SMAD1基因敲除A549细胞

SMAD1基因敲除A549细胞
货号:

EDJ-KQ18634

物种:

细胞名称:

A-549

基因名称:

SMAD1

基因ID:

4086

规格:

1×10⁶cells

SMAD1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-KQ18634
产品名称 SMAD1 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 SMAD1
基因ID
基因别名 BSP-1|BSP1|JV4-1|JV41|MADH1|MADR1
摘要
The protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signals of the bone morphogenetic proteins (BMPs), which are involved in a range of biological activities including cell growth, apoptosis, morphogenesis, development and immune responses. In response to BMP ligands, this protein can be phosphorylated and activated by the BMP receptor kinase. The phosphorylated form of this protein forms a complex with SMAD4, which is important for its function in the transcription regulation. This protein is a target for SMAD-specific E3 ubiquitin ligases, such as SMURF1 and SMURF2, and undergoes ubiquitination and proteasome-mediated degradation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]
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=3.9
The Journal of biological chemistry
该KO模型可能有助于: - 研究TGF-β信号通路及其在细胞运动中的作用 - 研究Rac1活性调控和ARHGAP介导的细胞骨架动力学 - 探索上皮-间质转化(EMT)的机制 - 验证SMAD1在癌细胞迁移和侵袭中的功能 - 筛选TGF-β驱动的转移通路中的治疗靶点

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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