纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | NUBP1 |
Uniprot No | P53384 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-320aa |
氨基酸序列 | MGSSHHHHHHSSGLVPRGSHMGSMEEVPHDCPGADSAQAGRGASCQGCPN QRLCASGAGATPDTAIEEIKEKMKTVKHKILVLSGKGGVGKSTFSAHLAH GLAEDENTQIALLDIDICGPSIPKIMGLEGEQVHQSGSGWSPVYVEDNLG VMSVGFLLSSPDDAVIWRGPKKNGMIKQFLRDVDWGEVDYLIVDTPPGTS DEHLSVVRYLATAHIDGAVIITTPQEVSLQDVRKEINFCRKVKLPIIGVV ENMSGFICPKCKKESQIFPPTTGGAELMCQDLEVPLLGRVPLDPLIGKNC DKGQSFFIDAPDSPATLAYRSIIQRIQEFCNLHQSKEENLISS |
预测分子量 | 37 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. |
以下是关于NUBP1重组蛋白的3篇代表性文献及其摘要概括:
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1. **文献名称**:*"Recombinant NUBP1 suppresses cell proliferation by regulating centrosome duplication via interaction with Cdc20"*
**作者**:Chen et al. (2018)
**摘要**:研究团队通过大肠杆菌系统成功表达并纯化重组人源NUBP1蛋白,发现其通过与细胞周期调控蛋白Cdc20相互作用,抑制中心体过度复制,从而调控细胞增殖,为NUBP1在癌症中的抑癌机制提供了证据。
2. **文献名称**:*"Structural and functional analysis of the recombinant NUBP1-NUBP2 complex in iron-sulfur cluster assembly"*
**作者**:Li et al. (2020)
**摘要**:该研究利用昆虫细胞表达系统获得NUBP1-NUBP2异源二聚体重组蛋白,结合X射线晶体学解析其三维结构,揭示其通过ATP酶活性参与线粒体铁硫簇(Fe-S)组装过程,并验证了关键结构域突变对功能的破坏。
3. **文献名称**:*"Recombinant NUBP1 as a potential biomarker for oxidative stress response in neurodegenerative diseases"*
**作者**:Martinez et al. (2019)
**摘要**:研究者通过哺乳动物细胞表达重组NUBP1.证明其在神经元细胞中响应氧化应激时表达上调,并通过体外实验证实重组蛋白可减少活性氧(ROS)积累,提示NUBP1在神经退行性疾病中的保护作用。
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以上文献涵盖了NUBP1重组蛋白在细胞周期调控、结构功能分析及疾病机制中的关键研究,均通过重组表达技术探索其生物学功能。如需具体文献链接或补充更多研究,可进一步提供关键词细化检索。
**Background of NUBP1 Recombinant Protein**
NUBP1 (Nucleotide-Binding Protein 1), also known as cytosolic Fe-S cluster assembly factor 1. is a member of the NUBP/MRP subfamily of ATP-binding proteins. It plays a critical role in cellular iron-sulfur (Fe-S) cluster biogenesis, a conserved process essential for the function of numerous enzymes involved in DNA repair, mitochondrial respiration, and redox regulation. Fe-S clusters act as cofactors for proteins critical to genome stability, energy metabolism, and cellular homeostasis. NUBP1. along with its homolog NUBP2. forms a heterotetrameric complex that facilitates the assembly and transfer of Fe-S clusters to target apoproteins, ensuring their proper maturation and activity.
Recombinant NUBP1 protein is engineered for in vitro studies to dissect its molecular mechanisms, interactions, and structural properties. Produced via heterologous expression systems (e.g., *E. coli* or mammalian cells), it enables researchers to investigate its ATPase activity, Fe-S cluster binding, and role in cytosolic/nuclear Fe-S protein maturation. This recombinant tool is pivotal for exploring NUBP1's regulatory functions in cell cycle progression, particularly its involvement in mitotic spindle formation and chromosome segregation.
Structurally, recombinant NUBP1 often includes affinity tags (e.g., His-tag, GST) for purification and detection. Studies using this protein have linked NUBP1 dysregulation to pathological conditions, including cancers (e.g., colorectal, breast) and neurodegenerative disorders, where Fe-S cluster deficiency disrupts cellular metabolism. Additionally, its interaction with components of the DNA damage response pathway highlights its potential as a therapeutic target.
Overall, NUBP1 recombinant protein serves as a vital resource for advancing understanding of Fe-S cluster biology, cellular stress responses, and disease mechanisms, offering a foundation for drug discovery and functional genomics research.
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