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ds2  (Tocris)


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    Structured Review

    Tocris ds2
    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM <t>DS2.</t> (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
    Ds2, supplied by Tocris, used in various techniques. Bioz Stars score: 92/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ds2/product/Tocris
    Average 92 stars, based on 47 article reviews
    ds2 - by Bioz Stars, 2026-04
    92/100 stars

    Images

    1) Product Images from "Compensatory responses to glaucoma pathology in the dorsolateral geniculate nucleus"

    Article Title: Compensatory responses to glaucoma pathology in the dorsolateral geniculate nucleus

    Journal: iScience

    doi: 10.1016/j.isci.2026.115176

    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM DS2. (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
    Figure Legend Snippet: Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM DS2. (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.

    Techniques Used: Inhibition, Activation Assay, Control, Transferring



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    ds2  (Tocris)
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    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM <t>DS2.</t> (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
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    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM <t>DS2.</t> (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
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    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM <t>DS2.</t> (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
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    (A) Schematic diagram and design rationale of monomer A. The design of monomer A was outlined (top). Substitutions unique to monomer A and <t>DS2</t> are labeled in black and gray, respectively. Substitutions shared among DS-Cav1, DS2, and monomer A are colored in red, and those shared between DS2 and monomer A are colored in blue. The dashed squares indicated the deleted residues. In the pre-F structure (PDB: 5k6i), Epitope I, II, III, IV, V, and Ø were labeled in magenta, green, purple, red, yellow, and blue, respectively and their neutralizing sensitivities are indicated. (B) Binding affinities of monomer A (top) and scDimer AA (bottom) with MAbs targeting six epitopes. Actual and fitted curves were represented by red and black lines, respectively. K D values were listed as mean ± SD of three experiments. (C) Endpoint titers of immunized antigen-binding IgG in murine sera were measured by ELISA. Groups of mice (n=4∼5) were intramuscularly immunized with 3 or 10 µg of monomer A or scDimer AA at 0, 3, and 6 weeks with Alhydrogel ® adjuvant. Serum samples were collected on day 56 (two weeks after the 3 rd immunization) and subjected for ELISA test. (D) Neutralization of RSV A2 strain in murine sera on day 56 was assessed. (E) Design of scDimer AA. Two truncated monomers A were tandemly linked, with the latter one starting at N27 residue. (F) Crystal structure of scDimer AA, with epitopes labeled as in panel A. Dotted lines represented areas with uncharacterized structures due to the flexibility of the regions. In (C) and (D), dotted lines indicated the lower limit of detection (LLD). Any value less than the LLD was assigned a value of 1⁄2 the LLD. Data were derived from two technical replicates of a single experiment, with bars indicating mean ± SD. P values were determined using Two-way ANOVA (ns indicated P > 0⋅05; * indicated P < 0⋅05; ** indicated P < 0⋅01, *** indicated P < 0⋅001, **** indicated P < 0⋅0001).
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    Image Search Results


    Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM DS2. (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.

    Journal: iScience

    Article Title: Compensatory responses to glaucoma pathology in the dorsolateral geniculate nucleus

    doi: 10.1016/j.isci.2026.115176

    Figure Lengend Snippet: Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM DS2. (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.

    Article Snippet: DS2 , Tocris , Cat # 3679.

    Techniques: Inhibition, Activation Assay, Control, Transferring

    (A) Schematic diagram and design rationale of monomer A. The design of monomer A was outlined (top). Substitutions unique to monomer A and DS2 are labeled in black and gray, respectively. Substitutions shared among DS-Cav1, DS2, and monomer A are colored in red, and those shared between DS2 and monomer A are colored in blue. The dashed squares indicated the deleted residues. In the pre-F structure (PDB: 5k6i), Epitope I, II, III, IV, V, and Ø were labeled in magenta, green, purple, red, yellow, and blue, respectively and their neutralizing sensitivities are indicated. (B) Binding affinities of monomer A (top) and scDimer AA (bottom) with MAbs targeting six epitopes. Actual and fitted curves were represented by red and black lines, respectively. K D values were listed as mean ± SD of three experiments. (C) Endpoint titers of immunized antigen-binding IgG in murine sera were measured by ELISA. Groups of mice (n=4∼5) were intramuscularly immunized with 3 or 10 µg of monomer A or scDimer AA at 0, 3, and 6 weeks with Alhydrogel ® adjuvant. Serum samples were collected on day 56 (two weeks after the 3 rd immunization) and subjected for ELISA test. (D) Neutralization of RSV A2 strain in murine sera on day 56 was assessed. (E) Design of scDimer AA. Two truncated monomers A were tandemly linked, with the latter one starting at N27 residue. (F) Crystal structure of scDimer AA, with epitopes labeled as in panel A. Dotted lines represented areas with uncharacterized structures due to the flexibility of the regions. In (C) and (D), dotted lines indicated the lower limit of detection (LLD). Any value less than the LLD was assigned a value of 1⁄2 the LLD. Data were derived from two technical replicates of a single experiment, with bars indicating mean ± SD. P values were determined using Two-way ANOVA (ns indicated P > 0⋅05; * indicated P < 0⋅05; ** indicated P < 0⋅01, *** indicated P < 0⋅001, **** indicated P < 0⋅0001).

    Journal: bioRxiv

    Article Title: Rational design of respiratory syncytial virus dimeric F-subunit vaccines in protein and mRNA forms

    doi: 10.1101/2025.05.31.655981

    Figure Lengend Snippet: (A) Schematic diagram and design rationale of monomer A. The design of monomer A was outlined (top). Substitutions unique to monomer A and DS2 are labeled in black and gray, respectively. Substitutions shared among DS-Cav1, DS2, and monomer A are colored in red, and those shared between DS2 and monomer A are colored in blue. The dashed squares indicated the deleted residues. In the pre-F structure (PDB: 5k6i), Epitope I, II, III, IV, V, and Ø were labeled in magenta, green, purple, red, yellow, and blue, respectively and their neutralizing sensitivities are indicated. (B) Binding affinities of monomer A (top) and scDimer AA (bottom) with MAbs targeting six epitopes. Actual and fitted curves were represented by red and black lines, respectively. K D values were listed as mean ± SD of three experiments. (C) Endpoint titers of immunized antigen-binding IgG in murine sera were measured by ELISA. Groups of mice (n=4∼5) were intramuscularly immunized with 3 or 10 µg of monomer A or scDimer AA at 0, 3, and 6 weeks with Alhydrogel ® adjuvant. Serum samples were collected on day 56 (two weeks after the 3 rd immunization) and subjected for ELISA test. (D) Neutralization of RSV A2 strain in murine sera on day 56 was assessed. (E) Design of scDimer AA. Two truncated monomers A were tandemly linked, with the latter one starting at N27 residue. (F) Crystal structure of scDimer AA, with epitopes labeled as in panel A. Dotted lines represented areas with uncharacterized structures due to the flexibility of the regions. In (C) and (D), dotted lines indicated the lower limit of detection (LLD). Any value less than the LLD was assigned a value of 1⁄2 the LLD. Data were derived from two technical replicates of a single experiment, with bars indicating mean ± SD. P values were determined using Two-way ANOVA (ns indicated P > 0⋅05; * indicated P < 0⋅05; ** indicated P < 0⋅01, *** indicated P < 0⋅001, **** indicated P < 0⋅0001).

    Article Snippet: DS-Cav1, a representative pre-F stabilized by introducing a disulfide bond and two cavity-filling substitutions, is adopted in the approved GSK protein-based vaccine, Arexvy., An enhanced version, DS2, with additional disulfide bonds and substitutions, was also adopted in Moderna’s licensed mRNA vaccine (mRNA-1345, mRESVIA).

    Techniques: Labeling, Binding Assay, Enzyme-linked Immunosorbent Assay, Adjuvant, Neutralization, Residue, Derivative Assay