REN基因敲除HCT116细胞

REN基因敲除HCT116细胞
货号:

EDJ-KQ71269

物种:

细胞名称:

HCT 116

基因名称:

REN

基因ID:

5972

规格:

1×10⁶ cells

REN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-KQ71269
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 REN
基因ID
基因别名 ADTKD4|HNFJ2|RTD
摘要
This gene encodes renin, an aspartic protease that is secreted by the kidneys. Renin is a part of the renin-angiotensin-aldosterone system involved in regulation of blood pressure, and electrolyte balance. This enzyme catalyzes the first step in the activation pathway of angiotensinogen by cleaving angiotensinogen to form angiotensin I, which is then converted to angiotensin II by angiotensin I converting enzyme. This cascade can result in aldosterone release, narrowing of blood vessels, and increase in blood pressure as angiotension II is a vasoconstrictive peptide. Transcript variants that encode different protein isoforms and that arise from alternative splicing and the use of alternative promoters have been described, but their full-length nature has not been determined. Mutations in this gene have been shown to cause hyperuricemic nephropathy familial juvenile 2, familial hyperproreninemia, and renal tubular dysgenesis. [provided by RefSeq, May 2020]
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=15.7
Nature communications
IF=2.8
Frontiers in genetics
该KO模型可能有助于: - 研究特定lncRNA和编码基因在结肠癌发生发展中的作用; - 研究结直肠癌中MAPK和EZH2介导的表观遗传调控等信号通路; - 评估免疫逃逸机制,包括PD-L1细胞内转运和抗肿瘤免疫; - 验证肿瘤抑制或致癌通路中候选基因的功能; - 在p53野生型结肠癌背景下进行针对形态学改变或细胞凋亡的药物筛选和表型分析。

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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