FADD基因敲除HCT116细胞

FADD基因敲除HCT116细胞
货号:

EDJ-KQ21050

物种:

细胞名称:

HCT 116

基因名称:

FADD

基因ID:

8772

规格:

1×10⁶ cells

FADD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-KQ21050
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 FADD
基因ID
基因别名 GIG3|IMD90|MORT1
摘要
The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development. [provided by RefSeq, Jul 2008]
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=5.1
Communications biology
Mind bomb 2 (MIB2) is an E3 ligase involved in Notch signalling and attenuates TNF-induced apoptosis through ubiquitylation of receptor-interacting protein kinase 1 (RIPK1) and cylindromatosis. Here we show that MIB2 bound and conjugated K48- and K63-linked polyubiquitin chains to a long-form of cellular FLICE-inhibitory protein (cFLIP), a catalytically inactive homologue of caspase 8. Deletion of MIB2 did not impair the TNF-induced complex I formation that mediates NF-κB activation but significantly enhanced formation of cytosolic death-inducing signalling complex II. TNF-induced RIPK1 Ser phosphorylation, a hallmark of RIPK1 death-inducing activity, was enhanced in MIB2 knockout cells, as was RIPK1 kinase activity-dependent and -independent apoptosis. Moreover, RIPK1 kinase activity-independent apoptosis was induced in cells expressing cFLIP mutants lacking MIB2-dependent ubiquitylation. Together, these results suggest that MIB2 suppresses both RIPK1 kinase activity-dependent and -independent apoptosis, through suppression of RIPK1 kinase activity and ubiquitylation of cFLIP, respectively.
该敲除模型可用于: - 研究FADD在RIPK1激酶活性依赖性和非依赖性凋亡通路中的作用。 - 研究MIND bomb 2介导的cFLIP泛素化在细胞死亡信号中的调节机制。 - 验证泛素连接酶介导的凋亡与坏死性凋亡细胞命运控制的功能。 - 筛选在结直肠癌背景下调节FADD依赖性凋亡的化合物。 - 解析FADD、RIPK1和cFLIP在死亡受体信号复合物中的相互作用。

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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