strain background ( m. musculus ) , dat-cre Search Results


86
Jackson Laboratory dat cre
Dat Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory vgat ires cre stock no 028862 mice
Vgat Ires Cre Stock No 028862 Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory emx1 cre mice
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Emx1 Cre Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Charles River Laboratories female wildtype c57bl 6 mice
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Female Wildtype C57bl 6 Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory floxed tdtomato mice
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Floxed Tdtomato Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory strain background
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Strain Background, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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Jackson Laboratory strain
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Strain, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Charles River Laboratories strain background
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Strain Background, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sintetica SA bupivicaine
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Bupivicaine, supplied by Sintetica SA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Enzo Biochem clozapine-noxide (cno
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
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Vetoquinol sa ketamin
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
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Provet NZ Pty Ltd xylazin hydrochlorine
Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− <t>:Emx1-Cre</t> , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.
Xylazin Hydrochlorine, supplied by Provet NZ Pty Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− :Emx1-Cre , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.

Journal: Neuropharmacology

Article Title: Sex-specific role for serotonin 5-HT 2A receptor in modulation of opioid-induced antinociception and reward in mice

doi: 10.1016/j.neuropharm.2022.108988

Figure Lengend Snippet: Serotonin 5-HT 2A R in DRG neurons represses oxycodone-induced antinociception in male mice. ( A ) Restoration of 5-HT 2A R expression in DRG neurons of 5-HT 2A R −/− male mice. By insertion of a “stop” cassette 5’ upstream of exon 1 (grey box) flanked by loxP sites (red arrows), we interrupted the translation of the 5-HT 2A R gene. Pirt-Cre excises the stop cassette and restores expression of 5-HT 2A R to areas where their promoter activities overlap. ( B ) Representative immunohistochemical images with anti-5-HT 2A R antibody and HRP-conjugated secondary antibody in DRG tissue samples of 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice. Note that 5-HT 2A R immunoreactivity is rescued in the DRG of 5-HT 2A R −/− :Pirt-Cre male mice. ( C ) Adjunctive effect of volinanserin (0.125 mg/kg) or vehicle on the cumulative dose-response induced by oxycodone in the TFR test in male 5-HT 2A R −/− and 5-HT 2A R −/− :Pirt-Cre mice (n = 10-12 mice per group) (Oxycodone effect F[7,244] = 90.34, p < 0.001, Volinanserin/Genotype effect F[4,244] = 6.90, p < 0.01). ( D and E ) Male 5-H 2A R −/− :Emx1-Cre , 5-HT 2A R −/− :DAT-Cre and 5-HT 2A R −/− mice were given oxycodone (8 mg/kg), volinanserin (0.125 mg/kg) and oxycodone, or vehicle once a day for 5 days, after which locomotor activity was evaluated. On day 8 (3 days after the last injection), all mice received a single dose of oxycodone (8 mg/kg), and then tested for locomotor activity (n = 9-20 mice per group). Two-way ANOVA ( D – days 0-5, Time effect F[5,522] = 24.44, p < 0.001, Volinanserin/Oxycodone/Genotype effect F[5,522] = 39.77, p < 0.001) or one-way ANOVA ( D – day 8 and E , F[6,85] = 9.45, p < 0.001) followed by Bonferroni’s multiple comparison test. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., not significant. Data are mean ± S.E.M.

Article Snippet: Mice expressing a monomeric red fluorescent protein (mCherry) knocked into the last exon of μ-OR on a C57BL/6J background ( μ-OR-mCherry) (Stock No. 029013), Emx1-Cre mice (Stock No. 005628) and DAT-Cre mice (Stock No. 006660) on a C57BL/6J background were obtained from The Jackson Laboratory (Bar Harbor, ME).

Techniques: Expressing, Immunohistochemical staining, Activity Assay, Injection, Comparison