Neural Stem Cell Marker (Nestin, SOX2, Occludin, E Cadherin, Hes1, Notch1) Antibody Panel - Mouse (ab254028) is part of the multiplex kits range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
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Required for brain and eye development. Promotes the disassembly of phosphorylated vimentin intermediate filaments (IF) during mitosis and may play a role in the trafficking and distribution of IF proteins and other cellular factors to daughter cells during progenitor cell division (By similarity). Required for survival, renewal and mitogen-stimulated proliferation of neural progenitor cells.
Hes1, Sox2, Ocln, Cdh1, Notch1
Nestin, Nes
Neural Stem Cell Marker (Nestin, SOX2, Occludin, E Cadherin, Hes1, Notch1) Antibody Panel - Mouse (ab254028) is part of the multiplex kits range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
Neural Stem Cell (Neuroepithelial) Marker Antibody Panel - Mouse ab254028 contains multiple trial-sized versions of anti-mouse antibody clones against Nestin, SOX2, Occludin, E Cadherin, Hes1, Notch1 specifically selected for high performance in various applications. This panel contains 4 recombinant rabbit monoclonal antibodies against mouse SOX2, Occludin, Hes1, Notch1, 1 rat monoclonal against E Cadherin and 1 mouse monoclonal against Nestin. They are provided as a sampler panel to allow you to easily evaluate each in your required applications.
For guidelines on how to use each antibody within the panel, please consult the individual datasheet for each antibody.
Panel contains:
- Mouse monoclonal [Rat 401] to Nestin (20 μg) ab6142
- Rabbit monoclonal [EPR3131] to SOX2 (20 μL) ab92494
- Rabbit monoclonal [EPR20992] to Occludin (20 μL) ab216327
- Rat monoclonal [DECMA-1] to E Cadherin (20 μg) ab11512
- Rabbit monoclonal [EPR4226] to Hes1 (20 μL) ab108937
- Rabbit monoclonal [EP1238Y] to Notch1 (20 μL) ab52627
Explore our range of antibody sample panels designed to provide you with a variety of trial-size antibodies in a convenient and cost-effective format.
Carrier-free formulations of our recombinant antibodies are also available for easy conjugation to labels of your choice and for multiplex applications. Use our intuitive search and select carrier-free or your label of choice. For bespoke conjugations or large volumes email bespoke@abcam.com.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
E-cadherin also known as cadherin-1 is a 120 kDa transmembrane protein important for cell-cell adhesion in epithelial tissues. It is primarily expressed in epithelial cells where it maintains cell structure and polarity. E-cadherin functions as an adhesion molecule in adherens junctions helping cells to bind tightly together. Nestin a marker of neural stem cells is an intermediate filament protein involved in cytoskeletal organisation with expression in neuronal precursor cells and certain adult stem cells. SOX2 a transcription factor weighing approximately 34 kDa plays a vital role in the regulation of embryonic stem cell pluripotency and neural progenitor cell maintenance. Notch1 Hes1 and Occludin each contribute to various physiological mechanisms. Notch1 a receptor around 300 kDa helps in cell fate determination while Hes1 serves as a transcriptional repressor in the Notch signaling pathway. Occludin about 65 kDa acts as an important player in forming tight junctions in epithelial and endothelial cells.
E-cadherin participates in maintaining the integrity and function of epithelial tissues. As part of the cadherin-catenin complex it connects the actin cytoskeleton to intercellular junctions creating a stable cell structure. Nestin contributes to cellular structural changes during neural development responding to environmental cues related to cell division and differentiation. SOX2's function centers around gene regulation necessary for sustaining pluripotency in multipotent cell populations. Notch1's involvement in cell differentiation signals within tissues with Hes1 functioning as part of feedback loops modulates downstream gene expression essential for developmental processes. Occludin forms part of the complex regulating paracellular permeability important for maintaining selective cellular barriers.
E-cadherin plays significant roles within the Wnt signaling pathway influencing processes related to cell fate and embryogenesis. This pathway also involves critical interactions with beta-catenin which stabilizes cell adhesion structures. Nestin engages in pathways related to neurogenesis guiding the specification and proliferation of neural stem cells. SOX2 is deeply integrated within both the pluripotency network and the Notch signaling pathway which cross-talks with other transcriptional regulators. Notch1 is an important component of the Notch signaling pathway affecting adjacent interactions between neighboring cells and often intersecting with Hes1 to influence gene expression patterns. Occludin participates in epithelial-mesenchymal transition pathways influencing cellular movement and plasticity.
Defects or dysregulation of E-cadherin are associated with cancer metastasis particularly in gastric and breast cancers where E-cadherin loss contributes to epithelial-mesenchymal transition. Nestin meanwhile provides markers for brain tumors and its abnormal expression links to certain aggressive cancer types. SOX2 has implications in ocular disorders notably those impairing vision due to developmental defects. Notch1 has links to T-cell acute lymphoblastic leukemia acting in concert with Hes1 to influence leukemogenesis. Occludin shows connection to inflammatory diseases like inflammatory bowel disease where its dysfunction may compromise the intestinal barrier.
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Lane 1 : Mouse E12 brain tissue lysate
Lane 2 : Mouse E14 brain tissue lysate
Lane 3 : Mouse E16 brain tissue lysate
Lane 4 : Mouse E18 brain tissue lysate
Lysates/proteins at 20 μg per lane.
Performed under reducing conditions.
Predicted band size: 200 kDa
This blot was produced using a 3-8% Tris-Acetate gel under the Tris-Acetate buffer system. The gel was run at 150V for 60 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with Anti-Nestin antibody [Rat-401] - Neural Stem Cell Marker ab6142 overnight at 4°C. Antibody binding was detected using Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) at 1/20000 dilution for 1 hour at room temperature before imaging.
Anti-Notch1 antibody [EP1238Y] (Anti-Notch1 antibody [EP1238Y] ab52627) at 1/2000 dilution (Purified) + Mouse brain at 10 μg
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Observed band size: 125 kDa
Blocking/Dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-Notch1 antibody [EP1238Y] (Anti-Notch1 antibody [EP1238Y] ab52627) at 1/2000 dilution
All lanes: Mouse brain at 10 µg
All lanes: HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 272 kDa
Observed band size: 110-120 kDa
Anti-E Cadherin antibody [DECMA-1] (Anti-E Cadherin antibody [DECMA-1] - Intercellular Junction Marker ab11512) used at a 1/5000 dilution for 16 hours at 4°C.
Goat polyclonal IRDye 800CW used as the secondary antibody at a 1/10,000 dilution.
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue labeling Occludin with Anti-Occludin antibody [EPR20992] ab216327 at 1/200 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Cytoplasmic staining on distal tubules of mouse kidney is observed. Counter stained with Hematoxylin.
Secondary antibody only control: Rabbit specific IHC polymer detection kit HRP/DAB ab209101 (Rabbit specific IHC polymer detection kit HRP/DAB).
Confocal image showing nuclear staining on F9 cells
Anti-SOX2 antibody [EPR3131] ab92494 staining SOX2 in the F9 (mouse embryonal carcinoma) cell line by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 4% PFA, permeabilized with 0.1% Triton-X. Samples were incubated with primary antibody (1/200). An Alexa Fluor® 488-conjugated Goat anti-Rabbit IgG, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 (1/1000) was used as the secondary antibody. Counterstained with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 anti-Tubulin (1/1000), Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 AlexaFluor®594 Goat anti-Mouse secondary (1/1000). DAPI was used as a nuclear counter stain.
Negative control 1 Anti-SOX2 antibody [EPR3131] ab92494 was used as the primary antibody at 1/200 and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 was used as the secondary at 1/1000.
Negative control 2 Ab7291was used as the primary antibody at 1/1000 and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 was used as the secondary at 1/1000.
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