bp1 antibody Search Results


98
Cell Signaling Technology Inc anti 4e bp1
Anti 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Cell Signaling Technology Inc anti phospho 4ebp1 ser65
Anti Phospho 4ebp1 Ser65, 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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95
Proteintech anti 4ebp1
Anti 4ebp1, supplied by Proteintech, 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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Average 95 stars, based on 1 article reviews
anti 4ebp1 - by Bioz Stars, 2026-04
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Cell Signaling Technology Inc phospho4e bp1 thr70
Phospho4e Bp1 Thr70, 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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93
Proteintech rabbit anti cpeb1
Rabbit Anti Cpeb1, supplied by Proteintech, 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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85
Proteintech anti siglec 6
Anti Siglec 6, supplied by Proteintech, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 85 stars, based on 1 article reviews
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96
Cell Signaling Technology Inc rabbit anti phospho 4ebp1
Rabbit Anti Phospho 4ebp1, 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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Average 96 stars, based on 1 article reviews
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95
Santa Cruz Biotechnology p 4ebp1
P 4ebp1, supplied by Santa Cruz Biotechnology, 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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94
Santa Cruz Biotechnology antibody to cugbp1
One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, <t>CUGBP1</t> levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.
Antibody To Cugbp1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Proteintech atf2
One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, <t>CUGBP1</t> levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.
Atf2, supplied by Proteintech, 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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93
Proteintech rabbit anti gorab
One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, <t>CUGBP1</t> levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.
Rabbit Anti Gorab, supplied by Proteintech, 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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93
Proteintech app
One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, <t>CUGBP1</t> levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.
App, supplied by Proteintech, 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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Average 93 stars, based on 1 article reviews
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Image Search Results


One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, CUGBP1 levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.

Journal: Cell Death & Disease

Article Title: CUGBP1, a crucial factor for heart regeneration in mice

doi: 10.1038/s41419-022-04570-w

Figure Lengend Snippet: One-day ( A ) or 8-day ( B ) old mice were performed sham or apical resection surgery, CUGBP1 levels in cardiac tissue samples were detected by western blot analysis at 1,4,7,14 days post resection. Western blot bands were quantified by densitometry and normalized to GAPDH. dpr, days post resection. Data are the mean ± SEM ( n = 4–6). * p < 0.05, ** p < 0.01 vs. control.

Article Snippet: Briefly, antibody to CUGBP1 (Santa Cruz Biotechnology, cat# sc-20003), and IgG (Santa Cruz Biotechnology, cat# sc-2025) was added to supernatant for immunoprecipitation (IP) and mock group, respectively.

Techniques: Western Blot, Control

A CUGBP1 was overexpressed in the 14-day old mice hearts and apical resection was performed simultaneously. Seven days after resection, cardiac tissue from apex zone was collected for paraffin section immunofluorescence detection of PH3 (red) and TNNI (green). Representative images are presented. B Statistical analysis of the number of PH3/TNNI-positive cells in apex and remote zone in the 14-day old mice heart following the Ad-virus infection and resection on seven days after resection. C Statistical analysis of the number of PH3/TNNI-positive cells by paraffin sections for immunofluorescence in the 14-day old mice heart following the Ad-virus infection and resection. Scale bars: 50 μm, 10 μm(inset). Data are presented as the mean ± SEM ( n = 8, 9 fields each mouse). * p < 0.05, ** p < 0.01 vs. control. dpi&r, days post injection & resection.

Journal: Cell Death & Disease

Article Title: CUGBP1, a crucial factor for heart regeneration in mice

doi: 10.1038/s41419-022-04570-w

Figure Lengend Snippet: A CUGBP1 was overexpressed in the 14-day old mice hearts and apical resection was performed simultaneously. Seven days after resection, cardiac tissue from apex zone was collected for paraffin section immunofluorescence detection of PH3 (red) and TNNI (green). Representative images are presented. B Statistical analysis of the number of PH3/TNNI-positive cells in apex and remote zone in the 14-day old mice heart following the Ad-virus infection and resection on seven days after resection. C Statistical analysis of the number of PH3/TNNI-positive cells by paraffin sections for immunofluorescence in the 14-day old mice heart following the Ad-virus infection and resection. Scale bars: 50 μm, 10 μm(inset). Data are presented as the mean ± SEM ( n = 8, 9 fields each mouse). * p < 0.05, ** p < 0.01 vs. control. dpi&r, days post injection & resection.

Article Snippet: Briefly, antibody to CUGBP1 (Santa Cruz Biotechnology, cat# sc-20003), and IgG (Santa Cruz Biotechnology, cat# sc-2025) was added to supernatant for immunoprecipitation (IP) and mock group, respectively.

Techniques: Paraffin Section, Immunofluorescence, Virus, Infection, Control, Injection

A , B Cardiac tissues from 14-day old mice with CUGBP1 over-expression and apical resection were collected at 7 days after the surgery and mRNA expression level of Sfrp5 and Wif1 were determined by real-time quantitative PCR. C Western blotting of ki67 in Ad-virus infected primary cardiomyocyte with IMR treatment. Bands were quantified by densitometry and normalized to GAPDH. D Statistical analysis of western blot with GATA4 expression upon CUGBP1 inactivation in 1-day old mice heart. E Statistical analysis of western blot with GATA4 abundance upon CUGBP1 over-expression and IWR-1 treatment. Data are the mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01 vs. control.

Journal: Cell Death & Disease

Article Title: CUGBP1, a crucial factor for heart regeneration in mice

doi: 10.1038/s41419-022-04570-w

Figure Lengend Snippet: A , B Cardiac tissues from 14-day old mice with CUGBP1 over-expression and apical resection were collected at 7 days after the surgery and mRNA expression level of Sfrp5 and Wif1 were determined by real-time quantitative PCR. C Western blotting of ki67 in Ad-virus infected primary cardiomyocyte with IMR treatment. Bands were quantified by densitometry and normalized to GAPDH. D Statistical analysis of western blot with GATA4 expression upon CUGBP1 inactivation in 1-day old mice heart. E Statistical analysis of western blot with GATA4 abundance upon CUGBP1 over-expression and IWR-1 treatment. Data are the mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01 vs. control.

Article Snippet: Briefly, antibody to CUGBP1 (Santa Cruz Biotechnology, cat# sc-20003), and IgG (Santa Cruz Biotechnology, cat# sc-2025) was added to supernatant for immunoprecipitation (IP) and mock group, respectively.

Techniques: Over Expression, Expressing, Real-time Polymerase Chain Reaction, Western Blot, Virus, Infection, Control

A RIP analysis was carried out using antibodies against CUGBP1 in NRVMs and RT-PCR assay was performed using primers targeting Wif1, Sfrp5, or GATA4, respectively. B Proposed mechanism of CUGBP1-Wnt/β-catenin-GATA4 regulatory axis. CUGBP1 abundance is upregulated upon apical resection. Therefore, altered levels of CUGBP1 interfere and downregulate the Sfrp5 and Wif1, which leads to activation of Wnt/β-catenin signaling. Consequently, cardiomyocyte proliferation and GATA4 levels is elevated, which could contribute to heart regeneration.

Journal: Cell Death & Disease

Article Title: CUGBP1, a crucial factor for heart regeneration in mice

doi: 10.1038/s41419-022-04570-w

Figure Lengend Snippet: A RIP analysis was carried out using antibodies against CUGBP1 in NRVMs and RT-PCR assay was performed using primers targeting Wif1, Sfrp5, or GATA4, respectively. B Proposed mechanism of CUGBP1-Wnt/β-catenin-GATA4 regulatory axis. CUGBP1 abundance is upregulated upon apical resection. Therefore, altered levels of CUGBP1 interfere and downregulate the Sfrp5 and Wif1, which leads to activation of Wnt/β-catenin signaling. Consequently, cardiomyocyte proliferation and GATA4 levels is elevated, which could contribute to heart regeneration.

Article Snippet: Briefly, antibody to CUGBP1 (Santa Cruz Biotechnology, cat# sc-20003), and IgG (Santa Cruz Biotechnology, cat# sc-2025) was added to supernatant for immunoprecipitation (IP) and mock group, respectively.

Techniques: Reverse Transcription Polymerase Chain Reaction, Activation Assay