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Proteintech ndufs3
DDIT4 facilitates the ubiquitination of <t>NDUFS3</t> resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.
Ndufs3, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/15066+1+ap/NDUFS3+Antibody/pmc12846758-356-79-81
Average 93 stars, based on 45 article reviews
ndufs3 - by Bioz Stars, 2026-09
93/100 stars

Images

1) Product Images from "Microvascular endothelial metabolic dysfunction drives cerebral edema through bioenergetic failure after ischemia-reperfusion"

Article Title: Microvascular endothelial metabolic dysfunction drives cerebral edema through bioenergetic failure after ischemia-reperfusion

Journal: Theranostics

doi: 10.7150/thno.127083

DDIT4 facilitates the ubiquitination of NDUFS3 resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.
Figure Legend Snippet: DDIT4 facilitates the ubiquitination of NDUFS3 resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.

Techniques Used: Ubiquitin Proteomics, Mass Spectrometry, Isolation, Expressing, Immunoprecipitation, Control, Western Blot, Knockdown, Co-Immunoprecipitation Assay, Over Expression, Staining

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Immunohistochemistry:

Article Title: Antihypertensive Drug Amlodipine Besylate Shows Potential in Alleviating Diabetic Peripheral Neuropathy
Article Snippet: .. Antibodies used for immunohistochemistry and western blotting Antibody name Company and catalog number anti-p-AMPK CST, 4185S anti-AMPK CST, 2532S anti-SIRT1 Abcam, ab110304 anti-PGC-1α Abcam, ab54481 anti-COXIV Proteintech, 11242-1-AP anti-NDUFS3 Proteintech, 15066-1-AP anti-PGP9.5 Abcam, ab108986 anti-NLRP3 CST, 15101S anti-IL-1β CST, 31202S anti-β-tubulin isotype III Sigma Aldrich, T8578 anti-β-arrestin2 Santa Cruz Biotechnology, SC-365445 anti-GPR40 Santa Cruz Biotechnology, SC-32905 anti-ASC CST, 67824S anti-Caspase-1 AdipoGen, AG-20B-0042 anti-LKB1 CST, 3047S anti-ZO-1 Santa Cruz Biotechnology, SC-33725 anti-Claudin-1 Santa Cruz Biotechnology, SC-166338 ..

Article Title: Antihypertensive drug amlodipine besylate shows potential in alleviating diabetic peripheral neuropathy.
Article Snippet: Schematic summary of the mechanism underlying the amelioration of AB on DPN in mice.. AB as a GPR40 agonist ameliorated DPN-like pathology in both T1DM and T2DM mice.. AB suppressed inflammation by regulating GPR40/β-arrestin2/NLRP3 pathway in sciatic nerves, improved mitochondrial dysfunction through GPR40/LKB1/AMPK/SIRT1/PGC-1α pathway in sciatic nerves and DRG tissues.

Western Blot:

Article Title: Antihypertensive Drug Amlodipine Besylate Shows Potential in Alleviating Diabetic Peripheral Neuropathy
Article Snippet: .. Antibodies used for immunohistochemistry and western blotting Antibody name Company and catalog number anti-p-AMPK CST, 4185S anti-AMPK CST, 2532S anti-SIRT1 Abcam, ab110304 anti-PGC-1α Abcam, ab54481 anti-COXIV Proteintech, 11242-1-AP anti-NDUFS3 Proteintech, 15066-1-AP anti-PGP9.5 Abcam, ab108986 anti-NLRP3 CST, 15101S anti-IL-1β CST, 31202S anti-β-tubulin isotype III Sigma Aldrich, T8578 anti-β-arrestin2 Santa Cruz Biotechnology, SC-365445 anti-GPR40 Santa Cruz Biotechnology, SC-32905 anti-ASC CST, 67824S anti-Caspase-1 AdipoGen, AG-20B-0042 anti-LKB1 CST, 3047S anti-ZO-1 Santa Cruz Biotechnology, SC-33725 anti-Claudin-1 Santa Cruz Biotechnology, SC-166338 ..

Article Title: Antihypertensive drug amlodipine besylate shows potential in alleviating diabetic peripheral neuropathy.
Article Snippet: Schematic summary of the mechanism underlying the amelioration of AB on DPN in mice.. AB as a GPR40 agonist ameliorated DPN-like pathology in both T1DM and T2DM mice.. AB suppressed inflammation by regulating GPR40/β-arrestin2/NLRP3 pathway in sciatic nerves, improved mitochondrial dysfunction through GPR40/LKB1/AMPK/SIRT1/PGC-1α pathway in sciatic nerves and DRG tissues.



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DDIT4 facilitates the ubiquitination of <t>NDUFS3</t> resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.
Ndufs3, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DDIT4 facilitates the ubiquitination of <t>NDUFS3</t> resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.
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DDIT4 facilitates the ubiquitination of <t>NDUFS3</t> resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.
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Image Search Results


DDIT4 facilitates the ubiquitination of NDUFS3 resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.

Journal: Theranostics

Article Title: Microvascular endothelial metabolic dysfunction drives cerebral edema through bioenergetic failure after ischemia-reperfusion

doi: 10.7150/thno.127083

Figure Lengend Snippet: DDIT4 facilitates the ubiquitination of NDUFS3 resulted in mitochondrial dysfunction. A, Mass spectrometry analysis of proteins pulled down by anti-DDIT4 antibodies identified potential DDIT4-interacting proteins. B, Volcano plot of differentially expressed proteins between mitochondria isolated from cerebral microvascular tissues before and after ischemia-reperfusion. C, Overlapping analysis of differential proteins in mitochondrial proteomic and interacting proteins of DDIT4. D, Heat map showed the expression of 11 overlapping proteins in mitochondrial proteomic. E, Co-immunoprecipitation of NDUFS3 (left) or DDIT4 (right) in ECs (IgG as a control antibody). F, Western blotting of NDUFS3 in indicated cells. Endothelial cell was treated with MG132 6h for harvest. And the quantification of protein was shown in below (n = 6 per group). G, Western blotting of NDUFS3 in cerebral microvascular tissues from conditional DDIT4 knockdown mice. The quantification of protein was shown in below (n = 6 per group). H, Co-IP of NDUFS3 and then western blotted with anti-ubiquitin in DDIT4 overexpression ECs. I, Representative images of staining with mitoSOX (red) and live cell nuclear stain hoechst33342 (blue). J, Phospho-MLKL aggregation in indicated cells. K, IntDen/cell measured using ImageJ (n = 6 per group). L, p-MLKL aggregates/nucleus quantified using Fiji (n = 6 per group). M, The OCR was measured in indicated cells. Data are mean ± SEM.

Article Snippet: The following primary antibody was utilized: Pan Kla (PTM-1401, PTM BIO), H3K9la (PTM-1419, PTM BIO), H3K14la (PTM-1414, PTM BIO), H3K18la (PTM-1406, PTM BIO), H4K5la (PTM-1407, PTM BIO), H4K8la (PTM-1415, PTM BIO), H4K12la (PTM-1411, PTM BIO), H4K16la (PTM-1417, PTM BIO), H3 (PTM-1001, PTM BIO), H4 (PTM-1015, PTM BIO), LDHA (19987-1-AP, Proteintech), β-actin (Abclonal), DDIT4 (10638-1-AP, Proteintech), p-MLKL (ab196436, Abcam), MLKL (37705, Cell Signaling Technology), p-RIP1 (65746S, Cell Signaling Technology), RIP1 (7519-1-AP, Proteintech), p-mTOR (5536S, Cell Signaling Technology), mTOR (66888-1-Ig, Proteintech), NDUFS3 (15066-1-AP, Proteintech), Ubiquitin (43124S, Cell Signaling Technology), ATF4 (60035-1-Ig, Proteintech).

Techniques: Ubiquitin Proteomics, Mass Spectrometry, Isolation, Expressing, Immunoprecipitation, Control, Western Blot, Knockdown, Co-Immunoprecipitation Assay, Over Expression, Staining