RAB8A基因敲除Hela细胞

RAB8A基因敲除Hela细胞
货号:

EDJ-KQ21773

物种:

细胞名称:

HeLa

基因名称:

RAB8A

基因ID:

4218

规格:

1×10⁶cells

RAB8A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-KQ21773
产品名称 RAB8A 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 RAB8A
基因ID
基因别名 MEL|RAB8
摘要
The protein encoded by this gene is a member of the RAS superfamily which are small GTP/GDP-binding proteins with an average size of 200 amino acids. The RAS-related proteins of the RAB/YPT family may play a role in the transport of proteins from the endoplasmic reticulum to the Golgi and the plasma membrane. This protein shares 97%, 96%, and 51% similarity with the dog RAB8, mouse MEL, and mouse YPT1 proteins, respectively and contains the 4 GTP/GDP-binding sites that are present in all the RAS proteins. The putative effector-binding site of this protein is similar to that of the RAB/YPT proteins. However, this protein contains a C-terminal CAAX motif that is characteristic of many RAS superfamily members but which is not found in YPT1 and the majority of RAB proteins. Although this gene was isolated as a transforming gene from a melanoma cell line, no linkage between MEL and malignant melanoma has been demonstrable. This oncogene is located 800 kb distal to MY09B on chromosome 19p13.1. [provided by RefSeq, Jul 2008]
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=1.3
Genes to cells : devoted to molecular & cellular mechanisms
该敲除模型可能有助于: - 研究 RAB8A 在囊泡运输和膜动力学中的作用。 - 研究 OPTN-RAB8A 在自噬和选择性运输中的相互作用的结构和功能。 - 阐明参与细胞稳态和蛋白质质量控制的信号通路。 - 验证 RAB8A 作为神经退行性疾病或炎症性疾病模型靶点的功能。 - 利用细胞分析筛选 RAB8A 依赖性运输或 OPTN 结合的调节因子。

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