GPX4基因敲除A549细胞

GPX4基因敲除A549细胞
货号:

EDJ-KQ61892

物种:

细胞名称:

A-549

基因名称:

GPX4

基因ID:

2879

规格:

1×10⁶cells

GPX4基因敲除细胞A549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-KQ61892
产品名称 GPX4 Knockout A549 Cell Line
细胞 A549
Cellosaurus ID CVCL_0023
细胞别名 A 549, A549, NCI-A549, A549/ATCC, A549 ATCC, A549ATCC, hA549
基因 GPX4
基因ID
基因别名 GPx-4|GSHPx-4|MCSP|PHGPx|SMDS|snGPx|snPHGPx
摘要
The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme has a high preference for lipid hydroperoxides and protects cells against membrane lipid peroxidation and cell death. It is also required for normal sperm development; thus, it has been identified as a 'moonlighting' protein because of its ability to serve dual functions as a peroxidase, as well as a structural protein in mature spermatozoa. Mutations in this gene are associated with Sedaghatian type of spondylometaphyseal dysplasia (SMDS). This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Transcript variants resulting from alternative splicing or use of alternate promoters have been described to encode isoforms with different subcellular localization. [provided by RefSeq, Dec 2018]
癌症类型 Non-Small Cell Lung Carcinoma
细胞形态 Adherent
传代比率 1/5-1/4 ,2days
完全培养基 F-12K + 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: A-549
细胞库细胞STR信息
细胞库细胞名: A-549
Allele1Allele2Allele1 Allele2
AmelogeninX YXY
CSF1PO10121012
D2S13382424
D3S13581616
D5S8181111
D7S820811811
D8S117913141314
D13S3171111
D16S53911121112
D18S5114171417
D19S4331313
D21S112929
FGA2323
Penta D99
Penta E711711
TH0189.389.3
TPOX811811
vWA1414
D6S10431113
D12S3911818
D2S44110131013
* 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=13
Journal of advanced research
IF=8.2
Free radical biology & medicine
该KO模型可能对以下方面有用: - 铁死亡机制研究,特别是GPX4依赖性降解途径 - EGFR野生型非小细胞肺癌中铁死亡诱导剂(例如β-榄香烯)的药物筛选 - 细胞凋亡和铁死亡的相互作用分析(例如Bim/Bax介导的线粒体途径) - 非小细胞肺癌靶向治疗耐药性研究 - 细胞死亡途径验证实验(细胞凋亡与铁死亡)

配套产品

相关产品

A-549(人非小细胞肺癌)A-549(人非小细胞肺癌)

相关服务

基因敲除细胞基因敲除细胞
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