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rabbit primary antibodies anti-glut3  (Millipore)

 
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    Millipore rabbit primary antibodies anti-glut3
    Rabbit Primary Antibodies Anti Glut3, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit primary antibodies anti-glut3/product/Millipore
    Average 90 stars, based on 1 article reviews
    rabbit primary antibodies anti-glut3 - by Bioz Stars, 2026-03
    90/100 stars

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    Tau pathology switches the energy metabolism to fatty acid oxidation. A-B Immunofluorescence staining of neuron-specific <t>glucose</t> <t>transporter</t> <t>3</t> <t>(GLUT3)</t> in the medulla oblongata from control and transgenic animals. Representative images of GLUT3 (green), NeuN (red), and DAPI staining (blue). C Representative images of 8-month-old control and transgenic animals. Scale bar 20 μm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p = 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p = 0.022; n = 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals)
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    A-B Immunofluorescence staining of neuron-specific <t>glucose</t> <t>transporter</t> <t>3</t> <t>(GLUT3).</t> Representative images of GLUT3 (green), NeuN (red), and DAPI staining in brain tissue from control and transgenic animals. C Representative images of 8-month-old control and transgenic animals. Scale bar 20 µm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p= 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p= 0.022; n= 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals).
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    Transcript and membrane protein abundance of GLUT1 in the placentas from dams in the 1×, 2×, and 4× choline groups at E15.5 (A). Membrane protein abundance of <t>GLUT3</t> in the placentas from dams in the 1×, 2×, and 4× choline groups at E18.5 (B). Values are given as means ± SEMs, n = 6–7 dams/group for each gestational day. Means without a common letter differ, P ≤ 0.05. E, gestational day; GLUT, glucose transporter.
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    Transcript and membrane protein abundance of GLUT1 in the placentas from dams in the 1×, 2×, and 4× choline groups at E15.5 (A). Membrane protein abundance of <t>GLUT3</t> in the placentas from dams in the 1×, 2×, and 4× choline groups at E18.5 (B). Values are given as means ± SEMs, n = 6–7 dams/group for each gestational day. Means without a common letter differ, P ≤ 0.05. E, gestational day; GLUT, glucose transporter.
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    Image Search Results


    Tau pathology switches the energy metabolism to fatty acid oxidation. A-B Immunofluorescence staining of neuron-specific glucose transporter 3 (GLUT3) in the medulla oblongata from control and transgenic animals. Representative images of GLUT3 (green), NeuN (red), and DAPI staining (blue). C Representative images of 8-month-old control and transgenic animals. Scale bar 20 μm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p = 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p = 0.022; n = 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals)

    Journal: Journal of Neuroinflammation

    Article Title: Changes in lipid metabolism track with the progression of neurofibrillary pathology in tauopathies

    doi: 10.1186/s12974-024-03060-4

    Figure Lengend Snippet: Tau pathology switches the energy metabolism to fatty acid oxidation. A-B Immunofluorescence staining of neuron-specific glucose transporter 3 (GLUT3) in the medulla oblongata from control and transgenic animals. Representative images of GLUT3 (green), NeuN (red), and DAPI staining (blue). C Representative images of 8-month-old control and transgenic animals. Scale bar 20 μm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p = 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p = 0.022; n = 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals)

    Article Snippet: Sections were incubated overnight in a polyclonal rabbit anti-IBA-1 primary antibody (1:1000, Wako), polyclonal rabbit anti-GLUT3 primary antibody (1:100, Invitrogen, Massachusetts, USA), and monoclonal mouse anti-NeuN primary antibody (1:1000, Abcam, Waltham, MA, USA).

    Techniques: Immunofluorescence, Staining, Transgenic Assay, Fluorescence

    A-B Immunofluorescence staining of neuron-specific glucose transporter 3 (GLUT3). Representative images of GLUT3 (green), NeuN (red), and DAPI staining in brain tissue from control and transgenic animals. C Representative images of 8-month-old control and transgenic animals. Scale bar 20 µm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p= 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p= 0.022; n= 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals).

    Journal: bioRxiv

    Article Title: Changes in lipid metabolism track with the progression of neurofibrillary pathology in tauopathies

    doi: 10.1101/2023.09.05.556321

    Figure Lengend Snippet: A-B Immunofluorescence staining of neuron-specific glucose transporter 3 (GLUT3). Representative images of GLUT3 (green), NeuN (red), and DAPI staining in brain tissue from control and transgenic animals. C Representative images of 8-month-old control and transgenic animals. Scale bar 20 µm. D . Quantification of GLUT3 mean fluorescence intensity in brain tissue. Quantification of relative fluorescent intensity showed a decrease of GLUT3 in transgenic animals (8-months old animals: CN: 25.07 ± 1.43, Tg: 20.91 ± 0.54; p= 0.035; 10-month-old animals: CN: 28.37 ± 1.03, Tg: 22.36 ± 1.67; p= 0.022; n= 5; mean ± SD, student’s t-test with p-value). E Changes of long-chain, hydroxylated, short-chain ACs and free carnitine in brain tissue of control and transgenic rats (data are presented as median intensities with 95% confidence intervals).

    Article Snippet: Sections were incubated overnight in a polyclonal rabbit anti-IBA-1 primary antibody (1:1000, Wako), polyclonal rabbit anti-GLUT3 primary antibody (1:100, Invitrogen, Massachusetts, USA), and monoclonal mouse anti-NeuN primary antibody (1:1000, Abcam, Waltham, MA, USA).

    Techniques: Immunofluorescence, Staining, Transgenic Assay, Fluorescence

    Transcript and membrane protein abundance of GLUT1 in the placentas from dams in the 1×, 2×, and 4× choline groups at E15.5 (A). Membrane protein abundance of GLUT3 in the placentas from dams in the 1×, 2×, and 4× choline groups at E18.5 (B). Values are given as means ± SEMs, n = 6–7 dams/group for each gestational day. Means without a common letter differ, P ≤ 0.05. E, gestational day; GLUT, glucose transporter.

    Journal: The Journal of Nutrition

    Article Title: Maternal Choline Supplementation Modulates Placental Nutrient Transport and Metabolism in Late Gestation of Mouse Pregnancy 1 2

    doi: 10.3945/jn.117.256107

    Figure Lengend Snippet: Transcript and membrane protein abundance of GLUT1 in the placentas from dams in the 1×, 2×, and 4× choline groups at E15.5 (A). Membrane protein abundance of GLUT3 in the placentas from dams in the 1×, 2×, and 4× choline groups at E18.5 (B). Values are given as means ± SEMs, n = 6–7 dams/group for each gestational day. Means without a common letter differ, P ≤ 0.05. E, gestational day; GLUT, glucose transporter.

    Article Snippet: Membranes were blocked in LI-COR blocking buffer and then incubated overnight with primary antibodies for GLUT1 (catalog no. 21829–1, 1:200; ProteinTech), GLUT3 (catalog no. AB1344, 1:1000; EMD Millipore), and β-actin (catalog no. 3700, 1:5000; Cell Signaling Technology).

    Techniques: