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Human R-Spondin 1 Affinity Purified PAb (25 UG)

货号: AF4645-SP 基本售价: 1407.8 元 规格: -

产品信息

概述
货号AF4645-SP
别名Cristin 3; CRISTIN3; FLJ40906Roof plate-specific spondin-1; hRspo1; roof plate-specific spondin; RSPO; RSPO1; R-spondin homolog (Xenopus laevis); RSPONDIN; R-spondin1; R-spondin-1
全称Roof Plate-specific Spondin 1
反应种属Human
应用Neutralization
目标/特异性Detects human R-Spondin 1 in direct ELISAs. In direct ELISAs, approximately 6% cross-reactivity with recombinant mouse R-Spondin 1 is observed and less than 1% cross-reactivity with recombinant human (rh) R-Spondin 2, rhR-Spondin 3, and rhR-Spondin 4 is observed.
使用方法Neutralization: Measured by its ability to neutralize R‑Spondin 1-induced activation of beta ‑Catenin response in the HEK293T human embryonic kidney cell line in a Topflash Luciferase assay. The Neutralization Dose (ND50) is typically 3-12 µg/mL in the presence of 100 ng/mL Recombinant Human R‑Spondin 1 and 5 ng/mL Recombinant Mouse Wnt‑3a.
来源Polyclonal Sheep IgG
产品组分
性能
供应商R&D Systems
Entrez Gene IDs284654 (Human); 192199 (Mouse)
应用文献
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.

R-Spondin1/LGR5 Activates TGF? Signaling and Suppresses Colon Cancer Metastasis
Authors: X Zhou, L Geng, D Wang, H Yi, G Talmon, J Wang
Cancer Res., 2017;0(0):.
Species: Human
Sample Type: Whole Cells
Application: Neut

纯化方式Antigen Affinity-purified
免疫原Chinese hamster ovary cell line CHO-derived human R-Spondin 1
Arg31-Ala263
Accession # Q2MKA7
内毒素水平<0.10 EU per 1 μg of the antibody by the LAL method.
生物活性Human
标记Unconjugated
溶解方法Sterile PBS to a final concentration of 0.2 mg/mL.
背景

R-Spondin 1 (RSPO1, Roof plate-specific Spondin 1), also known as cysteine-rich and single thrombospondin domain containing protein 3 (Cristin 3), is a 27 kDa secreted protein that shares ~40% amino acid (aa) identity with three otherR-Spondin family members (1, 2). All R-Spondins regulate Wnt/ beta -catenin signaling, but have distinct expression patterns (1‑3). Like other R-Spondins, R-Spondin 1 contains two adjacent cysteine-rich furin-like domains (aa 34‑135) with one potential N‑glycosylation site, followed by a thrombospondin (TSP-1) motif (aa 147‑207) and a region rich in basic residues (aa 211‑263). Only the furin-like domains are needed for beta -catenin stabilization (2, 4). A putative nuclear localization signal at the C-terminus may allow some expression in the nucleus (5). Potential isoforms of 200 and 236 aa have an alternate, shorter N‑terminus or are missing aa 146‑208, respectively (6). Over aa 21‑263, human R-Spondin 1 shares 89%, 87%, 92%, 91%, 91% and 89% aa identity with mouse, rat, equine, canine, caprine and bovine R-Spondin 1, respectively. R-Spondin 1 is expressed in early development at the roof plate boundary and is thought to contribute to dorsal neural tube development (3, 5). In humans, rare disruptions of the R-Spondin 1 gene are associated with tendencies for XX sex reversal (phenotypic male) or hermaphroditism, indicating a role for R-Spondin 1 in gender-specific differentiation (7, 8). Disruption is also associated with palmoplantar keratosis (7, 8). Postnatally, R-Spondin 1 is expressed by neuroendocrine cells in the intestine, adrenal gland and pancreas, and by epithelia in kidney and prostate (9). Injection of recombinant R-Spondin 1 in mice causes activation of beta -catenin and proliferation of intestinal crypt epithelial cells, and ameliorates experimental colitis (9, 10). R-Spondin 1 regulates Wnt/ beta -catenin by competing with the Wnt antagonist DKK-1 for binding to the Wnt co-receptors, Kremen and LRP-6, reducing their DKK-1-mediated internalization (11). Reports differ on whether R-Spondin 1 binds LRP-6 directly (11‑13).

运输条件Blue Ice
存放说明4℃
参考文献
  1. Chen, J-Z. et al. (2002) Mol. Biol. Rep. 29:287.
  2. Kim, K.-A. et al. (2006) Cell Cycle 5:23.
  3. Nam, J.-S. et al. (2007) Gene Expr. Patterns 7:306.
  4. Kazanskaya, O. et al. (2004) Dev. Cell 7:525.
  5. Kamata, T. et al. (2004) Biochim. Biophys. Acta 1676:51.
  6. Entrez accession # EAX07331, ABA54598.
  7. Tomaselli, S. et al. (2008) Hum. Mutat. 29:220.
  8. Parma, P. et al. (2006) Nat. Genet. 38:1304.
  9. Kim, K.-A. et al. (2005) Science 309:1256.
  10. Zhao, J. et al. (2007) Gastroenterology 132:1331.
  11. Binnerts, M.E. et al. (2007) Proc. Natl. Acad. Sci. USA 104:14700.
  12. Nam, J.-S. et al. (2006) J. Biol. Chem. 281:13247.
  13. Wei, Q. et al. (2007) J. Biol. Chem. 282:15903.