beta lactamase 3d structure Search Results


beta tricalcium phosphate (β-tcp) disk (9.5 diameter×1.6 thickness)  (3D Biotek LLC)
90
3D Biotek LLC beta tricalcium phosphate (β-tcp) disk (9.5 diameter×1.6 thickness)
Beta Tricalcium Phosphate (β Tcp) Disk (9.5 Diameter×1.6 Thickness), supplied by 3D Biotek LLC, 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/beta+lactamase+3d+structure/us09359694-269-0-4?v=3D+Biotek+LLC
Average 90 stars, based on 1 article reviews
beta tricalcium phosphate (β-tcp) disk (9.5 diameter×1.6 thickness) - by Bioz Stars, 2026-08
90/100 stars
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mouse inflammatory cytokine cytometric bead array kit  (Becton Dickinson)
90
Becton Dickinson mouse inflammatory cytokine cytometric bead array kit
Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
Mouse Inflammatory Cytokine Cytometric Bead Array Kit, supplied by Becton Dickinson, 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/beta+lactamase+3d+structure/pmc07168451-26-8-22?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
mouse inflammatory cytokine cytometric bead array kit - by Bioz Stars, 2026-08
90/100 stars
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ec-8042  (EntreChem)
90
EntreChem ec-8042
Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
Ec 8042, supplied by EntreChem, 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/beta+lactamase+3d+structure/pmc10127337-54-0-1?v=EntreChem
Average 90 stars, based on 1 article reviews
ec-8042 - by Bioz Stars, 2026-08
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rabbit polyclonal anti β1 adrenergic receptor  (Biorbyt)
91
Biorbyt rabbit polyclonal anti β1 adrenergic receptor
Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory <t>cytokine</t> (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and <t>IL‐12p70)</t> cytometric bead array kit. Bar shows the SEM ( n = 3).
Rabbit Polyclonal Anti β1 Adrenergic Receptor, 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
https://www.bioz.com/product/beta+lactamase+3d+structure/pmc07081352-270-184-196?v=Biorbyt
Average 91 stars, based on 1 article reviews
rabbit polyclonal anti β1 adrenergic receptor - by Bioz Stars, 2026-08
91/100 stars
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ubiquitin k48  (Danaher Inc)
99
Danaher Inc ubiquitin k48
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Ubiquitin K48, supplied by Danaher 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/product/beta+lactamase+3d+structure/pmc07334420-280-9-25?v=Danaher+Inc
Average 99 stars, based on 1 article reviews
ubiquitin k48 - by Bioz Stars, 2026-08
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rabbit antimouse active cleaved caspase 3 antibody  (Novus Biologicals)
95
Novus Biologicals rabbit antimouse active cleaved caspase 3 antibody
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Rabbit Antimouse Active Cleaved Caspase 3 Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/beta+lactamase+3d+structure/10__1161_slash_atvbaha__117__310467-44-26-32?v=Novus+Biologicals
Average 95 stars, based on 1 article reviews
rabbit antimouse active cleaved caspase 3 antibody - by Bioz Stars, 2026-08
95/100 stars
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polyclonal goat antihuman galectin 10 antibody  (R&D Systems)
92
R&D Systems polyclonal goat antihuman galectin 10 antibody
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Polyclonal Goat Antihuman Galectin 10 Antibody, supplied by R&D Systems, 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/beta+lactamase+3d+structure/pmc03361262-58-17-25?v=R%26D+Systems
Average 92 stars, based on 1 article reviews
polyclonal goat antihuman galectin 10 antibody - by Bioz Stars, 2026-08
92/100 stars
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full-length human gal-3 (residues 1–250)  (Promega)
90
Promega full-length human gal-3 (residues 1–250)
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Full Length Human Gal 3 (Residues 1–250), supplied by Promega, 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/beta+lactamase+3d+structure/pmc05018044-434-3-37?v=Promega
Average 90 stars, based on 1 article reviews
full-length human gal-3 (residues 1–250) - by Bioz Stars, 2026-08
90/100 stars
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commercial elisa kits  (PBL Assay)
90
PBL Assay commercial elisa kits
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Commercial Elisa Kits, supplied by PBL Assay, 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/beta+lactamase+3d+structure/pmc07722385__rmdopen___2020___001261supp001-131-10-13?v=PBL+Assay
Average 90 stars, based on 1 article reviews
commercial elisa kits - by Bioz Stars, 2026-08
90/100 stars
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cytokines  (Merck & Co)
86
Merck & Co cytokines
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Cytokines, supplied by Merck & Co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/beta+lactamase+3d+structure/10__1016_slash_j__athplu__2025__09__002-108-2-20?v=Merck+%26+Co
Average 86 stars, based on 1 article reviews
cytokines - by Bioz Stars, 2026-08
86/100 stars
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mouse igg2  (R&D Systems)
90
R&D Systems mouse igg2
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Mouse Igg2, supplied by R&D Systems, 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/beta+lactamase+3d+structure/pmc05927541-361-70-82?v=R%26D+Systems
Average 90 stars, based on 1 article reviews
mouse igg2 - by Bioz Stars, 2026-08
90/100 stars
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azd4076  (AstraZeneca ltd)
90
AstraZeneca ltd azd4076
AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked <t>ubiquitin</t> specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.
Azd4076, supplied by AstraZeneca ltd, 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/beta+lactamase+3d+structure/us11332497-1130-15-15?v=AstraZeneca+ltd
Average 90 stars, based on 1 article reviews
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Image Search Results


Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit. Bar shows the SEM ( n = 3).

Journal: Microbiology and Immunology

Article Title: Neutralizing antibody against severe acute respiratory syndrome (SARS)‐coronavirus spike is highly effective for the protection of mice in the murine SARS model

doi: 10.1111/j.1348-0421.2008.00097.x

Figure Lengend Snippet: Concentrations of TNF‐α, IL‐6 and MCP‐1 in the lung lavage of vaccinated mice. Cytokines and chemokines in the lung lavage of vaccinated and control mice on day 3 after SARS‐CoV infection were assayed by flow cytometry using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit. Bar shows the SEM ( n = 3).

Article Snippet: Cytokines and chemokines were assayed either using a mouse inflammatory cytokine (IL‐6, IL‐10, MCP‐1, IFN‐γ, TNF‐α and IL‐12p70) cytometric bead array kit (Becton Dickinson, San Jose, CA, USA) ( ) or using the Luminex 200 system (Luminex Co., Austin, TX, USA) as previously reported ( ).

Techniques: Control, Infection, Flow Cytometry

AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked ubiquitin specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.

Journal: Molecular Therapy. Methods & Clinical Development

Article Title: Enzyme Replacement Therapy Can Reverse Pathogenic Cascade in Pompe Disease

doi: 10.1016/j.omtm.2020.05.026

Figure Lengend Snippet: AT-GAA Reversed the Levels of the Autophagic Markers and Alleviated the Burden of Accumulated Protein Aggregates and ER-Stress in Muscle from KO Mice Muscle biopsies were collected from age and sex-matched WT, untreated (KO), and AT-GAA-treated KO (KO-ERT) mice. (A) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with the indicated antibodies (n = 4 for each group; n = 5 for western blot with LC3 antibody). (B) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with K63-linked ubiquitin specific antibody (n = 4 for each group). Western blot with anti-GAPDH and Ponceau S staining were used as loading controls. (C) Western blot analysis of muscle lysates from WT, untreated KO (KO), and treated KO (KO-ERT) mice with anti-Grp 78 antibody (ER-stress marker; n = 4 for each group); GAPDH was used as loading control. Each data point represents an individual mouse. Statistical significance was determined by one-way ANOVA. Graphs represent mean ± SD. ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ∗∗∗∗p < 0.0001.

Article Snippet: SQSTM1/p62 (#ab56416; mouse monoclonal), galectin 9 (#ab69630; rabbit polyclonal), Ubiquitin K48 (Linkage Specific) (#ab140601; rabbit monoclonal), and glyceraldehyde-3-phosphate dehydrogenase (#ab9485; rabbit polyclonal) were purchased from Abcam.

Techniques: Western Blot, Ubiquitin Proteomics, Staining, Marker, Control