GPX4基因敲除Hela细胞

GPX4基因敲除Hela细胞
货号:

EDJ-KQ53417

物种:

细胞名称:

HeLa

基因名称:

GPX4

基因ID:

2879

规格:

1×10⁶cells

GPX4基因敲除细胞Hela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-KQ53417
产品名称 GPX4 Knockout Hela Cell Line
细胞 Hela
Cellosaurus ID CVCL_0030
细胞别名 HELA, Hela, He La, He-La, HeLa-CCL2, Henrietta Lacks cells, Helacyton gartleri
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 Cervical Carcinoma
细胞形态 Adherent
传代比率 1/5, 2days
完全培养基 MEM + 10% FBS
冻存培养基 70%完全培养基+ 20% FBS+ 10% 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: HeLa
细胞库细胞STR信息
细胞库细胞名: HeLa
Allele1Allele2Allele1 Allele2
AmelogeninXX
CSF1PO910910
D1S165612151215
D2S13381717
D3S135815181518
D5S81811121112
D6S10431818
D7S820812812
D8S117912131213
D12S39120252025
D13S31712141214
D16S539910910
D18S511616
D19S43313141314
D21S1127282728
FGA18211821
Penta D815815
Penta E717717
TPOX812812
VWA16181618
* 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=3.7
Biochimica et biophysica acta. Molecular cell research
IF=3
Archives of biochemistry and biophysics
该KO模型可能有助于: - 研究GPX4在半胱氨酸饥饿和线粒体复合物III衍生的超氧化物产生条件下铁死亡执行中的作用。 - 研究erastin和RSL3诱导铁死亡的不同机制,特别是NCOA4介导的铁蛋白自噬。 - 在人宫颈癌细胞背景下验证铁死亡相关通路的功能。 - 筛选在GPX4缺失的情况下诱导或抑制铁死亡的化合物。 - 探索线粒体活性氧、铁代谢和脂质过氧化在细胞死亡实验中的相互作用。

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