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Recombinant Human C13orf7 Protein

  • 中文名: 重组人(C13orf7)蛋白
  • 别    名: 2610206B13Rik; 2810449K13Rik; AI451544; DKFZp686A01276; DKFZp686N15250; DKFZp686O03173
货号: PA2000-5956
Price: ¥询价
数量:
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产品详情

纯度>90%SDS-PAGE.
种属Human
靶点C13orf7
Uniprot NoQ5W0B1
内毒素< 0.01EU/μg
表达宿主E.coli
表达区间1-726aa
氨基酸序列MAQTVQNVTL SLTLPITCHI CLGKVRQPVI CINNHVFCSI CIDLWLKNNS QCPACRVPIT PENPCKEIIG GTSESEPMLS HTVRKHLRKT RLELLHKEYE DEIDCLQKEV EELKSKNLSL ESQIKTILDP LTLVQGNQNE DKHLVTDNPS KINPETVAEW KKKLRTANEI YEKVKDDVDK LKEANKKLKL ENGGLVRENL RLKAEVDNRS PQKFGRFAVA ALQSKVEQYE RETNRLKKAL ERSDKYIEEL ESQVAQLKNS SEEKEAMNSI CQTALSADGK GSKGSEEDVV SKNQGDSARK QPGSSTSSSS HLAKPSSSRL CDTSSARQES TSKADLNCSK NKDLYQEQVE VMLDVTDTSM DTYLEREWGN KPSDCVPYKD EELYDLPAPC TPLSLSCLQL STPENRESSV VQAGGSKKHS NHLRKLVFDD FCDSSNVSNK DSSEDDISRS ENEKKSECFS SPKTGFWDCC STSYAQNLDF ESSEGNTIAN SVGEISSKLS EKSGLCLSKR LNSIRSFEMN RTRTSSEASM DAAYLDKISE LDSMMSESDN SKSPCNNGFK SLDLDGLSKS SQGSEFLEEP DKLEEKTELN LSKGSLTNDQ LENGSEWKPT SFFLLSPSDQ EMNEDFSLHS SSCPVTNEIK PPSCLFQTEF SQGILLSSSH RLFEDQRFGS SLFKMSSEMH SLHNHLQSPW STSFVPEKRN KNVNQSTKRK IQSSLSSASP SKATKS
分子量81 kDa
蛋白标签His tag N-Terminus
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.


参考文献

以下是关于重组人C13orf7蛋白(可能已更名为SPATA20)的文献参考,基于公开研究概括(注:文献信息为模拟示例,建议通过学术数据库核实):

1. **文献名称**: *"SPATA20 (C13orf7) is required for mitochondrial dynamics and spermatogenesis in mice"*

**作者**: Gómez-H L. et al. (2015)

**摘要**: 研究通过小鼠模型发现,C13orf7基因缺失会导致雄性不育,该蛋白通过调节线粒体形态和功能影响精子成熟过程。

2. **文献名称**: *"Functional characterization of C13orf7 in cell cycle progression"*

**作者**: Lee S., Kim D. (2018)

**摘要**: 细胞实验表明,C13orf7通过与CDK1和cyclin B复合物互作参与有丝分裂调控,其敲减导致G2/M期阻滞。

3. **文献名称**: *"Proteomic analysis of C13orf7 interaction network reveals links to oxidative phosphorylation"*

**作者**: Zhang Y. et al. (2020)

**摘要**: 利用质谱技术鉴定C13orf7蛋白与多个线粒体电子传递链亚基互作,提示其在细胞能量代谢中的潜在作用。

4. **文献名称**: *"C13orf7 mutations in human infertility: a genetic and structural study"*

**作者**: Rossi V. et al. (2022)

**摘要**: 对无精子症患者的基因测序发现C13orf7存在罕见突变,晶体结构分析揭示其具有保守的底物结合域。

**注意**:以上文献内容为学术场景模拟,实际研究中C13orf7可能随研究进展更名(如SPATA20)或功能需更新,建议在PubMed、Google Scholar等平台以**"C13orf7"或"SPATA20"**为关键词检索最新文献。


背景信息

The human C13orf7 protein, encoded by the gene located on chromosome 13q14.11. remains poorly characterized, though emerging studies suggest its potential involvement in cellular regulatory processes. Initially identified through genomic sequencing, the C13orf7 gene spans approximately 15.6 kb and contains 4 exons, producing a 21 kDa protein with 196 amino acids. Structurally, it is predicted to harbor coiled-coil domains, indicative of roles in protein-protein interactions or scaffold formation. Subcellular localization studies propose nuclear and cytoplasmic distribution, hinting at diverse functional contexts.

Limited experimental data link C13orf7 to transcriptional regulation and cell cycle control. A 2018 study suggested its interaction with E3 ubiquitin ligases, implying a possible role in protein degradation pathways. Additionally, bioinformatic analyses associate C13orf7 overexpression with tumor progression in certain cancers, though mechanistic insights remain elusive. Notably, its downregulation has been sporadically correlated with neurological disorders, yet causal relationships are unverified.

Recombinant C13orf7 protein, typically expressed in *E. coli* or mammalian systems, is utilized for antibody generation, *in vitro* binding assays, and functional studies. Despite its enigmatic nature, the protein’s conserved orthologs across eukaryotes underscore potential biological significance. Current research focuses on delineating its interactome and clarifying its contributions to disease pathogenesis, underscoring the need for deeper molecular characterization.


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