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anti syp  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti syp
    Anti Syp, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 136 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+syp/PSD95+Mouse+mAb/pmc12805289-48-12-16
    Average 96 stars, based on 136 article reviews
    anti syp - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Membrane:

    Article Title: High cereblon expression in neuroendocrine cancer confers vulnerability to GSPT1 molecular glue degrader
    Article Snippet: .. The membrane was blocked with 5% skim milk and incubated overnight at 4 °C with primary antibodies, including anti-ASCL1 (#10585), anti-CRBN (#71810), anti-CUL4A (#2699), anti-DDB1 (#5428), anti-ENO2 (#9536), anti-NeuroD1 (#7019), anti-POU2F3 (#92579), and anti-SYP (#5461) from Cell Signaling Technology (Danvers, MA, USA); anti-eRF3/GSPT1 (ab234433) from Abcam (Cambridge, MA, USA); and anti-β-actin (#A2228), anti-GAPDH (CB1001), and anti-puromycin (MABE343) from Sigma-Aldrich (St. Louis, MO, USA). ..

    Article Title: High cereblon expression in neuroendocrine cancer confers vulnerability to GSPT1 molecular glue degrader.
    Article Snippet: .. The membrane was blocked with 5% skim milk and incubated overnight at 4 °C with primary antibodies, including anti-ASCL1 (#10585), anti-CRBN (#71810), anti-CUL4A (#2699), anti-DDB1 (#5428), antiENO2 (#9536), anti-NeuroD1 (#7019), anti-POU2F3 (#92579), and anti-SYP (#5461) from Cell Signaling Technology (Danvers, MA, USA); anti-eRF3/GSPT1 (ab234433) from Abcam (Cambridge, MA, USA); and anti-β-actin (#A2228), anti-GAPDH (CB1001), and anti-puromycin (MABE343) from Sigma-Aldrich (St. Louis, MO, USA). ..

    Incubation:

    Article Title: High cereblon expression in neuroendocrine cancer confers vulnerability to GSPT1 molecular glue degrader
    Article Snippet: .. The membrane was blocked with 5% skim milk and incubated overnight at 4 °C with primary antibodies, including anti-ASCL1 (#10585), anti-CRBN (#71810), anti-CUL4A (#2699), anti-DDB1 (#5428), anti-ENO2 (#9536), anti-NeuroD1 (#7019), anti-POU2F3 (#92579), and anti-SYP (#5461) from Cell Signaling Technology (Danvers, MA, USA); anti-eRF3/GSPT1 (ab234433) from Abcam (Cambridge, MA, USA); and anti-β-actin (#A2228), anti-GAPDH (CB1001), and anti-puromycin (MABE343) from Sigma-Aldrich (St. Louis, MO, USA). ..

    Article Title: High cereblon expression in neuroendocrine cancer confers vulnerability to GSPT1 molecular glue degrader.
    Article Snippet: .. The membrane was blocked with 5% skim milk and incubated overnight at 4 °C with primary antibodies, including anti-ASCL1 (#10585), anti-CRBN (#71810), anti-CUL4A (#2699), anti-DDB1 (#5428), antiENO2 (#9536), anti-NeuroD1 (#7019), anti-POU2F3 (#92579), and anti-SYP (#5461) from Cell Signaling Technology (Danvers, MA, USA); anti-eRF3/GSPT1 (ab234433) from Abcam (Cambridge, MA, USA); and anti-β-actin (#A2228), anti-GAPDH (CB1001), and anti-puromycin (MABE343) from Sigma-Aldrich (St. Louis, MO, USA). ..

    Article Title: Ondansetron reduces seizures and improves cognitive impairment in a rat model of temporal lobe epilepsy
    Article Snippet: .. Fixed neurons on coverslips were incubated overnight at 4°C with primary antibodies: Anti-SYP (mouse mAb, 1:200, CST)、Anti-NeuN (mouse mAb, 1:200, CST)、Anti-PSD95 (rabbit mAb, 1:300, CST). .. After PBS washes, samples were incubated with Alexa Fluor-conjugated secondary antibodies (goat anti-mouse 555 and goat anti-rabbit 647, 1:1000, CST) for 1 hr at RT in the dark.

    Western Blot:

    Article Title: Acetate utilization promotes hormone therapy resistance in prostate cancer through neuroendocrine differentiation.
    Article Snippet: .. Western blot analysis was performed as previously described(Xu et al., 2022a; Xu et al., 2022b), using the following antibodies: anti-ACSS2 (Proteintech, Rosemont, IL, USA; 16087), anti-NSE (Proteintech, 10149), anti-SYP (CST, Danvers, MA, USA; 4329), anti-c-Myc (Proteintech, 67447), anti-H3 (Proteintech, 17168), anti-H4 (Proteintech, 16047), anti-Ac-H3K9 (CST, 9649), anti-Ac-H3K14 (CST, 7627), anti-Ac-H3K27 (CST, 8173), and anti-Ac-H4 (Proteintech, 39244). .. Anti-GAPDH (CST, 5174), anti-tubulin (Proteintech, 66031), and anti-TBP (Proteintech, 22006) were used as the internal references.



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    Cell Signaling Technology Inc syp
    SHPL-49 at a dosage of 90 mg/kg enhances synaptic plasticity. (A) Representative Golgi-Cox staining images of rat brain tissue. (B) Quantitative analysis of dendritic spine density. (C–E) qRT-PCR analysis of key markers associated with synaptic remodeling: <t>SYP,</t> β-III tubulin and MAP-2. (F) Representative Western blot images showing the expression of presynaptic markers SYP <t>and</t> <t>SYN1,</t> as well as the postsynaptic marker PSD95, in rat brain tissue. (G) Quantification of SYP protein levels in rat brain tissue. (H) Quantification of SYN1 protein levels in rat brain tissue. (I) Quantification of PSD95 protein levels in rat brain tissue. (J) Immunofluorescence staining image of SYP, SYN1, PSD95, and the glial scar. Scale bars = 50 μm for synaptic markers; and 200 μm for the glial scar. (K) Quantification of SYP fluorescence intensity based on immunofluorescence staining. (L) Quantification of SYN1 fluorescence intensity based on immunofluorescence staining. (M) Quantification of PSD95 fluorescence intensity based on immunofluorescence staining. (N) Quantification of glial scar area based on immunofluorescence Staining. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, Model group vs. the Sham group, # P < 0.05, ## P < 0.01, ### P < 0.001, SHPL-49 group or SAL group vs. the Model group. n = 6 per group; & P < 0.05, &&& P < 0.001, SHPL-49 group vs. SAL group.
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    Cell Signaling Technology Inc synaptophysin syp
    SHPL-49 at a dosage of 90 mg/kg enhances synaptic plasticity. (A) Representative Golgi-Cox staining images of rat brain tissue. (B) Quantitative analysis of dendritic spine density. (C–E) qRT-PCR analysis of key markers associated with synaptic remodeling: <t>SYP,</t> β-III tubulin and MAP-2. (F) Representative Western blot images showing the expression of presynaptic markers SYP <t>and</t> <t>SYN1,</t> as well as the postsynaptic marker PSD95, in rat brain tissue. (G) Quantification of SYP protein levels in rat brain tissue. (H) Quantification of SYN1 protein levels in rat brain tissue. (I) Quantification of PSD95 protein levels in rat brain tissue. (J) Immunofluorescence staining image of SYP, SYN1, PSD95, and the glial scar. Scale bars = 50 μm for synaptic markers; and 200 μm for the glial scar. (K) Quantification of SYP fluorescence intensity based on immunofluorescence staining. (L) Quantification of SYN1 fluorescence intensity based on immunofluorescence staining. (M) Quantification of PSD95 fluorescence intensity based on immunofluorescence staining. (N) Quantification of glial scar area based on immunofluorescence Staining. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, Model group vs. the Sham group, # P < 0.05, ## P < 0.01, ### P < 0.001, SHPL-49 group or SAL group vs. the Model group. n = 6 per group; & P < 0.05, &&& P < 0.001, SHPL-49 group vs. SAL group.
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    Santa Cruz Biotechnology syp
    SHPL-49 at a dosage of 90 mg/kg enhances synaptic plasticity. (A) Representative Golgi-Cox staining images of rat brain tissue. (B) Quantitative analysis of dendritic spine density. (C–E) qRT-PCR analysis of key markers associated with synaptic remodeling: <t>SYP,</t> β-III tubulin and MAP-2. (F) Representative Western blot images showing the expression of presynaptic markers SYP <t>and</t> <t>SYN1,</t> as well as the postsynaptic marker PSD95, in rat brain tissue. (G) Quantification of SYP protein levels in rat brain tissue. (H) Quantification of SYN1 protein levels in rat brain tissue. (I) Quantification of PSD95 protein levels in rat brain tissue. (J) Immunofluorescence staining image of SYP, SYN1, PSD95, and the glial scar. Scale bars = 50 μm for synaptic markers; and 200 μm for the glial scar. (K) Quantification of SYP fluorescence intensity based on immunofluorescence staining. (L) Quantification of SYN1 fluorescence intensity based on immunofluorescence staining. (M) Quantification of PSD95 fluorescence intensity based on immunofluorescence staining. (N) Quantification of glial scar area based on immunofluorescence Staining. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, Model group vs. the Sham group, # P < 0.05, ## P < 0.01, ### P < 0.001, SHPL-49 group or SAL group vs. the Model group. n = 6 per group; & P < 0.05, &&& P < 0.001, SHPL-49 group vs. SAL group.
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    Image Search Results


    SHPL-49 at a dosage of 90 mg/kg enhances synaptic plasticity. (A) Representative Golgi-Cox staining images of rat brain tissue. (B) Quantitative analysis of dendritic spine density. (C–E) qRT-PCR analysis of key markers associated with synaptic remodeling: SYP, β-III tubulin and MAP-2. (F) Representative Western blot images showing the expression of presynaptic markers SYP and SYN1, as well as the postsynaptic marker PSD95, in rat brain tissue. (G) Quantification of SYP protein levels in rat brain tissue. (H) Quantification of SYN1 protein levels in rat brain tissue. (I) Quantification of PSD95 protein levels in rat brain tissue. (J) Immunofluorescence staining image of SYP, SYN1, PSD95, and the glial scar. Scale bars = 50 μm for synaptic markers; and 200 μm for the glial scar. (K) Quantification of SYP fluorescence intensity based on immunofluorescence staining. (L) Quantification of SYN1 fluorescence intensity based on immunofluorescence staining. (M) Quantification of PSD95 fluorescence intensity based on immunofluorescence staining. (N) Quantification of glial scar area based on immunofluorescence Staining. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, Model group vs. the Sham group, # P < 0.05, ## P < 0.01, ### P < 0.001, SHPL-49 group or SAL group vs. the Model group. n = 6 per group; & P < 0.05, &&& P < 0.001, SHPL-49 group vs. SAL group.

    Journal: Frontiers in Pharmacology

    Article Title: Salidroside derivative SHPL-49 enhances synaptic remodeling in BCCAO rats via the CDK5/p35/p25 signaling pathway

    doi: 10.3389/fphar.2026.1727177

    Figure Lengend Snippet: SHPL-49 at a dosage of 90 mg/kg enhances synaptic plasticity. (A) Representative Golgi-Cox staining images of rat brain tissue. (B) Quantitative analysis of dendritic spine density. (C–E) qRT-PCR analysis of key markers associated with synaptic remodeling: SYP, β-III tubulin and MAP-2. (F) Representative Western blot images showing the expression of presynaptic markers SYP and SYN1, as well as the postsynaptic marker PSD95, in rat brain tissue. (G) Quantification of SYP protein levels in rat brain tissue. (H) Quantification of SYN1 protein levels in rat brain tissue. (I) Quantification of PSD95 protein levels in rat brain tissue. (J) Immunofluorescence staining image of SYP, SYN1, PSD95, and the glial scar. Scale bars = 50 μm for synaptic markers; and 200 μm for the glial scar. (K) Quantification of SYP fluorescence intensity based on immunofluorescence staining. (L) Quantification of SYN1 fluorescence intensity based on immunofluorescence staining. (M) Quantification of PSD95 fluorescence intensity based on immunofluorescence staining. (N) Quantification of glial scar area based on immunofluorescence Staining. Data are presented as mean ± SD. * P < 0.05, ** P < 0.01, *** P < 0.001, Model group vs. the Sham group, # P < 0.05, ## P < 0.01, ### P < 0.001, SHPL-49 group or SAL group vs. the Model group. n = 6 per group; & P < 0.05, &&& P < 0.001, SHPL-49 group vs. SAL group.

    Article Snippet: Membranes were blocked with 5% non-fat milk (Beyotime, China) in Tris-buffered saline containing 0.1% Tween-20 (TBST) and incubated overnight at 4 °C with the following primary antibodies: SYP (1:1,000, CST, United States), SYN1 (1:1,000, Boster, China), PSD95 (1:1,000, ABCAM, United States), CDK5 (1:1,000, Boster, China), p35/25 (1:1,000, CST, United States), p-PSD95 (1:1,000, CST, United States).

    Techniques: Staining, Quantitative RT-PCR, Western Blot, Expressing, Marker, Immunofluorescence, Fluorescence