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hybridization solution  (Cytiva Europe)


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    Cytiva Europe hybridization solution
    Hybridization Solution, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 93/100, based on 116 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/microarray+blocking+solution/Microarray+Hybridization+Solution+v2%2E0/pmc08974173-72-32-31
    Average 93 stars, based on 116 article reviews
    hybridization solution - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Comprehensive analysis of peripheral blood non-coding RNAs identifies a diagnostic panel for fungal infection after transplantation
    Article Snippet: .. 1ul of the cDNA is mixed with 5ul 10X of blocking reagent and 1ul 25X of separation buffer at 60°C for 30 minutes, and then be diluted by 25ul 2X of GE hybridization solution. .. It was further transferred into Mouse LncRNA Array (Arraystar, USA, v2.0) and incubated in an Agilent hybridization oven at 65°C for 17 hours.

    Hybridization:

    Article Title: Comprehensive analysis of peripheral blood non-coding RNAs identifies a diagnostic panel for fungal infection after transplantation
    Article Snippet: .. 1ul of the cDNA is mixed with 5ul 10X of blocking reagent and 1ul 25X of separation buffer at 60°C for 30 minutes, and then be diluted by 25ul 2X of GE hybridization solution. .. It was further transferred into Mouse LncRNA Array (Arraystar, USA, v2.0) and incubated in an Agilent hybridization oven at 65°C for 17 hours.

    Article Title: A chemical defense deters cannibalism in migratory locusts
    Article Snippet: .. Subsequently, each slide was covered with 130 μl hybridization solution [50% formamide, 25% H2O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)] containing either the labeled antisense or sense RNA probe. ..

    Article Title: Expression and Functional Analysis of lncRNAs Involved in Platelet-Derived Growth Factor-BB-Induced Proliferation of Human Aortic Smooth Muscle Cells
    Article Snippet: Concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000; 1 μg of each labeled cRNA was fragmented by adding 5 μL of 10 × Blocking Agent and 1 μL of 25 × Fragmentation Buffer and then heated at 60°C for 30 min. .. Finally, 25 μL of 2 × GE Hybridization Buffer was added to dilute the labeled cRNA; 50 μL of hybridization solution was dispensed into the gasket slide and assembled to the lncRNA expression microarray slide. .. Slides were incubated for 17 h at 65°C in an Agilent Hybridization Oven.

    Article Title: Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription
    Article Snippet: .. From this, 4 μg of DNA was labeled with fluorescent Cy5 dye and used for the microarray hybridization (GE Amersham, USA). ..

    Article Title: Characterization of histopathology and gene-expression profiles of synovitis in early rheumatoid arthritis using targeted biopsy specimens
    Article Snippet: The PCR products were spotted in duplicate on type VII glass slides (Amersham Biosciences) with a Microarray Spotter Generation III (Amersham Biosciences). .. Labeled probes were mixed with Microarray Hybridization Solution Version 2 (Amersham Biosciences) and formamide (Sigma Chemical Co, St Louis, MO, USA) to a final concentration of 50%. ..

    Article Title: Long noncoding intronic RNAs are differentially expressed in primary and metastatic pancreatic cancer
    Article Snippet: .. For each sample, cRNA targets were ressuspended in a final volume of 200 μl of 1× Microarray Hybridization Solution v.2.0 (GE Healthcare) containing 25% formamide, denaturated at 92°C for 2 minutes and incubated with microarrays at 42°C for 16 hours using an automated slide processor (GE Healthcare). .. Following sequential washes in 1× SSC; 0.2% SDS, 0.1× SSC; 0.2% SDS and 0.1× SSC; 0.2% SDS, microarray slides were scanned immediately in a Generation III Microarray Systems Scanner (Molecular Dynamics/GE Healthcare).

    Article Title: A small number of male-biased candidate pheromone receptors are expressed in large subsets of the olfactory sensory neurons in the antennae of drones from the European honey bee Apis mellifera.
    Article Snippet: .. Each slide with tissue sections was covered with 130 μL hybridization solution 1 [50% formamide, 25% H2O, 25% Microarray hybridization solution version 2.0 (GE Healthcare, Freiburg, Germany)] supplemented with the labeled riboprobe. ..

    Article Title: The Sensilla-Specific Expression and Subcellular Localization of SNMP1 and SNMP2 Reveal Novel Insights into Their Roles in the Antenna of the Desert Locust Schistocerca gregaria
    Article Snippet: .. After sectioning, the samples were treated for 20 min at 4 °C with 4% paraformaldehyde dissolved in PBS, washed in PBS for 5 min, and then incubated in 0.2 M HCl for 10 min. After washing the samples two times for 2 min in PBS, the slides were transferred into pre-hybridization solution (5× SSC (0.75 M NaCl, 0.075 M sodium citrate, pH 7.0) and 50% formamide) for 10 min. Next, each slide was covered with 130 μL hybridization solution (50% formamide, 25% H 2 O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)) containing either the ORCO or the SNMP1 antisense riboprobe. ..

    Microarray:

    Article Title: A chemical defense deters cannibalism in migratory locusts
    Article Snippet: .. Subsequently, each slide was covered with 130 μl hybridization solution [50% formamide, 25% H2O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)] containing either the labeled antisense or sense RNA probe. ..

    Article Title: Expression and Functional Analysis of lncRNAs Involved in Platelet-Derived Growth Factor-BB-Induced Proliferation of Human Aortic Smooth Muscle Cells
    Article Snippet: Concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000; 1 μg of each labeled cRNA was fragmented by adding 5 μL of 10 × Blocking Agent and 1 μL of 25 × Fragmentation Buffer and then heated at 60°C for 30 min. .. Finally, 25 μL of 2 × GE Hybridization Buffer was added to dilute the labeled cRNA; 50 μL of hybridization solution was dispensed into the gasket slide and assembled to the lncRNA expression microarray slide. .. Slides were incubated for 17 h at 65°C in an Agilent Hybridization Oven.

    Article Title: Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription
    Article Snippet: .. From this, 4 μg of DNA was labeled with fluorescent Cy5 dye and used for the microarray hybridization (GE Amersham, USA). ..

    Article Title: Characterization of histopathology and gene-expression profiles of synovitis in early rheumatoid arthritis using targeted biopsy specimens
    Article Snippet: The PCR products were spotted in duplicate on type VII glass slides (Amersham Biosciences) with a Microarray Spotter Generation III (Amersham Biosciences). .. Labeled probes were mixed with Microarray Hybridization Solution Version 2 (Amersham Biosciences) and formamide (Sigma Chemical Co, St Louis, MO, USA) to a final concentration of 50%. ..

    Article Title: Long noncoding intronic RNAs are differentially expressed in primary and metastatic pancreatic cancer
    Article Snippet: .. For each sample, cRNA targets were ressuspended in a final volume of 200 μl of 1× Microarray Hybridization Solution v.2.0 (GE Healthcare) containing 25% formamide, denaturated at 92°C for 2 minutes and incubated with microarrays at 42°C for 16 hours using an automated slide processor (GE Healthcare). .. Following sequential washes in 1× SSC; 0.2% SDS, 0.1× SSC; 0.2% SDS and 0.1× SSC; 0.2% SDS, microarray slides were scanned immediately in a Generation III Microarray Systems Scanner (Molecular Dynamics/GE Healthcare).

    Article Title: A small number of male-biased candidate pheromone receptors are expressed in large subsets of the olfactory sensory neurons in the antennae of drones from the European honey bee Apis mellifera.
    Article Snippet: .. Each slide with tissue sections was covered with 130 μL hybridization solution 1 [50% formamide, 25% H2O, 25% Microarray hybridization solution version 2.0 (GE Healthcare, Freiburg, Germany)] supplemented with the labeled riboprobe. ..

    Article Title: The Sensilla-Specific Expression and Subcellular Localization of SNMP1 and SNMP2 Reveal Novel Insights into Their Roles in the Antenna of the Desert Locust Schistocerca gregaria
    Article Snippet: .. After sectioning, the samples were treated for 20 min at 4 °C with 4% paraformaldehyde dissolved in PBS, washed in PBS for 5 min, and then incubated in 0.2 M HCl for 10 min. After washing the samples two times for 2 min in PBS, the slides were transferred into pre-hybridization solution (5× SSC (0.75 M NaCl, 0.075 M sodium citrate, pH 7.0) and 50% formamide) for 10 min. Next, each slide was covered with 130 μL hybridization solution (50% formamide, 25% H 2 O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)) containing either the ORCO or the SNMP1 antisense riboprobe. ..

    Labeling:

    Article Title: A chemical defense deters cannibalism in migratory locusts
    Article Snippet: .. Subsequently, each slide was covered with 130 μl hybridization solution [50% formamide, 25% H2O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)] containing either the labeled antisense or sense RNA probe. ..

    Article Title: Expression and Functional Analysis of lncRNAs Involved in Platelet-Derived Growth Factor-BB-Induced Proliferation of Human Aortic Smooth Muscle Cells
    Article Snippet: Concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000; 1 μg of each labeled cRNA was fragmented by adding 5 μL of 10 × Blocking Agent and 1 μL of 25 × Fragmentation Buffer and then heated at 60°C for 30 min. .. Finally, 25 μL of 2 × GE Hybridization Buffer was added to dilute the labeled cRNA; 50 μL of hybridization solution was dispensed into the gasket slide and assembled to the lncRNA expression microarray slide. .. Slides were incubated for 17 h at 65°C in an Agilent Hybridization Oven.

    Article Title: Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription
    Article Snippet: .. From this, 4 μg of DNA was labeled with fluorescent Cy5 dye and used for the microarray hybridization (GE Amersham, USA). ..

    Article Title: Characterization of histopathology and gene-expression profiles of synovitis in early rheumatoid arthritis using targeted biopsy specimens
    Article Snippet: The PCR products were spotted in duplicate on type VII glass slides (Amersham Biosciences) with a Microarray Spotter Generation III (Amersham Biosciences). .. Labeled probes were mixed with Microarray Hybridization Solution Version 2 (Amersham Biosciences) and formamide (Sigma Chemical Co, St Louis, MO, USA) to a final concentration of 50%. ..

    Article Title: A small number of male-biased candidate pheromone receptors are expressed in large subsets of the olfactory sensory neurons in the antennae of drones from the European honey bee Apis mellifera.
    Article Snippet: .. Each slide with tissue sections was covered with 130 μL hybridization solution 1 [50% formamide, 25% H2O, 25% Microarray hybridization solution version 2.0 (GE Healthcare, Freiburg, Germany)] supplemented with the labeled riboprobe. ..

    Expressing:

    Article Title: Expression and Functional Analysis of lncRNAs Involved in Platelet-Derived Growth Factor-BB-Induced Proliferation of Human Aortic Smooth Muscle Cells
    Article Snippet: Concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000; 1 μg of each labeled cRNA was fragmented by adding 5 μL of 10 × Blocking Agent and 1 μL of 25 × Fragmentation Buffer and then heated at 60°C for 30 min. .. Finally, 25 μL of 2 × GE Hybridization Buffer was added to dilute the labeled cRNA; 50 μL of hybridization solution was dispensed into the gasket slide and assembled to the lncRNA expression microarray slide. .. Slides were incubated for 17 h at 65°C in an Agilent Hybridization Oven.

    Concentration Assay:

    Article Title: Characterization of histopathology and gene-expression profiles of synovitis in early rheumatoid arthritis using targeted biopsy specimens
    Article Snippet: The PCR products were spotted in duplicate on type VII glass slides (Amersham Biosciences) with a Microarray Spotter Generation III (Amersham Biosciences). .. Labeled probes were mixed with Microarray Hybridization Solution Version 2 (Amersham Biosciences) and formamide (Sigma Chemical Co, St Louis, MO, USA) to a final concentration of 50%. ..

    Incubation:

    Article Title: Long noncoding intronic RNAs are differentially expressed in primary and metastatic pancreatic cancer
    Article Snippet: .. For each sample, cRNA targets were ressuspended in a final volume of 200 μl of 1× Microarray Hybridization Solution v.2.0 (GE Healthcare) containing 25% formamide, denaturated at 92°C for 2 minutes and incubated with microarrays at 42°C for 16 hours using an automated slide processor (GE Healthcare). .. Following sequential washes in 1× SSC; 0.2% SDS, 0.1× SSC; 0.2% SDS and 0.1× SSC; 0.2% SDS, microarray slides were scanned immediately in a Generation III Microarray Systems Scanner (Molecular Dynamics/GE Healthcare).

    Article Title: The Sensilla-Specific Expression and Subcellular Localization of SNMP1 and SNMP2 Reveal Novel Insights into Their Roles in the Antenna of the Desert Locust Schistocerca gregaria
    Article Snippet: .. After sectioning, the samples were treated for 20 min at 4 °C with 4% paraformaldehyde dissolved in PBS, washed in PBS for 5 min, and then incubated in 0.2 M HCl for 10 min. After washing the samples two times for 2 min in PBS, the slides were transferred into pre-hybridization solution (5× SSC (0.75 M NaCl, 0.075 M sodium citrate, pH 7.0) and 50% formamide) for 10 min. Next, each slide was covered with 130 μL hybridization solution (50% formamide, 25% H 2 O, 25% Microarray Hybridization Solution Version 2.0 (GE Healthcare, Freiburg, Germany)) containing either the ORCO or the SNMP1 antisense riboprobe. ..



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    Image Search Results


    Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein microarray 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).

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Maternal Wnt/STOP signaling promotes cell division during early Xenopus embryogenesis

    doi: 10.1073/pnas.1423533112

    Figure Lengend Snippet: Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein microarray 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).

    Article Snippet: Briefly, the arrays were washed in TBST and blocked for 4 h at 4 °C using Microarray Blocking solution (Arrayit), followed by a wash in lysis buffer.

    Techniques: Microarray, Ubiquitin Proteomics, Control, Immunofluorescence, Transformation Assay, In Vitro, Inhibition, Biomarker Discovery, Functional Assay, Western Blot, Injection, Dominant Negative Mutation, Negative Control