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ChinaPeptides
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European Collection of Authenticated Cell Cultures
pc12 cell, a rat adrenal pheochromocytoma cell line ![]() Pc12 Cell, A Rat Adrenal Pheochromocytoma Cell Line, supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pc12+rat+cells/pmc07143819-37-0-12?v=European+Collection+of+Authenticated+Cell+Cultures Average 90 stars, based on 1 article reviews
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CH Instruments
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Biopharm GmbH
rat neuronal pc12 cell line ![]() Rat Neuronal Pc12 Cell Line, supplied by Biopharm GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pc12+rat+cells/pm30184529-76-3-10?v=Biopharm+GmbH Average 90 stars, based on 1 article reviews
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AddexBio Inc
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INCSTAR Corporation
mouse monoclonal antiserum against tyrosine hydroxylase isolated, and were purified from rat pc 12 cells ![]() Mouse Monoclonal Antiserum Against Tyrosine Hydroxylase Isolated, And Were Purified From Rat Pc 12 Cells, supplied by INCSTAR Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pc12+rat+cells/pm15113603-97-31-35?v=INCSTAR+Corporation Average 90 stars, based on 1 article reviews
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KeyGene Inc
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Beijing Centre Biology Co Ltd
rat pc12 cells ![]() Rat Pc12 Cells, supplied by Beijing Centre Biology Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pc12+rat+cells/pm28609839-9-9-26?v=Beijing+Centre+Biology+Co+Ltd Average 90 stars, based on 1 article reviews
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Medim GmbH
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Georg Thieme Verlag KG
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Dawley Inc
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PC 12 Rat adrenal pheochromocytoma Whole Cell Lysate
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Image Search Results
Journal: PLoS ONE
Article Title: The Anti-Tumor Histone Deacetylase Inhibitor SAHA and the Natural Flavonoid Curcumin Exhibit Synergistic Neuroprotection against Amyloid-Beta Toxicity
doi: 10.1371/journal.pone.0085570
Figure Lengend Snippet: A. PC12 cells were treated with different concentrations of Aβ 25–35 (n = 5). *, p <0.05; ***, p <0.001 vs Ctrl. B. PC12 cells were treated with different concentrations of SAHA (n = 5). *, p <0.05; ***, p <0.001 vs Ctrl. C. PC12 cells were treated with different concentrations of curcumin (n = 5). *, p <0.05; ***, p <0.001 vs Ctrl. D. MTT assay was performed to detect cell viability after treating with SAHA and curcumin against Aβ 25–35 -induced cytotoxicity in PC12 cells (n = 5). ***, p <0.001 vs Ctrl; **, p <0.01 vs Aβ 25–35 .
Article Snippet:
Techniques: MTT Assay
Journal: PLoS ONE
Article Title: The Anti-Tumor Histone Deacetylase Inhibitor SAHA and the Natural Flavonoid Curcumin Exhibit Synergistic Neuroprotection against Amyloid-Beta Toxicity
doi: 10.1371/journal.pone.0085570
Figure Lengend Snippet: A. Apoptotic cells were detected by TUNEL assay. Cells were stained with TUNEL positive nuclei (green) and nuclei of PC12 cells (blue). B. The percentage of TUNEL positive cells was determined (n = 5). ***, p <0.001 vs Ctrl; **, p <0.01 vs Aβ 25–35 . Ctrl: the control group. C. Western blot of cleaved caspase 3 (n = 3). ***, p <0.001 vs Ctrl; **, p <0.01 vs Aβ 25–35 . Ctrl: the control group; CASP3: caspase 3.
Article Snippet:
Techniques: TUNEL Assay, Staining, Control, Western Blot
Journal: PLoS ONE
Article Title: The Anti-Tumor Histone Deacetylase Inhibitor SAHA and the Natural Flavonoid Curcumin Exhibit Synergistic Neuroprotection against Amyloid-Beta Toxicity
doi: 10.1371/journal.pone.0085570
Figure Lengend Snippet: A. Representative western blot of the p -Akt (Ser 473) protein expression with SAHA treatment (n = 3). **, p <0.01 vs Ctrl. B. Representative western blot of the p -Akt (Ser 473) protein expression with curcumin treatment (n = 3). **, p <0.01 vs Ctrl. C. Representative western blot of the p -Akt (Ser 473) protein expression with co-treatment of SAHA and curcumin (n = 3) to the PC12 cells (n = 3). *, p <0.05 vs Ctrl; **, p <0.01 vs Aβ 25–35 ; Ctrl: the control group.
Article Snippet:
Techniques: Western Blot, Expressing, Control
Journal: Microorganisms
Article Title: Potential Effects of Indole-3-Lactic Acid, a Metabolite of Human Bifidobacteria, on NGF-Induced Neurite Outgrowth in PC12 Cells
doi: 10.3390/microorganisms8030398
Figure Lengend Snippet: Effects of indole-3-lactic acid (ILA) on nerve growth factor (NGF)-induced neurite outgrowth of PC12 cells. PC12 cells were treated with NGF (25 ng/mL) and the test compounds (RC, ILA or Trp at 1 nM, 10 nM, 100 nM, and 1 µM) for five consecutive days. ( A ) Percentage of neurite-bearing cells in PC12 cells. ( B ) Acetylcholinesterase (AchE) activity in PC12 cells. ( C ) Images of βIII-tubulin (green) immunostaining of PC12 cells treated with NGF (25 ng/mL) and the test compounds (RC, ILa or Trp at 100 nM) for five consecutive days at a magnification of ×100. Scale bars: 100 µm. Nuclei were counterstained with DAPI (blue). The data represent the mean ± SD of three replicates. One-way ANOVA with Tukey’s post hoc tests were used for statistical analysis. Means with different lowercase letters are significantly different between test groups ( p < 0.05). Means with different uppercase letters are significantly different within the same test group ( p < 0.05). NGF-treated control. NTC, nontreated control; papaverine hydrochloride was used as a reference control (RC); tryptophan (Trp) was used as a baseline compound.
Article Snippet:
Techniques: Activity Assay, Immunostaining
Journal: Microorganisms
Article Title: Potential Effects of Indole-3-Lactic Acid, a Metabolite of Human Bifidobacteria, on NGF-Induced Neurite Outgrowth in PC12 Cells
doi: 10.3390/microorganisms8030398
Figure Lengend Snippet: Effects of indole-3-lactic acid (ILA) on the phosphorylation of TrkA, ERK1/2, and CREB in PC12 cells. Phosphorylation of ( A ) TrkA, ( B ) ERK1/2, and ( C ) CREB in PC12 cells treated for 24 h with NGF (25 ng/mL) and RC, ILA, or Trp (100 nM) was detected using western blot analysis. The data represent the mean ± SD of three replicates. Means with different lowercase letters are significantly different between test groups ( p < 0.05) by one-way ANOVA with Tukey’s post hoc tests. NTC, nontreated control; Papavarine hydrochloride was used as a reference control (RC); Tryptophan (Trp) was used as a baseline compound.
Article Snippet:
Techniques: Western Blot
Journal: Microorganisms
Article Title: Potential Effects of Indole-3-Lactic Acid, a Metabolite of Human Bifidobacteria, on NGF-Induced Neurite Outgrowth in PC12 Cells
doi: 10.3390/microorganisms8030398
Figure Lengend Snippet: Effects of indole-3-lactic acid (ILA) on the aryl hydrocarbon receptor (AhR) in PC12 cells. PC12 cells were pretreated with the AhR antagonist, α-naphthoflavone (ANF; 1 µM), for 1 h and treated for five consecutive days with NGF (25 ng/mL) and RC, ILA or Trp (100 nM). Nonpretreated PC12 cells served as a null control. ( A ) AhR protein (95 kDa) in PC12 cells was detected by Western blot analysis using a monoclonal antibody specific for AhR. The corresponding β-actin blot served as a loading control. ( B ) Acetylcholinesterase (AchE) activity in PC12 cells. The data represent the mean ± SD of three replicates. * p < 0.05, ** p < 0.01 for intragroup differences compared by an independent Student’s t-test. Means with different lowercase letters are significantly different between test groups ( p < 0.05) by one-way ANOVA with Tukey’s post hoc tests. NTC, nontreated control; Papavarine hydrochloride was used as a reference control (RC); Tryptophan (Trp) was used as a baseline compound.
Article Snippet:
Techniques: Western Blot, Activity Assay
Journal: Microorganisms
Article Title: Potential Effects of Indole-3-Lactic Acid, a Metabolite of Human Bifidobacteria, on NGF-Induced Neurite Outgrowth in PC12 Cells
doi: 10.3390/microorganisms8030398
Figure Lengend Snippet: Effects of indole-3-lactic acid (ILA) on the aryl hydrocarbon receptor (AhR) in PC12 cells. PC12 cells were pretreated with the AhR antagonist, CH223191 (1 µM), for 1 h and treated for five consecutive days with NGF (25 ng/mL) and RC, ILA or Trp (100 nM). Nonpretreated PC12 cells served as a null control. ( A ) AhR protein (95 kDa) in PC12 cells was detected by Western blot analysis using a monoclonal antibody specific for AhR. The corresponding β-actin blot served as a loading control. ( B ) Acetylcholinesterase (AchE) activity in PC12 cells. The data represent the mean ± SD of three replicates. * p < 0.05, ** p < 0.01 for intragroup differences compared by an independent Student’s t -test. Means with different lowercase letters are significantly different between test groups ( p < 0.05) by one-way ANOVA with Tukey’s post hoc tests. NTC, nontreated control; Papavarine hydrochloride was used as a reference control (RC); Tryptophan (Trp) was used as a baseline compound.
Article Snippet:
Techniques: Western Blot, Activity Assay
Journal: Frontiers in Cell and Developmental Biology
Article Title: Detecting Key Functional Components Group and Speculating the Potential Mechanism of Xiao-Xu-Ming Decoction in Treating Stroke
doi: 10.3389/fcell.2022.753425
Figure Lengend Snippet: The comparation of effective components and non-KFCG components on cell viabilities induced PC12 cells. (A–E) The treatments with ferulic acid, vanillic acid, zingerone, caryophyllene oxide, and methylephedrine hydrochloride, respectively. (F) The structures of ferulic acid, vanillic acid, zingerone, caryophyllene oxide, methylephedrine hydrochloride, and edaravone. K represents the control group without the treatments of components and OGD; M represents the model group with OGD treatment and without components treatments; Eda represents edaravone (20 μM). ### represents the comparation of model group to control group ( p = 0.001); *, **, and *** represent the comparations of components groups to model group in the levels of p < 0.05, p < 0.01, and p < 0.001. (G) The screening process of components. Five components marked in red were selected for the in vitro experiments.
Article Snippet: The
Techniques: Control, In Vitro