primary antibodies against βactin Search Results


96
Proteintech antibodies against βactin
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
Antibodies Against βactin, supplied by Proteintech, 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
antibodies against βactin - by Bioz Stars, 2026-03
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90
Beyotime secondary antibodies (hpr)
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
Secondary Antibodies (Hpr), supplied by Beyotime, 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/result/secondary antibodies (hpr)/product/Beyotime
Average 90 stars, based on 1 article reviews
secondary antibodies (hpr) - by Bioz Stars, 2026-03
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95
Valiant Co Ltd antibody against betaactin
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
Antibody Against Betaactin, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antibody against betaactin/product/Valiant Co Ltd
Average 95 stars, based on 1 article reviews
antibody against betaactin - by Bioz Stars, 2026-03
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99
Cell Signaling Technology Inc c mouse antibody against βactin
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
C Mouse Antibody Against βactin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
c mouse antibody against βactin - by Bioz Stars, 2026-03
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90
Santa Cruz Biotechnology primary antibodies against βactin
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
Primary Antibodies Against βactin, supplied by Santa Cruz Biotechnology, 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/result/primary antibodies against βactin/product/Santa Cruz Biotechnology
Average 90 stars, based on 1 article reviews
primary antibodies against βactin - by Bioz Stars, 2026-03
90/100 stars
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96
Proteintech βactin
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
βactin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/βactin/product/Proteintech
Average 96 stars, based on 1 article reviews
βactin - by Bioz Stars, 2026-03
96/100 stars
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99
Cell Signaling Technology Inc anti βactin primary antibody
FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control <t>was</t> <t>GAPDH</t> and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.
Anti βactin Primary Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti βactin primary antibody/product/Cell Signaling Technology Inc
Average 99 stars, based on 1 article reviews
anti βactin primary antibody - by Bioz Stars, 2026-03
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96
Santa Cruz Biotechnology mouse monoclonal antibody moab anti βactin
Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).
Mouse Monoclonal Antibody Moab Anti βactin, supplied by Santa Cruz Biotechnology, 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
mouse monoclonal antibody moab anti βactin - by Bioz Stars, 2026-03
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90
Thermo Fisher rabbit anti-βactin primary antibody
Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).
Rabbit Anti βactin Primary Antibody, supplied by Thermo Fisher, 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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Cell Signaling Technology Inc primary antibodies against βactin
Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).
Primary Antibodies Against βactin, supplied by Cell Signaling Technology Inc, 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/result/primary antibodies against βactin/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
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Millipore primary antibodies against βactin
Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).
Primary Antibodies Against βactin, supplied by Millipore, 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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Average 90 stars, based on 1 article reviews
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Thermo Fisher mouse monoclonal antibody against βactin
Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).
Mouse Monoclonal Antibody Against βactin, supplied by Thermo Fisher, 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/result/mouse monoclonal antibody against βactin/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
mouse monoclonal antibody against βactin - by Bioz Stars, 2026-03
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Image Search Results


FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control was GAPDH and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.

Journal: Frontiers in cardiovascular medicine

Article Title: Deficiency of a novel lncRNA-HRAT protects against myocardial ischemia reperfusion injury by targeting miR-370-3p/RNF41 pathway.

doi: 10.3389/fcvm.2022.951463

Figure Lengend Snippet: FIGURE 3 Characterization of lncRNA-HRAT. (A) Assessment the protein-coding potential of lncRNA-HRAT by Coding Potential Calculator Online. (B) Schematic annotation of the lncRNA-HRAT genomic locus. (C) The analysis of Adora1 expression in Ctrl and H/R cells was conducted through qRT-PCR (n = 3). (D) The analysis of Adora1 expression in H9c2 cells infected with lncRNA-HRAT or control lentivirus was conducted through qRT-PCR (n = 3). (E) The localization of lncRNA-HRAT in H9c2 cells was tested via RNA FISH (n = 3). Nuclei was stained with 40,6-diamidino-2-phenylindole (DAPI; blue), 18S and lncRNA-HRAT appeared red. Scale bar, 10µm. (F) The analysis of lncRNA-HRAT expression in the nucleus and cytoplasm of H9c2 cells was employed through qRT-PCR (n = 3). The cytoplasmic control was GAPDH and β-actin, while the nuclear control was U6. All the data are described as the mean ± SD. *P < 0.05.

Article Snippet: After blocking with 5% milk at RT, the membrane was then incubated with antibodies against βactin (1:5000, Proteintech, 20536-1-AP), GAPDH (1:1000; Proteintech, 10494-1-AP), Caspase-3 (1:1000, CST, 9662S), cleaved Caspase-3 (1:1000, CST, 9664S), RNF41 (1:1000, Proteintech, 17233-1-AP) overnight at 4◦C. β-actin and GAPDH antibody was served as control.

Techniques: Expressing, Quantitative RT-PCR, Infection, Control, Staining

Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Journal: Nutrients

Article Title: Lentil Waste Extracts for Inflammatory Bowel Disease (IBD) Symptoms Control: Anti-Inflammatory and Spasmolytic Effects.

doi: 10.3390/nu16193327

Figure Lengend Snippet: Figure 2. Effects of different lentil hull extracts on TLR4 expression levels in Caco-2 cells treated with LPS (1 µg/mL) for 24 h. Immunoblotting detection in the Caco-2 cells of control, LPS, BEVa and BEVa plus LPS (A), BEVb and BEVb plus LPS (B), mBEVa and mBEVa plus LPS (C), and mBEVb and mBEVb plus LPS (D). Densitometric analysis of TLR4 expression, after normalization against β-actin, is reported. Data are presented as means ± SD of five independent experiments. (*** p < 0.001 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Article Snippet: Then, following a standard avidin-biotin complex procedure, membranes were incubated in the dark with primary mouse monoclonal antibody (moAb) anti-βactin (sc-47778), rabbit poAb anti-TLR4 (sc-10741) (all from Santa Cruz Biotechnology, Inc., Milan, Italy), at a 1:500 dilution.

Techniques: Expressing, Western Blot, Control

Figure 3. Analysis of pro-inflammatory responses. Real-time PCR analysis of iNOS mRNA expression levels in Caco2-untreated cells (control), treated with LPS alone (LPS) or treated with LPS after pre- treatment with different lentil hull extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (** p < 0.05 vs. control; ## p < 0.01 and # p < 0.05 vs. LPS).

Journal: Nutrients

Article Title: Lentil Waste Extracts for Inflammatory Bowel Disease (IBD) Symptoms Control: Anti-Inflammatory and Spasmolytic Effects.

doi: 10.3390/nu16193327

Figure Lengend Snippet: Figure 3. Analysis of pro-inflammatory responses. Real-time PCR analysis of iNOS mRNA expression levels in Caco2-untreated cells (control), treated with LPS alone (LPS) or treated with LPS after pre- treatment with different lentil hull extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (** p < 0.05 vs. control; ## p < 0.01 and # p < 0.05 vs. LPS).

Article Snippet: Then, following a standard avidin-biotin complex procedure, membranes were incubated in the dark with primary mouse monoclonal antibody (moAb) anti-βactin (sc-47778), rabbit poAb anti-TLR4 (sc-10741) (all from Santa Cruz Biotechnology, Inc., Milan, Italy), at a 1:500 dilution.

Techniques: Real-time Polymerase Chain Reaction, Expressing, Control

Figure 4. Analysis of pro-inflammatory IL-1 cytokine expression. Real-time PCR analysis of IL-1 mRNA expression levels in Caco-2 untreated cells (Control), treated with LPS alone (LPS) or treated with LPS after pre-treatment of different lentil peel extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (*** p < 0.001 and ** p < 0.01 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Journal: Nutrients

Article Title: Lentil Waste Extracts for Inflammatory Bowel Disease (IBD) Symptoms Control: Anti-Inflammatory and Spasmolytic Effects.

doi: 10.3390/nu16193327

Figure Lengend Snippet: Figure 4. Analysis of pro-inflammatory IL-1 cytokine expression. Real-time PCR analysis of IL-1 mRNA expression levels in Caco-2 untreated cells (Control), treated with LPS alone (LPS) or treated with LPS after pre-treatment of different lentil peel extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (*** p < 0.001 and ** p < 0.01 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Article Snippet: Then, following a standard avidin-biotin complex procedure, membranes were incubated in the dark with primary mouse monoclonal antibody (moAb) anti-βactin (sc-47778), rabbit poAb anti-TLR4 (sc-10741) (all from Santa Cruz Biotechnology, Inc., Milan, Italy), at a 1:500 dilution.

Techniques: Expressing, Real-time Polymerase Chain Reaction, Control

Figure 5. Analysis of anti-inflammatory cytokine expression. Real-time PCR analysis of IL-10 mRNA expression levels in Caco-2 untreated cells (Control), treated with LPS alone (LPS) or treated with LPS after pre-treatment of different lentil hull extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (*** p < 0.001 and ** p < 0.01 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Journal: Nutrients

Article Title: Lentil Waste Extracts for Inflammatory Bowel Disease (IBD) Symptoms Control: Anti-Inflammatory and Spasmolytic Effects.

doi: 10.3390/nu16193327

Figure Lengend Snippet: Figure 5. Analysis of anti-inflammatory cytokine expression. Real-time PCR analysis of IL-10 mRNA expression levels in Caco-2 untreated cells (Control), treated with LPS alone (LPS) or treated with LPS after pre-treatment of different lentil hull extracts: (A) BEVa and mBEVa and (B) BEVb and mBEVb. Values represent the mRNA fold changes relative to β-actin used as resident control and expressed as means ± SD of five independent experiments. (*** p < 0.001 and ** p < 0.01 vs. control; ### p < 0.001, ## p < 0.01, and # p < 0.05 vs. LPS).

Article Snippet: Then, following a standard avidin-biotin complex procedure, membranes were incubated in the dark with primary mouse monoclonal antibody (moAb) anti-βactin (sc-47778), rabbit poAb anti-TLR4 (sc-10741) (all from Santa Cruz Biotechnology, Inc., Milan, Italy), at a 1:500 dilution.

Techniques: Expressing, Real-time Polymerase Chain Reaction, Control