Mouse Monoclonal Nestin antibody. Neural Crest Stem Cell marker. Suitable for IHC-P, WB and reacts with Mouse, Rat samples. Cited in 228 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS, 6.97% L-Arginine
IHC-P | WB | IHC-Fr | |
---|---|---|---|
Human | Not recommended | Not recommended | Not recommended |
Mouse | Tested | Tested | Not recommended |
Rat | Tested | Tested | Not recommended |
Cat | Not recommended | Not recommended | Not recommended |
Monkey | Not recommended | Not recommended | Not recommended |
Sheep | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 0.05000-1.00000 µg/mL | Notes Tissue fixed with 4% paraformaldehyde at pH 7.4 for light microscopy. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Rat | Dilution info 0.05000-1.00000 µg/mL | Notes Tissue fixed with 4% paraformaldehyde at pH 7.4 for light microscopy. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Monkey | Dilution info - | Notes Tissue fixed with 4% paraformaldehyde at pH 7.4 for light microscopy. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Cat | Dilution info - | Notes Tissue fixed with 4% paraformaldehyde at pH 7.4 for light microscopy. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Sheep | Dilution info - | Notes Tissue fixed with 4% paraformaldehyde at pH 7.4 for light microscopy. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1 µg/mL | Notes Block with milk or BSA but do not dilute primary antibody in buffer containing milk. |
Species Rat | Dilution info 1 µg/mL | Notes Block with milk or BSA but do not dilute primary antibody in buffer containing milk. |
Species | Dilution info | Notes |
---|---|---|
Species Monkey | Dilution info - | Notes Block with milk or BSA but do not dilute primary antibody in buffer containing milk. |
Species Cat | Dilution info - | Notes Block with milk or BSA but do not dilute primary antibody in buffer containing milk. |
Species Sheep | Dilution info - | Notes Block with milk or BSA but do not dilute primary antibody in buffer containing milk. |
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat, Monkey, Cat, Sheep | Dilution info - | Notes - |
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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.
Nestin, Nes
Mouse Monoclonal Nestin antibody. Neural Crest Stem Cell marker. Suitable for IHC-P, WB and reacts with Mouse, Rat samples. Cited in 228 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS, 6.97% L-Arginine
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Nestin also known as NES is an intermediate filament protein with a molecular weight of about 220 kDa. Nestin features prominently in cells related to the nervous system including neural stem cells and it serves as a structural component in these cells. Nestin also appears in substantial amounts during the development of the nervous system and is important for cell structural organization. It is often used as a Nestin marker in research particularly with Nestin antibodies for identifying the presence of neural stem cells and tracking their developmental course. Researchers frequently utilize techniques like Nestin IHC (immunohistochemistry) and Nestin western blot to stain and detect Nestin allowing detailed investigations into its expression in various tissues.
Nestin plays a significant role in the dynamic remodeling of the cytoskeleton. It does not act as a solitary element but forms part of a larger protein complex involved in maintaining and organizing cellular structure. This property grants cells flexibility in shape and resilience during the rapid changes in development and specialization. The role of Nestin in the cellular architecture allows it to contribute to processes such as cell migration and proliferation critical during tissue development and repair.
Nestin integrates into networks that regulate stem cell behavior and neurogenesis. It tightly interacts within the pathways involving cell cycle regulation and differentiation. For example the Wnt and Notch signaling pathways modulate its expression to influence neural stem cell fate and patterning during development. Protein interactions between Nestin and other cytoskeletal elements like vimentin facilitate its roles in these pathways adapting the cellular environment for specific developmental activities.
Nestin associates with various pathological conditions including brain tumors and muscular dystrophies. Its expression is aberrant in many forms of gliomas where it often signifies a higher grade of malignancy. Within these tumors Nestin connects to oncogenic signaling pathways involving proteins such as the epidermal growth factor receptor (EGFR). Moreover in muscular dystrophies Nestin's expression in regenerating muscle fibers illustrates its involvement in cellular repair mechanisms potentially interacting with dystrophin a protein important for muscle integrity. Research on anti-Nestin antibodies continues to clarify its role in these diseases potentially offering diagnostic or therapeutic insights.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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ab6142 staining adult mouse brain tissue section by Immunohistochemistry (Formalin/PFA-fixed, paraffin embedded sections). Tissue underwent fixation in paraformaldehyde, heat mediated antigen retrieval in Sodium Citrate, permeabilization in 1% Triton buffer and blocking in 10% serum for 1 hour at 25°C. The primary antibody, diluted 1/200 (PBS, 2% Donkey serum, 0.2% Triton) for 16 hours at 4°C. An Alexa Fluor® 488 conjugated donkey polyclonal to mouse Ig, diluted 1/500 was used as the secondary.
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 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.
All lanes: Western blot - Anti-Nestin antibody [Rat-401] - Neural Stem Cell Marker (ab6142) at 1 µg/mL
Lane 1: Mouse E12 brain tissue lysate at 20 µg
Lane 2: Mouse E14 brain tissue lysate at 20 µg
Lane 3: Mouse E16 brain tissue lysate at 20 µg
Lane 4: Mouse E18 brain tissue lysate at 20 µg
Lane 5: Rat E12 brain tissue lysate at 20 µg
Lane 6: Rat E14 brain tissue lysate at 20 µg
Lane 7: Rat E16 brain tissue lysate at 20 µg
Lane 8: Rat E18 brain tissue lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 177 kDa
REST expression in N-hREST mouse brains correlates with stemness in embryonic neural stem cells. Immunofluorescence analysis of E18.5 N-hREST and LSL-hRESTcontrol littermate mouse brains with antibodies against REST (using an antibody that preferentially recognizes hREST over mouse REST) and Nestin (using ab6142)
Mice were anesthetized and perfused with phosphate-buffered saline followed by 4% paraformaldehyde (PFA). Brain tissues were then dissected and fixed in 4% PFA overnight at 4 °C. Fixed brain tissues were processed for paraffin embedding and then cut into 5-μm sections.
IHC image of Nestin staining in a section of formalin-fixed paraffin-embedded normal rat brain performed on a Leica BONDTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20mins. The section was then incubated with ab6142, 0.05ug/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with hematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
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