Neuron-specific beta -III Tubulin PerCP-conjugated Antibody
Neuron-specific beta -III Tubulin PerCP-conjugated Antibody Summary
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of beta ‑III Tubulin in HepG2 cells by Flow Cytometry. HepG2 cells were stained with Mouse Anti-Neuron-specific beta ‑III Tubulin PerCP‑conjugated Monoclonal Antibody (Catalog # IC1195C, filled histogram) or isotype control antibody (Catalog # IC003C, open histogram). To facilitate intracellular staining, cells were fixed with [[catalogNumber:FC012 ]]and permeabilized with FoxP3 Perm. View our protocol for Staining Intracellular Molecules.
Detection of beta ‑III Tubulin in Rat Cortical Stem Cells by Flow Cytometry. Eight-day differentiated Rat cortical stem cells were stained with Mouse Anti-Neuron-specific beta -III Tubulin PerCP-conjugated Monoclonal Antibody (IC1195C, filled histogram) or isotype control antibody (IC003C, open histogram). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (FC005). View our protocol for Staining Intracellular Molecules.
Detection of Human beta-III Tubulin by Flow Cytometry Flow cytometry analysis of neuronal cells from mock- and LACV-infected COs. Mock- (a–d) and LACV-infected (e–h) COs were non-enzymatically digested into a single cell suspension and analyzed via flow cytometry as described in the “Methods” section. Two representative examples are shown. Live cells were identified and interrogated for expression of activated poly-caspases (y-axis) and LACV expression (x-axis). a, e Active caspase and LACV staining from the whole live cell population. Gating within the whole live cell population for Sox2 (b, f), DCX (c, g) and beta III tubulin-positive cells allowed for examination of active poly-caspase and LACV staining within each neuronal population. Proportions of LACV-infected (i), activated poly-caspase (j), and LACV-infected/activated poly-caspase double-positive (k) neuronal cells within mock (closed circles) or infected (open squares) COs are shown. A two-way ANOVA with a Sidak’s multiple comparisons test was used to determine significance. **p < 0.001, ****p < 0.0001 Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/31739796), licensed under a CC-BY license. Not internally tested by R&D Systems.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: beta-III Tubulin
beta -III Tubulin, also known as tubulin beta -4, is regarded as a neuron-specific marker. The expression of beta -III Tubulin has been suggested to be one of the earliest markers to signal neuronal commitment in primitive neuroepithelium.
Product Datasheets
Citation for Neuron-specific beta -III Tubulin PerCP-conjugated Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
1 Citation: Showing 1 - 1
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Neuronal maturation reduces the type I IFN response to orthobunyavirus infection and leads to increased apoptosis of human neurons
Authors: CW Winkler, TA Woods, BR Groveman, AB Carmody, EE Speranza, CA Martens, SM Best, CL Haigh, KE Peterson
J Neuroinflammation, 2019-11-18;16(1):229.
Species: Human
Sample Types: Organoid
Applications: Flow Cytometry
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