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AGC-037  (alomone labs)


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    Structured Review

    alomone labs AGC-037
    Primary and secondary antibodies used for immunocytochemistry
    Agc 037, supplied by alomone labs, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/AGC-037/product/alomone labs
    Average 90 stars, based on 2 article reviews
    AGC-037 - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism"

    Article Title: Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism

    Journal: eNeuro

    doi: 10.1523/ENEURO.0106-19.2019

    Primary and secondary antibodies used for immunocytochemistry
    Figure Legend Snippet: Primary and secondary antibodies used for immunocytochemistry

    Techniques Used: Clone Assay, Recombinant, Purification, Isolation, Strep-tag



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    Image Search Results


    Primary and secondary antibodies used for immunocytochemistry

    Journal: eNeuro

    Article Title: Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism

    doi: 10.1523/ENEURO.0106-19.2019

    Figure Lengend Snippet: Primary and secondary antibodies used for immunocytochemistry

    Article Snippet: VGLUT3 , Peptide (C)ELNHEAFVSPRKK, corresponding to amino acid residues 533–545 of rat VGLUT3 (accession Q7TSF2); cytoplasmic, C terminus , Alomone Labs , AGC-037 , Rabbit , 1:300.

    Techniques: Clone Assay, Recombinant, Purification, Isolation, Strep-tag

    Primary and secondary antibodies used for immunocytochemistry

    Journal: eNeuro

    Article Title: Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism

    doi: 10.1523/ENEURO.0106-19.2019

    Figure Lengend Snippet: Primary and secondary antibodies used for immunocytochemistry

    Article Snippet: VGLUT3 , Peptide (C)ELNHEAFVSPRKK, corresponding to amino acid residues 533–545 of rat VGLUT3 (accession Q7TSF2); cytoplasmic, C terminus , Alomone Labs , AGC-037 , Rabbit , 1:300.

    Techniques: Clone Assay, Recombinant, Purification, Isolation, Strep-tag

    Primary and secondary antibodies used for immunocytochemistry

    Journal: eNeuro

    Article Title: Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism

    doi: 10.1523/ENEURO.0106-19.2019

    Figure Lengend Snippet: Primary and secondary antibodies used for immunocytochemistry

    Article Snippet: VGLUT3 , Peptide (C)ELNHEAFVSPRKK, corresponding to amino acid residues 533–545 of rat VGLUT3 (accession Q7TSF2); cytoplasmic, C terminus , Alomone Labs , AGC-037 , Rabbit , 1:300.

    Techniques: Clone Assay, Recombinant, Purification, Isolation, Strep-tag

    Histochemical profile of excitatory and inhibitory inputs to the SPN. A , B , D , E , G , H , Glycinergic input forms the most prominent input to SPN (white dotted circle in A , D , G ) and is depicted by neuronal GlyT2 (green) labeling. Immunolabeling for microtubule associated protein 2 (MAP2, blue) is used as a neuronal marker in all images. Glutamatergic inputs are shown by labeling for the VGLUTs (magenta): VGLUT1 ( A – C ), VGLUT2 ( D – F ), VGLUT3 ( G – I ). A–F , While both VGLUT1 ( B , white arrows) and VGLUT2 ( E , white arrows) positive synaptic boutons are present at the soma, VGLUT2 boutons are also seen in the neuropil ( E , white arrowheads). G–I , VGLUT3 shows only weak somatic but no presynaptic bouton labeling. Scale bars = 200 µm (left images) and 20 µm (middle and right images).

    Journal: eNeuro

    Article Title: Slow NMDA-Mediated Excitation Accelerates Offset-Response Latencies Generated via a Post-Inhibitory Rebound Mechanism

    doi: 10.1523/ENEURO.0106-19.2019

    Figure Lengend Snippet: Histochemical profile of excitatory and inhibitory inputs to the SPN. A , B , D , E , G , H , Glycinergic input forms the most prominent input to SPN (white dotted circle in A , D , G ) and is depicted by neuronal GlyT2 (green) labeling. Immunolabeling for microtubule associated protein 2 (MAP2, blue) is used as a neuronal marker in all images. Glutamatergic inputs are shown by labeling for the VGLUTs (magenta): VGLUT1 ( A – C ), VGLUT2 ( D – F ), VGLUT3 ( G – I ). A–F , While both VGLUT1 ( B , white arrows) and VGLUT2 ( E , white arrows) positive synaptic boutons are present at the soma, VGLUT2 boutons are also seen in the neuropil ( E , white arrowheads). G–I , VGLUT3 shows only weak somatic but no presynaptic bouton labeling. Scale bars = 200 µm (left images) and 20 µm (middle and right images).

    Article Snippet: VGLUT3 , Peptide (C)ELNHEAFVSPRKK, corresponding to amino acid residues 533–545 of rat VGLUT3 (accession Q7TSF2); cytoplasmic, C terminus , Alomone Labs , AGC-037 , Rabbit , 1:300.

    Techniques: Labeling, Immunolabeling, Marker