Plexin A1 (formerly Plexin 1) is a 200 kDa type I transmembrane protein that is a member of the Plexin family of Semaphorin signal transducers (1). Plexin signaling induces cytoskeletal remodeling, which mediates cell migration and axon repulsion (2). The mouse Plexin A1 cDNA encodes 1894 amino acids (aa) including a 27 aa signal sequence, a 1215 aa extracellular domain (ECD) with one Sema domain, a spacer, and four tandem IPT/TIG domains, a 21 aa transmembrane segment, and a 631 aa cytoplasmic domain (1). Within the ECD, human Plexin A1 shares 95%, 95%, 92%, 80% and 79% aa sequence identity with mouse, rat, bovine, chicken and Xenopus Plexin A1, respectively. The four mouse Plexin A molecules share 59‑67% aa identity with each other. Plexin A1 binds Class 3 (secreted) Semaphorins indirectly via Neuropilin (Npn)-1 and Npn-2, and binds transmembrane Semaphorin 6D directly (3‑5). Sema3A engagement of Plexin A1 and Npn-1 guides proprioceptive and sensory neurons during development, while Sema3B engagement guides floorplate neurons (5‑8). In contrast, T cell Sema6D engagement of dendritic cell Plexin A1 controls actin polymeration, which supports formation of immunological synapses and enhances the function of the dendritic cells (3, 4, 9). Complex formation with DAP12 allows Plexin A1 signaling through TREM family proteins (10, 11). However, the most striking effect of Plexin A1 deletion is on bone homeostasis, where Plexin A1-deficient mice show increased trabecular bone mass due to downregulated osteoclast differentiation (10). Plexin A1 and Sema6D are frequently expressed in malignant pleural mesothelioma, where they promote anchorage-independent growth through complexing with and activating VEGF R2 (12).
Human/Mouse Plexin A1 Antibody
R&D Systems | Catalog # AF4309
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Ser28-Pro1242
Accession # P70206
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human/Mouse Plexin A1 Antibody
Detection of Mouse Plexin A1 by Western Blot.
Western blot shows lysates of mouse embryonic heart tissue. PVDF Membrane was probed with 1 µg/mL of Mouse Plexin A1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4309) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF019). A specific band was detected for Plexin A1 at approximately 200 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.
Plexin A1 in Human Dendritic Cells.
Plexin A1 was detected in immersion fixed immature human dendritic cells using Goat Anti-Mouse Plexin A1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4309) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # NL001) and counterstained with DAPI (blue). Specific staining was localized to cell surfaces and cytoplasm. View our protocol for Fluorescent ICC Staining of Non-adherent Cells.
Plexin A1 in Mouse Spinal Cord.
Plexin A1 was detected in immersion fixed frozen sections of embryonic mouse spinal cord using Mouse Plexin A1 Affinity-purified Polyclonal Antibody (Catalog # AF4309) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS008) and counterstained with hematoxylin (blue). View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections.
Detection of Mouse Plexin A1 by Western Blot
Localization of PlexinA1 and Npn1 in the coronal sections of WT and PlexinA1 KO brains at E16.5 and E17.5.(A) Immunohistochemistry with anti-PlexinA1 antibody revealed the localization of PlexinA1 only in WT brains at E16.5 and E17.5 (a, b) as well as the lack of PlexinA1 in PlexinA1 KO brains (c, d). Scale bars: 200 μm. (B, C) Western blot analysis using anti-PlexinA1 antibodies was performed with tissue lysates from the medial regions covering the cingulate cortex, axons from the cingulate and neocortex, and the CC of E16.5 and E17.5 brains. PlexinA1 protein was detected in WT brains (B; E16.5, C; E17.5) but not in PlexinA1 KO brains (B; E16.5, C; E17.5). (D) Immunohistochemistry with anti-Npn1 antibodies revealed localization of Npn1 in both WT (a; E16.5, b; E17.5) and PlexinA1 KO (c; E16.5, d; E17.5) brains at E16.5 and E17.5. Scale bars: 200 μm. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/31430342), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Mouse Plexin A1 by Western Blot
Localization of PlexinA1 and Npn1 in the coronal sections of WT and PlexinA1 KO brains at E16.5 and E17.5.(A) Immunohistochemistry with anti-PlexinA1 antibody revealed the localization of PlexinA1 only in WT brains at E16.5 and E17.5 (a, b) as well as the lack of PlexinA1 in PlexinA1 KO brains (c, d). Scale bars: 200 μm. (B, C) Western blot analysis using anti-PlexinA1 antibodies was performed with tissue lysates from the medial regions covering the cingulate cortex, axons from the cingulate and neocortex, and the CC of E16.5 and E17.5 brains. PlexinA1 protein was detected in WT brains (B; E16.5, C; E17.5) but not in PlexinA1 KO brains (B; E16.5, C; E17.5). (D) Immunohistochemistry with anti-Npn1 antibodies revealed localization of Npn1 in both WT (a; E16.5, b; E17.5) and PlexinA1 KO (c; E16.5, d; E17.5) brains at E16.5 and E17.5. Scale bars: 200 μm. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/31430342), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Mouse Plexin A1 by Immunocytochemistry/ Immunofluorescence
Expression of Sema3A, NGF and BNDF receptors in adult TG and embryonic DRG neurons. The expression of Sema3A receptors (NRP1, NRP2, PlexinA1 and PlexinA3) and the NGF receptors TrkA, the BDNF receptor TrkB, and the neuropeptide CGRP in isolated TG and DRG neurons was evaluated by immunofluorescence staining. Representative images of TG neurons treated with Sema3A (A) show expression of all receptors both in the cell body as well as in the growing neurites. We found that 100% of neurons express the receptors and the neuropeptide CGRP. Similarly, all of these receptors were also expressed in DRG neurons treated with NGF (B). However, 100% of the neurons expressed NRP1, NRP2, PlexinA3, TrkA and CGRP, while 75% of the DRG neurons expressed PlexinA3 and TrkB. In general, there were no major differences in Sema3A receptor expression between the adult and embryonic sensory neurons. Additionally, no differences were observed in the expression of the neuropeptide CGRP. See Table 1 in “Materials and methods” for antibody information. All images were taken at same magnification, scale bar = 25 μm. The background effect generated by the secondary antibody (staining without primary antibody) is shown on Supplementary Fig. S4). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/34155284), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Mouse Plexin A1 by Immunocytochemistry/ Immunofluorescence
Expression of Sema3A, NGF and BNDF receptors in adult TG and embryonic DRG neurons. The expression of Sema3A receptors (NRP1, NRP2, PlexinA1 and PlexinA3) and the NGF receptors TrkA, the BDNF receptor TrkB, and the neuropeptide CGRP in isolated TG and DRG neurons was evaluated by immunofluorescence staining. Representative images of TG neurons treated with Sema3A (A) show expression of all receptors both in the cell body as well as in the growing neurites. We found that 100% of neurons express the receptors and the neuropeptide CGRP. Similarly, all of these receptors were also expressed in DRG neurons treated with NGF (B). However, 100% of the neurons expressed NRP1, NRP2, PlexinA3, TrkA and CGRP, while 75% of the DRG neurons expressed PlexinA3 and TrkB. In general, there were no major differences in Sema3A receptor expression between the adult and embryonic sensory neurons. Additionally, no differences were observed in the expression of the neuropeptide CGRP. See Table 1 in “Materials and methods” for antibody information. All images were taken at same magnification, scale bar = 25 μm. The background effect generated by the secondary antibody (staining without primary antibody) is shown on Supplementary Fig. S4). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/34155284), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human/Mouse Plexin A1 Antibody
Immunocytochemistry
Sample: Immersion fixed immature human dendritic cells
Immunohistochemistry
Sample: Immersion fixed frozen sections of embryonic mouse spinal cord
Western Blot
Sample: Mouse embryonic heart tissue
Formulation, Preparation, and Storage
Purification
Reconstitution
Sterile PBS to a final concentration of 0.2 mg/mL. 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: Plexin A1
References
- Kameyama, T. et al. (1996) Biochem. Biophys. Res. Commun. 226:524.
- Kruger, R.P. et al. (2005) Nat. Rev. Mol. Cell Biol. 6:789.
- Takamatsu, H. et al. (2010) Cell. Mol. Immunol. 7:83.
- O’Connor, B.P. and J.P.Y. Ting (2008) Immunol. Res. 41:217.
- Takahashi, T. et al. (1999) Cell 99:59.
- Yoshida, Y. et al. (2006) Neuron 52:775.
- Toyofuku, T. et al. (2005) Nat. Neurosci. 8:1712.
- Nawabi, H. et al. (2010) Genes Dev. 24:396.
- Eun, S-Y. et al. (2006) J. Immunol. 177:4271.
- Takegahara, N. et al. (2006) Nat. Cell Biol. 8:615.
- Watarai, H. et al. (2008) Proc. Natl. Acad. Sci. USA 105:2993.
- Catalano, A. et al. (2009) Cancer Res. 69:1485.
Alternate Names
Gene Symbol
UniProt
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Product Specific Notices for Human/Mouse Plexin A1 Antibody
For research use only
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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
- 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
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- 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 Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- 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 ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- 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
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars