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MedChemExpress temsirolimus cci 779
The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus <t>(CCI-779)</t> (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)
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Taylor Hobson talysurf cci lite optical profilometer
The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus <t>(CCI-779)</t> (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)
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Motic Group ccis ef-n plan achromat 10× lens
The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus <t>(CCI-779)</t> (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)
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Charles River Laboratories cci surgery
The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus <t>(CCI-779)</t> (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)
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Exosome Diagnostics cci group
The impact of exosomes on pain behavior in <t>CCI</t> rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, <t>and</t> <t>Exo</t> group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.
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MedChemExpress cci 779
The impact of exosomes on pain behavior in <t>CCI</t> rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, <t>and</t> <t>Exo</t> group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.
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Wolters Kluwer Health cci
The impact of exosomes on pain behavior in <t>CCI</t> rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, <t>and</t> <t>Exo</t> group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.
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Zhongshi Duqing Biotech Co Ltd impact cci device
The impact of exosomes on pain behavior in <t>CCI</t> rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, <t>and</t> <t>Exo</t> group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.
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The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus (CCI-779) (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)

Journal: BMC Cancer

Article Title: Oncolytic adenovirus type 11-induced ferroptosis of esophageal squamous cell carcinoma cells involves in mitochondrial impairment and the mTOR pathway

doi: 10.1186/s12885-026-15735-7

Figure Lengend Snippet: The PI3K/Akt/mTOR pathway is essential for HAdV-11 replication in ESCC cell lines. ( A ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, the mRNA expression levels were determined using quantitative polymerase chain reaction (qPCR). ( B , D , E , F , H and I ) Cells were treated with HAdV-11 for 72 h at an MOI of 2 PFU/cell, and Western blot analysis of mTOR, p-DRP1, PARK2, LC3 and GPX4 expression. ( C ) Cells were pretreated with Temsirolimus (CCI-779) (10 nM) for 2 h, and then infected with HAdV-11 at an MOI of 2 for 48 h. The mitochondrial mass was estimated by MTG staining. ( H ) After pretreatment with 0.5 µM mTOR agonist (MHY1485) for 2 h, cells were infected with HAdV-11 at a MOI of 2 for 48 h. Subsequently, the cells were stained with either C11-BODIPY or Fe 2+ and quantified using flow cytometry. ( J ) Cells were pretreated with CCI-779 for 2 h, and then infected with HAdV-11 at an MOI of 2 for 72 h. Infectious virus production was assessed by titration on JH293 cells and the titer as PFU/cell calculated. The half maximal effective concentration (EC50) for each sample was calculated. Data are cumulative results from 3 experiments ( A , J ) or are representative of 3 independent experiments ( B , C , D , E , F , G , H , I ). Data are presented as mean ± SD ( A , C , E , F , G , H , I , J ). Differences analyzed using a one-way ANOVA with Bonferroni’s post hoc correction ( C , E , F , G , H , I ) or two-tailed t-test ( A , J ) ( n = 3)

Article Snippet: Mitochondrial division inhibitor 1 (Mdivi-1), Ferrostatin-1, Erastin, MK2206, LY294002 and Temsirolimus (CCI-779) were purchased from MedChem Express (Shanghai, China).

Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot, Infection, Staining, Flow Cytometry, Virus, Titration, Concentration Assay, Two Tailed Test

The impact of exosomes on pain behavior in CCI rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, and Exo group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.

Journal: Molecular Pain

Article Title: Mechanism of human umbilical cord mesenchymal stem cell-derived exosomes in alleviating neuropathic pain in CCI rats

doi: 10.1177/17448069261417109

Figure Lengend Snippet: The impact of exosomes on pain behavior in CCI rats. (a) Mechanical paw withdrawal threshold (PWT) of rats in Sham group, CCI group, and Exo group. (b) Thermal withdrawal latency (PWL) of rats in Sham group, CCI group, and Exo group ns indicates p > 0.05; * denotes the difference between the Exo group and the CCI group; # denotes the difference between the Sham group and the CCI group; **** p < 0.001; #### p < 0.001.

Article Snippet: Relative to the CCI group, exosome-treated rats (Exo group) showed no statistically significant difference in PWT ( p > 0.05), but exhibited a marked increase in PWL ( p < 0.001).

Techniques:

The effect of exosomes on inflammatory factors in the spinal dorsal horn of CCI rats. (a–c) represent the intra-group and inter-group comparison results of NF-κB, TNF-α, and IL-6 at D7 and D14 in the spinal cord Sham group, CCI group, and Exo group, respectively. Here, ns p > 0.05; * p < 0.05; ** p < 0.01; **** p < 0.001.

Journal: Molecular Pain

Article Title: Mechanism of human umbilical cord mesenchymal stem cell-derived exosomes in alleviating neuropathic pain in CCI rats

doi: 10.1177/17448069261417109

Figure Lengend Snippet: The effect of exosomes on inflammatory factors in the spinal dorsal horn of CCI rats. (a–c) represent the intra-group and inter-group comparison results of NF-κB, TNF-α, and IL-6 at D7 and D14 in the spinal cord Sham group, CCI group, and Exo group, respectively. Here, ns p > 0.05; * p < 0.05; ** p < 0.01; **** p < 0.001.

Article Snippet: Relative to the CCI group, exosome-treated rats (Exo group) showed no statistically significant difference in PWT ( p > 0.05), but exhibited a marked increase in PWL ( p < 0.001).

Techniques: Comparison

Changes in mRNA content of A1, A2, and GFAP in spinal cord astrocytes of CCI rats treated with exosomes. (a–c) Represent the intra-group and inter-group comparison results of GFAP, S100A10 mRNA, and C3 mRNA in the spinal dorsal horn at D7 and D14 for the Sham group, CCI group, and Exo group, respectively. ns p > 0.05; * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Journal: Molecular Pain

Article Title: Mechanism of human umbilical cord mesenchymal stem cell-derived exosomes in alleviating neuropathic pain in CCI rats

doi: 10.1177/17448069261417109

Figure Lengend Snippet: Changes in mRNA content of A1, A2, and GFAP in spinal cord astrocytes of CCI rats treated with exosomes. (a–c) Represent the intra-group and inter-group comparison results of GFAP, S100A10 mRNA, and C3 mRNA in the spinal dorsal horn at D7 and D14 for the Sham group, CCI group, and Exo group, respectively. ns p > 0.05; * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Article Snippet: Relative to the CCI group, exosome-treated rats (Exo group) showed no statistically significant difference in PWT ( p > 0.05), but exhibited a marked increase in PWL ( p < 0.001).

Techniques: Comparison

Changes in A1 and A2 protein content in spinal cord astrocytes of CCI rats treated with exosomes. (a–d) Represent the intra-group and inter-group comparison results of C3 and S100A10 in the spinal dorsal horn at D7 and D14 for the Sham group, CCI group, and Exo group, respectively. Here, ns p > 0.05; * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Journal: Molecular Pain

Article Title: Mechanism of human umbilical cord mesenchymal stem cell-derived exosomes in alleviating neuropathic pain in CCI rats

doi: 10.1177/17448069261417109

Figure Lengend Snippet: Changes in A1 and A2 protein content in spinal cord astrocytes of CCI rats treated with exosomes. (a–d) Represent the intra-group and inter-group comparison results of C3 and S100A10 in the spinal dorsal horn at D7 and D14 for the Sham group, CCI group, and Exo group, respectively. Here, ns p > 0.05; * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Article Snippet: Relative to the CCI group, exosome-treated rats (Exo group) showed no statistically significant difference in PWT ( p > 0.05), but exhibited a marked increase in PWL ( p < 0.001).

Techniques: Comparison