Human F-Spondin/SPON1 Antibody Summary
Phe29-Cys807
Accession # Q9HCB6
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 Human F-Spondin/SPON1 antibody by Western Blot. Detection of Human F-Spondin/SPON1 antibody by Western Blot.](https://resources.rndsystems.com/images/datasheets/antibody/FSpondin_AF3135_Western_Blot_20824.jpg)
Detection of Human F‑Spondin/SPON1 by Western Blot. Western blot shows lysates of OVCAR-3 human ovarian carcinoma cell line. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human F-Spondin/SPON1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3135) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF017). A specific band was detected for F-Spondin/ SPON1 at approximately 110 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
![Detection of Human F-Spondin/SPON1 antibody by Simple Western<sup>TM</sup>. Detection of Human F-Spondin/SPON1 antibody by Simple Western<sup>TM</sup>.](https://resources.rndsystems.com/images/datasheets/antibody/FSpondin_AF3135_Simple_Western_20927.jpg)
Detection of Human F‑Spondin/SPON1 by Simple WesternTM. Simple Western lane view shows lysates of OVCAR-3 human ovarian carcinoma cell line, loaded at 0.2 mg/mL. A specific band was detected for F-Spondin/SPON1 at approximately 134 kDa (as indicated) using 10 µg/mL of Goat Anti-Human F-Spondin/SPON1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3135) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
Reconstitution Calculator
Preparation and 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.
Background: F-Spondin/SPON1
F-Spondin (“Floor plate” and “thrombospondin” homology; also Spondin-1 and VSGP) is a member of the F-Spondin family of proteins that collectively belong to a subgroup of TSR (thrombospondin) type I class molecules (1). Class I molecules are either membrane-bound or ECM-associated. F-Spondin is a 110 kDa, secreted, heparin-binding extracellular matrix glycoprotein first characterized in rat for its high expression in embryonic floor plate (2‑4). Human F-Spondin is synthesized as an 807 amino acid (aa) precursor that contains a 28 aa signal sequence and a 779 aa mature region (3, 4). The mature region includes an N-terminal reelin-like domain (aa 1‑200), a centrally placed F-Spondin (FS) type segment (aa 201‑440), and six C-terminal class 2 thrombospondin type I repeats (1, 3, 5). Class 1 and 2 repeats differ in the placement of their cysteine residues. The fifth and sixth TSP repeats (aa 668‑806) apparently bind ECM, while TSP repeats 1‑4 (aa 442‑666), plus the spondin segment, are suggested to mediate either repulsive activity (on motor neurons), or outgrowth promoting activity (on sensory neurons) (1, 6). At least two isoforms of F-Spondin are known. Both are proteolytically-generated, one by plasmin, another by an unidentified protease. Plasmin cleaves the C-terminus at two points, generating a soluble, 95 kDa, 656 aa F‑Spondin that contains all but TSP repeats #5 and 6 (7). The unidentified protease appears to cleave F-Spondin between the FS segment and the first TSP repeat, generating 60 kDa and 50 kDa fragments, respectively (6). F-Spondin shows highly unusual glycosylation, exhibiting both C-mannosylation (mannose bound to Trp) and O-fucosylation (fucose bound to Ser/Thr) (4). The significance of these glycosidic modifications is unknown. Mature human F-Spondin is 98%, 97%, 98%, and 97% aa identical to mature canine, rat, bovine and mouse F-Spondin, respectively. Mammalian cells known to express F‑Spondin include floor plate epithelium, ventral motor neurons, Schwann cells, fibroblasts, hippocampal pyramidal cells, endothelial cells, vascular smooth muscle cells and some tumor cells (6, 8, 9).
- Feinstein, Y. and A. Klar (2004) Int. J. Biochem. Cell Biol. 36:975.
- Klar, A. et al. (1992) Cell 69:95.
- Miyamoto, K. et al. (2001) Arch. Biochem. Biophys. 390:93.
- Gonzalez de Peredo, A. et al. (2002) Mol. Cell. Proteomics 1:11.
- Adams, J.C. and R.P. Tucker (2000) Dev. Dyn. 218:280.
- Burstyn-Cohen, T. et al. (1998) J. Neurosci. 18:8875.
- Tzarfaty-Majar, V. et al. (2001) J. Biol. Chem. 276:28233.
- Feinstein, Y. et al. (1999) Development 126:3637.
- Pyle-Chenault, R.A. et al. (2005) Tumor Biol. 26:245.
- Mattes, J. and P.S. Foster (2003) Curr. Drug Targets Inflamm. Allergy 2:169.
Product Datasheets
Citations for Human F-Spondin/SPON1 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.
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F-Spondin Is the Signal by Which 2-Methoxyestradiol Induces Apoptosis in the Endometrial Cancer Cell Line Ishikawa
Authors: Ramiro Rincón-Rodriguez, Dennise Mena, Javier Mena, Patricia Díaz-Saldivar, Emanuel Guajardo-Correa, Carlos Godoy-Guzman et al.
International Journal of Molecular Sciences
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A multiplex immunoassay of serum biomarkers for the detection of uveal melanoma
Authors: J Song, SL Merbs, LJ Sokoll, DW Chan, Z Zhang
Clin Proteomics, 2019-03-05;16(0):10.
Species: Human
Sample Types: Serum
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