Recombinant Human Semaphorin 3E Protein, CF Summary
Product Specifications
Thr25-Ser775 (Arg557Ala and Arg560Ala), with an N-terminal 10-His tag
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
3239-S3
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS and Tween® 20. |
Reconstitution | Reconstitute at 100 μg/mL in sterile PBS. |
Shipping | The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Reconstitution Calculator
Background: Semaphorin 3E
Semaphorin 3E (Sema3E), previously known as SemaH, is one of six Class 3 (secreted) semaphorins which function in axon guidance and/or vascular tip cell guidance during development (1). Sema3E contains a seven-blade beta -propeller sema domain, a cysteine-knot PSI domain, an Ig-like domain, and a basic region. Dimerization and cleavage within the basic region are required for the repulsing activity of class 3 semaphorins (2). Sema3E can also be cleaved at a furin consensus sequence C-terminal to the sema domain, resulting in a 61 kDa form that does not dimerize and is highly expressed in tumor cell lines with metastatic potential (3, 4). Mature human Sema3E shares 90% aa sequence identity with mouse and rat Sema3E. Alternative splicing generates a short isoform that lacks the signal peptide and the N-terminal 35 residues of the mature protein. Sema3E signaling is transduced by Plexin D1 which may also be associated with Neuropilin 1 and/or VEGF R2 (2, 5, 6). Its interaction with Plexin D1 inhibits axon migration in the neocortex and forebrain (6, 7), although it can attract axons that express both Plexin D1 and Neuropilin 1 (6). Sema3E promotes axonal growth (5), the development of glutamatergic synaptic specificity (8, 9), and the development of GnRH producing neurons (10). Genetic disruption of either Sema3E or Plexin D1 in mouse causes excessive and disorganized vascular growth and branching, indicating the importance of this ligand-receptor pair for vascular guidance (11, 12). In addition, Sema3E is up-regulated by inflammatory macrophages and damaged hepatocytes (13-15). It inhibits smooth muscle cell proliferation and migration in the asthmatic airway (16), promotes hepatic stellate cell activation and wound healing (15), and regulates the migration of developing thymocytes (17).
- Oh, W.J. and C. Gu (2013) Semin. Cell Dev. Biol. 24:156.
- Adams, R. H. et al. (1997) EMBO J. 16:6077.
- Christensen, C. et al. (2005) Cancer Res. 65:6167.
- Casazza, A. et al. (2010) J. Clin. Invest. 120:2684.
- Bellon, A. et al. (2010) Neuron 66:205.
- Chauvet, S. et al. (2007) Neuron 56:807.
- Bribian, A. et al. (2014) Nat. Commun. 5:4265.
- Ding, J.B. et al. (2011) Nat. Neurosci. 15:215.
- Pecho-Vrieseling, E. et al. (2009) Nature 459:842.
- Cariboni, A. et al. (2015) J. Clin. Invest. 125:2413.
- Gu, C. et al. (2005) Science 307:265.
- Gitler, A. D. et al. (2004) Developmental Cell 7:107.
- Wanschel, A. et al. (2013) Arterioscler. Thromb. Vasc. Biol. 33:886.
- Shimizu, I. et al. (2013) Cell Metab. 18:491.
- Yagai, T. et al. (2014) Am. J. Pathol. 184:2250.
- Movassagh, H. et al. (2014) J. Allergy Clin. Immunol. 133:560.
- Choi, Y.I. et al. (2014) Proc. Natl. Acad. Sci. USA 111:379.
Citations for Recombinant Human Semaphorin 3E Protein, CF
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.
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Breast cancer bone metastases are attenuated in a Tgif1-deficient bone microenvironment
Authors: MT Haider, H Saito, J Zarrer, K Uzhunnumpu, S Nagarajan, V Kari, M Horn-Gland, S Werner, E Hesse, H Taipaleenm
Breast Cancer Res., 2020-04-09;22(1):34.
Species: Human
Sample Types: Whole Cells
Applications: Migration Bioassay -
Coronary vasculature patterning requires a novel endothelial ErbB2 holoreceptor
Nat Commun, 2016-06-30;7(0):12038.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Arhgef15 promotes retinal angiogenesis by mediating VEGF-induced Cdc42 activation and potentiating RhoJ inactivation in endothelial cells.
Authors: Kusuhara, Sentaro, Fukushima, Yoko, Fukuhara, Shigetom, Jakt, Lars Mar, Okada, Mitsuhir, Shimizu, Yuri, Hata, Masayuki, Nishida, Kohji, Negi, Akira, Hirashima, Masanori, Mochizuki, Naoki, Nishikawa, Shin-Ich, Uemura, Akiyoshi
PLoS ONE, 2012-09-21;7(9):e45858.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Semaphorin 4A exerts a proangiogenic effect by enhancing vascular endothelial growth factor-A expression in macrophages.
Authors: Meda C, Molla F, De Pizzol M
J. Immunol., 2012-03-21;188(8):4081-92.
Species: Human
Sample Types: Whole Cells
Applications: Bioassay -
Sema3E-PlexinD1 signaling selectively suppresses disoriented angiogenesis in ischemic retinopathy in mice.
Authors: Fukushima Y, Okada M, Kataoka H
J. Clin. Invest., 2011-04-18;121(5):1974-85.
Species: Human, Mouse
Sample Types: In Vivo, Whole Cells
Applications: Bioassay, In Vivo
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