hybridization buffer (Molecular Instruments)
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Hybridization Buffer, supplied by Molecular Instruments, 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/hybridization+buffer/buffer+hybridization+probe/us12655444-546-78-70
Average 86 stars, based on 1 article reviews
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Hybridization:Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. After rinsing in SSCT, sections were pre-hybridized in Article Title: Artificial expression constructs for selectively modulating gene expression in non-neuronal brain cells Article Snippet: For sectioning, hemispheres were embedded in 1% low-melt agarose in PBS and cut 50 μm sagittal sections on a Leica VT1000S vibratome in cold PBS buffer. .. Sections were post-fixed in 4% PFA in PBS for 2 hours and then rinsed in PBS at room temperature, then dehydrated with 70% ethanol at 4° C. Afterwards sections could be stored for up to a month in 4° C. For staining, sections were cleared with 8% SDS in PBS for 2 hours at room temperature then washed three times in 2×SSC for 1 hour each, then with Article Title: Retinoic Acid Informs the Positional Identity of Frontonasal Neural Crest Cells Through Alx Family of Transcription Factors Article Snippet: .. After pre- hybridizing in 500 μL Article Title: Engulfment by brain macrophages in a short-lived vertebrate Article Snippet: .. After the overnight incubation with probes sets diluted in Article Title: Elevated phagocytic capacity directs innate spinal cord repair. Article Snippet: .. For blocking, sections were incubated in prewarmed Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. Probes were added to the Article Title: An antagonistically pleiotropic gene regulates vertebrate growth, maturity, and lifespan. Article Snippet: Part of the fin was dissected, finely minced with scissors, and digested with 0.2% Collagenase Type P (Merck Millipore) and 0.12% Dispase II (Sigma Aldrich) in Leibovitz’s L-15 Medium (Gibco) for 30min atRT.Cellswerefilteredusing aFalcon40 μmfilter, centrifuged at 0.4 g for 10min, resuspended in L15 with 10% FBS, and injected dorsally in rag2Δ250/Δ250 and WT recipients. .. Slides were pre-hybridized in the Incubation:Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. After rinsing in SSCT, sections were pre-hybridized in Article Title: Retinoic Acid Informs the Positional Identity of Frontonasal Neural Crest Cells Through Alx Family of Transcription Factors Article Snippet: .. After pre- hybridizing in 500 μL Article Title: Engulfment by brain macrophages in a short-lived vertebrate Article Snippet: .. After the overnight incubation with probes sets diluted in Article Title: Elevated phagocytic capacity directs innate spinal cord repair. Article Snippet: .. For blocking, sections were incubated in prewarmed Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. Probes were added to the Concentration Assay:Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. After rinsing in SSCT, sections were pre-hybridized in Article Title: Evolutionary origins and transcriptomic innovations of vertebrate Cajal-Retzius cells. Article Snippet: .. Probes were added to the Staining:Article Title: Artificial expression constructs for selectively modulating gene expression in non-neuronal brain cells Article Snippet: For sectioning, hemispheres were embedded in 1% low-melt agarose in PBS and cut 50 μm sagittal sections on a Leica VT1000S vibratome in cold PBS buffer. .. Sections were post-fixed in 4% PFA in PBS for 2 hours and then rinsed in PBS at room temperature, then dehydrated with 70% ethanol at 4° C. Afterwards sections could be stored for up to a month in 4° C. For staining, sections were cleared with 8% SDS in PBS for 2 hours at room temperature then washed three times in 2×SSC for 1 hour each, then with Blocking Assay:Article Title: Elevated phagocytic capacity directs innate spinal cord repair. Article Snippet: .. For blocking, sections were incubated in prewarmed other:Article Title: Methods, culture medias and devices for generating embryos in vitro from stem cells Article Snippet: Samples were transferred to a cryomold, carefully positioned in OCT compound solution (Agar Scientific), and frozen in dry ice ethanol. |
