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TCPP and TNPP downregulate CEBPA expression through inhibiting the phosphorylation of ERK1/2. ( A ) Western blot analysis of <t>p38,</t> p-p38, ERK1/2, and p-ERK1/2 protein expression in HEK293T after treatment with TCPP and TNPP. ( B ) Quantization of protein levels from Western blot analysis in HEK293T after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( C ) Quantization of protein levels from Western blot analysis in HEK293T after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( D ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HK-2 after treatment with TCPP and TNPP. ( E ) Quantization of protein levels from Western blot analysis in HK-2 after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( F ) Quantization of protein levels from Western blot analysis in HK-2 after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3).
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TCPP and TNPP downregulate CEBPA expression through inhibiting the phosphorylation of ERK1/2. ( A ) Western blot analysis of <t>p38,</t> p-p38, ERK1/2, and p-ERK1/2 protein expression in HEK293T after treatment with TCPP and TNPP. ( B ) Quantization of protein levels from Western blot analysis in HEK293T after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( C ) Quantization of protein levels from Western blot analysis in HEK293T after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( D ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HK-2 after treatment with TCPP and TNPP. ( E ) Quantization of protein levels from Western blot analysis in HK-2 after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( F ) Quantization of protein levels from Western blot analysis in HK-2 after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3).
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TCPP and TNPP downregulate CEBPA expression through inhibiting the phosphorylation of ERK1/2. ( A ) Western blot analysis of <t>p38,</t> p-p38, ERK1/2, and p-ERK1/2 protein expression in HEK293T after treatment with TCPP and TNPP. ( B ) Quantization of protein levels from Western blot analysis in HEK293T after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( C ) Quantization of protein levels from Western blot analysis in HEK293T after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( D ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HK-2 after treatment with TCPP and TNPP. ( E ) Quantization of protein levels from Western blot analysis in HK-2 after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( F ) Quantization of protein levels from Western blot analysis in HK-2 after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3).
Anti Phospho P38 Mapk (Thr180/Tyr182) Polyclonal Antibody #28796 1 Ap, supplied by Proteintech, 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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TCPP and TNPP downregulate CEBPA expression through inhibiting the phosphorylation of ERK1/2. ( A ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HEK293T after treatment with TCPP and TNPP. ( B ) Quantization of protein levels from Western blot analysis in HEK293T after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( C ) Quantization of protein levels from Western blot analysis in HEK293T after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( D ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HK-2 after treatment with TCPP and TNPP. ( E ) Quantization of protein levels from Western blot analysis in HK-2 after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( F ) Quantization of protein levels from Western blot analysis in HK-2 after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3).

Journal: Toxics

Article Title: Tris (2-chloroisopropyl) phosphate and Tris (nonylphenyl) phosphite Promote Human Renal Cell Apoptosis through the ERK/CEPBA/Long Non-Coding RNA Cytoskeleton Regulator Axis

doi: 10.3390/toxics12070452

Figure Lengend Snippet: TCPP and TNPP downregulate CEBPA expression through inhibiting the phosphorylation of ERK1/2. ( A ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HEK293T after treatment with TCPP and TNPP. ( B ) Quantization of protein levels from Western blot analysis in HEK293T after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( C ) Quantization of protein levels from Western blot analysis in HEK293T after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( D ) Western blot analysis of p38, p-p38, ERK1/2, and p-ERK1/2 protein expression in HK-2 after treatment with TCPP and TNPP. ( E ) Quantization of protein levels from Western blot analysis in HK-2 after TCPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3). ( F ) Quantization of protein levels from Western blot analysis in HK-2 after TNPP treatment. Data are presented as the mean ± SD (** p < 0.01, n = 3).

Article Snippet: The primary antibodies used included phosph-p38 (Cat No. 28796-1-AP, 1:1000), p38 (Cat No. 14064-1-AP, 1:2000), phosph-ERK1/2 (Cat No. 80031-1-RR, 1:2000), ERK1/2 (Cat No. 11257-1-AP, 1:2000), CEBPA (Cat No. 29388-1-AP, 1:1000), GAPDH (Cat No. 80570-1-RR, 1:2000), and the secondary antibody Goat Anti-Rabbit IgG(H+L) (Cat No. SA00001-2, 1:10,000); all were from Proteintech Group, Inc (Wuhan, China).

Techniques: Expressing, Phospho-proteomics, Western Blot