anti ire1a Search Results


92
Bioss ire1a (ser726) polyclonal antibody
Ire1a (Ser726) Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/IRE1a+(Ser726)+Polyclonal+Antibody/custom%40bs-4308r%4030455644
Average 92 stars, based on 1 article reviews
ire1a (ser726) polyclonal antibody - by Bioz Stars, 2026-09
92/100 stars
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91
Rockland Immunochemicals anti ire1
Anti Ire1, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/Ire1+Antibody/10__1128_slash_mcb__01089___08-76-41-46
Average 91 stars, based on 1 article reviews
anti ire1 - by Bioz Stars, 2026-09
91/100 stars
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93
Boster Bio hydration
Hydration, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/Anti-MCU+Antibody+Picoband/pmc12417712-57-1-14
Average 93 stars, based on 1 article reviews
hydration - by Bioz Stars, 2026-09
93/100 stars
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93
Boster Bio ire1 α
MSCs attenuated EMT via the <t>IRE1</t> <t>α</t> /XBP1 pathway. (a) The protein expression levels of <t>IRE1</t> <t>α</t> and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).
Ire1 α, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/Anti-IRE1p+ERN1+Antibody/pmc10397497-55-54-57
Average 93 stars, based on 1 article reviews
ire1 α - by Bioz Stars, 2026-09
93/100 stars
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93
Boster Bio anti ire 1
MSCs attenuated EMT via the <t>IRE1</t> <t>α</t> /XBP1 pathway. (a) The protein expression levels of <t>IRE1</t> <t>α</t> and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).
Anti Ire 1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/Anti-IRE1%2FERN1+Antibody+Picoband/pm32938905-199-31-32
Average 93 stars, based on 1 article reviews
anti ire 1 - by Bioz Stars, 2026-09
93/100 stars
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91
Boster Bio anti phospho ire1 s724 rabbit monoclonal antibody
MSCs attenuated EMT via the <t>IRE1</t> <t>α</t> /XBP1 pathway. (a) The protein expression levels of <t>IRE1</t> <t>α</t> and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).
Anti Phospho Ire1 S724 Rabbit Monoclonal Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ire1a/Anti-Phospho-IRE1+(S724)+ERN1+Rabbit+Monoclonal+Antibody/pmc09323824-33-26-31
Average 91 stars, based on 1 article reviews
anti phospho ire1 s724 rabbit monoclonal antibody - by Bioz Stars, 2026-09
91/100 stars
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90
Boster Bio anti atp7b antibody
MSCs attenuated EMT via the <t>IRE1</t> <t>α</t> /XBP1 pathway. (a) The protein expression levels of <t>IRE1</t> <t>α</t> and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).
Anti Atp7b Antibody, supplied by Boster Bio, 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/anti+ire1a/Anti-ATP7B+Antibody+Picoband/pmc04088055-65-0-8
Average 90 stars, based on 1 article reviews
anti atp7b antibody - by Bioz Stars, 2026-09
90/100 stars
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90
GeneTex anti-ire1a
MSCs attenuated EMT via the <t>IRE1</t> <t>α</t> /XBP1 pathway. (a) The protein expression levels of <t>IRE1</t> <t>α</t> and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).
Anti Ire1a, supplied by GeneTex, 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/anti+ire1a/anti+ire1a/pmc08357971-217-14-22
Average 90 stars, based on 1 article reviews
anti-ire1a - by Bioz Stars, 2026-09
90/100 stars
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N/A
Goat Anti-Human ERN1 / IRE1a, (internal region)
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Image Search Results


MSCs attenuated EMT via the IRE1 α /XBP1 pathway. (a) The protein expression levels of IRE1 α and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).

Journal: Stem Cells International

Article Title: Mesenchymal Stem Cells Inhibit Epithelial-to-Mesenchymal Transition by Modulating the IRE1 α Branch of the Endoplasmic Reticulum Stress Response

doi: 10.1155/2023/4483776

Figure Lengend Snippet: MSCs attenuated EMT via the IRE1 α /XBP1 pathway. (a) The protein expression levels of IRE1 α and p-IRE1 α were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (b) The mRNA expression level of IRE1 α was measured using Q-PCR ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) A549 cells were treated with 4 μ 8c (5 and 10 μ M) for 48 hr, and the protein expression levels of IRE1 α and XBP-1s were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). (d) A549 cells were treated with 10 ng/ml TGF- β 1 in the presence or absence of 4 μ 8c for 72 hr. The protein expression levels of p-IRE1 α , XBP-1s, E-cadherin and vimentin were measured using western blotting and quantified using densitometry in ImageJ software ( n = 4, one-way ANOVA with Duncan's post hoc test). The data are shown as the means ± SEMs ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the TGF- β 1 group).

Article Snippet: After the proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, they were transferred to membranes, which were blocked with Protein Free Rapid Blocking Buffer (PS108, EpiZyme) and incubated with primary antibodies against CHOP (A5462, Bimake), BiP (11587-1-AP; Proteintech, Wuhan, China), ATF6 (D262665, Sangon, China), ATF4 (A5514, Bimake), XBP-1s (24868-1-AP, Proteintech), XBP-1u (25997-1-AP, Proteintech), IRE1 α (A00683-1, Boster, Wuhan, China), phospho-IRE1 α (S724, human) (ab124945, Abcam, Cambridge, UK), phospho-IRE1 α (S724, mouse) (530878, ZEN-BIO, Chengdu, China), Vimentin (ET1610-39, HuaBio, Hangzhou, China), and E-cadherin (340341, ZEN-BIO) overnight.

Techniques: Expressing, Western Blot, Software, Control

MSCs attenuated ER stress and EMT in the lungs of mice with lung fibrosis. (a) The mRNA expression levels of E-cadherin and Vimentin in lung tissues were measured using Q-PCR ( n = 5, one-way ANOVA with Duncan's post hoc test). (b) The protein expression levels of E-cadherin and vimentin in lung tissues were measured using western blotting, and the results were quantified via densitometry by using ImageJ software ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) The mRNA expression levels of Bip , Atf6 , Atf4 , Xbp-1s , Ire1α and Chop in lung tissues were measured using Q-PCR ( n = 5, one-way ANOVA with Duncan's post hoc test). (d) The protein expression levels of ATF6, ATF4, IRE1 α , p-IRE1 α , XBP-1s, XBP-1u, BiP and CHOP in lung tissues were measured using western blotting, and the results were quantified via densitometry by using ImageJ software ( n = 3, one-way ANOVA with Duncan's post hoc test). (e) Images of immunofluorescence staining of BiP (green) and vimentin (red) in the lung tissues of mice. Scale bar, 100 μ m. The data are shown as the means ± SEMs ( ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; # P < 0.05, ## P < 0.01 vs. the BLM group).

Journal: Stem Cells International

Article Title: Mesenchymal Stem Cells Inhibit Epithelial-to-Mesenchymal Transition by Modulating the IRE1 α Branch of the Endoplasmic Reticulum Stress Response

doi: 10.1155/2023/4483776

Figure Lengend Snippet: MSCs attenuated ER stress and EMT in the lungs of mice with lung fibrosis. (a) The mRNA expression levels of E-cadherin and Vimentin in lung tissues were measured using Q-PCR ( n = 5, one-way ANOVA with Duncan's post hoc test). (b) The protein expression levels of E-cadherin and vimentin in lung tissues were measured using western blotting, and the results were quantified via densitometry by using ImageJ software ( n = 3, one-way ANOVA with Duncan's post hoc test). (c) The mRNA expression levels of Bip , Atf6 , Atf4 , Xbp-1s , Ire1α and Chop in lung tissues were measured using Q-PCR ( n = 5, one-way ANOVA with Duncan's post hoc test). (d) The protein expression levels of ATF6, ATF4, IRE1 α , p-IRE1 α , XBP-1s, XBP-1u, BiP and CHOP in lung tissues were measured using western blotting, and the results were quantified via densitometry by using ImageJ software ( n = 3, one-way ANOVA with Duncan's post hoc test). (e) Images of immunofluorescence staining of BiP (green) and vimentin (red) in the lung tissues of mice. Scale bar, 100 μ m. The data are shown as the means ± SEMs ( ∗∗ P < 0.01, ∗ P < 0.05 vs. the control group; # P < 0.05, ## P < 0.01 vs. the BLM group).

Article Snippet: After the proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, they were transferred to membranes, which were blocked with Protein Free Rapid Blocking Buffer (PS108, EpiZyme) and incubated with primary antibodies against CHOP (A5462, Bimake), BiP (11587-1-AP; Proteintech, Wuhan, China), ATF6 (D262665, Sangon, China), ATF4 (A5514, Bimake), XBP-1s (24868-1-AP, Proteintech), XBP-1u (25997-1-AP, Proteintech), IRE1 α (A00683-1, Boster, Wuhan, China), phospho-IRE1 α (S724, human) (ab124945, Abcam, Cambridge, UK), phospho-IRE1 α (S724, mouse) (530878, ZEN-BIO, Chengdu, China), Vimentin (ET1610-39, HuaBio, Hangzhou, China), and E-cadherin (340341, ZEN-BIO) overnight.

Techniques: Expressing, Western Blot, Software, Immunofluorescence, Staining, Control