CXCR2基因敲除Hela细胞

CXCR2基因敲除Hela细胞
货号:

EDJ-KQ53642

物种:

细胞名称:

HeLa

基因名称:

CXCR2

基因ID:

3579

规格:

1×10⁶cells

CXCR2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-KQ53642
产品名称 CXCR2 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 CXCR2
基因ID
基因别名 CD182|CDw128b|CMKAR2|IL8R2|IL8RA|IL8RB|WHIMS2
摘要
The protein encoded by this gene is a member of the G-protein-coupled receptor family. This protein is a receptor for interleukin 8 (IL8). It binds to IL8 with high affinity, and transduces the signal through a G-protein activated second messenger system. This receptor also binds to chemokine (C-X-C motif) ligand 1 (CXCL1/MGSA), a protein with melanoma growth stimulating activity, and has been shown to be a major component required for serum-dependent melanoma cell growth. This receptor mediates neutrophil migration to sites of inflammation. The angiogenic effects of IL8 in intestinal microvascular endothelial cells are found to be mediated by this receptor. Knockout studies in mice suggested that this receptor controls the positioning of oligodendrocyte precursors in developing spinal cord by arresting their migration. This gene, IL8RA, a gene encoding another high affinity IL8 receptor, as well as IL8RBP, a pseudogene of IL8RB, form a gene cluster in a region mapped to chromosome 2q33-q36. Alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2009]
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

该敲除模型可用于: - 研究受CXCR2缺陷影响的编码基因和非编码RNA的调控网络。 - 研究CXCR2在宫颈癌细胞中调控基因表达和信号通路的功能。 - 探索CXCR2在肿瘤生物学中的作用,包括增殖、迁移和侵袭。 - 评估CXCR2敲除对非编码RNA介导的调控机制的影响。 - 作为靶向药物筛选和针对CXCR2相关通路治疗药物开发的细胞模型。

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