automated hybridization station hs4800 (Tecan Systems)
90
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Tecan Systems
automated hybridization station hs4800
Automated Hybridization Station Hs4800, supplied by Tecan 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/automated+hybridization+station/hs4800+hybridization+station/pm40664182-92-7-10
Average 90 stars, based on 1 article reviews
Automated Hybridization Station Hs4800, supplied by Tecan 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/automated+hybridization+station/hs4800+hybridization+station/pm40664182-92-7-10
Average 90 stars, based on 1 article reviews
automated hybridization station hs4800 - by Bioz Stars,
2026-10
90/100 stars
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Hybridization:Article Title: Functional genomics analysis of foliar condensed tannin and phenolic glycoside regulation in natural cottonwood hybrids. Article Snippet: .. Hybridization was carried out in an automated Article Title: Inter-individual and inter-regional variability of breast milk antibody reactivity to bacterial lipopolysaccharides Article Snippet: .. All following processing steps were performed in an automated Article Title: Article Snippet: All array experiments were carried out in two colours, Cy5 and Cy3, using the cRNA linear amplification and fluorescent labelling kit from Agilent Technologies. .. All arrays were processed in an automated Article Title: Array CGH demonstrates characteristic aberration signatures in human papillary thyroid carcinomas governed by RET/PTC. Article Snippet: For each experiment, 450ng of either female or male reference DNA (Promega, Mannheim, Germany) and 450ng tumour DNA were labelled with Cy3-dCTP and Cy5-dCTP (Perkin Elmer, Shelton, USA), respectively, in an overnight incubation at 37 1C using the BioPrime-Labelling Kit (Invitrogen, Karlsruhe, Germany). .. Test and reference DNAs were co-hybridized for 40h with 135mg cot-1 DNA (Invitrogen), washed and dried in an automated Article Title: Method for preventing the unfolding of a (poly)peptide and/or inducing the (re-)folding of a (poly)peptide Article Snippet: The protein microarrays were blocked in 2% (w/v) bovine serum albumin (BSA/TBST, 0.1% [v/v] Tween 20) at room temperature for 1 h. The antibody was added to 2% (w/v) BSA/TBST and was incubated in a humidified atmosphere for 16 h. Following three TBST washes and subsequent incubation with the secondary antibody (goat-anti-human-IgG-Cy3 (Dianova, Hamburg, Germany) at 0.002 mg/ml for 1 h at room temperature in 2% (w/v) BSA/TBST, the protein microarrays were washed three times in TBST. .. All antibody incubation steps were carried out in a volume of 200 μl in an automated Article Title: Clonal success of piliated penicillin nonsusceptible pneumococci Article Snippet: .. The hybridization was carried out at 42°C for 14 h in an automated Control:Article Title: Inter-individual and inter-regional variability of breast milk antibody reactivity to bacterial lipopolysaccharides Article Snippet: .. All following processing steps were performed in an automated Incubation:Article Title: Inter-individual and inter-regional variability of breast milk antibody reactivity to bacterial lipopolysaccharides Article Snippet: .. All following processing steps were performed in an automated Article Title: Method for preventing the unfolding of a (poly)peptide and/or inducing the (re-)folding of a (poly)peptide Article Snippet: The protein microarrays were blocked in 2% (w/v) bovine serum albumin (BSA/TBST, 0.1% [v/v] Tween 20) at room temperature for 1 h. The antibody was added to 2% (w/v) BSA/TBST and was incubated in a humidified atmosphere for 16 h. Following three TBST washes and subsequent incubation with the secondary antibody (goat-anti-human-IgG-Cy3 (Dianova, Hamburg, Germany) at 0.002 mg/ml for 1 h at room temperature in 2% (w/v) BSA/TBST, the protein microarrays were washed three times in TBST. .. All antibody incubation steps were carried out in a volume of 200 μl in an automated other:Article Title: Linking molecular biomarkers with higher level condition indicators to identify effects of copper exposures on the endangered delta smelt (Hypomesus transpacificus). Article Snippet: The delta smelt (Hypomesus transpacificus) is an endangered pelagic fish species endemic to the Sacramento–San Joaquin estuary (CA, USA), and considered an indicator of ecosystem health.. Copper is a contaminant of concern in Californian waterways that may affect the development and survival of this endangered species.. The experimental combination of molecular biomarkers with higher level effects may allow for interpretation of responses in a functional context that can be used to predict detrimental outcomes caused by exposure. Article Title: Linking mechanistic and behavioral responses to sublethal esfenvalerate exposure in the endangered delta smelt; Hypomesus transpacificus (Fam. Osmeridae) Article Snippet: Each experimental sample and control was combined with a reference pool cDNA prior to hybridization using an automated Software:Article Title: Article Snippet: All array experiments were carried out in two colours, Cy5 and Cy3, using the cRNA linear amplification and fluorescent labelling kit from Agilent Technologies. .. All arrays were processed in an automated Automated:Article Title: Method for preventing the unfolding of a (poly)peptide and/or inducing the (re-)folding of a (poly)peptide Article Snippet: The protein microarrays were blocked in 2% (w/v) bovine serum albumin (BSA/TBST, 0.1% [v/v] Tween 20) at room temperature for 1 h. The antibody was added to 2% (w/v) BSA/TBST and was incubated in a humidified atmosphere for 16 h. Following three TBST washes and subsequent incubation with the secondary antibody (goat-anti-human-IgG-Cy3 (Dianova, Hamburg, Germany) at 0.002 mg/ml for 1 h at room temperature in 2% (w/v) BSA/TBST, the protein microarrays were washed three times in TBST. .. All antibody incubation steps were carried out in a volume of 200 μl in an automated |