polyclonal guinea pig anti-map2 Search Results


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NSJ Bioreagents map2 antibody
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Cell Signaling Technology Inc anti map2 immunostaining

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Cell Signaling Technology Inc d1r1r cell signaling 23706 guinea pig anti map2 synaptic systems 188004 rabbit anti tyrosine hydroxylase th

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Millipore guinea pig map2
( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, <t>MAP2,</t> and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).
Guinea Pig Map2, 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
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Biorbyt mouse anti-mcherry orb66657
( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, <t>MAP2,</t> and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).
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Image Search Results


Journal: Neuron

Article Title: Targeted proteoform mapping uncovers specific Neurexin-3 variants required for dendritic inhibition

doi: 10.1016/j.neuron.2022.04.017

Figure Lengend Snippet:

Article Snippet: The following antibodies were used in this study: rabbit polyclonal anti-β-actin (Abcam; Cat# ab8227; RRID: AB_2305186; LOT# GR3314266-1), mouse monoclonal anti-calbindin (Swant; Cat# 300; RRID: AB_10000347; LOT# 17 (F)), goat polyclonal anti-calretinin (Swant; Cat# CG1; RRID: AB_10000342; LOT# 1§.1), mouse monoclonal anti-CamKII alpha (Thermo Fisher Scientific; 6G9; Cat# Ma1-048; RRID: AB_325403; LOT# TH269517), mouse monoclonal anti-cannabinoid receptor 1 (Immunogene; IMG-3C2; Cat# IMG-CB1R-mAb001; LOT# CJ03), guinea pig polyclonal anti-cholecystokinin (Synaptic Systems, Cat# 438004; RRID: AB_2814938; LOT# 1-1), mouse monoclonal anti-GAD67 (Millipore; 1G10.2; Cat# MAB5406; RRID: AB_2278725; LOT# 3015328), rabbit polyclonal anti-GAPDH (Enogene; Cat# E1C604; LOT# R14Q12), mouse monoclonal anti-gephyrin (Synaptic Systems; mAb7a; Cat# 147021; RRID: AB_2232546; LOT# 147021/15), mouse monoclonal anti-gephyrin (Synaptic Systems; mAb7a; Cat# 147011; RRID: AB_887717; LOT# 147011/54), rat monoclonal anti-HA (Roche; 3F10; Cat# 11867431001; RRID: AB_390919; LOT# 34502100), rabbit monoclonal anti-HA (Cell Signaling; 3724; Cat# 3724; RRID: AB_1549585; LOT# 9), guinea pig polyclonal anti-MAP2 (Synaptic Systems; Cat# 188004; RRID: AB_2138181; LOT# 2-26), mouse monoclonal anti-MAP2 (Synaptic Systems; 198A5; Cat# 188011; RRID: AB_2147096; LOT# 1-10), rabbit polyclonal anti-neurexin , chicken anti-neurexin , rabbit anti-neuroligin , rabbit monoclonal anti-nNOS (Cell Signaling; C7D7; Cat# 4231; RRID: AB_2152485; LOT# 2), goat polyclonal anti-parvalbumin (Swant, Cat# PVG214; RRID: AB_10000345), mouse monoclonal anti-PSD95 (Santa Cruz; 7E3; Cat# sc32290; RRID: AB_628114; LOT# J1509), goat polyclonal anti-somatostatin (Santa Cruz; Cat# sc7819; RRID: AB_2302603; LOT# L1611), mouse monoclonal anti-Synaptotagmin 2 (Zebrafish International Resource Center; Cat# znp-1; RRID: AB_10013783), mouse monoclonal anti-V5 (Biorad; SV5-PK1; Cat# MCA1360; RRID: AB_322378; LOT# 148239), guinea pig polyclonal anti-vGAT (Synaptic Systems; Cat# 131004; RRID: AB_887873; LOT# 2-42), guinea pig polyclonal anti-vGlut1 (Millipore; Cat# AB5905; RRID: AB_2301751; LOT# 3308226), rabbit polyclonal anti-VIP (Immunostar; Cat# 20077; RRID: AB_572270; LOT# 1513001), guinea pig anti-somatostatin (raised in the present study against amino acid residues 35-88 of mouse pro-somatostatin, GenBank: #BC010770.1), goat anti-cannabinoid receptor 1 (Nittobo Medical, MSFR100600; RRID: AB_2571592), guinea pig anti-GABAA receptor alpha 1 (Nittobo Medical, MSFR101540; RRID: AB_2571572), goat anti-vGAT (Nittobo Medical, MSFR106130; RRID: AB_2571623), guinea pig anti-PSD95 (Nittobo Medical, MSFR105180; RRID: AB_2571612).

Techniques: Recombinant, Reporter Assay, Multiplex Assay, Plasmid Preparation, Software, Microscopy

( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, MAP2, and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).

Journal: bioRxiv

Article Title: Cell specificity of adeno-associated virus (AAV) serotypes in human cortical organoids

doi: 10.1101/2023.04.13.536491

Figure Lengend Snippet: ( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, MAP2, and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).

Article Snippet: For staining, slides were rinsed with PBS, then incubated in 0.25% Triton X-100 with 4% Donkey serum (EMD Millipore, S30) for 1 hour, followed by incubation in primary antibodies overnight: chicken GFP (1:3000, Aves Labs, GFP-1010) and guinea pig MAP2 (1:1000, Millipore-Sigma, MAB3418).

Techniques: Transduction, Labeling, Staining, Flow Cytometry