etoh Search Results


94
ATCC c showae
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96
MedChemExpress u0126
U0126, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Selleck Chemicals u0126
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
U0126, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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91
Revvity 3h n deoxy d glucose
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
3h N Deoxy D Glucose, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Revvity c deoxyglucose
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
C Deoxyglucose, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
DSMZ showae dsm 19458 dna
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
Showae Dsm 19458 Dna, supplied by DSMZ, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Revvity h d glucose
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
H D Glucose, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 91 stars, based on 1 article reviews
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90
Revvity myo 2 3 h n inositol
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
Myo 2 3 H N Inositol, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Revvity h thymidine
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
H Thymidine, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Revvity citrate
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
Citrate, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
Chem Impex International methylamine in thf
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
Methylamine In Thf, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
National Research Council Canada high concentration certified reference materials
Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, <t>U0126,</t> LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.
High Concentration Certified Reference Materials, supplied by National Research Council Canada, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, U0126, LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.

Journal: Cells

Article Title: Long-Term Treatment with Low-Level Arsenite Induces Aberrant Proliferation and Migration via Redox Rebalance in Human Urothelial Cells.

doi: 10.3390/cells14120912

Figure Lengend Snippet: Figure 8. Effects of JNK, p38, ERK, AKT, or NF-κB on the cell proliferation and migration and enhancement of HSP90, TGFα, and EGF following long-term arsenite treatment. Either SP600125, SB203580, U0126, LY294002, or PDTC was added to cells treated continuously with 0.5 µM arsenite for 40 weeks. (A) Cell viability was determined according to the MTS assay. (B) Cell migration capacities were estimated using wound-healing assays. (C,E) Western blots showing the effects on protein levels of EGF, TGFα, and HSP90 (C), and p65 and p-p65 (E). (D) Effects on EGF and TGFα levels in cell culture media. The outcomes are reported as mean ± SD, and a minimum of three separate experiments were conducted. * p < 0.05, vs. arsenite-treated group. T40 W, cells cultured for 40 weeks with arsenite treatment; SP, SP600125; SB, SB203580; LY, LY294002. The scale bars in the photos represent 100 µM for wound healing assay.

Article Snippet: The antibodies, reagents, and kits used in this study are as follows: ERK (Cell Signaling Technology, Danvers, MA, USA, 9102); p-ERK (Cell Signaling Technology, 9101); p38 (Cell Signaling Technology, 9212); p-p38(Cell Signaling Technology, 9211); JNK (Cell Signaling Technology, 9252); p-JNK (Cell Signaling Technology, 9251); AKT (Cell Signaling Technology, 9272); p-AKT (Cell Signaling Technology, 9271); Grx1 (ABclonal Technology, Wuhan, China, A23246); Trx1 (ABclonal Technology, A4024,); TrxR1 (ABclonal Technology, A4725); NLRP3 (ABclonal Technology, A24294,); TXNIP (ABclonal Technology, A9342); Caspase1 (ABclonal Technology, A0964); ASC (ABclonal Technology, A22046); IL-18 (ABclonal Technology, A23999); IL-1β (ABclonal Technology, A22257); P65 (Proteintech, Wuhan, China, 10745-1-AP); p-p65 (Proteintech, 82335-1-RR); EGF (ABclonal Technology, A26211); HSP90 (ABclonal Technology, A5027); TGFα (ABclonal Technology, A0337); Nrf2 (ABclonal Technology, A3577); β-actin (ABclonal Technology, AC038); U0126 (Selleck Chemicals, Houston, TX, USA, S1102); SB203580 (Selleck Chemicals, S1076); SP600125 (Selleck Chemicals, S1460), LY294002 (Selleck Chemicals, S1105); PDTC (Selleck Chemicals, S3633); BSO (Selleck Chemicals, S9728); PX-12 (MedChemExpress, Monmouth Junction, NJ, USA, HY13734); auranofin (MedChemExpress, HY-B1123); MCC950 (MedChemExpress, HY-12815); melatonin (MedChemExpress, HY-B0075); TBHQ (MedChemExpress, HY-100489); ML385 (MedChemExpress, HY-100523).

Techniques: Migration, MTS Assay, Western Blot, Cell Culture, Wound Healing Assay