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Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Ser27-His901
Accession # Q9WVB4
Specificity
Clonality
Host
Isotype
Endotoxin Level
Scientific Data Images for Slit3 Antibody
Slit3 in 13 D.P.C. Mouse Embryo.
Slit3 was detected in immersion fixed paraffin-embedded sections of 13 d.p.c. mouse embryo using Goat Anti-Human/Mouse/Rat Slit3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3629) at 5 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Goat IgG VisUCyte™ HRP Polymer Antibody (VC004). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (CTS013). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to developing braiin and cartillage.Detection of Slit3 by Western Blot
VDC stimulates the expression of osteoblast‐specific proteins by the Wnt/SHN3 pathway. A) Representative images and corresponding quantitative analysis of immunofluorescence staining results of OCN and beta ‐catenin treated with 1, 5, and 10 µm VDC for 5 days (n = 5). Scale bar, 50 µm. B) Representative images and quantitative analysis of immunofluorescence staining of OCN and beta ‐catenin treated with VDC (5 µm) for 3 days, 5 days, and 8 days (n = 5). Scale bar, 50 µm. C) Representative images of western blot showing the expression levels of beta ‐catenin, NF‐ kappa B, GSK‐3 beta, phosphorylated (p)‐GSK‐3 beta, ERK1/2, p‐ERK1/2, Slit3 and normalized to the expression of GAPDH. Under induction conditions (50 µg mL−1 ascorbic acid and 5 mm beta ‐glycerophosphate), MC3T3‐E1 cells were cultured with VDC (1, 5, 10 µm) or 0.1% DMSO (control group) for 5 days. The solvent control group (Control) was treated with 0.1% DMSO (n = 3). D) Quantitative analysis of the relative protein expression for beta ‐catenin, NF‐ kappa B, p‐GSK‐3 beta and p‐ERK1/2 and Slit3. Data represent mean ± SD, ns: not significant, *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 versus the Control group by one‐way ANOVA with Tukey's post‐hoc test. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/40192033), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Slit3 Antibody
Immunohistochemistry
Sample: Immersion-fixed paraffin-embedded 13 d.p.c. mouse embryo
Neutralization
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: Slit3
References
- Yuan, W. et al. (1999) Dev. Biol. 212:290.
- Howitt, J. A. et al. (2004) EMBO J. 23:4406.
- Long, H. et al. (2004) Neuron 42:213.
- Greenberg, J. M. et al. (2004) Dev. Dyn. 230:350.
- Liu, J. et al. (2003) Mech. Dev. 120:1059.
- Yuan, W. et al. (2003) Proc. Natl. Acad. Sci. USA 100:5217.
- Little, M. H. et al. (2001) Am. J. Physiol. Cell Physiol. 281:C486.
Long Name
Alternate Names
Gene Symbol
UniProt
Additional Slit3 Products
Product Documents for Slit3 Antibody
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Slit3 Antibody
For research use only
Citations for Slit3 Antibody
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars