FITC标记的RSPO4蛋白抗体
产品名称: FITC标记的RSPO4蛋白抗体
英文名称: Anti-RSPO4/FITC
产品编号: HZ-18878R-FITC
产品价格: null
产品产地: 中国/上海
品牌商标: HZbscience
更新时间: 2023-08-17T10:24:20
使用范围: ICC=1:50-200 IF=1:50-200
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Rabbit Anti-RSPO4/FITC Conjugated antibody
FITC标记的RSPO4蛋白抗体
英文名称 | Anti-RSPO4/FITC |
中文名称 | FITC标记的RSPO4蛋白抗体 |
别 名 | C20orf182; CRISTIN4; hRspo4; R-spondin family, member 4; R-spondin-4; Roof plate-specific spondin-4; RSPO4; RSPO4_HUMAN. |
规格价格 | 100ul/2980元 购买 大包装/询价 |
说 明 书 | 100ul |
研究领域 | 细胞生物 发育生物学 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, Pig, Cow, Horse, Sheep, |
产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 24kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human RSPO4 |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
产品介绍 | background: This gene encodes a member of the R-spondin family of proteins that share a common domain organization consisting of a signal peptide, cysteine-rich/furin-like domain, thrombospondin domain and a C-terminal basic region. The encoded protein may be involved in activation of Wnt/beta-catenin signaling pathways. Mutations in this gene are associated with anonychia congenital. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009] Function: Activator of the beta-catenin signaling cascade, leading to TCF-dependent gene activation. Acts both in the canonical Wnt/beta-catenin-dependent pathway, possibly via a direct interaction with Wnt proteins, and in a Wnt-independent beta catenin pathway through a receptor signaling pathway that may not use frizzled/LRP receptors. Subcellular Location: Secreted. Post-translational modifications: Tyr-112 may be phosphorylated; however as this position is probably extracellular, the vivo relevance is not proven. DISEASE: Defects in RSPO4 are the cause of anonychia congenita (ANONC) [MIM:206800]. A rare condition characterized by the absence or severe hypoplasia of all fingernails and toenails without significant bone anomalies. Similarity: Belongs to the R-spondin family. Contains 1 FU (furin-like) repeat. Contains 1 TSP type-1 domain. Database links: Entrez Gene: 343637 Human Entrez Gene: 228770 Mouse Entrez Gene: 499918 Rat Omim: 610573 Human SwissProt: Q2I0M5 Human SwissProt: Q8BJ73 Mouse Unigene: 444980 Human Unigene: 159868 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
该基因编码一个蛋白家族的成员,该家族成员共有一个由信号肽、富含半胱氨酸/呋喃样结构域、凝血酶敏感蛋白结构域和C-末端基本区组成的共同结构域。编码的蛋白可能参与Wnt/β-catenin信号通路的激活。该基因突变与先天性甲沟炎有关。交替剪接导致多个转录变体。(RefSeq,SEP 2009提供)