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low stringency wash buffer  (Thermo Fisher)


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    Thermo Fisher low stringency wash buffer
    Low Stringency Wash Buffer, supplied by Thermo Fisher, 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/low+stringency+wash+buffer/pmc11109757-171-10-15
    Average 86 stars, based on 1 article reviews
    low stringency wash buffer - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Membrane:

    Article Title: Bacterial virulence factors and uses thereof
    Article Snippet: The DNA was cross-linked to the membrane by exposing the membrane to UV light for 2 min, followed by 30 min of baking at 80° C. The membrane was prehybridized by washing it in 10 ml of ULTRAhyb Ultrasensitive Hybridization Buffer (Ambion) at 42° C. for 30 min. .. Ten microliters of the prepared probe were then added to the prehybridized membrane in buffer and the probe was hybridized to the membrane overnight at 42° C. Membrane was washed 2 times 5 min in low stringency wash buffer (Ambion) and 2 times 15 min in high stringency wash buffer (Ambion) at room temperature. .. The hybridized probe was detected using BrightStar BioDetect Nonisotopic Detection Kit (Ambion), followed by exposure to Kodak film.

    Article Title: Bacterial virulence factors and uses thereof
    Article Snippet: The DNA was cross-linked to the membrane by exposing the membrane to UV light for 2 min, followed by 30 min of baking at 80° C. The membrane was prehybridized by washing it in 10 ml of ULTRAhyb Ultrasensitive Hybridization Buffer (Ambion) at 42° C. for 30 min. .. Ten microliters of the prepared probe were then added to the prehybridized membrane in buffer and the probe was hybridized to the membrane overnight at 42° C. Membrane was washed 2 times 5 min in low stringency wash buffer (Ambion) and 2 times 15 min in high stringency wash buffer (Ambion) at room temperature. .. The hybridized probe was detected using BrightStar BioDetect Nonisotopic Detection Kit (Ambion), followed by exposure to Kodak film.

    Incubation:

    Article Title: Jaagsiekte Sheep Retrovirus Encodes a Regulatory Factor, Rej, Required for Synthesis of Gag Protein
    Article Snippet: Briefly, RNA (7 g) was denatured in glyoxal-dimethyl sulfoxide loading dye (Ambion, Austin, TX) at 50°C for 30 min, subjected to agarose gel (0.9%) electrophoresis, and transferred to nylon membranes (Hybond-N Plus; GE Healthcare) using transfer buffer (Ambion) as recommended by the manufacturer. .. Membranes were incubated with rotation in hybridization buffer (GE Healthcare) at 42°C for at least 30 min followed by the addition of 32P-labeled JSRV gag- or mammalian GAPDH-specific probes (5 105 cpm/ml; carried in 4 mg salmon sperm DNA) and incubated at 58°C for 12 to 24 h. Membranes were subsequently washed two times in high-stringency wash buffer (300 mM NaCl, 30 mM sodium citrate, 0.1% SDS) at room temperature for 10 min and then washed two times in low-stringency wash buffer (15 mM NaCl, 1.5 mM sodium citrate, 0.1% SDS) at 55°C for 20 min. Membranes were exposed to phosphorimager plates, followed by phosphorimager analysis on an ABI Typhoon phosphorimager with ImageQuant version 4.2 software (Molecular Dynamics, Sunnyvale, CA). .. PCR-generated gag (nt 929 to 1110 [49]) or plasmid GAPDH DNA templates were labeled with [ -32P]dATP (PerkinElmer, Waltham, MA) by random hexamer-Klenow exonuclease using the DECA Prime II kit (Ambion), as recommended by the manufacturer.

    Hybridization:

    Article Title: Jaagsiekte Sheep Retrovirus Encodes a Regulatory Factor, Rej, Required for Synthesis of Gag Protein
    Article Snippet: Briefly, RNA (7 g) was denatured in glyoxal-dimethyl sulfoxide loading dye (Ambion, Austin, TX) at 50°C for 30 min, subjected to agarose gel (0.9%) electrophoresis, and transferred to nylon membranes (Hybond-N Plus; GE Healthcare) using transfer buffer (Ambion) as recommended by the manufacturer. .. Membranes were incubated with rotation in hybridization buffer (GE Healthcare) at 42°C for at least 30 min followed by the addition of 32P-labeled JSRV gag- or mammalian GAPDH-specific probes (5 105 cpm/ml; carried in 4 mg salmon sperm DNA) and incubated at 58°C for 12 to 24 h. Membranes were subsequently washed two times in high-stringency wash buffer (300 mM NaCl, 30 mM sodium citrate, 0.1% SDS) at room temperature for 10 min and then washed two times in low-stringency wash buffer (15 mM NaCl, 1.5 mM sodium citrate, 0.1% SDS) at 55°C for 20 min. Membranes were exposed to phosphorimager plates, followed by phosphorimager analysis on an ABI Typhoon phosphorimager with ImageQuant version 4.2 software (Molecular Dynamics, Sunnyvale, CA). .. PCR-generated gag (nt 929 to 1110 [49]) or plasmid GAPDH DNA templates were labeled with [ -32P]dATP (PerkinElmer, Waltham, MA) by random hexamer-Klenow exonuclease using the DECA Prime II kit (Ambion), as recommended by the manufacturer.

    Software:

    Article Title: Jaagsiekte Sheep Retrovirus Encodes a Regulatory Factor, Rej, Required for Synthesis of Gag Protein
    Article Snippet: Briefly, RNA (7 g) was denatured in glyoxal-dimethyl sulfoxide loading dye (Ambion, Austin, TX) at 50°C for 30 min, subjected to agarose gel (0.9%) electrophoresis, and transferred to nylon membranes (Hybond-N Plus; GE Healthcare) using transfer buffer (Ambion) as recommended by the manufacturer. .. Membranes were incubated with rotation in hybridization buffer (GE Healthcare) at 42°C for at least 30 min followed by the addition of 32P-labeled JSRV gag- or mammalian GAPDH-specific probes (5 105 cpm/ml; carried in 4 mg salmon sperm DNA) and incubated at 58°C for 12 to 24 h. Membranes were subsequently washed two times in high-stringency wash buffer (300 mM NaCl, 30 mM sodium citrate, 0.1% SDS) at room temperature for 10 min and then washed two times in low-stringency wash buffer (15 mM NaCl, 1.5 mM sodium citrate, 0.1% SDS) at 55°C for 20 min. Membranes were exposed to phosphorimager plates, followed by phosphorimager analysis on an ABI Typhoon phosphorimager with ImageQuant version 4.2 software (Molecular Dynamics, Sunnyvale, CA). .. PCR-generated gag (nt 929 to 1110 [49]) or plasmid GAPDH DNA templates were labeled with [ -32P]dATP (PerkinElmer, Waltham, MA) by random hexamer-Klenow exonuclease using the DECA Prime II kit (Ambion), as recommended by the manufacturer.

    Control:

    Article Title: IGHMBP2 deletion suppresses translation and activates the integrated stress response
    Article Snippet: Membranes were pre-hybridized with pre-warmed ULTRAhyb ultrasensitive hybridization buffer (AM8670; Invitrogen ) at 52°C for 1 h, followed by addition of 10 pmol of each probe. .. The membranes were hybridized overnight and washed two times with Low Stringency Wash Buffer (AM8673; Invitrogen ) with rotation at RT for 5 min. Membranes were probed with either tRNA-Tyr, tRNA-Val mAC , or tRNA-Val TAC , stripped, re-probed for tRNA-Gly sCC as an internal control, and imaged using a LI-COR Odyssey DLx. tRNA-Tyr and tRNA-Val probes were labeled with IRDye800 RD and the tRNA-Gly probe was labeled with IRDye680RD (LI-COR). ..

    Labeling:

    Article Title: IGHMBP2 deletion suppresses translation and activates the integrated stress response
    Article Snippet: Membranes were pre-hybridized with pre-warmed ULTRAhyb ultrasensitive hybridization buffer (AM8670; Invitrogen ) at 52°C for 1 h, followed by addition of 10 pmol of each probe. .. The membranes were hybridized overnight and washed two times with Low Stringency Wash Buffer (AM8673; Invitrogen ) with rotation at RT for 5 min. Membranes were probed with either tRNA-Tyr, tRNA-Val mAC , or tRNA-Val TAC , stripped, re-probed for tRNA-Gly sCC as an internal control, and imaged using a LI-COR Odyssey DLx. tRNA-Tyr and tRNA-Val probes were labeled with IRDye800 RD and the tRNA-Gly probe was labeled with IRDye680RD (LI-COR). ..



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    Key Resources Table

    Journal: Cell

    Article Title: Promoter of lncRNA gene PVT1 is a tumor suppressor DNA boundary element

    doi: 10.1016/j.cell.2018.03.068

    Figure Lengend Snippet: Key Resources Table

    Article Snippet: NorthernMaxTM Low Stringency Wash Buffer , Thermo Fisher , Cat#AM8673.

    Techniques: Virus, Recombinant, Ligation, Transfection, Immunoprecipitation, Bradford Assay, Reverse Transcription, Membrane, Blocking Assay, SYBR Green Assay, Sample Prep, Luciferase, Reporter Assay, Clone Assay, Northern Blot, Plasmid Preparation, Cloning, Software