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Avantor h2 o2
H2 O2, supplied by Avantor, 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/result/h2 o2/product/Avantor
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
h2 o2 - by Bioz Stars, 2021-03
86/100 stars

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Related Articles

Next-Generation Sequencing:

Article Title: Increased intestinal permeability and gut dysbiosis in the R6/2 mouse model of Huntington’s disease
Article Snippet: .. Thereafter, sections were treated in 80% formic acid for 10 min and washed with dH2 O. Antigen retrieval was performed at 95 °C in 0.01 M citrate buffer pH 8.5, whereas the endogenous peroxidase was blocked with 3% H2 O2 for 15 min. After the wash steps, the sections were blocked in 5% normal goat serum (NGS), 2% (bovine serum albumin) BSA (VWR, Sweden) and 0.25% Triton-X in PBS and probed overnight at 4 °C with the primary antibody occludin (anti-rabbit, ab216327, 1:200). .. The following day sections were washed, incubated for 2 h with the secondary antibody (1:6000 Dnk anti-Rb IgG HPR Abcam, ab16284) at room temperature.

other:

Article Title: The three-dimensional distribution of minerals in potato tubers
Article Snippet: Dried and powdered samples (100 mg) were digested with 3 mL of 69 % HNO3 (Aristar grade, VWR) and 1 mL of 30 % H2 O2 (Aristar grade, VWR) in a 1600 W microwave oven (MARS Xpress) with the following program: 2 min at 100 °C, 1 min at 120 °C, 2 min at 160 °C, 20 min at 180 °C and 20 min cooling time.

Article Title: Energy reserves and respiration rate in the earthworm Eisenia andrei after exposure to zinc in nanoparticle or ionic form
Article Snippet: CHCl3 (chloroform), CH3 OH (methanol), C6 H6 O (phenol), NaOH, HCl, H2 SO4 , MgSO4 , and HNO3 (69.9–70.0%; Baker Instra-Analyzed) were purchased from Avantor Performance Materials S.A., and H2 O2 (30.0%; Baker Analyzed) was purchased from WITKO®.

Immunohistochemistry:

Article Title: Comparison of mHTT Antibodies in Huntington’s Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development
Article Snippet: Staining with all of the primary antibodies was optimised based on previous reports prior to the study to determine the optimal parameters for visualisation of mHTT staining. .. mHTT Primary antibody immunohistochemistry Endogenous peroxidise activity was inhibited by incubation in methanol containing 3% H2 O2 (VWR International, UK) for 5 min. Non-specific binding sites were blocked with 3% horse serum in TBS for 1 h, and the sections were incubated with ubiquitin (1:1000:1μl in 1ml TXTBS containing 1% horse serum), S830 (1:20000: 1μl in 20ml TXTBS containing 1% horse serum), EM48 (1:500: 0.5μl in 1ml TXTBS containing 1% horse serum), MW8 (1:1000: 1μl in 1ml TXTBS containing 1% horse serum), or 1C2 (1:4000: 0.25μl in 1ml TXTBS containing 1% horse serum) antibodies overnight (~16 hours) at room temperature (21°± 2°C). .. After several washes in TBS, the sections were incubated with a horse anti-goat secondary antibody for S830 or horse anti-mouse secondary antibody (diluted 1:200, Vector Laboratories, Burlingame, CA, USA) for MW8, EM48, ubiquitin and 1C2 for 2 h at 21° ± 2°C.

Activity Assay:

Article Title: Comparison of mHTT Antibodies in Huntington’s Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development
Article Snippet: Staining with all of the primary antibodies was optimised based on previous reports prior to the study to determine the optimal parameters for visualisation of mHTT staining. .. mHTT Primary antibody immunohistochemistry Endogenous peroxidise activity was inhibited by incubation in methanol containing 3% H2 O2 (VWR International, UK) for 5 min. Non-specific binding sites were blocked with 3% horse serum in TBS for 1 h, and the sections were incubated with ubiquitin (1:1000:1μl in 1ml TXTBS containing 1% horse serum), S830 (1:20000: 1μl in 20ml TXTBS containing 1% horse serum), EM48 (1:500: 0.5μl in 1ml TXTBS containing 1% horse serum), MW8 (1:1000: 1μl in 1ml TXTBS containing 1% horse serum), or 1C2 (1:4000: 0.25μl in 1ml TXTBS containing 1% horse serum) antibodies overnight (~16 hours) at room temperature (21°± 2°C). .. After several washes in TBS, the sections were incubated with a horse anti-goat secondary antibody for S830 or horse anti-mouse secondary antibody (diluted 1:200, Vector Laboratories, Burlingame, CA, USA) for MW8, EM48, ubiquitin and 1C2 for 2 h at 21° ± 2°C.

Incubation:

Article Title: Comparison of mHTT Antibodies in Huntington’s Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development
Article Snippet: Staining with all of the primary antibodies was optimised based on previous reports prior to the study to determine the optimal parameters for visualisation of mHTT staining. .. mHTT Primary antibody immunohistochemistry Endogenous peroxidise activity was inhibited by incubation in methanol containing 3% H2 O2 (VWR International, UK) for 5 min. Non-specific binding sites were blocked with 3% horse serum in TBS for 1 h, and the sections were incubated with ubiquitin (1:1000:1μl in 1ml TXTBS containing 1% horse serum), S830 (1:20000: 1μl in 20ml TXTBS containing 1% horse serum), EM48 (1:500: 0.5μl in 1ml TXTBS containing 1% horse serum), MW8 (1:1000: 1μl in 1ml TXTBS containing 1% horse serum), or 1C2 (1:4000: 0.25μl in 1ml TXTBS containing 1% horse serum) antibodies overnight (~16 hours) at room temperature (21°± 2°C). .. After several washes in TBS, the sections were incubated with a horse anti-goat secondary antibody for S830 or horse anti-mouse secondary antibody (diluted 1:200, Vector Laboratories, Burlingame, CA, USA) for MW8, EM48, ubiquitin and 1C2 for 2 h at 21° ± 2°C.

Binding Assay:

Article Title: Comparison of mHTT Antibodies in Huntington’s Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development
Article Snippet: Staining with all of the primary antibodies was optimised based on previous reports prior to the study to determine the optimal parameters for visualisation of mHTT staining. .. mHTT Primary antibody immunohistochemistry Endogenous peroxidise activity was inhibited by incubation in methanol containing 3% H2 O2 (VWR International, UK) for 5 min. Non-specific binding sites were blocked with 3% horse serum in TBS for 1 h, and the sections were incubated with ubiquitin (1:1000:1μl in 1ml TXTBS containing 1% horse serum), S830 (1:20000: 1μl in 20ml TXTBS containing 1% horse serum), EM48 (1:500: 0.5μl in 1ml TXTBS containing 1% horse serum), MW8 (1:1000: 1μl in 1ml TXTBS containing 1% horse serum), or 1C2 (1:4000: 0.25μl in 1ml TXTBS containing 1% horse serum) antibodies overnight (~16 hours) at room temperature (21°± 2°C). .. After several washes in TBS, the sections were incubated with a horse anti-goat secondary antibody for S830 or horse anti-mouse secondary antibody (diluted 1:200, Vector Laboratories, Burlingame, CA, USA) for MW8, EM48, ubiquitin and 1C2 for 2 h at 21° ± 2°C.

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