normal goat serum (Vector Laboratories)
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Vector Laboratories
normal goat serum
Normal Goat Serum, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 6362 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microarray+blocking+solution/Normal+Goat+Serum+Blocking+Solution/pm36509287-257-22-37
Average 96 stars, based on 6362 article reviews
Normal Goat Serum, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 6362 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microarray+blocking+solution/Normal+Goat+Serum+Blocking+Solution/pm36509287-257-22-37
Average 96 stars, based on 6362 article reviews
normal goat serum - by Bioz Stars,
2026-10
96/100 stars
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Activity Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Plasmid Preparation:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Binding Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Incubation:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Recombinant:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( DC Protein Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Staining:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Enzyme-linked Immunosorbent Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Chloramphenicol Acetyltransferase Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Nonspecific Binding:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Blocking Assay:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Polymer:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Saline:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Immunohistochemistry:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Agarose Gel Electrophoresis:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Fractionation:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Size-exclusion Chromatography:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Ethanol Precipitation:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Purification:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Extraction:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( Chromatography:Article Title: Systematic discovery of immunomodulatory plant-derived nanoparticles reveals RNA-mediated macrophage reprogramming Article Snippet: cam) for 10 min, followed by cooling at room temperature for 2 h. Endogenous peroxidase activity was quenched using 3% hydrogen peroxide, and nonspecific binding was blocked with 5% normal goat serum ( |
![Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein <t>microarray</t> experiment to assess Gsk3-dependent polyubiquitination. Interphase egg extracts were supplemented with ubiquitin, pretreated with LiCl or NaCl (Control), and then applied on protein arrays containing ∼9,000 proteins. Polyubiquitination of arrayed proteins (PolyUb) was monitored using anti-polyubiquitin antibodies and immunofluorescence detection using an array scanner. Signal intensities were transformed and are displayed as heat-map. (B) Distribution plot of polyubiquitination changes of 3,873 in vitro polyubiquitinated proteins after Gsk3 inhibition by LiCl (Log2[Control/LiCl]). Arrays were treated with 30 mM LiCl or 30 mM NaCl (Control). LiCl reduced polyubiquitination of 864 proteins >1.8-fold. Some candidates, associated with cell cycle progression and selected for further validation are indicated in the plot. (C) Cluster of mitotic associated proteins that are significantly regulated by LiCl in B. The functional network was determined using String 9.1 and color-coded based on the fold change in the microarray (Dataset S1). (D) Western blots of indicated proteins from Xenopus eggs (naturally arrested in metaphase II) and released into interphase with the Ca2+ ionophore A23187 for 25 min, treated with LiCl, or mock treated (NaCl). β-cat, β-catenin; cycE, cyclin E; Interph., interphase; M. II, metaphase II; pH3, phosphorylated histone 3. (E) Western blots of stage VI oocytes in Prophase I and Progesterone-matured (Prog.) oocytes in metaphase II. Oocytes were injected (Inj.) with Morpholinos (MO) or mRNA as indicated. Co, control; dnWnt11, dominant negative Wnt11; pH3, phosphorylated histone 3; PPL, preprolactin (negative control).](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_6427/pmc04426427/pmc04426427__pnas.1423533112fig02.jpg)