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anti mtr polyclonal antibody  (Proteintech)


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    Proteintech anti mtr polyclonal antibody
    Anti Mtr Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+mtr+polyclonal+antibody/MTR+Antibody/pmc13006396-2-0-4
    Average 93 stars, based on 17 article reviews
    anti mtr polyclonal antibody - by Bioz Stars, 2026-10
    93/100 stars

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    Article Title: SIRT1 mediates brain metabolic and developmental consequences of methionine synthase deficiency in inborn errors of cobalamin metabolism
    Article Snippet: Anti-Mtr Polyclonal Antibody , Protein Tech , Cat25896-1-AP; RRID: AB_2880287.



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    Assessment of placental transfer of Oxt and its impact on <t>Oxtr</t> in the developing brain (A) Schematic for placental Oxt transfer experiments. (B‒D) Dot plots with bar graphs showing Oxt concentration in the maternal plasma, fetal plasma, and the fetal brain, respectively, showing a nearly 2-fold elevation of Oxt in the fetal plasma and brain after Oxt infusion. (E) Schematic for stable isotope labeled Oxt (SIL-Oxt) experiments. (F) Retention time and precursor ion, 1014.46 m/z , of SIL-Oxt and the PRM (parallel reaction monitoring) transitions. The topmost intense fragment ion, 730.28 m/z , was selected. (G) Bar graph showing the presence of maternally administered SIL-Oxt in the newborn circulation confirming transplacental transfer of Oxt. (H) Schematic of the experimental timeline for impact of Oxt on Oxtr in the developing brain. (I) Dot plots with bar graphs showing a significant decrease in Oxtr gene expression in the fetal cortex. (J) Immunoblots showing a decrease in the expression of OXTR protein in the fetal brain after maternal Oxt infusion. Lanes were run on the same gel but were non-contiguous. (K) Dot plots with bar graphs showing densitometric quantification of the decrease in OXTR expression. (L) Dot plots with bar graphs showing a dose-dependent decrease in Oxtr gene expression in the fetal cortex suggesting that the consequences for the fetus could be dependent on maternal Oxt dose. (M) Details of the DNA methylation assay for the Oxtr. (N) Oxt exposure was associated with a significant decrease in the % methylation of selected CpG sites in the Oxtr promoter region. (O) Dot plots with bar graphs showing a decrease in Oxtr gene expression in the cortex of 1-day old vaginally born pups. Each data point represents a dam and/or its litter (n = 5–8 per condition except SIL-Oxt experiments). Data were analyzed with Welch’s t-test or one-way ANOVA and expressed as mean ± SEM; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.
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    OriGene rabbit anti oxtr antibody
    Validation of the model for labor induction with oxytocin. ( A ) Visualization of uterine contraction. Upper panel: uterine myometrium harvested from pregnant E21 rats at least 8 h after either saline (control) or intravenous Oxt infusion and stained with hematoxylin. 20 × photomicrographs showing lack of clustering of uterine myocytes in saline-treated myometrium (left) compared to extensive clustering in the Oxt-exposed myometrium (right). Lower panel: 5-μm frozen sections from Oxt-exposed myometrium stained without (left) or with rabbit anti-mouse phosphomyosin light chain kinase showing prominent staining among clustered uterine myocytes revealed with anti-rabbit HRP conjugate (marked by arrows) (right). Nuclei counterstained with hematoxylin. Scale bar = 100 μM. ( B ) Labor induction with Oxt causes cyclical increases in intrauterine pressure. Labor was induced with Oxt at 48 h after pump implantation (around 12 noon, light cycle, E20) and intrauterine pressure changes were monitored with telemetry. Oxt initiation was associated with acute and cyclical increases in intrauterine pressure until birth (first pup delivered around 21:00 h, dark cycle, E20). Light and dark cycle from 07:00–19:00 and 19:00–07:00, respectively. ( C ) Labor induction with Oxt was associated with a significant increase in <t>OxtR</t> gene expression at 8–12 h. ( D ) Labor induction with Oxt decreases OxtR immunoreactivity in the rat uterus. Sample 20 × photomicrographs from 5-µm sections of the uterine myometrium stained with goat anti-rat OxtR antibody (1:100) and revealed with Alexa Fluor® 594 labeled rabbit anti-goat antibody (1:300). Note naïve uterine myometrium with bright staining for OxtR in the upper panel, in sharp contrast to Oxt-exposed myometrial tissue in the lower panel where staining was scant, suggesting downregulation of OxtR. Scale bar = 50 μM. ( E ) Representative cropped western blot images showing a decrease <t>in</t> <t>membrane</t> associated OxtR protein expression after labor induction with Oxt and quantified with densitometry. Full length blot is presented in Supplementary Figure . Please note that the Oxt and Con lanes have been cropped and reversed to present the data in a manner consistent with the rest of the manuscript (i.e., Con followed by Oxt data). Data analyzed with Welch’s t-test and presented as mean ± SEM; * p ≤ 0.05, ** p ≤ 0.01.
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    Image Search Results


    Assessment of placental transfer of Oxt and its impact on Oxtr in the developing brain (A) Schematic for placental Oxt transfer experiments. (B‒D) Dot plots with bar graphs showing Oxt concentration in the maternal plasma, fetal plasma, and the fetal brain, respectively, showing a nearly 2-fold elevation of Oxt in the fetal plasma and brain after Oxt infusion. (E) Schematic for stable isotope labeled Oxt (SIL-Oxt) experiments. (F) Retention time and precursor ion, 1014.46 m/z , of SIL-Oxt and the PRM (parallel reaction monitoring) transitions. The topmost intense fragment ion, 730.28 m/z , was selected. (G) Bar graph showing the presence of maternally administered SIL-Oxt in the newborn circulation confirming transplacental transfer of Oxt. (H) Schematic of the experimental timeline for impact of Oxt on Oxtr in the developing brain. (I) Dot plots with bar graphs showing a significant decrease in Oxtr gene expression in the fetal cortex. (J) Immunoblots showing a decrease in the expression of OXTR protein in the fetal brain after maternal Oxt infusion. Lanes were run on the same gel but were non-contiguous. (K) Dot plots with bar graphs showing densitometric quantification of the decrease in OXTR expression. (L) Dot plots with bar graphs showing a dose-dependent decrease in Oxtr gene expression in the fetal cortex suggesting that the consequences for the fetus could be dependent on maternal Oxt dose. (M) Details of the DNA methylation assay for the Oxtr. (N) Oxt exposure was associated with a significant decrease in the % methylation of selected CpG sites in the Oxtr promoter region. (O) Dot plots with bar graphs showing a decrease in Oxtr gene expression in the cortex of 1-day old vaginally born pups. Each data point represents a dam and/or its litter (n = 5–8 per condition except SIL-Oxt experiments). Data were analyzed with Welch’s t-test or one-way ANOVA and expressed as mean ± SEM; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Journal: iScience

    Article Title: Oxytocin-induced birth causes sex-specific behavioral and brain connectivity changes in developing rat offspring

    doi: 10.1016/j.isci.2024.108960

    Figure Lengend Snippet: Assessment of placental transfer of Oxt and its impact on Oxtr in the developing brain (A) Schematic for placental Oxt transfer experiments. (B‒D) Dot plots with bar graphs showing Oxt concentration in the maternal plasma, fetal plasma, and the fetal brain, respectively, showing a nearly 2-fold elevation of Oxt in the fetal plasma and brain after Oxt infusion. (E) Schematic for stable isotope labeled Oxt (SIL-Oxt) experiments. (F) Retention time and precursor ion, 1014.46 m/z , of SIL-Oxt and the PRM (parallel reaction monitoring) transitions. The topmost intense fragment ion, 730.28 m/z , was selected. (G) Bar graph showing the presence of maternally administered SIL-Oxt in the newborn circulation confirming transplacental transfer of Oxt. (H) Schematic of the experimental timeline for impact of Oxt on Oxtr in the developing brain. (I) Dot plots with bar graphs showing a significant decrease in Oxtr gene expression in the fetal cortex. (J) Immunoblots showing a decrease in the expression of OXTR protein in the fetal brain after maternal Oxt infusion. Lanes were run on the same gel but were non-contiguous. (K) Dot plots with bar graphs showing densitometric quantification of the decrease in OXTR expression. (L) Dot plots with bar graphs showing a dose-dependent decrease in Oxtr gene expression in the fetal cortex suggesting that the consequences for the fetus could be dependent on maternal Oxt dose. (M) Details of the DNA methylation assay for the Oxtr. (N) Oxt exposure was associated with a significant decrease in the % methylation of selected CpG sites in the Oxtr promoter region. (O) Dot plots with bar graphs showing a decrease in Oxtr gene expression in the cortex of 1-day old vaginally born pups. Each data point represents a dam and/or its litter (n = 5–8 per condition except SIL-Oxt experiments). Data were analyzed with Welch’s t-test or one-way ANOVA and expressed as mean ± SEM; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Article Snippet: Rabbit polyclonal anti-OxtR antibody , www.origene.com , TA351476.

    Techniques: Concentration Assay, Clinical Proteomics, Labeling, Targeted Proteomics, Gene Expression, Western Blot, Expressing, DNA Methylation Assay, Methylation

    Neurobehavioral and transcriptomic changes in the offspring after induced birth with Oxt (A) Schematic of the timeline of behavioral experiments from P8-P49. (B) Reduced number of ultrasonic vocalizations (USV) and phrases in Oxt-exposed P8 offspring. (C) Frequency of interaction during social play was not different after Oxt exposure. (D) Social investigation, shown as social preference index, was largely preserved in both female and male offspring after Oxt-induced birth. (E) Despite comparable freezing response at baseline, Oxt-exposed male pups displayed a significantly diminished freezing response during observational fear testing. Oxtr gene expression in the mPFC (F) and the BLA (G) was unaltered after Oxt exposure in both female and male P40 offspring. (H) Plasma Oxt was no different in the P40 offspring whose birth was induced. (I) Heatmap showing differentially expressed genes in male and female Oxt-exposed offspring, with sex of the offspring being the most important source of variation. Top 25 FDR-significant genes for gene ontology (GO) biological processes (J) suggesting upregulation of immune/inflammatory pathways. (K) Significantly differentially expressed gene pathways identified with KEGG (Kyoto Encyclopedia of Genes and Genomes) analyses. Behavioral and assay data are expressed as mean ± SEM (n = 4–8 per treatment condition per sex, except <xref ref-type=Figure 3 B where n = 16 per treatment condition with sexes combined); ∗p < 0.05, and ∗∗∗p < 0.001. RNA-seq data were analyzed with Limma generalized linear models and GAGE as described (n = 6 per sex per treatment condition). " width="100%" height="100%">

    Journal: iScience

    Article Title: Oxytocin-induced birth causes sex-specific behavioral and brain connectivity changes in developing rat offspring

    doi: 10.1016/j.isci.2024.108960

    Figure Lengend Snippet: Neurobehavioral and transcriptomic changes in the offspring after induced birth with Oxt (A) Schematic of the timeline of behavioral experiments from P8-P49. (B) Reduced number of ultrasonic vocalizations (USV) and phrases in Oxt-exposed P8 offspring. (C) Frequency of interaction during social play was not different after Oxt exposure. (D) Social investigation, shown as social preference index, was largely preserved in both female and male offspring after Oxt-induced birth. (E) Despite comparable freezing response at baseline, Oxt-exposed male pups displayed a significantly diminished freezing response during observational fear testing. Oxtr gene expression in the mPFC (F) and the BLA (G) was unaltered after Oxt exposure in both female and male P40 offspring. (H) Plasma Oxt was no different in the P40 offspring whose birth was induced. (I) Heatmap showing differentially expressed genes in male and female Oxt-exposed offspring, with sex of the offspring being the most important source of variation. Top 25 FDR-significant genes for gene ontology (GO) biological processes (J) suggesting upregulation of immune/inflammatory pathways. (K) Significantly differentially expressed gene pathways identified with KEGG (Kyoto Encyclopedia of Genes and Genomes) analyses. Behavioral and assay data are expressed as mean ± SEM (n = 4–8 per treatment condition per sex, except Figure 3 B where n = 16 per treatment condition with sexes combined); ∗p < 0.05, and ∗∗∗p < 0.001. RNA-seq data were analyzed with Limma generalized linear models and GAGE as described (n = 6 per sex per treatment condition).

    Article Snippet: Rabbit polyclonal anti-OxtR antibody , www.origene.com , TA351476.

    Techniques: Gene Expression, Clinical Proteomics, RNA Sequencing

    Journal: iScience

    Article Title: Oxytocin-induced birth causes sex-specific behavioral and brain connectivity changes in developing rat offspring

    doi: 10.1016/j.isci.2024.108960

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-OxtR antibody , www.origene.com , TA351476.

    Techniques: Recombinant, Protease Inhibitor, Labeling, Enzyme-linked Immunosorbent Assay, Fractionation, Methylation, DNA Extraction, Sequencing, RNA Sequencing, Gene Expression, Real-time Polymerase Chain Reaction, Software, Imaging

    Journal: iScience

    Article Title: Oxytocin-induced birth causes sex-specific behavioral and brain connectivity changes in developing rat offspring

    doi: 10.1016/j.isci.2024.108960

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-OxtR antibody , www.origene.com , TA351476.

    Techniques: Recombinant, Protease Inhibitor, Labeling, Enzyme-linked Immunosorbent Assay, Fractionation, Methylation, DNA Extraction, Sequencing, RNA Sequencing Assay, Expressing, Real-time Polymerase Chain Reaction, Software, Imaging

    Validation of the model for labor induction with oxytocin. ( A ) Visualization of uterine contraction. Upper panel: uterine myometrium harvested from pregnant E21 rats at least 8 h after either saline (control) or intravenous Oxt infusion and stained with hematoxylin. 20 × photomicrographs showing lack of clustering of uterine myocytes in saline-treated myometrium (left) compared to extensive clustering in the Oxt-exposed myometrium (right). Lower panel: 5-μm frozen sections from Oxt-exposed myometrium stained without (left) or with rabbit anti-mouse phosphomyosin light chain kinase showing prominent staining among clustered uterine myocytes revealed with anti-rabbit HRP conjugate (marked by arrows) (right). Nuclei counterstained with hematoxylin. Scale bar = 100 μM. ( B ) Labor induction with Oxt causes cyclical increases in intrauterine pressure. Labor was induced with Oxt at 48 h after pump implantation (around 12 noon, light cycle, E20) and intrauterine pressure changes were monitored with telemetry. Oxt initiation was associated with acute and cyclical increases in intrauterine pressure until birth (first pup delivered around 21:00 h, dark cycle, E20). Light and dark cycle from 07:00–19:00 and 19:00–07:00, respectively. ( C ) Labor induction with Oxt was associated with a significant increase in OxtR gene expression at 8–12 h. ( D ) Labor induction with Oxt decreases OxtR immunoreactivity in the rat uterus. Sample 20 × photomicrographs from 5-µm sections of the uterine myometrium stained with goat anti-rat OxtR antibody (1:100) and revealed with Alexa Fluor® 594 labeled rabbit anti-goat antibody (1:300). Note naïve uterine myometrium with bright staining for OxtR in the upper panel, in sharp contrast to Oxt-exposed myometrial tissue in the lower panel where staining was scant, suggesting downregulation of OxtR. Scale bar = 50 μM. ( E ) Representative cropped western blot images showing a decrease in membrane associated OxtR protein expression after labor induction with Oxt and quantified with densitometry. Full length blot is presented in Supplementary Figure . Please note that the Oxt and Con lanes have been cropped and reversed to present the data in a manner consistent with the rest of the manuscript (i.e., Con followed by Oxt data). Data analyzed with Welch’s t-test and presented as mean ± SEM; * p ≤ 0.05, ** p ≤ 0.01.

    Journal: Scientific Reports

    Article Title: Labor induction with oxytocin in pregnant rats is not associated with oxidative stress in the fetal brain

    doi: 10.1038/s41598-022-07236-x

    Figure Lengend Snippet: Validation of the model for labor induction with oxytocin. ( A ) Visualization of uterine contraction. Upper panel: uterine myometrium harvested from pregnant E21 rats at least 8 h after either saline (control) or intravenous Oxt infusion and stained with hematoxylin. 20 × photomicrographs showing lack of clustering of uterine myocytes in saline-treated myometrium (left) compared to extensive clustering in the Oxt-exposed myometrium (right). Lower panel: 5-μm frozen sections from Oxt-exposed myometrium stained without (left) or with rabbit anti-mouse phosphomyosin light chain kinase showing prominent staining among clustered uterine myocytes revealed with anti-rabbit HRP conjugate (marked by arrows) (right). Nuclei counterstained with hematoxylin. Scale bar = 100 μM. ( B ) Labor induction with Oxt causes cyclical increases in intrauterine pressure. Labor was induced with Oxt at 48 h after pump implantation (around 12 noon, light cycle, E20) and intrauterine pressure changes were monitored with telemetry. Oxt initiation was associated with acute and cyclical increases in intrauterine pressure until birth (first pup delivered around 21:00 h, dark cycle, E20). Light and dark cycle from 07:00–19:00 and 19:00–07:00, respectively. ( C ) Labor induction with Oxt was associated with a significant increase in OxtR gene expression at 8–12 h. ( D ) Labor induction with Oxt decreases OxtR immunoreactivity in the rat uterus. Sample 20 × photomicrographs from 5-µm sections of the uterine myometrium stained with goat anti-rat OxtR antibody (1:100) and revealed with Alexa Fluor® 594 labeled rabbit anti-goat antibody (1:300). Note naïve uterine myometrium with bright staining for OxtR in the upper panel, in sharp contrast to Oxt-exposed myometrial tissue in the lower panel where staining was scant, suggesting downregulation of OxtR. Scale bar = 50 μM. ( E ) Representative cropped western blot images showing a decrease in membrane associated OxtR protein expression after labor induction with Oxt and quantified with densitometry. Full length blot is presented in Supplementary Figure . Please note that the Oxt and Con lanes have been cropped and reversed to present the data in a manner consistent with the rest of the manuscript (i.e., Con followed by Oxt data). Data analyzed with Welch’s t-test and presented as mean ± SEM; * p ≤ 0.05, ** p ≤ 0.01.

    Article Snippet: Following a brief wash with TBST buffer, the membrane was immunoblotted overnight at 4 °C on a shaker with primary rabbit anti-OxtR antibody (catalog # TA351476, OriGene Technologies), at a dilution of 1:250 in 5% milk-TBST buffer.

    Techniques: Biomarker Discovery, Saline, Control, Staining, Gene Expression, Labeling, Western Blot, Membrane, Expressing