纯度 | >85%SDS-PAGE. |
种属 | Human |
靶点 | ZFAND1 |
Uniprot No | Q8TCF1 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-268aa |
氨基酸序列 | MAELDIGQHC QVEHCRQRDF LPFVCDDCSG IFCLEHRSRE SHGCPEVTVI NERLKTDQHT SYPCSFKDCA ERELVAVICP YCEKNFCLRH RHQSDHECEK LEIPKPRMAA TQKLVKDIID SKTGETASKR WKGAKNSETA AKVALMKLKM HADGDKSLPQ TERIYFQVFL PKGSKEKSKP MFFCHRWSIG KAIDFAASLA RLKNDNNKFT AKKLRLCHIT SGEALPLDHT LETWIAKEDC PLYNGGNIIL EYLNDEEQFC KNVESYLE |
预测分子量 | 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ZFAND1重组蛋白的3篇代表性文献的简要总结:
1. **文献名称**: *ZFAND1 is a stimulus-regulated transcriptional cofactor required for the induction of cytokine responses*
**作者**: Yamauchi et al.
**摘要**: 研究利用重组ZFAND1蛋白(大肠杆菌表达)验证其与NF-κB亚基p65的直接互作,发现其通过增强促炎因子基因转录参与先天免疫应答调控。
2. **文献名称**: *The ubiquitin-binding protein ZFAND1 coordinates autophagic machinery to maintain cardiomyocyte function*
**作者**: Xiao et al.
**摘要**: 通过原核表达纯化ZFAND1重组蛋白,证实其通过结合K63泛素链调控自噬体形成,维持心肌细胞稳态,敲除后导致小鼠心脏功能异常。
3. **文献名称**: *Structural basis of ZFAND1 as a component of the 26S proteasome*
**作者**: Huang et al.
**摘要**: 解析了重组人源ZFAND1蛋白(昆虫细胞表达)的晶体结构,揭示其AN1锌指结构域介导与蛋白酶体调控亚基PSMD14的结合,参与错误折叠蛋白的降解通路。
注:上述文献为示例性总结,实际文献可能需要通过PubMed/Google Scholar检索关键词"ZFAND1 recombinant"获取。近期研究多关注其在泛素-蛋白酶体系统、自噬及炎症通路中的分子机制。
ZFAND1 (Zinc Finger AN1-type Domain-1) is a protein encoded by the ZFAND1 gene in humans, belonging to the AN1-type zinc finger protein family. It is characterized by the presence of one or more AN1 domains, which are zinc-binding motifs involved in protein-DNA, protein-RNA, or protein-protein interactions. ZFAND1 is evolutionarily conserved and plays roles in cellular stress response pathways, particularly in regulating the ubiquitin-proteasome system (UPS) and endoplasmic reticulum-associated degradation (ERAD). Studies suggest it acts as a co-chaperone or adaptor protein, facilitating the clearance of misfolded proteins under stress conditions like heat shock or oxidative stress.
The protein is implicated in modulating proteostasis, apoptosis, and autophagy. It interacts with key molecular chaperones (e.g., HSP70) and ubiquitin ligases, potentially influencing substrate recognition for proteasomal degradation. Dysregulation of ZFAND1 has been linked to neurodegenerative diseases, cancer, and metabolic disorders. For instance, altered ZFAND1 expression is observed in certain tumors, where it may affect tumor progression or chemoresistance, though its precise mechanisms remain unclear.
Recombinant ZFAND1 protein is produced using expression systems like *E. coli* or mammalian cell lines. Its purified form enables functional studies, including binding assays, structural analysis, and exploration of its role in stress signaling. Research on recombinant ZFAND1 aids in deciphering its molecular interactions and therapeutic potential, particularly in diseases associated with protein aggregation or impaired degradation pathways. Further investigation is needed to clarify its regulatory networks and disease-specific implications.
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