纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | SLC25A24 |
Uniprot No | Q6NUK1 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-477 aa |
活性数据 | MLRWLRDFVLPTAACQDAEQPTRYETLFQALDRNGDGVVDIGELQEGLRNLGIPLGQDAEEKIFTTGDVNKDGKLDFEEFMKYLKDHEKKMKLAFKSLDKNNDGKIEASEIVQSLQTLGLTISEQQAELILQSIDVDGTMTVDWNEWRDYFLFNPVTDIEEIIRFWKHSTGIDIGDSLTIPDEFTEDEKKSGQWWRQLLAGGIAGAVSRTSTAPLDRLKIMMQVHGSKSDKMNIFGGFRQMVKEGGIRSLWRGNGTNVIKIAPETAVKFWAYEQYKKLLTEEGQKIGTFERFISGSMAGATAQTFIYPMEVMKTRLAVGKTGQYSGIYDCAKKILKHEGLGAFYKGYVPNLLGIIPYAGIDLAVYELLKSYWLDNFAKDSVNPGVMVLLGCGALSSTCGQLASYPLALVRTRMQAQAMLEGSPQLNMVGLFRRIISKEGIPGLYRGITPNFMKVLPAVGISYVVYENMKQTLGVTQK |
分子量 | 79.8 kDa |
蛋白标签 | GST-tag at N-terminal |
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. |
以下是关于重组人**SLC25A24**蛋白的参考文献示例(注:文献为示例性质,建议通过学术数据库验证详细信息):
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1. **文献名称**: *"Structural and functional analysis of the mitochondrial carrier SLC25A24 reveals a role in cellular energy homeostasis"*
**作者**: Smith J, et al.
**摘要**: 本研究通过重组表达人SLC25A24蛋白,解析了其晶体结构,发现其作为ATP-Mg/Pi转运体参与线粒体能量代谢。实验表明,SLC25A24的活性受钙离子浓度调节,突变会导致线粒体膜电位异常。
2. **文献名称**: *"SLC25A24 mutations cause a novel syndrome with craniofacial dysmorphism and mitochondrial dysfunction"*
**作者**: García-Castaño A, et al.
**摘要**: 研究报道了SLC25A24基因突变与Goel综合征的关联。通过重组蛋白功能实验,发现突变体损害线粒体ATP转运能力,导致细胞增殖缺陷和氧化应激反应增强。
3. **文献名称**: *"Reconstitution of recombinant SLC25A24 in proteoliposomes reveals pH-dependent transport activity"*
**作者**: Lee C, et al.
**摘要**: 使用重组SLC25A24蛋白在脂质体重建转运系统,证实其在酸性pH环境下优先转运磷酸盐。研究揭示了该蛋白在调节线粒体基质离子平衡中的关键作用。
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**备注**:
- 若需真实文献,建议在PubMed或Google Scholar检索关键词(如“SLC25A24 recombinant”“SLC25A24 function”)。
- SLC25A24主要参与线粒体代谢调控,突变体研究多与发育性疾病相关。
SLC25A24. a member of the mitochondrial carrier family (SLC25), is a nuclear-encoded transporter protein localized in the mitochondrial inner membrane. It facilitates the exchange of metabolites and ions across the membrane, playing a critical role in mitochondrial bioenergetics and cellular metabolism. Predominantly expressed in tissues with high metabolic demands (e.g., heart, skeletal muscle, and brain), SLC25A24 is implicated in transporting ATP-Mg/phosphate or other nucleotides, though its exact substrate specificity remains partially debated. Structurally, it features six transmembrane α-helices and a conserved tripartite sequence motif characteristic of mitochondrial carriers.
Mutations in SLC25A24 are linked to severe developmental disorders, including Gorlin-Chaudhry-Moss syndrome and Fontaine progeroid syndrome, characterized by craniofacial abnormalities, premature aging, and metabolic dysregulation. These disorders highlight its role in mitochondrial homeostasis and stress response pathways. Recombinant human SLC25A24 protein (rhSLC25A24) is produced via heterologous expression systems (e.g., *E. coli* or mammalian cells) for functional studies, structural analysis, and drug screening. Its recombinant form enables exploration of transport kinetics, interactions with regulatory molecules, and mechanistic insights into disease-associated variants. Current research aims to elucidate its physiological roles and therapeutic potential in mitochondrial disorders.
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