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Proteintech prrt1
Prrt1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 452 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+prrt1/PSD95-Specific%2CDLG4+Antibody/pm41912502-131-82-83
Average 96 stars, based on 452 article reviews
prrt1 - by Bioz Stars, 2026-09
96/100 stars

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Article Title: Interaction and Subcellular Association of PRRT1/SynDIG4 With AMPA Receptors
Article Snippet: The following primary antibodies were used: anti-PRRT1 (ProteinTech, 17261-1-AP, RRID:AB_2878371 ), anti-PRRT1 (NeuroMab, 75-409, RRID:AB_2531894 ), anti-GluA1 (Abcam, ab109450, RRID:AB_10860361 ), anti-GluA1 (NeuroMab, 75-327, RRID:AB_2315840 ), anti-MAP2 (EnCor, CPCA-MAP2, RRID:AB_2138173 ), anti-VGLUT1 (Synaptic Systems, 135 303, RRID:AB_887875 ), anti-EEA1 (Cell Signaling, C45B10, RRID:AB_2096811 ), anti-Rab7 (Cell Signaling, D95F2, RRID:AB_1904103 ), anti-Flag (Sigma, F3165, RRID:AB_259529 ), anti-HA (Thermo Fisher Scientific, 71-5500, RRID:AB_2533988 ), anti-HA (Biolegend, 16B12, RRID:AB_10064068 ), anti-GFP (Thermo Fisher Scientific, A-11122, RRID:AB_221569 ), and anti-β tubulin (Millipore, 05-661, RRID:AB_309885 ).

Incubation:

Article Title: Uncovering the epigenetic regulatory clues of PRRT1 in Alzheimer's disease: a strategy integrating multi-omics analysis with explainable machine learning.
Article Snippet: .. The membranes were then incubated with primary antibodies including anti-PRRT1 (rabbit, 1:1000, 17261-1-AP, Proteintech) and internal reference antibodies Na, K-ATPase (rabbit, 1:5000, #3010, CST), anti-MAZ (rabbit, 1:1000, 21068-1- AP, Proteintech), anti-LC3 (rabbit, 1:1000, 14600-1-AP, Proteintech), anti-phosphorylated-tau (rabbit, 1:1000, 28866-1-AP, Proteintech), anti-tau (rabbit, 1:2000,10274- 1-AP, Proteintech), anti-actin (rabbit, 1:10000, TDY051, TDY Biotech), followed by incubation with secondary antibodies. ..

Article Title: Uncovering the epigenetic regulatory clues of PRRT1 in Alzheimer’s disease: a strategy integrating multi-omics analysis with explainable machine learning
Article Snippet: .. The membranes were then incubated with primary antibodies including anti-PRRT1 (rabbit, 1:1000, 17261-1-AP, Proteintech) and internal reference antibodies Na, K-ATPase (rabbit, 1:5000, #3010, CST), anti-MAZ (rabbit, 1:1000, 21068-1-AP, Proteintech), anti-LC3 (rabbit, 1:1000, 14600-1-AP, Proteintech), anti-phosphorylated-tau (rabbit, 1:1000, 28866-1-AP, Proteintech), anti-tau (rabbit, 1:2000,10274-1-AP, Proteintech), anti-actin (rabbit, 1:10000, TDY051, TDY Biotech), followed by incubation with secondary antibodies. ..

Western Blot:

Article Title: PRRT1 regulates basal and plasticity-induced AMPA receptor trafficking.
Article Snippet: Accepted Manuscript PRRT1 regulates basal and plasticity-induced AMPA receptor trafficking Eva Troyano-Rodriguez, Shivani Mann, Raja Ullah, Mohiuddin Ahmad PII: S1044-7431(19)30004-1 DOI: https://doi.org/10.1016/j.mcn.2019.06.008 Reference: YMCNE 3388 To appear in: Molecular and Cellular Neuroscience Received date: 10 January 2019 Revised date: 7 June 2019 Accepted date: 13 June 2019 Please cite this article as: E. Troyano-Rodriguez, S. Mann, R. Ullah, et al., PRRT1 regulates basal and plasticity-induced AMPA receptor trafficking, Molecular and Cellular Neuroscience, https://doi.org/10.1016/j.mcn.2019.06.008 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.



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Proteintech rabbit antibodies against syndig4
Synapse composition is unaltered in SynDIG1-deficient synapses. A , Representative immunoblots of biochemical fractions isolated from WT and SynDIG1 β-gal homozygous mutant P14 mouse brain tissue showing levels of GluA1, GluA2, GluN1, GluN2B, PSD-93, PSD-95, synaptophysin (Synapto), SynDIG1, <t>SynDIG4,</t> and PICK-1 present in the S1-, P2-, Syn-, and PSD-enriched fractions. Loading controls are provided by β-actin and β-tubulin immunoreactivity. B–D , Graphs depict the ratio of SynDIG1 β-gal homozygous mutant protein relative to WT levels of AMPA receptor subunits ( B ), NMDA receptor subunits ( C ), and PSD-93 and PSD-95 ( D ) in the PSD-enriched fractions. Data are the average of three independent biochemical fractionation experiments; each experiment used four to six mouse brains of each genotype. Error bars represent ±SEM.
Rabbit Antibodies Against Syndig4, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Synapse composition is unaltered in SynDIG1-deficient synapses. A , Representative immunoblots of biochemical fractions isolated from WT and SynDIG1 β-gal homozygous mutant P14 mouse brain tissue showing levels of GluA1, GluA2, GluN1, GluN2B, PSD-93, PSD-95, synaptophysin (Synapto), SynDIG1, SynDIG4, and PICK-1 present in the S1-, P2-, Syn-, and PSD-enriched fractions. Loading controls are provided by β-actin and β-tubulin immunoreactivity. B–D , Graphs depict the ratio of SynDIG1 β-gal homozygous mutant protein relative to WT levels of AMPA receptor subunits ( B ), NMDA receptor subunits ( C ), and PSD-93 and PSD-95 ( D ) in the PSD-enriched fractions. Data are the average of three independent biochemical fractionation experiments; each experiment used four to six mouse brains of each genotype. Error bars represent ±SEM.

Journal: eNeuro

Article Title: Loss of SynDIG1 Reduces Excitatory Synapse Maturation But Not Formation In Vivo

doi: 10.1523/ENEURO.0130-16.2016

Figure Lengend Snippet: Synapse composition is unaltered in SynDIG1-deficient synapses. A , Representative immunoblots of biochemical fractions isolated from WT and SynDIG1 β-gal homozygous mutant P14 mouse brain tissue showing levels of GluA1, GluA2, GluN1, GluN2B, PSD-93, PSD-95, synaptophysin (Synapto), SynDIG1, SynDIG4, and PICK-1 present in the S1-, P2-, Syn-, and PSD-enriched fractions. Loading controls are provided by β-actin and β-tubulin immunoreactivity. B–D , Graphs depict the ratio of SynDIG1 β-gal homozygous mutant protein relative to WT levels of AMPA receptor subunits ( B ), NMDA receptor subunits ( C ), and PSD-93 and PSD-95 ( D ) in the PSD-enriched fractions. Data are the average of three independent biochemical fractionation experiments; each experiment used four to six mouse brains of each genotype. Error bars represent ±SEM.

Article Snippet: Membranes were blotted with the following primary antibodies: mouse antibodies against PSD-95 [catalog #75-028, NeuroMab (RRID:AB_2292909)], synaptophysin [catalog #101011, Synaptic Systems (RRID:AB_887824)], SynDIG1 [catalog #75-251, NeuroMab (RRID:AB_10999753)], GluA2 [catalog #75-002, NeuroMab (RRID:AB_2232661)], PSD-93 [catalog #75-057, NeuroMab (RRID:AB_2277296)], β-tubulin [catalog #05-661, Millipore (RRID:AB_309885)], GluN1 [catalog #556308, BD Biosciences (RRID:AB_396353)], and Pick1 [catalog #73-040, NeuroMab (RRID:AB_10672986)]; rabbit antibodies against SynDIG4 (Anti-Prrt1, catalog #17261-1-AP, ProteinTech), β-actin [catalog #ab8224, Abcam (RRID:AB_449644)], GluA1 [catalog #AB1504, Millipore (RRID:AB_2113602)], and GluN2B (provided by J.W.H.

Techniques: Western Blot, Isolation, Mutagenesis, Fractionation