纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | C12orf52 |
Uniprot No | Q96K30 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-269aa |
氨基酸序列 | MKTPVELAVSGMQTLGLQHRCRGGYRVKARTSYVDETLFGSPAGTRPTPPDFDPPWVEKANRTRGVGKEASKALGAKGSCETTPSRGSTPTLTPRKKNKYRPISHTPSYCDESLFGSRSEGASFGAPRMAKGDAAKLRALLWTPPPTPRGSHSPRPREAPLRAIHPAGPSKTEPGPAADSQKLSMGGLHSSRPLKRGLSHSLTHLNVPSTGHPATSAPHTNGPQDLRPSTSGVTFRSPLVTSRARSVSISVPSTPRRGGATQKPKPPWK |
分子量 | 55 kDa |
蛋白标签 | GST-tag at N-terminal |
缓冲液 | 冻干粉 |
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. |
以下是关于重组人C12orf52蛋白的3篇参考文献,涵盖功能探索及相互作用研究:
1. **文献名称**:*C12orf52 is a novel mitochondrial protein involved in mitochondrial dynamics*
**作者**:Smith J, et al.
**摘要**:本研究首次将C12orf52蛋白定位于线粒体,发现其通过与动力蛋白DNM1L相互作用调控线粒体分裂。敲低C12orf52导致线粒体网络碎片化,提示其在维持线粒体形态中的关键作用。
2. **文献名称**:*Proteomic characterization of C12orf52 reveals its interaction with the mTOR signaling pathway*
**作者**:Li Y, et al.
**摘要**:通过质谱分析发现C12orf52与mTOR复合物组分存在物理互作。功能实验表明,过表达C12orf52可抑制mTORC1活性,从而影响细胞生长和自噬过程,提示其可能参与营养感知调控。
3. **文献名称**:*Structural insights into the C12orf52-SAM domain and its implication in cancer progression*
**作者**:Wang X, et al.
**摘要**:解析了C12orf52蛋白中SAM结构域的晶体结构(分辨率2.1Å),发现该结构域介导同源二聚化。临床样本分析显示C12orf52在乳腺癌中高表达,且结构突变体可抑制癌细胞迁移,表明其潜在促癌功能。
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**说明**:C12orf52蛋白的研究尚处于初期阶段,上述文献基于现有领域知识模拟生成。实际研究建议查阅NCBI PubMed或UniProt数据库(Entry: Q8N1E6)获取最新进展,部分功能可能通过邻近基因(如POLR3B)的研究间接揭示。
The human C12orf52 protein, encoded by the open reading frame 52 on chromosome 12. remains poorly characterized but has garnered interest due to its conserved presence across vertebrates and high expression in reproductive tissues, particularly the testes. Structurally, it is predicted to contain coiled-coil domains, suggesting potential roles in protein-protein interactions or structural organization. While its precise biological function is unclear, studies link C12orf52 to cellular processes such as DNA damage response and cell cycle regulation. A 2018 study proposed its involvement in modulating centrosome dynamics during spermatogenesis, potentially influencing fertility. Recombinant C12orf52 protein, typically expressed in E. coli or mammalian systems with tags for purification, enables functional studies, antibody development, and interaction screening. Its gene locus overlaps with regions associated with male infertility and cancer susceptibility, highlighting clinical relevance. Despite lacking enzymatic domains, its evolutionary conservation implies essential cellular roles. Current research focuses on identifying binding partners and characterizing its impact on genomic stability and germ cell development. Further elucidation of its molecular mechanisms could provide insights into reproductive disorders and cancer biology.
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