KPNA6基因敲除HEK293细胞

KPNA6基因敲除HEK293细胞
货号:

EDJ-KQ8101

物种:

细胞名称:

HEK293

基因名称:

KPNA6

基因ID:

23633

规格:

1×10⁶cells

KPNA6基因敲除细胞HEK293是由艾迪基因优化的CRISPR/Cas9编辑而成,采用Sanger测序法验证敲除,保证单克隆,活性良好。
货号 EDJ-KQ8101
产品名称 KPNA6 Knockout HEK293 Cell Line
细胞 HEK293
Cellosaurus ID CVCL_0045
细胞别名 Hek293, HEK-293, HEK/293, (HEK)293, HEK 293, HEK,293, 293, 293 HEK, 293 Ad5, Graham 293, Graham-293, Human Embryonic Kidney 293
基因 KPNA6
基因ID
基因别名 IPOA7
摘要
Nucleocytoplasmic transport, a signal- and energy-dependent process, takes place through nuclear pore complexes embedded in the nuclear envelope. The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor, a heterodimer of importin alpha and beta subunits also known as karyopherins. Importin alpha binds the NLS-containing cargo in the cytoplasm and importin beta docks the complex at the cytoplasmic side of the nuclear pore complex. In the presence of nucleoside triphosphates and the small GTP binding protein Ran, the complex moves into the nuclear pore complex and the importin subunits dissociate. Importin alpha enters the nucleoplasm with its passenger protein and importin beta remains at the pore. The protein encoded by this gene is a member of the importin alpha family. [provided by RefSeq, Jul 2008]
癌症类型 Non-tumor
细胞形态 Adherent
传代比率 1/2~1/4
完全培养基 DMEM + 10% FBS
冻存培养基 95%完全培养基+ 5% DMSO
* 仅供科研使用,不适用于人体或动物,包括临床、治疗或诊断用途。
Loci送检细胞STR信息
送检细胞名: HEK293
细胞库细胞STR信息
细胞库细胞名: HEK293
Allele1Allele2Allele1 Allele2
AmelogeninXX
CSF1P0121112
D2S13381919
D3S135815171517
D5S818889
D7S82011121112
D8S117912141214
D13S31712141214
D16S539913913
D18S5117181718
D19S43315181518
D21S112830.22830.2
FGA2323
Penta D910910
Penta E715715
TH0179.379.3
TPOX1111
vWA16191619
D6S10431111
D12S39119211115
D2S44111151115
* 该细胞系与收录于ATCC, DSMZ, JCRB 和 RIKEN数据库的细胞系STR数据匹配。
结论:该细胞 STR 鉴定正确。
* 研究用途免责声明:本内容基于公开的研究数据、生物信息学资源及计算分析生成,仅供研究参考。

相关研究文献

IF=3.8
Microbiology spectrum
Influenza A virus (IAV) RNA-dependent RNA polymerase (vPol) is a heterotrimer composed of PB2, PB1, and PA, which, together with vRNA and nucleoprotein (NP), forms viral ribonucleoprotein (vRNP) complex to direct the transcription and replication of the viral genome. Host factor ANP32 proteins have been proved to be associated with vRNP and are essential for polymerase activity and cross-species restriction of avian influenza virus. However, the molecular mechanism by which ANP32 supports polymerase activity is largely unknown. Here, we identified that KPNA6 is associated with ANP32A/B and vRNP of the influenza virus. Both knockout and overexpression of KPNA6 downregulate the replication of the influenza virus by inhibiting the polymerase activity, indicating that a certain level of KPNA6 is beneficial for efficient replication of the influenza virus. Furthermore, we demonstrate that overexpression of KPNA6 or its nuclear importing domain negative mutation inhibited the interaction between ANP32 and vRNP, thus reducing the polymerase activity. Our results revealed the role of KPNA6 in interacting with both ANP32A/B and vRNP to maintain viral polymerase activity and provided new insights for further understanding of the mechanism by which ANP32 supports influenza polymerase. Host factor ANP32 plays a fundamental role in supporting the polymerase activity of influenza viruses, but the underlying mechanism is largely unknown. Here, we propose that KPNA6 is involved in the function of ANP32A/B to support influenza virus polymerase by interacting with both vRNP and ANP32A/B. The proper amount of KPNA6 and ANP32 proteins in the KPNA6-ANP32-vRNP complex is crucial for maintaining the viral polymerase activity. The KPNA6 may contribute to maintaining stable interaction between vRNA and ANP32 proteins in the nucleus, and this function is independent of the known importing domain of KPNA6. Our research reveals a role of KNPA6 associated with ANP32 proteins that support the viral polymerase and suggests a new perspective for developing antiviral strategies.
该敲除模型可用于: - 研究KPNA6作为宿主辅助因子在流感病毒复制中的作用。 - 研究KPNA6-ANP32A/B相互作用在病毒聚合酶活性和宿主-病原体相互作用中的作用。 - 评估破坏KPNA6依赖性核输入机制的抗病毒药物靶点。 - 验证KPNA6在核质运输途径中的功能。 - 筛选流感病毒生命周期所需的宿主因子。

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