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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| rp146167-10μg |
10μg |
现货 ![]() |
| |
| rp146167-50μg |
50μg |
现货 ![]() |
| |
| rp146167-100μg |
100μg |
现货 ![]() |
| |
| rp146167-1mg |
1mg |
期货 ![]() |
|
| 产品名称 | Recombinant Human Frizzled-4 Protein |
|---|---|
| 别名 | 卷曲同源物4(FZD4)重组蛋白 |
| 英文别名 | Fz-4 | FzE4 | hFz4 | CD344 | CD344 antigen | EVR1 | exudative vitreoretinopathy 1 | FEVR | frizzled (Drosophila) homolog 4 | frizzled homolog 4 (Drosophila) | Frizzled4 | Frizzled-4 | Fz-4 | FZD4 | FZD4S | FzE4 | GPCR | hFz4 | MGC34390 | WNT receptor friz |
| 规格或纯度 | ActiBioPure™, 生物活性, 无动物源, Carrier Free, ≥95%(SDS-PAGE) |
| 产品介绍 |
Receptor for Wnt proteins. Most of frizzled receptors are coupled to the beta-catenin (CTNNB1) canonical signaling pathway, which leads to the activation of disheveled proteins, inhibition of GSK-3 kinase, nuclear accumulation of beta-catenin (CTNNB1) and activation of Wnt target genes. Plays a critical role in retinal vascularization by acting as a receptor for Wnt proteins and norrin (NDP). In retina, it can be both activated by Wnt protein-binding, but also by a Wnt-independent signaling via binding of norrin (NDP), promoting in both cases beta-catenin (CTNNB1) accumulation and stimulation of LEF/TCF-mediated transcriptional programs. A second signaling pathway involving PKC and calcium fluxes has been seen for some family members, but it is not yet clear if it represents a distinct pathway or if it can be integrated in the canonical pathway, as PKC seems to be required for Wnt-mediated inactivation of GSK-3 kinase. Both pathways seem to involve interactions with G-proteins. May be involved in transduction and intercellular transmission of polarity information during tissue morphogenesis and/or in differentiated tissues.
|
| 生物活性 | Measured by its binding ability in a functional ELISA. In a 100 µL reaction mixture containing biotinylated rmWnt-5a at 100 ng/mL and rhFrizzled-4/Fc Chimera dilutions at 0.1-2,000 ng/mL, the concentration of rhFrizzled-4/Fc Chimera that produces 50% of the optimal binding response is found to be approximately 15-60 ng/mL. |
| 内毒素水平 | <0.1 EU/μg |
| 表达系统 | HEK293 |
| 种属 | 人(Human) |
| 氨基酸 | 37-180 aa |
| 序列 | FGDEEERRCDPIRISMCQNLGYNVTKMPNLVGHELQTDAELQLTTFTPLIQYGCSSQLQFFLCSVYVPMCTEKINIPIGPCGGMCLSVKRRCEPVLKEFGFAWPESLNCSKFPPQNDHNHMCMEGPGDEEVPLPHKTPIQPGEEENLYFQGMDPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKHHHHHH |
| 蛋白标签 | C-hFc & His |
| 无载体 | Yes |
| 无动物源 | Yes |
| Accession # | Q9ULV1 |
| 来源 | 重组表达 |
| 预测分子量 | 44.1 kDa |
| SDS-PAGE | 55 kDa, under reducing conditions; 115 kDa, under non-reducing conditions. |
| 物理形态 | 冻干(Lyophilized) |
|---|---|
| 储存缓冲液 | Lyophilized from 10mM PBS, 5% Trehalose, 5% Mannitol, pH 7.4 |
| 复溶 | Reconstitute in sterile water to a concentration of 0.1-0.5 mg/ml. |
| 储存温度 | -20°C储存,避免反复冻融 |
| 运输条件 | 超低温冰袋运输 |
| 稳定性与储存 | 在 -20~-80℃ 下可保存 1 年以上。收货后建议分装。避免冷冻/解冻循环。 |
| 分子类型 | 蛋白质 |
Recombinant Human Frizzled-4 Protein (rp146167) - SDS-PAGE
2 μg/lane of Recombinant Human Frizzled-4 Protein was resolved with SDS-PAGE under reducing (R) and non-reducing (N) conditions and visualized by Coomassie® Blue staining, showing the band at 55 kDa under reducing condition and 115 kDa under non-reducing condition.
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | rp146167 | |
| 分析证书 | rp146167 | |
| 分析证书 | rp146167 |
| 1. Kirikoshi H, Sagara N, Koike J, Tanaka K, Sekihara H, Hirai M, Katoh M. (1999) Molecular cloning and characterization of human Frizzled-4 on chromosome 11q14-q21.. Biochem Biophys Res Commun, 264 (3): (955-61). [PMID:10544037] |
| 2. Xu Q, Wang Y, Dabdoub A, Smallwood PM, Williams J, Woods C, Kelley MW, Jiang L, Tasman W, Zhang K et al.. (2004) Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair.. Cell, 116 (6): (883-95). [PMID:15035989] |
| 3. Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME. (2002) Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.. Nat Genet, 32 (326-330). [PMID:12172548] |
| 4. Yoshida S, Arita R, Yoshida A, Tada H, Emori A, Noda Y, Nakao S, Fujisawa K, Ishibashi T. (2004) Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy.. Am J Ophthalmol, 138 (4): (670-1). [PMID:15488808] |
| 5. Qin M, Hayashi H, Oshima K, Tahira T, Hayashi K, Kondo H. (2005) Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.. Hum Mutat, 26 (2): (104-12). [PMID:15981244] |
| 6. MacDonald ML, Goldberg YP, Macfarlane J, Samuels ME, Trese MT, Shastry BS. (2005) Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.. Clin Genet, 67 (4): (363-6). [PMID:15733276] |
| 7. Kondo H, Hayashi H, Oshima K, Tahira T, Hayashi K. (2003) Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity.. Br J Ophthalmol, 87 (10): (1291-5). [PMID:14507768] |
| 8. Tanaka S, Akiyoshi T, Mori M, Wands JR, Sugimachi K. (1998) A novel frizzled gene identified in human esophageal carcinoma mediates APC/beta-catenin signals.. Proc Natl Acad Sci USA, 95 (17): (10164-9). [PMID:9707618] |
| 9. Yang S, Wu Y, Xu TH, de Waal PW, He Y, Pu M, Chen Y, DeBruine ZJ, Zhang B, Zaidi SA et al.. (2018) Crystal structure of the Frizzled 4 receptor in a ligand-free state.. Nature, 560 (7720): (666-670). [PMID:30135577] |
| 10. Riccio G, Bottone S, La Regina G, Badolati N, Passacantilli S, Rossi GB, Accardo A, Dentice M, Silvestri R, Novellino E et al.. (2018) A Negative Allosteric Modulator of WNT Receptor Frizzled 4 Switches into an Allosteric Agonist.. Biochemistry, 57 (5): (839-851). [PMID:29293331] |
| 11. Generoso SF, Giustiniano M, La Regina G, Bottone S, Passacantilli S, Di Maro S, Cassese H, Bruno A, Mallardo M, Dentice M et al.. (2015) Pharmacological folding chaperones act as allosteric ligands of Frizzled4.. Nat Chem Biol, 11 (4): (280-6). [PMID:25751279] |
| 12. Todd D Taylor,Hideki Noguchi,Yasushi Totoki,Atsushi Toyoda,Yoko Kuroki,Ken Dewar,Christine Lloyd,Takehiko Itoh,Tadayuki Takeda,Dae-Won Kim,Xinwei She,Karen F Barlow,Toby Bloom,Elspeth Bruford,Jean L Chang,Christina A Cuomo,Evan Eichler,Michael G FitzGerald,David B Jaffe,Kurt LaButti,Robert Nicol,Hong-Seog Park,Christopher Seaman,Carrie Sougnez,Xiaoping Yang,Andrew R Zimmer,Michael C Zody,Bruce W Birren,Chad Nusbaum,Asao Fujiyama,Masahira Hattori,Jane Rogers,Eric S Lander,Yoshiyuki Sakaki. (2006-03-24) Human chromosome 11 DNA sequence and analysis including novel gene identification.. Nature, 440 ((7083)): (497-500). [PMID:16554811] |
| 13. Toomes, Carmel C and 12 more authors.. (2004) Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.. Investigative ophthalmology & visual science, [PMID:15223780] |
| 14. Omoto, Satoshi S, Hayashi, Takaaki T, Kitahara, Kenji K, Takeuchi, Tomokazu T and Ueoka, Yasuo Y.. (2004) Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R).. Ophthalmic genetics, [PMID:15370539] |
| 15. Nallathambi, Jeyabalan J and 5 more authors.. (2006) Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.. Molecular vision, (21): [PMID:17093393] |
| 16. Qin, Minghui M, Kondo, Hiroyuki H, Tahira, Tomoko T and Hayashi, Kenshi K.. (2008) Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.. Human genetics, [PMID:17955262] |
| 17. Robitaille, Johane M JM and 6 more authors.. (2009) Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees.. Ophthalmic genetics, [PMID:19172507] |
| 18. Boonstra, F Nienke FN and 10 more authors.. (2009) Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy.. Investigative ophthalmology & visual science, [PMID:19324841] |
| 19. Ells, Anna A and 11 more authors.. (2010) Severe retinopathy of prematurity associated with FZD4 mutations.. Ophthalmic genetics, [PMID:20141357] |
| 20. Nikopoulos, Konstantinos K and 16 more authors.. (2010) Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP.. Human mutation, [PMID:20340138] |
| 21. Hao, Huai-Xiang HX and 18 more authors.. (2012) ZNRF3 promotes Wnt receptor turnover in an R-spondin-sensitive manner.. Nature, (29): [PMID:22575959] |
| 22. Capurro, Mariana M, Martin, Tonya T, Shi, Wen W and Filmus, Jorge J.. (2014) Glypican-3 binds to Frizzled and plays a direct role in the stimulation of canonical Wnt signaling.. Journal of cell science, (1): [PMID:24496449] |