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anti synapsin1  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti synapsin1
    Anti Synapsin1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 379 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+synapsin1/Synapsin-1+XP+Rabbit+mAb/pm41106508-82-48-51
    Average 96 stars, based on 379 article reviews
    anti synapsin1 - by Bioz Stars, 2026-11
    96/100 stars

    Images

    Related Articles

    Incubation:

    Article Title: Human iPSC-Derived Cortical Neurons Display Homeostatic Plasticity
    Article Snippet: Fixed cells were then permeabilized using a PBS solution containing 0.2% Triton X-100 (Merck Life Science) for 15 min and blocked with the same solution supplemented with 5% goat serum (Merck Life Science) for 20 min at room temperature. .. Cells were then incubated with primary antibodies overnight at 4 °C using the following dilutions: mouse anti-PAX6 (sc81649 Santa Cruz Biotechnology, 1:50), chicken anti-MAP2 (ab5392 Abcam, 1:2000), rabbit anti-β-TUBULIN III (TUJ1) (T2200 Merck Life Science, 1:2000), mouse anti-GFAP (MAB360 Merck Life Science, 1:500), rabbit anti-PSD95 (3450 Cell Signaling, Danvers, MA; USA, 1:250), mouse anti-VGLUT1 (135303 Synaptic Systems, Göttingen, Germany, 1:250), rabbit anti-synapsin1 (D12G5 Cell Signaling, 1:200), and mouse anti-GAD67 (sc-28376 Santa Cruz, 1:250) [ ]. .. The second day, cells were incubated with AlexaFluor secondary antibodies (1 h at room temperature; Thermo Fisher Scientific; 1:750); DAPI (Merck Life Science) was used for nuclei staining.

    Article Title: Human iPSC-Derived Cortical Neurons Display Homeostatic Plasticity.
    Article Snippet: Fixed cells were then permeabilized using a PBS solution containing 0.2% Triton X-100 (Merck Life Science) for 15 min and blocked with the same solution supplemented with 5% goat serum (Merck Life Science) for 20 min at room temperature. .. Cells were then incubated with primary antibodies overnight at 4 ◦C using the following dilutions: mouse anti-PAX6 (sc81649 Santa Cruz Biotechnology, 1:50), chicken anti-MAP2 (ab5392 Abcam, 1:2000), rabbit anti-β-TUBULIN III (TUJ1) (T2200 Merck Life Science, 1:2000), mouse anti-GFAP (MAB360 Merck Life Science, 1:500), rabbit anti-PSD95 (3450 Cell Signaling, Danvers, MA; USA, 1:250), mouse anti-VGLUT1 (135303 Synaptic Systems, Göttingen, Germany, 1:250), rabbit anti-synapsin1 (D12G5 Cell Signaling, 1:200), and mouse anti-GAD67 (sc-28376 Santa Cruz, 1:250) [33]. .. The second day, cells were incubated with AlexaFluor secondary antibodies (1 h at room temperature; Thermo Fisher Scientific; 1:750); DAPI (Merck Life Science) was used for nuclei staining.

    Article Title: Cognitive impairments in a Down syndrome model with abnormal hippocampal and prefrontal dynamics and cytoarchitecture.
    Article Snippet: They were mixed with 4X NuPAGE LDS Sample Buffer (Thermo Fisher Scientific) containing b-mercaptoethanol, denaturalized at 95 C for 5 min and resolved onto NuPAGE 4 to 12% Bis-Tris polyacrylamide gels (Thermo Fisher Scientific) using NuPAGE MOPS SDS Running Buffer (20X; Thermofisher) for mediumsize to big targeted-proteins and NuPAGE MES SDS Running Buffer (20X; Thermofisher) for small ones. .. Proteins were then transferred onto 0.2 mmnitrocellulosemembranes using Trans-Blot Turbo transfer system (Bio-Rad) at 1.3 A for 10 min. Membranes were blocked for 1 h with Intercept (PBS) Blocking Buffer and incubated overnight at 4 C with the corresponding primary antibodies (rabbit anti-Synapsin1 (Cell Signaling; 1:60000), rabbit anti-PSD95 (abcam, 1:1000), mouse anti-Drebrin (Enzo Life Sciences, 1:1000), rabbit anti-GAPDH (Sigma Aldrich, 1:200000), beta-actin (Proteintech, 1:300000) diluted in blocking buffer. .. After blocking, membranes were washed 3 times (10 min each) in PBST (0.05% Tween in PBS) and incubated for 1 h with the pertinent IRDye-secondary antibody (LI-COR Biosciences) diluted in blocking buffer.

    Western Blot:

    Article Title: N-Methyl-D-aspartate receptor antagonist d -methadone produces rapid, mTORC1-dependent antidepressant effects
    Article Snippet: .. Homogenates were submitted to western blot analysis and the bands quantified as previously described [ 7 , 10 ] (primary antibodies: rabbit anti-phospho-p70S6K, rabbit anti-p70S6K, rabbit anti-phospho-p44-42 ERK, rabbit anti-p44-42 ERK, rabbit anti-phospho-4EBP1, rabbit anti-phospho-mTOR, rabbit anti-mTOR, rabbit anti-GluA1, rabbit anti-Synapsin1, rabbit anti-PSD95, 1:1000, Cell Signaling. .. Secondary antibody: anti-rabbit, 1:5000, Vector Laboratories).

    Blocking Assay:

    Article Title: Cognitive impairments in a Down syndrome model with abnormal hippocampal and prefrontal dynamics and cytoarchitecture.
    Article Snippet: They were mixed with 4X NuPAGE LDS Sample Buffer (Thermo Fisher Scientific) containing b-mercaptoethanol, denaturalized at 95 C for 5 min and resolved onto NuPAGE 4 to 12% Bis-Tris polyacrylamide gels (Thermo Fisher Scientific) using NuPAGE MOPS SDS Running Buffer (20X; Thermofisher) for mediumsize to big targeted-proteins and NuPAGE MES SDS Running Buffer (20X; Thermofisher) for small ones. .. Proteins were then transferred onto 0.2 mmnitrocellulosemembranes using Trans-Blot Turbo transfer system (Bio-Rad) at 1.3 A for 10 min. Membranes were blocked for 1 h with Intercept (PBS) Blocking Buffer and incubated overnight at 4 C with the corresponding primary antibodies (rabbit anti-Synapsin1 (Cell Signaling; 1:60000), rabbit anti-PSD95 (abcam, 1:1000), mouse anti-Drebrin (Enzo Life Sciences, 1:1000), rabbit anti-GAPDH (Sigma Aldrich, 1:200000), beta-actin (Proteintech, 1:300000) diluted in blocking buffer. .. After blocking, membranes were washed 3 times (10 min each) in PBST (0.05% Tween in PBS) and incubated for 1 h with the pertinent IRDye-secondary antibody (LI-COR Biosciences) diluted in blocking buffer.

    Immunohistochemistry:

    Article Title: Chronic maternal exposure to low-dose PM 2.5 impacts cognitive outcomes in a sex-dependent manner.
    Article Snippet: .. After deparaffinisation and rehydration through graded ethanol solutions, antigen retrieval was performed by immersing all slides in citrate antigen retrieval solution buffer (Sangon Biotech, China) (pH=6.0) at 100 ◦C for 15 min. Immunohistochemistry was carried out using the following primary antibodies: mouse anti-Tuj1 (1:500, MMS435P, Biolegend, USA), rabbit anti-MAP2 (1:500, 4542s, CST, USA), rabbit anti-Synapsin1 (1:1000, 5297s, CST, USA), rabbit anti-PSD95 (1:500, GTX133091, GeneTex, USA), rabbit anti-Cleaved caspase3 (1:1000, 9661s, CST, USA), rat anti-MBP (1:500, GTX133091, Millipore, USA), and goat anti-Iba-1 (1:500, ab5076, Abcam, USA). ..



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    Cell Signaling Technology Inc phospho synapsin1 ser603
    FIGURE 1 Presynaptic changes in the striatum of DAT+/+ and DAT/ rats. Protein levels of (a) VGLUT1, (b) VGLUT2, the ratio of (d) <t>pSynapsinSer603/Synapsin1,</t> (e) GLT-1 and (f) xCT were measured in the whole homogenate of the striatum of DAT+/+ and DAT/ rats. The ratio (c) pαCaMKIIThr286/αCaMKII was investigated in the postsynaptic density. (g) Representative immunoblots are shown for VGLUT1, VGLUT2, pαCaMKIIThr286, αCaMKII, pSynapsinSer603, Synapsin1, GLT-1, xCT and β-actin. Results are expressed as mean percentage ± mean standard error from five independent determinations for each experimental group. Unpaired Student's t test *P < 0.05 versus DAT+/+ rats.
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    Cell Signaling Technology Inc rabbit anti synapsin1 antibody
    Evidence of synaptic dysfunction in animal model of Wilson’s disease (WD). (A) Total dendritic lengths in wild type (WT) and toxic milk (TX) mice ( n = 3). (B) Number of dendrites in TX mice compared to the number in control mice ( n = 3). (C) Images of hippocampal neurons of TX and WT mice. Scale bar, 10 μm. (D,E) Microplate reader results showing hippocampal GDH and GOGAT activities ( n = 3). (F) LC/MS quantitative results for glutamate/GABA metabolic loop-related indicators in WT and TX mice ( n = 3). (G) RT-qPCR results for mRNA expressions of Synapsin-1, Syn and Vamp2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3). (H) Levels of <t>synapsin1,</t> synaptophysin, and VAMP2 in presynaptic membranes, and of PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3), as quantified using western blots (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.
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    Cell Signaling Technology Inc synapsin1 d12g5 rb mab
    Evidence of synaptic dysfunction in animal model of Wilson’s disease (WD). (A) Total dendritic lengths in wild type (WT) and toxic milk (TX) mice ( n = 3). (B) Number of dendrites in TX mice compared to the number in control mice ( n = 3). (C) Images of hippocampal neurons of TX and WT mice. Scale bar, 10 μm. (D,E) Microplate reader results showing hippocampal GDH and GOGAT activities ( n = 3). (F) LC/MS quantitative results for glutamate/GABA metabolic loop-related indicators in WT and TX mice ( n = 3). (G) RT-qPCR results for mRNA expressions of Synapsin-1, Syn and Vamp2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3). (H) Levels of <t>synapsin1,</t> synaptophysin, and VAMP2 in presynaptic membranes, and of PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3), as quantified using western blots (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.
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    Image Search Results


    FIGURE 1 Presynaptic changes in the striatum of DAT+/+ and DAT/ rats. Protein levels of (a) VGLUT1, (b) VGLUT2, the ratio of (d) pSynapsinSer603/Synapsin1, (e) GLT-1 and (f) xCT were measured in the whole homogenate of the striatum of DAT+/+ and DAT/ rats. The ratio (c) pαCaMKIIThr286/αCaMKII was investigated in the postsynaptic density. (g) Representative immunoblots are shown for VGLUT1, VGLUT2, pαCaMKIIThr286, αCaMKII, pSynapsinSer603, Synapsin1, GLT-1, xCT and β-actin. Results are expressed as mean percentage ± mean standard error from five independent determinations for each experimental group. Unpaired Student's t test *P < 0.05 versus DAT+/+ rats.

    Journal: British journal of pharmacology

    Article Title: Memantine-induced functional rewiring of the glutamate synapse in the striatum of dopamine transporter knockout rats.

    doi: 10.1111/bph.17403

    Figure Lengend Snippet: FIGURE 1 Presynaptic changes in the striatum of DAT+/+ and DAT/ rats. Protein levels of (a) VGLUT1, (b) VGLUT2, the ratio of (d) pSynapsinSer603/Synapsin1, (e) GLT-1 and (f) xCT were measured in the whole homogenate of the striatum of DAT+/+ and DAT/ rats. The ratio (c) pαCaMKIIThr286/αCaMKII was investigated in the postsynaptic density. (g) Representative immunoblots are shown for VGLUT1, VGLUT2, pαCaMKIIThr286, αCaMKII, pSynapsinSer603, Synapsin1, GLT-1, xCT and β-actin. Results are expressed as mean percentage ± mean standard error from five independent determinations for each experimental group. Unpaired Student's t test *P < 0.05 versus DAT+/+ rats.

    Article Snippet: The conditions of the primary antibodies were the following:- anti-GLT-1 (1:2000, Abcam, Cat# Ab41621, RRID:AB_ 941782), anti-vGluT1 (1:1000, Cell Signalling Technology, Cat# 12331, RRID:AB_2797887), anti vGluT2 (1:1000, Cell Signalling Technology, Cat# 71555, RRID:AB_2799805), anti xCT [SLC7A11] (1:1000, Abcam, Cat# ab216876), anti phospho-Synapsin1 Ser603 (1:1000, Cell Signalling Technology, Cat# 88246, RRID:AB_2800119), anti Synapsin1 (1:2000, Santa Cruz Biotechnology, Cat# sc-8295, RRID:AB_677472), anti phospho-αCaMKII Thr286 (1:1000, Thermo Fisher Scientific, Cat# MA1047, RRID:AB_325402), anti αCaMKII (1:2000, Millipore, Cat# 05-532, RRID:AB_309787), anti GluN1 (1:1000, Cell Signalling Technology, Cat# 5704, RRID:AB_1904067), anti GluN2A (1:1000, Cell Signalling Technology, Cat# 4205, RRID: nloaded from https://bpspubs.onlinelibrary.w iley.com /doi/10.1111/bph.17403 by IN A SP - N E PA L , W iley O nline L ibrary on [13/12/2024].

    Techniques: Western Blot

    Evidence of synaptic dysfunction in animal model of Wilson’s disease (WD). (A) Total dendritic lengths in wild type (WT) and toxic milk (TX) mice ( n = 3). (B) Number of dendrites in TX mice compared to the number in control mice ( n = 3). (C) Images of hippocampal neurons of TX and WT mice. Scale bar, 10 μm. (D,E) Microplate reader results showing hippocampal GDH and GOGAT activities ( n = 3). (F) LC/MS quantitative results for glutamate/GABA metabolic loop-related indicators in WT and TX mice ( n = 3). (G) RT-qPCR results for mRNA expressions of Synapsin-1, Syn and Vamp2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3). (H) Levels of synapsin1, synaptophysin, and VAMP2 in presynaptic membranes, and of PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3), as quantified using western blots (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Neuroscience

    Article Title: PKR downregulation prevents copper-induced synaptic dysfunction and cognitive impairment in a murine model of Wilson’s disease

    doi: 10.3389/fnins.2024.1447304

    Figure Lengend Snippet: Evidence of synaptic dysfunction in animal model of Wilson’s disease (WD). (A) Total dendritic lengths in wild type (WT) and toxic milk (TX) mice ( n = 3). (B) Number of dendrites in TX mice compared to the number in control mice ( n = 3). (C) Images of hippocampal neurons of TX and WT mice. Scale bar, 10 μm. (D,E) Microplate reader results showing hippocampal GDH and GOGAT activities ( n = 3). (F) LC/MS quantitative results for glutamate/GABA metabolic loop-related indicators in WT and TX mice ( n = 3). (G) RT-qPCR results for mRNA expressions of Synapsin-1, Syn and Vamp2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3). (H) Levels of synapsin1, synaptophysin, and VAMP2 in presynaptic membranes, and of PSD93 and PSD95 in postsynaptic membranes of WT and TX mice ( n = 3), as quantified using western blots (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: We incubated the membranes with different antibodies, namely rabbit anti-PKR antibody (1:2000 dilution, ab184257, Abcam), rabbit anti-Phospho-PKR (Thr451) antibody (1:1000 dilution, 44-668G, Invitrogen), rabbit anti-eIF2α antibody (1:1000 dilution, 5324, Cell Signaling Technology), rabbit anti-Phospho-eIF2α (Ser51) antibody (1:1000 dilution, 3398, Cell Signaling Technology), rabbit anti-ATF-4 antibody (1:1000 dilution, 11815, Cell Signaling Technology), rabbit anti-CREB antibody (1:1000 dilution, 9197, Cell Signaling Technology), rabbit anti-Phospho-CREB (Ser133) antibody (1:1000 dilution, 9198, Cell Signaling Technology), rabbit anti-CHOP antibody (1:1000 dilution, 5554, Cell Signaling Technology), rabbit anti-Synapsin1 antibody (1:1000 dilution, 5297, Cell Signaling Technology), rabbit anti-Synaptophysin antibody (1:1000 dilution, 36406, Cell Signaling Technology), rabbit anti-PSD-93 antibody (1:1000 dilution, 19046, Cell Signaling Technology), rabbit anti-PSD-95 antibody (1:1000 dilution, 3450, Cell Signaling Technology), and rabbit anti-VAMP2 antibody (1:1000 dilution, GB11451, Service bio) at 4°C overnight.

    Techniques: Animal Model, Control, Liquid Chromatography with Mass Spectroscopy, Quantitative RT-PCR, Western Blot

    C16, a PKR inhibitor, attenuates the synaptic dysfunction of Wilson’s disease (WD) in murine model. (A) Ultrastructural organization of hippocampal organotypic slices in saline- or C16-treated toxic milk (TX) and wild type (WT) mice by transmission electron microscope. The right-side images are enlarged versions of the black boxes on the left images, and the arrow points to synaptic vesicles and the pre- and post-synaptic membranes. Scale bars on the left represent 1 μm, and those on the right represent 500 nm. (B) Schematic photomicrographs of neurons with dendrites between repeated 20 mm-spaced concentric rings in the hippocampus of untreated or C16-treated TX and WT mice quantified using Golgi-Cox staining. (C) Total dendritic length and number of dendrites in the hippocampus of untreated or C16-treated TX and WT mice quantified using Golgi-Cox staining. (D,E) Levels of synapsin1, synaptophysin, VAMP2, PSD93, and PSD95 in the hippocampus of saline- or C16-treated TX and WT mice quantified using western blotting ( n = 3) (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). (F,G) RT-qPCR results for mRNA expressions of Synapsin-1 , Syn and Vamp 2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of saline- or C16-treated TX and WT mice ( n = 3). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Neuroscience

    Article Title: PKR downregulation prevents copper-induced synaptic dysfunction and cognitive impairment in a murine model of Wilson’s disease

    doi: 10.3389/fnins.2024.1447304

    Figure Lengend Snippet: C16, a PKR inhibitor, attenuates the synaptic dysfunction of Wilson’s disease (WD) in murine model. (A) Ultrastructural organization of hippocampal organotypic slices in saline- or C16-treated toxic milk (TX) and wild type (WT) mice by transmission electron microscope. The right-side images are enlarged versions of the black boxes on the left images, and the arrow points to synaptic vesicles and the pre- and post-synaptic membranes. Scale bars on the left represent 1 μm, and those on the right represent 500 nm. (B) Schematic photomicrographs of neurons with dendrites between repeated 20 mm-spaced concentric rings in the hippocampus of untreated or C16-treated TX and WT mice quantified using Golgi-Cox staining. (C) Total dendritic length and number of dendrites in the hippocampus of untreated or C16-treated TX and WT mice quantified using Golgi-Cox staining. (D,E) Levels of synapsin1, synaptophysin, VAMP2, PSD93, and PSD95 in the hippocampus of saline- or C16-treated TX and WT mice quantified using western blotting ( n = 3) (we normalized the relative protein levels against those of the tubulin loading control and present them as relative protein levels compared to the control). (F,G) RT-qPCR results for mRNA expressions of Synapsin-1 , Syn and Vamp 2 in presynaptic membranes, and PSD93 and PSD95 in postsynaptic membranes of saline- or C16-treated TX and WT mice ( n = 3). Numeric values represent means ± SEM; * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: We incubated the membranes with different antibodies, namely rabbit anti-PKR antibody (1:2000 dilution, ab184257, Abcam), rabbit anti-Phospho-PKR (Thr451) antibody (1:1000 dilution, 44-668G, Invitrogen), rabbit anti-eIF2α antibody (1:1000 dilution, 5324, Cell Signaling Technology), rabbit anti-Phospho-eIF2α (Ser51) antibody (1:1000 dilution, 3398, Cell Signaling Technology), rabbit anti-ATF-4 antibody (1:1000 dilution, 11815, Cell Signaling Technology), rabbit anti-CREB antibody (1:1000 dilution, 9197, Cell Signaling Technology), rabbit anti-Phospho-CREB (Ser133) antibody (1:1000 dilution, 9198, Cell Signaling Technology), rabbit anti-CHOP antibody (1:1000 dilution, 5554, Cell Signaling Technology), rabbit anti-Synapsin1 antibody (1:1000 dilution, 5297, Cell Signaling Technology), rabbit anti-Synaptophysin antibody (1:1000 dilution, 36406, Cell Signaling Technology), rabbit anti-PSD-93 antibody (1:1000 dilution, 19046, Cell Signaling Technology), rabbit anti-PSD-95 antibody (1:1000 dilution, 3450, Cell Signaling Technology), and rabbit anti-VAMP2 antibody (1:1000 dilution, GB11451, Service bio) at 4°C overnight.

    Techniques: Saline, Transmission Assay, Microscopy, Staining, Western Blot, Control, Quantitative RT-PCR