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MAPK1基因敲除细胞池(HEK293)
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原料试剂 研发实验室
价格
¥5499.00
品牌 粒曼生物
地区 中国,湖北省,武汉市
货号 LM01024100030
产地 国产
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1×10^6 cells/ 冻存管
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粒曼生物科技(武汉)有限公司
粒曼生物科技(武汉)有限公司
中国湖北武汉
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粒曼生物专注于提供高通量细胞编辑解决方案,服务新药研发与基础科研。 粒曼生物是一家专注于高通量细胞编辑工具研发的技术驱动型公司,核心技术来自加州大学伯克利分校,公司已完成人全基因组19883个基因的敲除实验验证。基于粒曼工业智能化高通量体外细胞编辑平台,为客户提供基因敲除、过表达、点突变、原位/定点敲入定制服务及基因编辑细胞现货、基因敲除试剂盒等系列产品,助力新药研发与基础研究。 粒曼作为国内高通量基因敲除阵列文库领域的领导者,已建成自动化、高通量基因敲除平台,实现每月1000+ KO 细胞的生产产能。粒曼基于自身构建的 Harbor 细胞和 pCargo 质粒载体系统,实现 2 周高效构建稳定细胞系。
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产品规格
品牌名称
粒曼生物
货号
LM01024100030
国产/进口
国产
规格
1×10^6 cells/ 冻存管
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细胞基因敲除效率:>70%

MAPK1 NCBI Gene ID:5594

MAPK1 Ensembl ID:ENSG00000100030

MAPK1 Uniprot ID:P28482

MAPK1 基因介绍:Acts as a transcriptional repressor. Binds to a [GC]AAA[GC] consensus sequence. Repress the expression of interferon gamma-induced genes. Seems to bind to the promoter of CCL5, DMP1, IFIH1, IFITM1, IRF7, IRF9, LAMP3, OAS1, OAS2, OAS3 and STAT1. Transcriptional activity is independent of kinase activity.||Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway. MAPK1/ERK2 and MAPK3/ERK1 are the 2 MAPKs which play an important role in the MAPK/ERK cascade. They participate also in a signaling cascade initiated by activated KIT and KITLG/SCF. Depending on the cellular context, the MAPK/ERK cascade mediates diverse biological functions such as cell growth, adhesion, survival and differentiation through the regulation of transcription, translation, cytoskeletal rearrangements. The MAPK/ERK cascade plays also a role in initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors. About 160 substrates have already been discovered for ERKs. Many of these substrates are localized in the nucleus, and seem to participate in the regulation of transcription upon stimulation. However, other substrates are found in the cytosol as well as in other cellular organelles, and those are responsible for processes such as translation, mitosis and apoptosis. Moreover, the MAPK/ERK cascade is also involved in the regulation of the endosomal dynamics, including lysosome processing and endosome cycling through the perinuclear recycling compartment (PNRC); as well as in the fragmentation of the Golgi apparatus during mitosis. The substrates include transcription factors (such as ATF2, BCL6, ELK1, ERF, FOS, HSF4 or SPZ1), cytoskeletal elements (such as CANX, CTTN, GJA1, MAP2, MAPT, PXN, SORBS3 or STMN1), regulators of apoptosis (such as BAD, BTG2, CASP9, DAPK1, IER3, MCL1 or PPARG), regulators of translation (such as EIF4EBP1) and a variety of other signaling-related molecules (like ARHGEF2, DCC, FRS2 or GRB10). Protein kinases (such as RAF1, RPS6KA1/RSK1, RPS6KA3/RSK2, RPS6KA2/RSK3, RPS6KA6/RSK4, SYK, MKNK1/MNK1, MKNK2/MNK2, RPS6KA5/MSK1, RPS6KA4/MSK2, MAPKAPK3 or MAPKAPK5) and phosphatases (such as DUSP1, DUSP4, DUSP6 or DUSP16) are other substrates which enable the propagation the MAPK/ERK signal to additional cytosolic and nuclear targets, thereby extending the specificity of the cascade. Mediates phosphorylation of TPR in respons to EGF stimulation. May play a role in the spindle assembly checkpoint. Phosphorylates PML and promotes its interaction with PIN1, leading to PML degradation. Phosphorylates CDK2AP2 (By similarity).

细胞生长培养基:DMEM+10% FBS+1% P,S

细胞培养条件:37℃,5% CO2 的培养箱,1/3到 1/4 传代

细胞倍增时间:~24-45 hours

细胞支原体检测结果:阴性

细胞开发路径:采用CRISPR-RNP方法生成稳定KO Cell Pool;Sanger 测序结果显示KO Cell Pool敲除效率>70%

细胞应用:高敲除效率的基因敲除细胞池(KO Cell Pool),特别适用于初步功能分析、复杂疾病模型的开发、精准药物筛选以及广泛的基因发现研究。

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