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, 2026-03
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, 2026-03
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rabbit anti brl1  (Proteintech)
96
Proteintech rabbit anti brl1
Rabbit Anti Brl1, 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
rabbit anti brl1 - by Bioz Stars, 2026-03
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trans blot1 turbotm transfer system  (Bio-Rad)
99
Bio-Rad trans blot1 turbotm transfer system
Trans Blot1 Turbotm Transfer System, supplied by Bio-Rad, 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/trans blot1 turbotm transfer system/product/Bio-Rad
Average 99 stars, based on 1 article reviews
trans blot1 turbotm transfer system - by Bioz Stars, 2026-03
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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, 2026-03
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anti-synaptophysin  (Millipore)
90
Millipore anti-synaptophysin
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
Anti Synaptophysin, 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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90/100 stars
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mouse monoclonal antibody against gapdh  (Abcam)
98
Abcam mouse monoclonal antibody against gapdh
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
Mouse Monoclonal Antibody Against Gapdh, supplied by Abcam, 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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Average 98 stars, based on 1 article reviews
mouse monoclonal antibody against gapdh - by Bioz Stars, 2026-03
98/100 stars
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goat anti-ndcbe  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology goat anti-ndcbe
(A) Western blot and (B) summary quantification <t>of</t> <t>pendrin,</t> <t>NDCBE,</t> AE4, AE1, the B1 subunit of V-ATPase, and CA15 in WT versus SPAK KO mice. Data represent the mean ± SEM. n = 4 animals per group. *P < 0.05 by 2-tailed t test for WT versus KO. (C). Each of the upregulated molecules comprise elements of the electroneutral NaCl reabsorption system. Proposed transport model (see Discussion).
Goat Anti Ndcbe, 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
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Average 90 stars, based on 1 article reviews
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antibody goat anti–ca-xv  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology antibody goat anti–ca-xv
(A) Western blot and (B) summary quantification <t>of</t> <t>pendrin,</t> <t>NDCBE,</t> AE4, AE1, the B1 subunit of V-ATPase, and CA15 in WT versus SPAK KO mice. Data represent the mean ± SEM. n = 4 animals per group. *P < 0.05 by 2-tailed t test for WT versus KO. (C). Each of the upregulated molecules comprise elements of the electroneutral NaCl reabsorption system. Proposed transport model (see Discussion).
Antibody Goat Anti–Ca Xv, 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
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Average 90 stars, based on 1 article reviews
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western blot k56 acetyl  (Millipore)
90
Millipore western blot k56 acetyl
(A) Western blot and (B) summary quantification <t>of</t> <t>pendrin,</t> <t>NDCBE,</t> AE4, AE1, the B1 subunit of V-ATPase, and CA15 in WT versus SPAK KO mice. Data represent the mean ± SEM. n = 4 animals per group. *P < 0.05 by 2-tailed t test for WT versus KO. (C). Each of the upregulated molecules comprise elements of the electroneutral NaCl reabsorption system. Proposed transport model (see Discussion).
Western Blot K56 Acetyl, 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
https://www.bioz.com/result/western blot k56 acetyl/product/Millipore
Average 90 stars, based on 1 article reviews
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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, 2026-03
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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, 2026-03
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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

(A) Western blot and (B) summary quantification of pendrin, NDCBE, AE4, AE1, the B1 subunit of V-ATPase, and CA15 in WT versus SPAK KO mice. Data represent the mean ± SEM. n = 4 animals per group. *P < 0.05 by 2-tailed t test for WT versus KO. (C). Each of the upregulated molecules comprise elements of the electroneutral NaCl reabsorption system. Proposed transport model (see Discussion).

Journal: The Journal of Clinical Investigation

Article Title: Integrated compensatory network is activated in the absence of NCC phosphorylation

doi: 10.1172/JCI78558

Figure Lengend Snippet: (A) Western blot and (B) summary quantification of pendrin, NDCBE, AE4, AE1, the B1 subunit of V-ATPase, and CA15 in WT versus SPAK KO mice. Data represent the mean ± SEM. n = 4 animals per group. *P < 0.05 by 2-tailed t test for WT versus KO. (C). Each of the upregulated molecules comprise elements of the electroneutral NaCl reabsorption system. Proposed transport model (see Discussion).

Article Snippet: The following antibodies were used for Western blot analysis and/or immunolocalization studies: mouse anti-calbindin D-28K (IHC 1:600; catalog c-9848; Sigma-Aldrich); chicken anti-AQP2 (from James Wade; IHC 1:100); rabbit anti-pendrin (from Susan Wall; Western blot 1:5,000, IHC 1:50,000); goat anti-pendrin (IHC 1:50; catalog sc-16894; Santa Cruz Biotechnology Inc.); goat anti-NDCBE (Western blot 1:100; catalog sc-169346; Santa Cruz Biotechnology Inc.); goat anti-B1-VATPase (Western blot 1:50; catalog sc-21206; Santa Cruz Biotechnology Inc.); goat anti–CA-XV (Western blot 1:100; catalog sc-54772; Santa Cruz Biotechnology Inc.); rabbit anti-AE4 (Western blot 1:100; catalog AE41-A; Alpha Diagnostic International); rabbit anti-AE1 (Western blot 1:1,000, IHC 1:50; catalog AE11-A; Alpha Diagnostic International); rabbit anti-tubulin (Western blot 1:2,000; catalog 2144s; Cell Signaling Technology); rabbit anti-HES1 (Western blot 1:1,000, IHC 1:3,000; catalog 11988s; Cell Signaling Technology); rabbit anti-OXGR1 (Western blot 1:100, IHC 1:25; catalog PA5-32960; Thermo Scientific); and goat anti-JAG1 (Western blot 1:200, IHC 1:100; catalog sc-6011; Santa Cruz Biotechnology Inc.).

Techniques: 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

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