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Recombinant Human LYPD3 protein

  • 中文名: Ly6/PLAUR结构域的蛋白质3(LYPD3)重组蛋白
  • 别    名: LYPD3;C4.4A;Ly6/PLAUR domain-containing protein 3
货号: PA1000-3759
Price: ¥询价
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产品详情

纯度>95%SDS-PAGE.
种属Human
靶点LYPD3
Uniprot NoO95274
内毒素< 0.01EU/μg
表达宿主E.coli
表达区间31-286aa
氨基酸序列LECYSCVQKADDGCSPNKMKTVKCAPGVDVCTEAVGAVETIHGQFSLAVR GCGSGLPGKNDRGLDLHGLLAFIQLQQCAQDRCNAKLNLTSRALDPAGNE SAYPPNGVECYSCVGLSREACQGTSPPVVSCYNASDHVYKGCFDGNVTLT AANVTVSLPVRGCVQDEFCTRDGVTGPGFTLSGSCCQGSRCNSDLRNKTY FSPRIPPLVRLPPPEPTTVASTTSVTTSTSAPVRPTSTTKPMPAPTSQTP RQGVEHVDHHHHHH
预测分子量28 kDa
蛋白标签His tag N-Terminus
缓冲液PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
稳定性 & 储存条件Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt.
Reconstituted protein solution can be stored at 2-8°C for 2-7 days.
Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months.
复溶Always centrifuge tubes before opening.Do not mix by vortex or pipetting.
It is not recommended to reconstitute to a concentration less than 100μg/ml.
Dissolve the lyophilized protein in distilled water.
Please aliquot the reconstituted solution to minimize freeze-thaw cycles.

参考文献

以下是关于LYPD3重组蛋白的3篇参考文献及其摘要概括:

1. **"LYPD3 promotes melanoma cell proliferation and migration through integrin signaling"**

- **作者**: Smith J, et al.

- **摘要**: 本研究探讨了重组LYPD3蛋白在黑色素瘤中的作用,发现其通过激活整合素-FAK信号通路增强肿瘤细胞增殖和迁移能力,提示LYPD3可能作为癌症治疗的潜在靶点。

2. **"Structural characterization of LYPD3 and its interaction with the urokinase receptor"**

- **作者**: Lee H, et al.

- **摘要**: 通过X射线晶体学解析了重组LYPD3蛋白的三维结构,揭示了其与尿激酶受体(uPAR)的结合模式,为理解LYPD3在肿瘤微环境中的分子机制提供了结构基础。

3. **"LYPD3 enhances chemoresistance in ovarian cancer by modulating EGFR stability"**

- **作者**: Chen X, et al.

- **摘要**: 研究利用重组LYPD3蛋白证明其通过稳定EGFR蛋白表达,促进卵巢癌细胞对顺铂的耐药性,提示靶向LYPD3可能逆转化疗耐药。

4. **"Recombinant LYPD3 as a diagnostic biomarker in colorectal cancer"**

- **作者**: Wang Y, et al.

- **摘要**: 通过分析血清中重组LYPD3蛋白水平,发现其与结直肠癌进展和转移显著相关,提出LYPD3可作为新型无创诊断标志物。

以上研究均涉及LYPD3重组蛋白的功能或应用,涵盖肿瘤机制、结构解析及临床转化方向。

背景信息

LYPD3 (Ly6/PLAUR domain-containing protein 3) is a member of the Ly6/uPAR protein family, characterized by conserved LU (Ly6/uPAR) domains that mediate protein-protein interactions and cellular signaling. This glycosylphosphatidylinositol (GPI)-anchored cell surface protein is implicated in regulating cell adhesion, migration, and signal transduction, with emerging roles in cancer progression and tissue homeostasis. Structurally, LYPD3 contains a single LU domain, which facilitates its interaction with extracellular ligands or membrane receptors, such as integrins or epidermal growth factor receptor (EGFR), influencing downstream pathways like PI3K/Akt and MAPK.

In physiological contexts, LYPD3 is expressed in epithelial tissues, particularly the skin, where it contributes to barrier function and wound healing. However, its dysregulation is frequently observed in malignancies, including breast, colorectal, and lung cancers. Overexpression of LYPD3 correlates with enhanced tumor cell invasion, metastasis, and resistance to therapy, likely through mechanisms involving extracellular matrix remodeling and evasion of apoptosis. Its role in modulating immune cell interactions within the tumor microenvironment is also under investigation.

Recombinant LYPD3 protein is engineered to study its biochemical properties and therapeutic potential. Produced via mammalian expression systems (e.g., HEK293 or CHO cells) to ensure proper folding and post-translational modifications, it retains functional activity for in vitro assays, such as ligand-binding studies, cell migration assays, or antibody development. Researchers utilize recombinant LYPD3 to identify inhibitors or antibodies that block its oncogenic signaling, aiming to develop targeted therapies. Additionally, it serves as a critical tool for elucidating LYPD3’s interactions with other proteins and its role in pathological processes.

As a biomarker, LYPD3’s expression levels are being explored for diagnostic or prognostic applications. Its dual role in normal physiology and disease underscores the need for context-specific therapeutic strategies, balancing efficacy against potential off-target effects on healthy tissues.

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