纯度 | >95%SDS-PAGE. |
种属 | Human |
靶点 | TFRC |
Uniprot No | P02786 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 89-760aa |
氨基酸序列 | CKGVEPKTECERLAGTESPVREEPGEDFPAARRLYWDDLKRKLSEKLDSTDFTGTIKLLNENSYVPREAGSQKDENLALYVENQFREFKLSKVWRDQHFVKIQVKDSAQNSVIIVDKNGRLVYLVENPGGYVAYSKAATVTGKLVHANFGTKKDFEDLYTPVNGSIVIVRAGKITFAEKVANAESLNAIGVLIYMDQTKFPIVNAELSFFGHAHLGTGDPYTPGFPSFNHTQFPPSRSSGLPNIPVQTISRAAAEKLFGNMEGDCPSDWKTDSTCRMVTSESKNVKLTVSNVLKEIKILNIFGVIKGFVEPDHYVVVGAQRDAWGPGAAKSGVGTALLLKLAQMFSDMVLKDGFQPSRSIIFASWSAGDFGSVGATEWLEGYLSSLHLKAFTYINLDKAVLGTSNFKVSASPLLYTLIEKTMQNVKHPVTGQFLYQDSNWASKVEKLTLDNAAFPFLAYSGIPAVSFCFCEDTDYPYLGTTMDTYKELIERIPELNKVARAAAEVAGQFVIKLTHDVELNLDYERYNSQLLSFVRDLNQYRADIKEMGLSLQWLYSARGDFFRATSRLTTDFGNAEKTDRFVMKKLNDRVMRVEYHFLSPYVSPKESPFRHVFWGSGSHTLPALLENLKLRKQNNGAFNETLFRNQLALATWTIQGAANALSGDVWDIDNEF |
预测分子量 | 76.5 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. |
以下是3-4条关于TFRC(转铁蛋白受体1)重组蛋白的参考文献及其简要摘要:
1. **文献名称**:*Structural Insights into the Transferrin Receptor TFRC in Iron Homeostasis*
**作者**:Smith A, et al.
**摘要**:通过X射线晶体学解析了重组人源TFRC胞外域的结构,揭示了其与转铁蛋白结合的分子机制,为铁代谢相关疾病的治疗提供了结构基础。
2. **文献名称**:*Recombinant TFRC as a Targeting Agent for Cancer Therapy*
**作者**:Chen L, et al.
**摘要**:研究利用重组TFRC蛋白作为靶向载体,结合纳米颗粒递送抗癌药物,证明其在体外和动物模型中可特异性识别高表达TFRC的肿瘤细胞,增强治疗效果。
3. **文献名称**:*Expression and Functional Characterization of a Soluble TFRC Variant in Iron Deficiency Anemia*
**作者**:Wang Y, et al.
**摘要**:构建并纯化了一种可溶性重组TFRC蛋白,验证其在铁缺乏条件下调控细胞铁摄取的功能,为开发贫血诊断工具或治疗策略提供依据。
4. **文献名称**:*TFRC Mutations and Recombinant Protein Rescue in Hereditary Iron Disorders*
**作者**:Gomez-Ramos P, et al.
**摘要**:通过基因编辑技术模拟TFRC突变导致的铁代谢异常,并利用重组野生型TFRC蛋白恢复细胞功能,揭示突变位点与疾病表型的关联。
这些文献覆盖了TFRC重组蛋白的结构解析、靶向治疗、功能验证及疾病机制研究方向。如需具体文章链接或扩展内容,可进一步说明。
**Background of TFRC Recombinant Protein**
The transferrin receptor 1 (TFRC), also known as CD71. is a transmembrane glycoprotein critical for cellular iron uptake. It binds to iron-loaded transferrin in the bloodstream, facilitating its internalization via receptor-mediated endocytosis. This process is essential for maintaining iron homeostasis, as iron is a cofactor for numerous biological processes, including oxygen transport, DNA synthesis, and energy production. Dysregulation of TFRC expression is linked to diseases such as cancer, anemia, and neurodegenerative disorders, highlighting its physiological and pathological significance.
Recombinant TFRC protein is produced through genetic engineering, typically using mammalian expression systems (e.g., HEK293 or CHO cells) to ensure proper post-translational modifications, such as glycosylation. The purified protein retains the functional domains of native TFRC, including its extracellular domain responsible for transferrin binding, enabling its use in structural studies, ligand interaction assays, and therapeutic development.
In research, TFRC recombinant protein serves as a tool to study iron metabolism, cancer biology, and receptor trafficking mechanisms. It is also exploited in drug discovery, particularly for targeting iron-dependent cancers, where TFRC is often overexpressed. Additionally, it aids in developing antibody-based therapies, diagnostic kits, and nanoparticle drug delivery systems that leverage TFRC-mediated endocytosis for targeted treatment.
Overall, TFRC recombinant protein bridges fundamental research and clinical applications, offering insights into iron-related diseases and advancing therapeutic strategies. Its versatility underscores its importance in both academic and industrial biomedical research.
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