GPX4基因敲除HCT116细胞

GPX4基因敲除HCT116细胞
货号:

EDJ-KQ70373

物种:

细胞名称:

HCT 116

基因名称:

GPX4

基因ID:

2879

规格:

1×10⁶ cells

GPX4基因敲除细胞HCT116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-KQ70373
细胞 HCT116
Cellosaurus ID CVCL_0291
细胞别名 HCT-116, HCT.116, HCT_116, HCT116, HCT116wt, HCT-116/P, HCT-116/parental, CoCL2
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 Colorectal Carcinoma
细胞形态 Adherent
传代比率 1/5-1/4,2days
完全培养基 mcCoy5A+10% FBS
冻存培养基 90% FBS/完培+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: HCT 116
细胞库细胞STR信息
细胞库细胞名: HCT 116
Allele1Allele2Allele3Allele4Allele1 Allele2 Allele3 Allele4
AmelogeninXX
CSF1PO710791011
D2S13381616
D3S135812171819121819
D5S81810111011
D7S82011121112
D8S11791012141510121415
D13S31710121012
D16S539111311121314
D18S5116171617
D19S433121312
D21S1129302930
FGA18231823
Penta D913913
Penta E121314121314
TH018989
TPOX88
vWA1721222317212223
D6S104313
D12S391172122
D2S4411112
* 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=4.8
Pharmaceuticals (Basel, Switzerland)
该基因敲除模型可用于: - 研究铁死亡抵抗机制和补偿途径 - 筛选铁死亡诱导化合物并评估药物疗效 - 研究GPX4依赖性细胞死亡调控和氧化还原生物学 - 模拟氧化应激相关疾病和治疗干预措施 - 验证癌症研究中的合成致死靶点

配套产品

相关产品

HCT 116(人结直肠腺癌细胞)HCT 116(人结直肠腺癌细胞)

相关服务

基因敲除细胞基因敲除细胞
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