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mouse monoclonal anti-glua1  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology mouse monoclonal anti-glua1
    Mouse Monoclonal Anti Glua1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 119 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse monoclonal anti-glua1/product/Santa Cruz Biotechnology
    Average 94 stars, based on 119 article reviews
    mouse monoclonal anti-glua1 - by Bioz Stars, 2026-04
    94/100 stars

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    Cell Signaling Technology Inc incubation with glur1
    A.Percent change PSD95 expression from saline (control) in mice treated with G-CSF (50 ug/kg), cocaine (7.5 mg/kg), or G-CSF+cocaine (50 ug/kg + 7.5 mg/kg). B . Percent change <t>GluR1</t> expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. C . Percent change GluR2 expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. D . Example PSD95 blot. E . Example GluR1 blot. F . Example GluR2 blot. * p < 0.05.
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    Cell Signaling Technology Inc glua1
    Synaptic plasticity, circulating neurofilament light chain, and glutamate receptor subunit expression. (A) Time course of field excitatory postsynaptic potential (fEPSP) response expressed as mean peak fEPSP (% baseline) following theta burst stimulation (TBS) in hippocampal slices from saline- and morphine-treated rats. ***p < 0.001 (B) Circulating neurofilament light chain (Nf-L) concentrations measured 30 days post-surgery in saline- and morphine-treated rats. Data are presented as mean ± SEM with individual data points shown. *p < 0.05. (C-G) Protein expression of glutamate receptor subunits <t>GluA1</t> (C), GluA2/3 (D), GluN1 (E), GluN2a (F), and GluN2b (G) measured in hippocampal synaptoneurosomes under baseline conditions and following a learning experience, expressed as percent of laparotomy saline baseline control. (H) Representative immunoblots for glutamate receptor subunits and GAPDH corresponding to quantified data shown in panels C-G. Data are presented as mean ± SEM with individual data points shown. *p < 0.05.
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    Image Search Results


    A.Percent change PSD95 expression from saline (control) in mice treated with G-CSF (50 ug/kg), cocaine (7.5 mg/kg), or G-CSF+cocaine (50 ug/kg + 7.5 mg/kg). B . Percent change GluR1 expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. C . Percent change GluR2 expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. D . Example PSD95 blot. E . Example GluR1 blot. F . Example GluR2 blot. * p < 0.05.

    Journal: bioRxiv

    Article Title: Granulocyte colony-stimulating factor acts through calcium-permeable AMPA receptors to potentiate cocaine reward

    doi: 10.64898/2026.01.30.702629

    Figure Lengend Snippet: A.Percent change PSD95 expression from saline (control) in mice treated with G-CSF (50 ug/kg), cocaine (7.5 mg/kg), or G-CSF+cocaine (50 ug/kg + 7.5 mg/kg). B . Percent change GluR1 expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. C . Percent change GluR2 expression from saline (control) in mice treated with G-CSF, cocaine, or G-CSF+cocaine. D . Example PSD95 blot. E . Example GluR1 blot. F . Example GluR2 blot. * p < 0.05.

    Article Snippet: Proteins were transferred to a PVDF membrane and blocked with Intercept blocking buffer (LiCor) before incubation with GluR1 (1:1000, Cell Signaling Technology #13185), PSD95 (1:1000, Cell Signaling Technology #36233), or GluR2 (1:1000, Cell Signaling Technology #13607), and actin (1:5000, MP Biomedicals #691001) antibodies overnight at 4°C.

    Techniques: Expressing, Saline, Control

    Synaptic plasticity, circulating neurofilament light chain, and glutamate receptor subunit expression. (A) Time course of field excitatory postsynaptic potential (fEPSP) response expressed as mean peak fEPSP (% baseline) following theta burst stimulation (TBS) in hippocampal slices from saline- and morphine-treated rats. ***p < 0.001 (B) Circulating neurofilament light chain (Nf-L) concentrations measured 30 days post-surgery in saline- and morphine-treated rats. Data are presented as mean ± SEM with individual data points shown. *p < 0.05. (C-G) Protein expression of glutamate receptor subunits GluA1 (C), GluA2/3 (D), GluN1 (E), GluN2a (F), and GluN2b (G) measured in hippocampal synaptoneurosomes under baseline conditions and following a learning experience, expressed as percent of laparotomy saline baseline control. (H) Representative immunoblots for glutamate receptor subunits and GAPDH corresponding to quantified data shown in panels C-G. Data are presented as mean ± SEM with individual data points shown. *p < 0.05.

    Journal: bioRxiv

    Article Title: Disruption of hippocampal mitochondrial function underlies opioid-induced postoperative cognitive dysfunction in aged rats

    doi: 10.64898/2026.01.30.702943

    Figure Lengend Snippet: Synaptic plasticity, circulating neurofilament light chain, and glutamate receptor subunit expression. (A) Time course of field excitatory postsynaptic potential (fEPSP) response expressed as mean peak fEPSP (% baseline) following theta burst stimulation (TBS) in hippocampal slices from saline- and morphine-treated rats. ***p < 0.001 (B) Circulating neurofilament light chain (Nf-L) concentrations measured 30 days post-surgery in saline- and morphine-treated rats. Data are presented as mean ± SEM with individual data points shown. *p < 0.05. (C-G) Protein expression of glutamate receptor subunits GluA1 (C), GluA2/3 (D), GluN1 (E), GluN2a (F), and GluN2b (G) measured in hippocampal synaptoneurosomes under baseline conditions and following a learning experience, expressed as percent of laparotomy saline baseline control. (H) Representative immunoblots for glutamate receptor subunits and GAPDH corresponding to quantified data shown in panels C-G. Data are presented as mean ± SEM with individual data points shown. *p < 0.05.

    Article Snippet: Primary antibodies, in Odyssey blocking solution containing 0.2% Tween20 (overnight at 4°C), were: SYP (1:1,000; sc-17750; Santa Cruz), PSD95 (1:1,000; 2507S; Cell Signaling), GluA1 (1:1000; 13185S; Cell Signaling) GluA2/3 (1:1000, 07-598; Millipore Sigma), GluN1 (1:500; MAB1586; Millipore Sigma), GluN2A (1:500; 07-632; Millipore Sigma) and GluN2B (1:1000; ab254356; Abcam),

    Techniques: Expressing, Saline, Control, Western Blot