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o bis  (Thermo Fisher)


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    Structured Review

    Thermo Fisher o bis
    O Bis, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/argon/N%2CO-Bis(trimethylsilyl)trifluoroacetamide%2C+with+1%25+TMCS%2C+packaged+under+Argon+in+resealable+ChemSeal+bottles/pm42332570-97-27-53
    Average 94 stars, based on 1 article reviews
    o bis - by Bioz Stars, 2026-11
    94/100 stars

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    Related Articles

    other:

    Article Title: Validation of ICNIRP estimates of toxicity thresholds for NIR (785 nm) light in the retinas of pigmented rabbits.
    Article Snippet: The International Commission on Non-Ionizing Radiation Protection (ICNIRP) established eye-safe exposure limits for laser light based on estimates of the 50% exposure dose (ED50) for retinal damage in animals.. The ED50 has not been determined for continuous-wave near-infrared (NIR) light, as may be used in instruments for spectroscopic analysis of the eye.. The purpose of this study is to determine the ED50 of 785-nm light delivered by a Raman spectroscopy instrument on the retinas of pigmented rabbits, and to compare that ED50 to the ICNIRP estimates.

    Article Title: The effect of the Fermi resonance on the Raman scattering cross sections of the Fermi doublet ν1 and 2ν2 of liquid carbon disulfide in benzene.
    Article Snippet: The effect of the Fermi resonance (FR) on the Raman scattering cross sections (RSCSs) of the Fermi doublet 1, 2 2 of liquid CS2 in C6H6 using the method of changing the volume concentration of the solution is investigated.. We have calculated the RSCSs of the Fermi doublet 1, 2 2 using Onsager’s theory with the 992 cm−1 Raman line of C6H6 as the internal standard.. The result shows that the RSCS of the 1 line decreases with decreasing the volume concentration of CS2, while that of the 2 2 line unexpectedly increases.

    Article Title: New Volatile Sulfur-Containing Constituents in a Simultaneous Distillation−Extraction Extract of Red Bell Peppers (Capsicum annuum)
    Article Snippet: An extract of red bell peppers (Capsicum annuum) was prepared by simultaneous distillation-extraction (SDE, Likens-Nickerson).. In addition to the already known (3E)-3-hepten-2-one (1), the unsaturated C9-ketones 1-nonen-4-one (2), (2E)-2-nonen-4-one (3), and (2E,5E)-2,5-nonadien-4-one (4), 2-methoxy-3-isobutylpyrazine (5), and heptane-2-thiol (6), we identified 19 new thiols (the aliphatic saturated and unsaturated thiols 14–16, and 22–27, the mercapto-ketones 12 and 13, the mercapto-alcohols 17, 18, and 30, the dithiols 19 and 28, the methylthio-thiols 20 and 21, and the thiophene-thiol 31) and the two new dithiolanes 10 and 29.. All of them are structurally related to the unsaturated C7and C9-ketones 1-4.

    Fluorescence:

    Article Title: Nuclear translocation of the p65 subunit of NF-kappaB in L5178Y sublines differing in antioxidant defense.
    Article Snippet: We examined the induction of nuclear translocation of the p65 subunit of NF-κB in L5178Y (LY) cells.. We used two LY sublines which are inversely cross-sensitive to hydrogen peroxide and x-rays: LY-R cells are radioresistant and oxidant-sensitive, whereas LY-S cells are radiosensitive and oxidant-resistant.. Hydrogen peroxide, phorbol ester and x-rays caused a marked translocation of p65-NF-κB in LY-R cells and a weak translocation in LY-S cells.

    Polymer:

    Article Title: Combination of main-chain and side-chain sulfonation of PFCB-6F high-temperature fuel cell membranes
    Article Snippet: .. The mixture is heated in an oil bath set at 130° C., and the polymer starts to dissolve rapidly between 80 and 95° C. While the stirred solution is being heated in the oil bath at 130° C. under argon, copper powder (15.47 g, 45-micrometer particles, Acros 196575000) is rapidly added and the mixture is stirred for 2 hours. ..



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    ( A ) Previously developed sulfonyl‐based solid support strategy for the incorporation of amino modifiers ( S ‐CPG). In some implementations, S ‐CPG can also be conjugated to the solid support through a carbamate linkage. ( B ) This work focuses on the use of CPR II CPG to incorporate amino modifiers via initial activation with N , N ′‐disuccinimidyl carbonate (DSC), generating R ‐CPG. A trifunctional ligand (protected 1,3‐diamino‐2‐propanol) enables anchoring to the solid support, followed by selective conjugation at the amine and subsequent strand elongation from the hydroxyl group.

    Journal: Current Protocols

    Article Title: A Facile Strategy for 3′‐Terminal Functionalization of DNA and RNA via On‐Column Conjugation with Integration into Tandem Oligonucleotide Synthesis

    doi: 10.1002/cpz1.70374

    Figure Lengend Snippet: ( A ) Previously developed sulfonyl‐based solid support strategy for the incorporation of amino modifiers ( S ‐CPG). In some implementations, S ‐CPG can also be conjugated to the solid support through a carbamate linkage. ( B ) This work focuses on the use of CPR II CPG to incorporate amino modifiers via initial activation with N , N ′‐disuccinimidyl carbonate (DSC), generating R ‐CPG. A trifunctional ligand (protected 1,3‐diamino‐2‐propanol) enables anchoring to the solid support, followed by selective conjugation at the amine and subsequent strand elongation from the hydroxyl group.

    Article Snippet: Argon gas 1,3‐Diamino‐2‐propanol (Fisher Scientific, cat. no. AAA1961809) 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU; Combi‐Blocks, cat. no. QA‐1443) 4‐Methoxytrityl chloride (MMTr‐Cl; Tokyo Chemical Industry, cat. no. M0790) Dichloromethane (DCM; ACS grade, Sigma‐Aldrich, cat. no. 34856) Methanol (MeOH; HPLC grade, Sigma‐Aldrich, cat. no. 34860) Silica gel (60 Å, 230‐400 mesh; Fisher Chemical, S82525) Deuterated DMSO (DMSO‐d 6 ; Sigma‐Aldrich, cat. no. 151874‐10 × 0.75ML) 2,5‐Dioxopyrrolidin‐1‐yl 2‐(prop‐2‐yn‐1‐yloxy)acetate (NHS‐ester propargyl; Combi‐Blocks, cat. no. JP‐4311) 200 mM HEPES buffer, pH 8 4 × 35‐cm (diameter × height) flash chromatography column 300‐MHz nuclear magnetic resonance (NMR) instrument (other instruments may be used)

    Techniques: Activation Assay, Conjugation Assay

    Synthesis of protected 1,3‐diamino‐2‐propanol ( A ) for on‐column coupling and subsequent conjugation using NHS‐ester chemistry, illustrated here with propargyl ( B ).

    Journal: Current Protocols

    Article Title: A Facile Strategy for 3′‐Terminal Functionalization of DNA and RNA via On‐Column Conjugation with Integration into Tandem Oligonucleotide Synthesis

    doi: 10.1002/cpz1.70374

    Figure Lengend Snippet: Synthesis of protected 1,3‐diamino‐2‐propanol ( A ) for on‐column coupling and subsequent conjugation using NHS‐ester chemistry, illustrated here with propargyl ( B ).

    Article Snippet: Argon gas 1,3‐Diamino‐2‐propanol (Fisher Scientific, cat. no. AAA1961809) 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU; Combi‐Blocks, cat. no. QA‐1443) 4‐Methoxytrityl chloride (MMTr‐Cl; Tokyo Chemical Industry, cat. no. M0790) Dichloromethane (DCM; ACS grade, Sigma‐Aldrich, cat. no. 34856) Methanol (MeOH; HPLC grade, Sigma‐Aldrich, cat. no. 34860) Silica gel (60 Å, 230‐400 mesh; Fisher Chemical, S82525) Deuterated DMSO (DMSO‐d 6 ; Sigma‐Aldrich, cat. no. 151874‐10 × 0.75ML) 2,5‐Dioxopyrrolidin‐1‐yl 2‐(prop‐2‐yn‐1‐yloxy)acetate (NHS‐ester propargyl; Combi‐Blocks, cat. no. JP‐4311) 200 mM HEPES buffer, pH 8 4 × 35‐cm (diameter × height) flash chromatography column 300‐MHz nuclear magnetic resonance (NMR) instrument (other instruments may be used)

    Techniques: Conjugation Assay