PABPC4基因敲除Hela细胞

PABPC4基因敲除Hela细胞
货号:

EDJ-KQ30306

物种:

细胞名称:

HeLa

基因名称:

PABPC4

基因ID:

8761

规格:

1×10⁶cells

PABPC4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-KQ30306
产品名称 PABPC4 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 PABPC4
基因ID
基因别名 APP-1|APP1|PABP4|iPABP
摘要
Poly(A)-binding proteins (PABPs) bind to the poly(A) tail present at the 3-prime ends of most eukaryotic mRNAs. PABPC4 or IPABP (inducible PABP) was isolated as an activation-induced T-cell mRNA encoding a protein. Activation of T cells increased PABPC4 mRNA levels in T cells approximately 5-fold. PABPC4 contains 4 RNA-binding domains and proline-rich C terminus. PABPC4 is localized primarily to the cytoplasm. It is suggested that PABPC4 might be necessary for regulation of stability of labile mRNA species in activated T cells. PABPC4 was also identified as an antigen, APP1 (activated-platelet protein-1), expressed on thrombin-activated rabbit platelets. PABPC4 may also be involved in the regulation of protein translation in platelets and megakaryocytes or may participate in the binding or stabilization of polyadenylates in platelet dense granules. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. This protein has also been found to interact with coronavirus nucleocapsid proteins and is thought to inhibit coronavirus replication. [provided by RefSeq, Nov 2021]
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=13.1
Nucleic acids research
该KO模型可能有助于: - 研究PABPC4在青春期泛素化介导的mRNA稳定性及翻译调控中的作用; - 研究神经内分泌信号通路中GNRH1表达的调控机制; - 探索MKRN3依赖的poly(A)结合蛋白的转录后调控; - 模拟与mRNA代谢改变相关的青春期发育障碍; - 验证PABPC4在与生殖生物学相关的RNA-蛋白质相互作用网络中的功能。

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