeletal muscle endothelial dysfunction through the activin A-PGC1α axis drives progression of cancer cachexia.
    Article Snippet: The secondary antibodies used were goat anti-rat IgM cross-adsorbed secondary antibody DyLight 488 (Thermo Fisher, SA5-10010, 1:400 dilution) or goat anti-rabbit IgG (H + L) cross-adsorbed secondary antibody Alexa Fluor 633 (Thermo Fisher, A21070; 1:500 dilution) for 1 h at room temperature. .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1-04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    Incubation:

    Article Title: Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress.
    Article Snippet: After separating equal amounts of total protein by SDSPAGE gels, the proteins were transferred to a PVDF membrane (Millipore) and blocked with 5% milk (fatty-acid free) for 1 h at room temperature. .. Followed primary antibodies: Anti-UCP1 (Abcam,ab10983, 1:1000), anti-Hsc70 (Abcam, ab51052, 1:1000), total OXPHOS Rodent WB Antibody Cocktail (Abcam, ab110413, 1:250), anti-PPARα/NR1C1 (novus, NB300-537, 1:1000), anti-PPARγ (CST, 2435, 1:1000), anti-LAMP-2A (Invitrogen, 51-2200, 1:1000), anti-PGC1α (novus, NBP1-04676, 1:1000), anti-CPT-1α (novus, NB100-53791, 1:1000), anti-CPT1β (ABclonal, A6796, 1:1000), anti-Flag (ABclonal, AE005, 1:2000), anti-DJ-1/PARK7 (ABclonal, A19097, 1:1000), anti-βtubulin (Cowin Biotech, CW0098M, 1:2000), anti-HA (Proteintech, 51064-2-AP, 1:2000), anti-V5(CST, 13202, 1:2000), anti-LAMP2a (Abmart, T55518, 1:1000) were incubated with the membranes, which were then washed three times in TBST (Tris-buffered saline containing 0.1% Tween 20) before visualization using the ECL. .. Western blot images were analyzed for densitometry using ImageJ (National Institutes of Health)58.

    Saline:

    Article Title: Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress.
    Article Snippet: After separating equal amounts of total protein by SDSPAGE gels, the proteins were transferred to a PVDF membrane (Millipore) and blocked with 5% milk (fatty-acid free) for 1 h at room temperature. .. Followed primary antibodies: Anti-UCP1 (Abcam,ab10983, 1:1000), anti-Hsc70 (Abcam, ab51052, 1:1000), total OXPHOS Rodent WB Antibody Cocktail (Abcam, ab110413, 1:250), anti-PPARα/NR1C1 (novus, NB300-537, 1:1000), anti-PPARγ (CST, 2435, 1:1000), anti-LAMP-2A (Invitrogen, 51-2200, 1:1000), anti-PGC1α (novus, NBP1-04676, 1:1000), anti-CPT-1α (novus, NB100-53791, 1:1000), anti-CPT1β (ABclonal, A6796, 1:1000), anti-Flag (ABclonal, AE005, 1:2000), anti-DJ-1/PARK7 (ABclonal, A19097, 1:1000), anti-βtubulin (Cowin Biotech, CW0098M, 1:2000), anti-HA (Proteintech, 51064-2-AP, 1:2000), anti-V5(CST, 13202, 1:2000), anti-LAMP2a (Abmart, T55518, 1:1000) were incubated with the membranes, which were then washed three times in TBST (Tris-buffered saline containing 0.1% Tween 20) before visualization using the ECL. .. Western blot images were analyzed for densitometry using ImageJ (National Institutes of Health)58.

    Concentration Assay:

    Article Title: Skeletal muscle endothelial dysfunction through the activin A–PGC1α axis drives progression of cancer cachexia
    Article Snippet: .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1–04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    Article Title: Skeletal muscle endothelial dysfunction through the activin A-PGC1α axis drives progression of cancer cachexia.
    Article Snippet: The secondary antibodies used were goat anti-rat IgM cross-adsorbed secondary antibody DyLight 488 (Thermo Fisher, SA5-10010, 1:400 dilution) or goat anti-rabbit IgG (H + L) cross-adsorbed secondary antibody Alexa Fluor 633 (Thermo Fisher, A21070; 1:500 dilution) for 1 h at room temperature. .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1-04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    Bradford Protein Assay:

    Article Title: Skeletal muscle endothelial dysfunction through the activin A–PGC1α axis drives progression of cancer cachexia
    Article Snippet: .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1–04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    Article Title: Skeletal muscle endothelial dysfunction through the activin A-PGC1α axis drives progression of cancer cachexia.
    Article Snippet: The secondary antibodies used were goat anti-rat IgM cross-adsorbed secondary antibody DyLight 488 (Thermo Fisher, SA5-10010, 1:400 dilution) or goat anti-rabbit IgG (H + L) cross-adsorbed secondary antibody Alexa Fluor 633 (Thermo Fisher, A21070; 1:500 dilution) for 1 h at room temperature. .. The concentration of protein was measured with Bradford protein assay solution (Bio-Red, 5000006) and the same amount of total protein was loaded in SDS–PAGE for western blotting and probed with specific antibodies: anti-PGC1α (NOVUS, NBP1-04676; 1:1,000 dilution), anti-actin (Santa Cruz, sc-517582 horseradish peroxidase; 1:1,000 dilution) or anti-VE-cadherin (Cayman, 160840; 1:1,000 dilution). ..

    other:

    Article Title: Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress.
    Article Snippet: Western blot images were analyzed for densitometry using ImageJ (National Institutes of Health)58.



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    SAC promotes <t>PGC1α/FBP1</t> axis in AKI mouse kidneys. (A) Representative images of multiplex immunofluorescence staining in renal tissues showing DAPI (blue, nuclei), LRP2 (green, proximal tubules), and FBP1 (red) (original magnification ×40; Scale bar: 50 μm). (B) Quantitative assessment of FBP1-positive area. (C) Representative photomicrographs of FOXO1 staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (D) Quantitative assessment of FOXO1-positive cells. (E) Representative photomicrographs of PGC1α staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (F) Quantitative assessment of PGC1α-positive Area. NS represents not significant. * p < 0.05. ** p < 0.01. *** p < 0.001.
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    Image Search Results


    SAC promotes PGC1α/FBP1 axis in AKI mouse kidneys. (A) Representative images of multiplex immunofluorescence staining in renal tissues showing DAPI (blue, nuclei), LRP2 (green, proximal tubules), and FBP1 (red) (original magnification ×40; Scale bar: 50 μm). (B) Quantitative assessment of FBP1-positive area. (C) Representative photomicrographs of FOXO1 staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (D) Quantitative assessment of FOXO1-positive cells. (E) Representative photomicrographs of PGC1α staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (F) Quantitative assessment of PGC1α-positive Area. NS represents not significant. * p < 0.05. ** p < 0.01. *** p < 0.001.

    Journal: Renal Failure

    Article Title: Salvianolic acid C alleviates acute kidney injury by restoring fructose-1,6-bisphosphatase 1-mediated gluconeogenesis

    doi: 10.1080/0886022X.2026.2629902

    Figure Lengend Snippet: SAC promotes PGC1α/FBP1 axis in AKI mouse kidneys. (A) Representative images of multiplex immunofluorescence staining in renal tissues showing DAPI (blue, nuclei), LRP2 (green, proximal tubules), and FBP1 (red) (original magnification ×40; Scale bar: 50 μm). (B) Quantitative assessment of FBP1-positive area. (C) Representative photomicrographs of FOXO1 staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (D) Quantitative assessment of FOXO1-positive cells. (E) Representative photomicrographs of PGC1α staining in renal tissues (original magnification ×40; Scale bar: 50 μm). (F) Quantitative assessment of PGC1α-positive Area. NS represents not significant. * p < 0.05. ** p < 0.01. *** p < 0.001.

    Article Snippet: Primary antibodies used were Cleaved-caspase-3 (Cat# 9661, Cell Signaling Technology, Danvers, MA, USA), FOXO1 (Cat# GB12286, Servicebio, Wuhan, China), and PGC1α (Cat# 66369-1-IG, Servicebio, Wuhan, Hubei, China).

    Techniques: Multiplex Assay, Immunofluorescence, Staining