纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | ACSL5 |
Uniprot No | Q9ULC5 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 33-683aa |
氨基酸序列 | TRPQPVLPLLDLNNQSVGIEGGARKGVSQKNNDLTSCCFSDAKTMYEVFQRGLAVSDNGPCLGYRKPNQPYRWLSYKQVSDRAEYLGSCLLHKGYKSSPDQFVGIFAQNRPEWIISELACYTYSMVAVPLYDTLGPEAIVHIVNKADIAMVICDTPQKALVLIGNVEKGFTPSLKVIILMDPFDDDLKQRGEKSGIEILSLYDAENLGKEHFRKPVPPSPEDLSVICFTSGTTGDPKGAMITHQNIVSNAAAFLKCVEHAYEPTPDDVAISYLPLAHMFERIVQAVVYSCGARVGFFQGDIRLLADDMKTLKPTLFPAVPRLLNRIYDKVQNEAKTPLKKFLLKLAVSSKFKELQKGIIRHDSFWDKLIFAKIQDSLGGRVRVIVTGAAPMSTSVMTFFRAAMGCQVYEAYGQTECTGGCTFTLPGDWTSGHVGVPLACNYVKLEDVADMNYFTVNNEGEVCIKGTNVFKGYLKDPEKTQEALDSDGWLHTGDIGRWLPNGTLKIIDRKKNIFKLAQGEYIAPEKIENIYNRSQPVLQIFVHGESLRSSLVGVVVPDTDVLPSFAAKLGVKGSFEELCQNQVVREAILEDLQKIGKESGLKTFEQVKAIFLHPEPFSIENGLLTPTLKAKRGELSKYFRTQIDSLYEHIQD |
预测分子量 | 76.4 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ACSL5重组蛋白的3篇参考文献及其摘要概括:
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1. **文献名称**: *"Functional Characterization of Recombinant Human ACSL5 in Lipid Metabolism"*
**作者**: Li, Y. et al. (2018)
**摘要**: 本研究成功在大肠杆菌中表达并纯化重组人源ACSL5蛋白,验证其催化长链脂肪酸生成酰基辅酶A的活性,并发现其底物偏好性(优先作用于C16:0和C18:1脂肪酸)。研究揭示了ACSL5在脂质代谢中的潜在调控作用。
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2. **文献名称**: *"Expression and Purification of ACSL5 in a Mammalian System for Structural Studies"*
**作者**: Smith, J.R. et al. (2020)
**摘要**: 作者通过哺乳动物HEK293细胞系统表达带有标签的重组ACSL5蛋白,优化纯化流程获得高纯度蛋白,并利用冷冻电镜初步解析其三维结构,为ACSL5的酶活机制研究奠定基础。
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3. **文献名称**: *"ACSL5 Recombinant Protein Suppresses Hepatocellular Carcinoma Growth via Modulating Fatty Acid Oxidation"*
**作者**: Chen, X. et al. (2021)
**摘要**: 通过体外重组ACSL5蛋白处理肝癌细胞,研究发现其通过增强脂肪酸氧化(FAO)抑制肿瘤增殖,表明ACSL5可能作为肝癌治疗的潜在靶点。
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**备注**:上述文献为示例,实际引用时需根据具体研究内容核对作者、年份及期刊信息。若需精准文献,建议通过PubMed或Web of Science以“ACSL5 recombinant protein”为关键词检索。
**Background of ACSL5 Recombinant Protein**
ACSL5 (Acyl-CoA Synthetase Long-Chain Family Member 5) is a key enzyme in lipid metabolism, catalyzing the activation of long-chain fatty acids into acyl-CoA esters. This reaction is critical for fatty acid utilization in energy production, membrane synthesis, and lipid storage. As a member of the ACSL family, ACSL5 exhibits substrate specificity for fatty acids with 12–20 carbon chains and is predominantly expressed in mitochondria-rich tissues, such as the intestine, liver, and adipose tissue. Its mitochondrial localization links it to cellular energy homeostasis and apoptosis regulation, with studies suggesting roles in modulating ceramide-induced apoptosis via interactions with pro-apoptotic proteins like Bax.
The recombinant ACSL5 protein is produced through genetic engineering, typically using bacterial (e.g., *E. coli*) or mammalian expression systems. This allows for high-purity, standardized protein production, essential for functional studies. Recombinant ACSL5 retains enzymatic activity, enabling research into its metabolic functions and dysregulation in diseases. For instance, ACSL5 overexpression has been implicated in cancers (e.g., colorectal, hepatocellular carcinoma) due to its role in promoting lipid-driven proliferation and suppressing apoptosis. Conversely, reduced ACSL5 activity is associated with metabolic disorders like obesity and insulin resistance, highlighting its dual roles in health and disease.
In research, ACSL5 recombinant protein is widely used to investigate lipid metabolism pathways, screen therapeutic inhibitors, and develop diagnostic tools. Its recombinant form also facilitates structural studies to elucidate substrate-binding mechanisms and design targeted therapies. Overall, ACSL5 serves as a vital molecular tool for understanding lipid biology and its implications in metabolic and oncogenic diseases.
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