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Genechem ad5 cmv 3flag egfp
Ad5 Cmv 3flag Egfp, supplied by Genechem, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Genechem recombinant pad4 adenovirus ad-pad4 adeno-cmv-mcs-padi4-3flag-sv40-egfp serotype ad5
<t>PAD4</t> promotes neuroinflammation and neuronal death via IRE1α/ASK1/JNK signaling pathway after TBI. A Schematic image of adeno-PAD4-EGFP and overexpression of PAD4 in the cortex of the mouse. B , C mNSS test on day 1 ( B ) and days 3 ( C ) post-TBI. **p < 0.01, ***p < 0.001, n = 10 per group. D , E Rotarod test on day 1 ( D ) and days 3 ( E ) post-TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 10 per group. F Representative western blot bands and densitometric quantification of Iba-1, CD16, and CD206 in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group. G Representative image of the FJC (green) staining and representative images of TUNEL (green) co-localization with neurons (NeuN, red) in the contused cortex at 3 days after TBI. Nuclei were stained with DAPI (blue). Scale bar = 100 μm. H , I Quantitative analysis of FJC-positive cells ( H ) and quantitative analysis of TUNEL-positive neurons ( I ) in the contused cortex at 3 days after TBI. *p < 0.05, **p < 0.01, n = 6 per group. J Representative western blot bands and densitometric quantification of pIRE1α, pASK1, and pJNK in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group
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PAD4 promotes neuroinflammation and neuronal death via IRE1α/ASK1/JNK signaling pathway after TBI. A Schematic image of adeno-PAD4-EGFP and overexpression of PAD4 in the cortex of the mouse. B , C mNSS test on day 1 ( B ) and days 3 ( C ) post-TBI. **p < 0.01, ***p < 0.001, n = 10 per group. D , E Rotarod test on day 1 ( D ) and days 3 ( E ) post-TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 10 per group. F Representative western blot bands and densitometric quantification of Iba-1, CD16, and CD206 in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group. G Representative image of the FJC (green) staining and representative images of TUNEL (green) co-localization with neurons (NeuN, red) in the contused cortex at 3 days after TBI. Nuclei were stained with DAPI (blue). Scale bar = 100 μm. H , I Quantitative analysis of FJC-positive cells ( H ) and quantitative analysis of TUNEL-positive neurons ( I ) in the contused cortex at 3 days after TBI. *p < 0.05, **p < 0.01, n = 6 per group. J Representative western blot bands and densitometric quantification of pIRE1α, pASK1, and pJNK in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group

Journal: Journal of Neuroinflammation

Article Title: Inhibition of neutrophil extracellular trap formation ameliorates neuroinflammation and neuronal apoptosis via STING-dependent IRE1α/ASK1/JNK signaling pathway in mice with traumatic brain injury

doi: 10.1186/s12974-023-02903-w

Figure Lengend Snippet: PAD4 promotes neuroinflammation and neuronal death via IRE1α/ASK1/JNK signaling pathway after TBI. A Schematic image of adeno-PAD4-EGFP and overexpression of PAD4 in the cortex of the mouse. B , C mNSS test on day 1 ( B ) and days 3 ( C ) post-TBI. **p < 0.01, ***p < 0.001, n = 10 per group. D , E Rotarod test on day 1 ( D ) and days 3 ( E ) post-TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 10 per group. F Representative western blot bands and densitometric quantification of Iba-1, CD16, and CD206 in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group. G Representative image of the FJC (green) staining and representative images of TUNEL (green) co-localization with neurons (NeuN, red) in the contused cortex at 3 days after TBI. Nuclei were stained with DAPI (blue). Scale bar = 100 μm. H , I Quantitative analysis of FJC-positive cells ( H ) and quantitative analysis of TUNEL-positive neurons ( I ) in the contused cortex at 3 days after TBI. *p < 0.05, **p < 0.01, n = 6 per group. J Representative western blot bands and densitometric quantification of pIRE1α, pASK1, and pJNK in the contused cortex after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group

Article Snippet: Recombinant PAD4 adenovirus (Ad-PAD4; Adeno-CMV-MCS-Padi4-3FLAG- SV40-EGFP, serotype Ad5, 4 × 10 10 plaque-forming-unit/mL) and empty control adenovirus (Ad-con, Adeno-CMV-MCS-3-FLAG-SV40-EGFP) were produced by Genechem (Shanghai, China).

Techniques: Over Expression, Western Blot, Staining, TUNEL Assay

Inhibition of IRE1α abolished the neurodestructive effects caused by PAD4 overexpression after TBI. A , B mNSS test ( A ) and Rotarod test ( B ) at 1 day post-TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 10 per group C, D mNSS test ( C ) and Rotarod test ( D ) at 3 days post-TBI. **p < 0.01, ***p < 0.001, n = 10 per group. E Representative western blot bands and densitometric quantification of pIRE1α, pASK1, pJNK, IL-1β, INOs, Arginase-1, Bax, and Bcl-2 after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group

Journal: Journal of Neuroinflammation

Article Title: Inhibition of neutrophil extracellular trap formation ameliorates neuroinflammation and neuronal apoptosis via STING-dependent IRE1α/ASK1/JNK signaling pathway in mice with traumatic brain injury

doi: 10.1186/s12974-023-02903-w

Figure Lengend Snippet: Inhibition of IRE1α abolished the neurodestructive effects caused by PAD4 overexpression after TBI. A , B mNSS test ( A ) and Rotarod test ( B ) at 1 day post-TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 10 per group C, D mNSS test ( C ) and Rotarod test ( D ) at 3 days post-TBI. **p < 0.01, ***p < 0.001, n = 10 per group. E Representative western blot bands and densitometric quantification of pIRE1α, pASK1, pJNK, IL-1β, INOs, Arginase-1, Bax, and Bcl-2 after TBI. *p < 0.05, **p < 0.01, ***p < 0.001, n = 6 per group

Article Snippet: Recombinant PAD4 adenovirus (Ad-PAD4; Adeno-CMV-MCS-Padi4-3FLAG- SV40-EGFP, serotype Ad5, 4 × 10 10 plaque-forming-unit/mL) and empty control adenovirus (Ad-con, Adeno-CMV-MCS-3-FLAG-SV40-EGFP) were produced by Genechem (Shanghai, China).

Techniques: Inhibition, Over Expression, Western Blot