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lo bind eppendorf tubes  (Eppendorf AG)


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    Structured Review

    Eppendorf AG lo bind eppendorf tubes
    Lo Bind Eppendorf Tubes, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 99/100, based on 71175 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lo+bind+eppendorf+tubes/Eppendorf+Tubes/10__22175_slash_mmb__17305-65-7-8
    Average 99 stars, based on 71175 article reviews
    lo bind eppendorf tubes - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Extraction:

    Article Title: Astrocyte-neuron mitochondrial transfer via mitoEVs supports neuronal energy metabolism and is impaired in early Alzheimer’s disease
    Article Snippet: In-gel digestion was performed using a trypsin solution (25 ng/μL trypsin (MS grade, Sigma) in 10 mM AMBIC and 10% Acetonitrile), followed by 100 mM AMBIC overnight at 37°C. .. Using an extraction buffer (5% Formic Acid in 50% Acetonitrile), the supernatants containing the peptides were transferred to Lo-Bind Eppendorf tubes. .. Extractions were repeated and the pooled supernatants were concentrated in an Eppendorf Speedvac.

    Virus:

    Article Title: Sensitive, flexible, and affordable serum RNA sequencing for pathogen detection on the Oxford Nanopore platform
    Article Snippet: The produced sgRNAs were purified using the Monarch RNA cleanup kit (T2040, NEB), eluted in water or IDTE pH 7.5 buffer (11–01–02–02, IDT), and measured using the Qubit 4 broad range RNA kit ( Q10210 , Thermo Fisher Scientific) after which they were aliquoted and stored at −80 °C for further use. .. Nucleic acids were extracted from 200 μL spiked serum using Macherey Nagel’s NucleoSpin Virus Mini kit (740,983.50) following the manufacturer’s protocol but replacing carrier RNA with 8 μl of linear polyacrylamide (LPA, AM9520, Thermo Fisher Scientific), using 400 μL instead of 200 μL lysis buffer VL, and eluting with 50 μL water in Lo-Bind Eppendorf tubes. .. 44 μL of extract was transferred to tube strips (Thermo Fisher Scientific) to which a mix of 5 μL TURBO buffer and 1 μL TURBO DNase (AM2238, Thermo Fisher Scientific) was added and subsequently incubated for 30 min at 37 °C.

    Article Title: Sensitive, flexible, and affordable serum RNA sequencing for pathogen detection on the Oxford Nanopore platform.
    Article Snippet: The produced sgRNAs were purified using the Monarch RNA cleanup kit (T2040, NEB), eluted in water or IDTE pH 7.5 buffer (11–01–02–02, IDT), and measured using the Qubit 4 broad range RNA kit (Q10210, Thermo Fisher Scientific) after which they were aliquoted and stored at −80 °C for further use. .. Nucleic acids were extracted from 200 μL spiked serum using Macherey Nagel’s NucleoSpin Virus Mini kit (740,983.50) following the manufacturer’s protocol but replacing carrier RNA with 8 μl of linear polyacrylamide (LPA, AM9520, Thermo Fisher Scientific), using 400 μL instead of 200 μL lysis buffer VL, and eluting with 50 μL water in Lo-Bind Eppendorf tubes. .. 44 μL of extract was transferred to tube strips (Thermo Fisher Scientific) to which a mix of 5 μL TURBO buffer and 1 μL TURBO DNase (AM2238, Thermo Fisher Scientific) was added and subsequently incubated for 30 min at 37 °C.

    Lysis:

    Article Title: Sensitive, flexible, and affordable serum RNA sequencing for pathogen detection on the Oxford Nanopore platform
    Article Snippet: The produced sgRNAs were purified using the Monarch RNA cleanup kit (T2040, NEB), eluted in water or IDTE pH 7.5 buffer (11–01–02–02, IDT), and measured using the Qubit 4 broad range RNA kit ( Q10210 , Thermo Fisher Scientific) after which they were aliquoted and stored at −80 °C for further use. .. Nucleic acids were extracted from 200 μL spiked serum using Macherey Nagel’s NucleoSpin Virus Mini kit (740,983.50) following the manufacturer’s protocol but replacing carrier RNA with 8 μl of linear polyacrylamide (LPA, AM9520, Thermo Fisher Scientific), using 400 μL instead of 200 μL lysis buffer VL, and eluting with 50 μL water in Lo-Bind Eppendorf tubes. .. 44 μL of extract was transferred to tube strips (Thermo Fisher Scientific) to which a mix of 5 μL TURBO buffer and 1 μL TURBO DNase (AM2238, Thermo Fisher Scientific) was added and subsequently incubated for 30 min at 37 °C.

    Article Title: Sensitive, flexible, and affordable serum RNA sequencing for pathogen detection on the Oxford Nanopore platform.
    Article Snippet: The produced sgRNAs were purified using the Monarch RNA cleanup kit (T2040, NEB), eluted in water or IDTE pH 7.5 buffer (11–01–02–02, IDT), and measured using the Qubit 4 broad range RNA kit (Q10210, Thermo Fisher Scientific) after which they were aliquoted and stored at −80 °C for further use. .. Nucleic acids were extracted from 200 μL spiked serum using Macherey Nagel’s NucleoSpin Virus Mini kit (740,983.50) following the manufacturer’s protocol but replacing carrier RNA with 8 μl of linear polyacrylamide (LPA, AM9520, Thermo Fisher Scientific), using 400 μL instead of 200 μL lysis buffer VL, and eluting with 50 μL water in Lo-Bind Eppendorf tubes. .. 44 μL of extract was transferred to tube strips (Thermo Fisher Scientific) to which a mix of 5 μL TURBO buffer and 1 μL TURBO DNase (AM2238, Thermo Fisher Scientific) was added and subsequently incubated for 30 min at 37 °C.

    Infection:

    Article Title: CFTR modulators partially restore the epithelial interferome in Aspergillus infection to improve clinical outcome
    Article Snippet: .. After 3 h of infection the cells were lysed using 0.05% PBS-TWEEN and the lysates moved into 1.5 ml lo-bind Eppendorf tubes. ..

    Article Title: CFTR modulators partially restore the epithelial interferome in Aspergillus infection to improve clinical outcome.
    Article Snippet: .. After 3 h of infection the cells were lysed using 0.05% PBS-TWEEN and the lysates moved into 1.5 ml lo-bind Eppendorf tubes. ..

    Solvent:

    Article Title: The antigen-presenting molecule MR1 binds host-generated riboflavin catabolites
    Article Snippet: .. The supernatant was transferred to fresh lo-bind Eppendorf tubes and evaporated off using a centrifugal evaporator set to 38°C, reaching dryness after ∼1 h. The tubes were then reconstituted into an LC-MS–matched solvent (mobile phase A; 0.1% formic acid, 2% ACN in Optima Water). ..



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