claudin 1 Search Results


anti claudin 1 antibody  (R&D Systems)
91
R&D Systems anti claudin 1 antibody
Anti Claudin 1 Antibody, supplied by R&D Systems, 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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claudin 1  (Proteintech)
96
Proteintech claudin 1
Claudin 1, 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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claudin 1  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc claudin 1
Claudin 1, supplied by Cell Signaling Technology Inc, 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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anti claudin 1  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology anti claudin 1
Anti Claudin 1, 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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claudin 1  (Biorbyt)
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Biorbyt claudin 1
Claudin 1, supplied by Biorbyt, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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small interfering rna targeting  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology small interfering rna targeting
FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated <t>by</t> <t>claudin-1.</t> The <t>RNA</t> interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.
Small Interfering Rna Targeting, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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claudin 1  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology claudin 1
FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated <t>by</t> <t>claudin-1.</t> The <t>RNA</t> interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.
Claudin 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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primary rabbit antibody  (Cell Signaling Technology Inc)
95
Cell Signaling Technology Inc primary rabbit antibody
FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated <t>by</t> <t>claudin-1.</t> The <t>RNA</t> interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.
Primary Rabbit Antibody, supplied by Cell Signaling Technology Inc, 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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cldn 1 csb el005490hu elisa kit는  (Cusabio)
93
Cusabio cldn 1 csb el005490hu elisa kit는
FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated <t>by</t> <t>claudin-1.</t> The <t>RNA</t> interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.
Cldn 1 Csb El005490hu Elisa Kit는, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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polyclonal rabbit anti claudin 1  (Biorbyt)
91
Biorbyt polyclonal rabbit anti claudin 1
FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated <t>by</t> <t>claudin-1.</t> The <t>RNA</t> interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.
Polyclonal Rabbit Anti Claudin 1, supplied by Biorbyt, 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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rabbit polyclonal anti claudin 1 antibody  (OriGene)
91
OriGene rabbit polyclonal anti claudin 1 antibody
Effects of MRPs on the mRNA and protein expression levels of <t>claudin-1</t> and ZO-1 in duodenal tissues. (A) The mRNA expression levels of claudin-1. (B) The mRNA expression levels of ZO-1. (C) The protein expression levels of claudin-1. (D) The protein expression levels of ZO-1. The mRNA levels of claudin-1and ZO-1 were quantified with β-actin as reference gene. The protein expression levels of claudin-1and ZO-1 were quantified with β-actin as the internal control. Values are mean ± SD (n = 6). *P < 0.05, compared with the control group; △P < 0.05, compared with the S-R-HGF group
Rabbit Polyclonal Anti Claudin 1 Antibody, supplied by OriGene, 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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Image Search Results


FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated by claudin-1. The RNA interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.

Journal: Frontiers in pharmacology

Article Title: Andrographolide Inhibits Cholangiocarcinoma Cell Migration by Down-Regulation of Claudin-1 via the p-38 Signaling Pathway.

doi: 10.3389/fphar.2019.00827

Figure Lengend Snippet: FIGURE 4 | Inhibitory effect of andrographolide on cell migration mediated by claudin-1. The RNA interference of claudin-1 was used to knock down the claudin-1 gene in KKU-M213 cells. KKU-M213 were treated with 0 μM (1% DMSO), 50 μM of andrographolide, scramble, and si-claudin-1 prior to harvesting RNA and cellular proteins for the detection of claudin-1. (A) The expression of claudin-1 mRNA from real-time RT-PCR; (B) The level of claudin-1 protein from Western blot analysis. Actin was used as internal standard. (C) With those treatments, KKU-M213 was scratched to make a wound and photographed at 0 and 12 h to measure the wound length for migration index analysis. (D) The results of bar graph are represented by the average of relative intensity compared with that of control. Data were derived from three independent experiments and are presented as mean ± SE, *p < 0.05, **p < 0.01.

Article Snippet: Small Interfering RNA Targeting of Claudin-1 Synthetic small interfering RNAs (siRNA) were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Migration, Knockdown, Expressing, Quantitative RT-PCR, Western Blot, Control, Derivative Assay

Effects of MRPs on the mRNA and protein expression levels of claudin-1 and ZO-1 in duodenal tissues. (A) The mRNA expression levels of claudin-1. (B) The mRNA expression levels of ZO-1. (C) The protein expression levels of claudin-1. (D) The protein expression levels of ZO-1. The mRNA levels of claudin-1and ZO-1 were quantified with β-actin as reference gene. The protein expression levels of claudin-1and ZO-1 were quantified with β-actin as the internal control. Values are mean ± SD (n = 6). *P < 0.05, compared with the control group; △P < 0.05, compared with the S-R-HGF group

Journal: Food Science and Biotechnology

Article Title: Promoting effect of the Maillard reaction products produced during the stir-frying process of Hordei Fructus Germinatus on the intestinal absorption of active ingredients in Hordei Fructus Germinatus

doi: 10.1007/s10068-021-00911-1

Figure Lengend Snippet: Effects of MRPs on the mRNA and protein expression levels of claudin-1 and ZO-1 in duodenal tissues. (A) The mRNA expression levels of claudin-1. (B) The mRNA expression levels of ZO-1. (C) The protein expression levels of claudin-1. (D) The protein expression levels of ZO-1. The mRNA levels of claudin-1and ZO-1 were quantified with β-actin as reference gene. The protein expression levels of claudin-1and ZO-1 were quantified with β-actin as the internal control. Values are mean ± SD (n = 6). *P < 0.05, compared with the control group; △P < 0.05, compared with the S-R-HGF group

Article Snippet: Rabbit polyclonal anti-ZO-1 antibody and Rabbit polyclonal anti-Claudin-1 antibody were provided by Beijing OriGene Technology Co., Ltd. (Beijing, China).

Techniques: Expressing