trans blot1 turbo transfer system Search Results


pcr dot blot pcr dot blot 1 v cholerae o1 14035  (ATCC)
96
ATCC pcr dot blot pcr dot blot 1 v cholerae o1 14035
Pcr Dot Blot Pcr Dot Blot 1 V Cholerae O1 14035, supplied by ATCC, 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/pcr dot blot pcr dot blot 1 v cholerae o1 14035/product/ATCC
Average 96 stars, based on 1 article reviews
pcr dot blot pcr dot blot 1 v cholerae o1 14035 - by Bioz Stars, 2026-05
96/100 stars
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n3200s phusion new england biolabs  (New England Biolabs)
99
New England Biolabs n3200s phusion new england biolabs
N3200s Phusion New England Biolabs, supplied by New England Biolabs, 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/n3200s phusion new england biolabs/product/New England Biolabs
Average 99 stars, based on 1 article reviews
n3200s phusion new england biolabs - by Bioz Stars, 2026-05
99/100 stars
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p65  (Cell Signaling Technology Inc)
99
Cell Signaling Technology Inc p65
HDAC3 deficiency in macrophages results in impaired RIP1-dependent NF-κB signaling activity. A , B Western blot analysis of phosphorylated and total RIP1 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. C , D Western blot analysis of phosphorylated and total <t>P65</t> in control and HDAC3 deficient RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. E , F Confocal micrographs of RAW264.7 stimulated or unstimulated with TNFα (20 ng/ml) for 15 min stained with DAPI (blue, DNA) and antibodies against P65 (AF488). The nuclear P65 positive cells were calculated. Scale bar: 100/10 μm. Ctl, Control. G PCR analysis of Il1β , Mcp1 , Mip2 and Cox2 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for 1 h. Data are representative of three independent experiments and showed as mean ± SEM; * P < 0.05 and ** P < 0.01
P65, 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/p65/product/Cell Signaling Technology Inc
Average 99 stars, based on 1 article reviews
p65 - by Bioz Stars, 2026-05
99/100 stars
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β catenin mouse monoclonal  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology β catenin mouse monoclonal
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution <t>of</t> <t>β-catenin</t> and E-cadherin by western blotting. Controls for the integrity of the fractions were vimentin for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
β Catenin Mouse Monoclonal, 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
https://www.bioz.com/result/β catenin mouse monoclonal/product/Santa Cruz Biotechnology
Average 96 stars, based on 1 article reviews
β catenin mouse monoclonal - by Bioz Stars, 2026-05
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anti vimentin mouse monoclonal  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology anti vimentin mouse monoclonal
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Anti Vimentin Mouse Monoclonal, 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
https://www.bioz.com/result/anti vimentin mouse monoclonal/product/Santa Cruz Biotechnology
Average 96 stars, based on 1 article reviews
anti vimentin mouse monoclonal - by Bioz Stars, 2026-05
96/100 stars
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gapdh  (Santa Cruz Biotechnology)
97
Santa Cruz Biotechnology gapdh
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Gapdh, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gapdh/product/Santa Cruz Biotechnology
Average 97 stars, based on 1 article reviews
gapdh - by Bioz Stars, 2026-05
97/100 stars
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anti e cadherin  (Cell Signaling Technology Inc)
91
Cell Signaling Technology Inc anti e cadherin
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Anti E Cadherin, supplied by Cell Signaling Technology Inc, 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/result/anti e cadherin/product/Cell Signaling Technology Inc
Average 91 stars, based on 1 article reviews
anti e cadherin - by Bioz Stars, 2026-05
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anti ace2  (Proteintech)
96
Proteintech anti ace2
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Anti Ace2, 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/anti ace2/product/Proteintech
Average 96 stars, based on 1 article reviews
anti ace2 - by Bioz Stars, 2026-05
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af3628 histone 3  (R&D Systems)
98
R&D Systems af3628 histone 3
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Af3628 Histone 3, supplied by R&D Systems, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/af3628 histone 3/product/R&D Systems
Average 98 stars, based on 1 article reviews
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phospho aktt308  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc phospho aktt308
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Phospho Aktt308, 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
phospho aktt308 - by Bioz Stars, 2026-05
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dot blot  (Biorbyt)
91
Biorbyt dot blot
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Dot Blot, 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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Average 91 stars, based on 1 article reviews
dot blot - by Bioz Stars, 2026-05
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goat polyclonal anti pick1  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology goat polyclonal anti pick1
Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were <t>vimentin</t> for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.
Goat Polyclonal Anti Pick1, 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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Average 93 stars, based on 1 article reviews
goat polyclonal anti pick1 - by Bioz Stars, 2026-05
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Image Search Results


HDAC3 deficiency in macrophages results in impaired RIP1-dependent NF-κB signaling activity. A , B Western blot analysis of phosphorylated and total RIP1 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. C , D Western blot analysis of phosphorylated and total P65 in control and HDAC3 deficient RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. E , F Confocal micrographs of RAW264.7 stimulated or unstimulated with TNFα (20 ng/ml) for 15 min stained with DAPI (blue, DNA) and antibodies against P65 (AF488). The nuclear P65 positive cells were calculated. Scale bar: 100/10 μm. Ctl, Control. G PCR analysis of Il1β , Mcp1 , Mip2 and Cox2 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for 1 h. Data are representative of three independent experiments and showed as mean ± SEM; * P < 0.05 and ** P < 0.01

Journal: Cell & Bioscience

Article Title: Histone deacetylase 3 facilitates TNFα-mediated NF-κB activation through suppressing CTSB induced RIP1 degradation and is required for host defense against bacterial infection

doi: 10.1186/s13578-022-00814-6

Figure Lengend Snippet: HDAC3 deficiency in macrophages results in impaired RIP1-dependent NF-κB signaling activity. A , B Western blot analysis of phosphorylated and total RIP1 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. C , D Western blot analysis of phosphorylated and total P65 in control and HDAC3 deficient RAW264.7 stimulated with TNFα (20 ng/ml) for indicated time. E , F Confocal micrographs of RAW264.7 stimulated or unstimulated with TNFα (20 ng/ml) for 15 min stained with DAPI (blue, DNA) and antibodies against P65 (AF488). The nuclear P65 positive cells were calculated. Scale bar: 100/10 μm. Ctl, Control. G PCR analysis of Il1β , Mcp1 , Mip2 and Cox2 in Vector and Hdac3 −/− RAW264.7 stimulated with TNFα (20 ng/ml) for 1 h. Data are representative of three independent experiments and showed as mean ± SEM; * P < 0.05 and ** P < 0.01

Article Snippet: Antibodies against HDAC3 (#85057, 1:1000 for western blot; #3949, 1:100 for immunofluorescence staining), HDAC1 (#5356, 1:1000), HDAC2 (#5113, 1:1000), HDAC8 (#66042, 1:1000), CTSB (#31718, 1:1000 for western blot; 1:100 for immunofluorescence staining), CTSD (#69854, 1:1000), RIP1 (#3493, 1:1000), GAPDH (#2118, 1:2000), β-ACTIN (#4970, 1:2000), Phosphorylated-RIP1 (#38662, 1:1000), Phosphorylated-P65 (#3033, 1:1000), P65 (#8242, 1:1000 for western blot; 1:100 for immunofluorescence staining), H3K27ac (#8173, 1:50 for CHIPseq) were purchased from Cell Signaling Technology (CST).

Techniques: Activity Assay, Western Blot, Plasmid Preparation, Control, Staining

Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were vimentin for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.

Journal: PLoS ONE

Article Title: Differential Regulation of Cell-Cell Contact, Invasion and Anoikis by hScrib and hDlg in Keratinocytes

doi: 10.1371/journal.pone.0040279

Figure Lengend Snippet: Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were vimentin for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.

Article Snippet: The following commercial antibodies were used at the dilution indicated: anti-hScrib goat polyclonal antibody (Santa Cruz, CA, USA; Western Blot 1∶1000), anti-hDlg1 mouse monoclonal antibody (Santa Cruz, CA, USA; Western Blot 1∶1000), anti-γ-tubulin mouse monoclonal antibody (Abcam; Western Blot 1∶5000), anti-ZO-1 rabbit polyclonal antibody (Santa Cruz; CA,USA; Immuofluorescence 1∶100), anti β-catenin mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶500), anti E-Cadherin rabbit polyclonal (Santa Cruz; CA, USA; Western Blot 1∶500), anti- Vimentin mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶1000), anti-p84 mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶1000), anti-transferrin receptor mouse monoclonal (Santa Cruz, USA; Wesern Blot 1∶1000).

Techniques: Membrane, Western Blot

Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were vimentin for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.

Journal: PLoS ONE

Article Title: Differential Regulation of Cell-Cell Contact, Invasion and Anoikis by hScrib and hDlg in Keratinocytes

doi: 10.1371/journal.pone.0040279

Figure Lengend Snippet: Cells were grown to 80% confluency and then extracted into cytosolic (F1), membrane (F2), nuclear (F3) and cytoskeletal (F4) fractions. These were then analysed for the distribution of β-catenin and E-cadherin by western blotting. Controls for the integrity of the fractions were vimentin for the cytoskeletal fraction, p84 for the nuclear fraction, α-tubulin for the cytosolic fraction and transferrin receptor for the membrane fraction.

Article Snippet: The following commercial antibodies were used at the dilution indicated: anti-hScrib goat polyclonal antibody (Santa Cruz, CA, USA; Western Blot 1∶1000), anti-hDlg1 mouse monoclonal antibody (Santa Cruz, CA, USA; Western Blot 1∶1000), anti-γ-tubulin mouse monoclonal antibody (Abcam; Western Blot 1∶5000), anti-ZO-1 rabbit polyclonal antibody (Santa Cruz; CA,USA; Immuofluorescence 1∶100), anti β-catenin mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶500), anti E-Cadherin rabbit polyclonal (Santa Cruz; CA, USA; Western Blot 1∶500), anti- Vimentin mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶1000), anti-p84 mouse monoclonal (Santa Cruz; CA, USA; Western Blot 1∶1000), anti-transferrin receptor mouse monoclonal (Santa Cruz, USA; Wesern Blot 1∶1000).

Techniques: Membrane, Western Blot