Antibodies for Neuroscience Research

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Formalin fixed, paraffin-embedded rat brain cerebellum region showing staining of VGlut2 with anti-VGlut2 recombinant chicken monoclonal antibody (green)  (Cat. 78-067) at 1:100 dilution. The sections were mounted with FluoroshieldTM with DAPI and DABCO mounting medium (Cat. AR-6505). DAPI nuclear stain (blue) shows cell nuclei. Anti-VGlut2 specifically stains the mossy fiber terminals in the granular layer and climbing climbing fiber terminals in the molecular layer of the cerebellum.​ Magnification 100X.Western blotting of rat brain membrane fraction with Aves Labs anti-Vglut2 recombinant chicken m (Cat. 78-067) antibody and detected with anti-chicken-HRP. Aves Labs recombinant chicken anti-VGlut2 mAb recognizes endogenous Vglut2 in the rat brain membrane fraction at ~60 kDa.
Aves Labs Anti-VGlut2 Recombinant Chicken Chimeric mAb
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Formalin fixed, paraffin-embedded rat brain cerebellum region showing staining of VGlut1. The sections were stained with anti-VGlut1 recombinant chicken monoclonal antibody (green)  (Cat. 78-066) at 1:100 dilution. The stained sections were mounted with Antibodies Incorporated FluoroshieldTM with DAPI and DABCO mounting medium (Cat. AR-6505). DAPI nuclear stain (blue) shows cell nuclei. Anti-VGlut1 specifically stains the axonal synapses in the granular layer of the cerebellum.​ Magnification 100X.Western blotting of rat brain membrane fraction with Aves Labs anti-Vglut1 recombinant chicken Mab (Cat. 78-066) antibody at various concentrations and detected with anti-chicken-HRP. Aves Labs Recombinant Chicken anti-VGlut1 Mab recognizes endogenous Vglut1 in the rat brain membrane fraction at ~52 kDa.
Aves Labs Anti-VGlut1 Recombinant Chicken Chimeric mAb
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Anti-ADAM11 Antibody (BSA and Azide free)
NeuroMab Anti-ADAM11 Antibody (BSA and Azide free)
$486
Anti-LRRK2/Dardarin, C-Terminus Antibody (BSA and Azide free)
NeuroMab Anti-LRRK2/Dardarin, C-Terminus Antibody (BSA and Azide free)
$486
Anti-Nav1.8 Na+ Channel Antibody (BSA and Azide free)
NeuroMab Anti-Nav1.8 Na+ Channel Antibody (BSA and Azide free)
$486
Anti-Nav1.7 Na+ Channel Antibody (BSA and Azide free)
NeuroMab Anti-Nav1.7 Na+ Channel Antibody (BSA and Azide free)
$486
Anti-PSD-95 Antibody (BSA and Azide free)
NeuroMab Anti-PSD-95 Antibody (BSA and Azide free)
$486
Representative image of 4% paraformaldehyde fixed free-floating mouse cerebellum sections stained with Aves Labs anti-Calretinin recombinant chicken monoclonal antibody (red, Cat No. 78-488) at 1:1000 dilution and co-stained with anti-Calbindin mouse monoclonal antibody (green). DAPI nuclear stain (blue) shows cell nuclei. Anti-Calretinin specifically stains the interneurons in the granule cell layer of the cerebellum. Image courtesy of EnCor Biotechnology.Representative image of 4% paraformaldehyde fixed free-floating rat cerebellum sections stained with Aves Labs anti-Calretinin recombinant chicken monoclonal antibody (Cat No. 78-488) at 1:1000 dilution. Anti-Calretinin specifically stains the interneurons in the granule cell layer of the cerebellum. Magnification 200X. Image courtesy of EnCor Biotechnology.
Aves Labs Anti-Calretinin Recombinant Chicken Chimeric mAb
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Western blot analysis of A431 cells treated with calyculin A (100 nM) for 30 min (lane 1 and 2) then treated with lambda phosphatase (lane 3). The blot was probed with anti-Phosphoserine/threonine mouse monoclonal at 1:250 (lane 1) or 1:1000 (lanes 2 & 3).Immunocytochemical labeling of phosphoserine and phosphothreonine in control and calyculin A-treated A431 cells. The cells were labeled with mouse monoclonal anti-Phosphoserine/threonine (PM3801) and rabbit polyclonal anti-Phosphoserine/threonine (PP2551), then the antibodies were detected using appropriate secondary antibodies conjugated to Cy3.
PhosphoSolutions Anti-Phosphoserine/threonine Antibody
$348
Paraformaldehyde-fixed zebrafish embryos were probed with anti-EphA4 (Tyr-602) (EP2731) then detected using Alexa Fluor 647 goat anti-rabbit. Arrows show labeling of somite boundaries and the notochord. (Image provided by Dr. Scott Holley at the Department of Molecular, Cellular and Developmental Biology, Yale University.)Western blot analysis of human umbilical vein endothelial cells untreated (lanes 1, 3, 5, & 7) or treated with pervanadate (1 mM) for 30 min. (lanes 2, 4, 6, & 8). The blot was probed with anti-EphA4 (N-terminal region) (lanes 1 & 2), anti-EphA4 (Tyr-779) (lanes 3 & 4), anti-EphA4 (Tyr-602) (lanes 5 & 6), or anti-EphA4 (C-terminal region) (lanes 7 & 8).
PhosphoSolutions Anti-EphA4 (Tyr-602) [conserved site], Phosphospecific Antibody
$348
Western blot of human A431 cells treated with Calyculin A (100 nM) for 30 min. Blot lanes were untreated (lanes 1 & 3) or treated with lambda phosphatase (lanes 2 & 4) then probed with anti-Arp2 (C-terminal) (lanes 1 & 2) or anti-Arp2 (Thr-237/Thr-238) (lanes 3 & 4).Immunocytochemical labeling of Arp2 phosphorylation in rat PC12 cells differentiated with NGF. The cells were probed with Arp2 (C-terminal region) and Arp2 (Thr-237/Thr-238) rabbit polyclonal antibodies, then the antibodies were detected using appropriate secondary antibody conjugated to Cy3.
PhosphoSolutions Anti-Arp2 (C-terminal region) Antibody
$348
Immunofluorescence of healthy human kidney. The antibody specifically labels pre-pro-vasopressin (white) in the collecting ducts (DBA, red), but not in the proximal tubules (LTL, green) of human kidney. DNA is labeled with DAPI (blue). Image kindly provided by JP Arroyo, Vanderbilt University.Western blot of mouse whole brain lysate showing specific immunolabeling of the ~20 kDa uncleaved pre-pro vasopressin protein.
PhosphoSolutions Anti-Pre-Pro-Vasopressin
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Western blot of mouse heart lysate showing specific immunolabeling of the ~25 kDa cardiac troponin I protein phosphorylated at Ser43 in the first lane (-). Phosphospecificity is shown in the second lane (+) where the immunolabeling is greatly decreased by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 minutes).
PhosphoSolutions Anti-Troponin I (cardiac) Ser43 Antibody
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Western blot of mouse heart lysate showing specific immunolabeling of ~25 kDa cardiac troponin I protein phosphorylated at Ser150 in the first lane (-). Phosphospecificity is shown in the second lane (+) where the immunolabeling is completely greatly decreased by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 minutes).
PhosphoSolutions Anti-Troponin I (cardiac) Ser150 Antibody
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Western blot of Jurkat cell lysate showing specific immunolabeling of the ~62 kDa p62 phosphorylated at Thr269/Ser272 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is blocked by preadsorption of the phosphopeptide used as antigen, but not by the corresponding non-phosphopeptide (not shown). AD293, A375 and MDA-MB-231 cells were treated with DMSO (control), or MG132 (2 μM), and Doramapimod (50 μM), alone or in combination for 14 h. The whole-cell lysates were subjected to western blot analysis with indicated antibodies. Image from publication CC-BY-4.0. PMID: 35840557
PhosphoSolutions Anti-p62 (Thr269, Ser272) Antibody
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Western blot of human T47D cells showing specific immunolabeling of the ~45 kDa MEK 1 protein phosphorylated at Thr386 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 min).
PhosphoSolutions Anti-MEK1 (Thr386) Antibody
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Western blot of HeLa cell lysate showing specific labeling of the ~95 kDa IR protein phosphorylated at Thr1160 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 min).
PhosphoSolutions Anti-Insulin Receptor (Thr1160) Antibody
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Western blot of PC-12 cell lysate incubated in the absence (-) and presence (+) of okadaic acid (OA, 1 µM for 60 min) showing specific immunolabeling of the ~60 kDa tyrosine hydroxylase phosphorylated at Ser31.
PhosphoSolutions Anti-Tyrosine Hydroxylase (Ser31) Antibody
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Immunostaining of cultured mouse caudate neurons showing synapsin I when phosphorylated at Ser9 (Cat. p1560-9, 1:500, red). Cells and photo courtesy of QBMCellScience.Western blot of rat cortical lysate showing specific immunolabeling of the ~78 kDa synapsin I phosphorylated at Ser9 in the first lane (-). Phosphospecificity is shown in the second lane (+) where the immunolabeling is completely eliminated by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 minutes).
PhosphoSolutions Anti-Synapsin I (Ser9) Antibody
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Western blot of rat neonatal brain lysate showing specific immunolabeling of the ~32 kDa form of the Olig2 protein phosphorylated at Ser10,13,14 in the first lane (-). Phosphospecificity is shown in the second lane (+) where Immunolabeling is blocked by the phosphopeptide used as the antigen but not by the corresponding non-phosphopeptide (not shown).
PhosphoSolutions Anti-Olig2 (Ser10/13/14) Antibody
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Western blot of mouse hippocampal lysate showing specific immunolabeling of the ~50 kDa eEF1A2 protein phosphorylated at Ser358 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by lysate treatment with lambda phosphatase (λ-Ptase, 800 units/1mg protein for 30 min).
PhosphoSolutions Anti-eEF1A2 (Ser358) Antibody
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Western blot of rat hippocampal lysate showing specific immunolabeling of the ~180 kDa NR2B subunit phosphorylated at Tyr1252 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by blot treatment with lambda phosphatase (λ-Ptase, 1200 units for 30 min).Immunostaining of 14 DIV rat cortical neurons showing NR2B phosphorylated at Tyr1252 (red, 1:400) and PSD95 (green). Photo courtesy of Gang Liu.
PhosphoSolutions Anti-NMDA NR2B Subunit (Tyr1252) Antibody
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Western blot of rat hippocampal lysate showing specific immunolabeling of the ~180 kDa NR2A subunit of the NMDAR phosphorylated at Tyr1325 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by lysate treatment with lambda phosphatase (400 units/100uL lysate for 30 min).
PhosphoSolutions Anti-NMDA NR2A Subunit (Tyr1325) Antibody
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Western blot of human T47D cells showing specific immunolabeling of the ~34 kDa cdc2 phosphorylated at Tyr15 (Control, Lane 1). Treatment with EGF (30 ng per ml for 30 min) caused dephosphorylation of the Tyr15 on cdc2 (Lane 2). Phosphospecificity is shown in lanes 3 and 4, where the immunolabeling is completely eliminated by blot treatment with lambda phosphatase, λ-Ptase (1200 units for 30 min).
PhosphoSolutions Anti-cdc2 (Tyr15) Antibody
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