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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 提供商:
云舟生物科技(广州)有限公司
- 服务名称:
病毒套装
- 规格:
小规格/中规格/大规格
| 规格: | 小规格 | 产品价格: | ¥7180.0 |
|---|---|---|---|
| 规格: | 中规格 | 产品价格: | ¥9480.0 |
| 规格: | 大规格 | 产品价格: | ¥14480.0 |
技术详情
当前我们提供慢病毒类型的CRISPR(3+1)和CRISPRi(3+1)套装。这些CRISPR载体系统均经过我们专门优化,在大肠杆菌中具有高拷贝复制、可包装产生高滴度病毒并且对于靶细胞具有可靠的转导效率。
我们的CRISPR慢病毒载体能将CRISPR/Cas9系统整合进细胞基因组中,随细胞分裂而分裂,实现Cas9和gRNA的长期稳定表达。如果选择非整合型慢病毒进行包装,这种慢病毒转导细胞后由于其突变的整合酶没有功能,病毒DNA不插入细胞基因组并且以非复制型游离体存在于转导细胞中,则转导进细胞的Cas9和gRNA不能持续表达,有助于降低脱靶风险。
在CRISPRi系统中,dCas9是与KRAB和MeCP2阻遏域融合在一起的,具有强大的基因阻遏功能。与shRNA相比,CRISPRi系统可以沉默更多类型基因,如蛋白编码基因、非编码RNA、microRNA等。对于我们的CRISPRi慢病毒套装,其gRNA慢病毒携带Puromycin抗性基因,而dCas9-KRAB-MeCP2慢病毒携带Hygromycin抗性基因。进行实验时,使用Puromycin和Hygromycin两种抗生素筛选转导细胞。
订购信息
注意:以上价格和周期包含载体构建
点击查看我们的慢病毒包装详情
CRISPRi(3+1)慢病毒套装

注意:以上价格和周期包含载体构建
常见问题解答
我们如何测定病毒滴度?
我应该选择单gRNA还是双gRNA用于CRISPR介导的基因敲除?
与shRNA相比,CRISPRi基因沉默具有什么特点?
如何计算gRNA特异性分值?
关注“载体家”公众号,为您详情解答。
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文献和实验- KMT2D deficiency drives lung squamous cell carcinoma and hypersensitivity to RTK-RAS inhibition
Cancer Cell. 2022. doi: 10.1016/j.ccell.2022.11.015. IF: 38.585 - Glycine decarboxylase maintains mitochondrial protein lipoylation to support tumor growth
Cell Metab. 2022. doi: 10.1016/j.cmet.2022.04.006. IF: 31.373 - The RNA-binding protein SRSF3 has an essential role in megakaryocyte maturation and platelet production
Blood. 2022. doi: 10.1182/blood.2021013826. IF: 25.476 - A Myb enhancer-guided analysis of basophil and mast cell differentiation
Nat Commun. 2022. doi: 10.1038/s41467-022-34906-1. IF: 17.694 - Inhibition of FGF receptor blocks adaptive resistance to RET inhibition in CCDC6-RET–rearranged thyroid cancer
J Exp Med. 2022. doi: 10.1084/jem.20210390. IF: 17.579 - Loss of selenoprotein W in murine macrophages alters the hierarchy of selenoprotein expression, redox tone, and mitochondrial functions during inflammation
Redox Biol. 2022. doi: 10.1016/j.redox.2022.102571. IF: 10.787 - Genome-wide CRISPR screen for HSV-1 host factors reveals PAPSS1 contributes to heparan sulfate synthesis
Commun Biol. 2022. doi: 10.1038/s42003-022-03581-9. IF: 6.548 - PINK1 Phosphorylates Drp1S616 to Improve Mitochondrial Fission and Inhibit the Progression of Hypertension-Induced HFpEF
Int J Mol Sci. 2022. doi: 10.3390/ijms231911934. IF: 6.208 - Biofabrication of synthetic human liver tissue with advanced programmable functions
iScience. 2022. doi: 10.1016/j.isci.2022.105503. IF: 6.107 - Stratification of lung squamous cell carcinoma based on ferroptosis regulators: Potential for new therapeutic strategies involving ferroptosis induction
Lung Cancer. 2022. doi: 10.1016/j.lungcan.2022.01.012. IF: 6.081 - Angioplasty induces epigenomic remodeling in injured arteries
Life Sci Alliance. 2022. doi: 10.26508/lsa.202101114. IF: 5.781 - Exosomes/microvesicles target SARS-CoV-2 via innate and RNA-induced immunity with PIWI-piRNA system
Life Sci Alliance. 2022. doi: 10.26508/lsa.202101240. IF: 5.781 - Enhanced Orai1-mediated store-operated Ca2+ channel/calpain signaling contributes to high glucose-induced podocyte injury
J Biol Chem. 2022. doi: 10.1016/j.jbc.2022.101990. IF: 5.486 - Stress granules and mTOR are regulated by membrane atg8ylation during lysosomal damage
J Cell Biol. 2022. doi: 10.1083/jcb.202207091. IF: 5.486 - The influence of CD26+ and CD26− fibroblasts on the regeneration of human dermo-epidermal skin substitutes
Sci Rep. 2022. doi: 10.1038/s41598-022-05309-5. IF: 4.996 - The Chd4 subunit of the NuRD complex regulates Pdx1-controlled genes involved in β-cell function
J Mol Endocrinol. 2022. doi: 10.1530/JME-22-0011. IF: 4.869 - The cytotoxic action of BCI is not dependent on its stated DUSP1 or DUSP6 targets in neuroblastoma cells
FEBS Open Bio. 2022. doi: 10.1002/2211-5463.13418. IF: 2.792 - CRISPR/Cas9 mediated approach to generate YAP-depleted human embryonic stem cell line (MUSIe002-A-1)
Stem Cell Res. 2022. doi: 10.1016/j.scr.2022.102990. IF: 1.587 - Transcriptional super-enhancers control cancer stemness and metastasis genes in squamous cell carcinoma
Nat Commun. 2021. doi: 10.1038/s41467-021-24137-1. IF: 17.694 - Desmosomal proteins of DSC2 and PKP1 promote cancer cells survival and metastasis by increasing cluster formation in circulatory system
Sci Adv. 2021. doi: 10.1126/sciadv.abg7265. IF: 14.957 - TNF leads to mtDNA release and cGAS/STING-dependent interferon responses that support inflammatory arthritis
Cell Rep. 2021. doi: 10.1016/j.celrep.2021.109977. IF: 9.995 - Upregulation of the Clock Gene E4BP4 in Macrophages Induces an Anti-Inflammatory Phenotype Promoting Recovery From Colitis
Cell Rep. 2021. doi: 10.2139/ssrn.3981898. IF: 9.995 - Enhancing CRISPR deletion via pharmacological delay of DNA-PKcs
Genome Res. 2021. doi: 10.1101/gr.265736.120. IF: 9.438 - Thioredoxin reductase is a major regulator of metabolism in leukemia cells
Oncogene. 2021. doi: 10.1038/s41388-021-01924-0. IF: 8.756 - Therapeutic Potential of EWSR1–FLI1 Inactivation by CRISPR/Cas9 in Ewing Sarcoma
Cancers (Basel). 2021. doi: 10.3390/cancers13153783. IF: 6.575 - Discovery and validation of FBLN1 and ANT3 as potential biomarkers for early detection of cervical cancer
Cancer Cell Int. 2021. doi: 10.1186/s12935-021-01802-5. IF: 6.429 - Apoptotic Neuron-Derived Histone Amyloid Fibrils Induce α-Synuclein Aggregation
Mol Neurobiol. 2021. doi: 10.1007/s12035-020-02167-y. IF: 5.682 - Tumor elastography and its association with cell-free tumor DNA in the plasma of breast tumor patients: a pilot study
Quant Imaging Med Surg. 2021. doi: 10.21037/qims-20-443. IF: 4.63 - TET2 directs mammary luminal cell differentiation and endocrine response
Nat Commun. 2020. doi: 10.1038/s41467-020-18129-w. IF: 17.694 - A Single-Cell Transcriptomics CRISPR-Activation Screen Identifies Epigenetic Regulators of the Zygotic Genome Activation Program
Cell Syst. 2020. doi: 10.1016/j.cels.2020.06.004. IF: 11.091
157(6) (2014) 1262-1278. [5] K.H. Siu, W. Chen, Riboregulated toehold-gated gRNA for programmable CRISPR-Cas9 function, Nat Chem Biol 15(3) (2019) 217-220. [6] X.W. Wang, L.F. Hu, J. Hao, L.Q. Liao, Y.T. Chiu, M. Shi, Y. Wang, A microRNA-inducible
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genome elucidates the conquest of land by vertebrates。该工作对 澳洲肺鱼进行全基因组(其基因组是人基因组的 14 倍)测序,其巨大体积归因于富含重复序列及活跃的转座子元件。 研究人员通过贝叶斯系统发育分析确认了肺鱼与陆地两栖爬行类脊椎动物的亲缘关系,对深入理解脊椎动物进化过程的主要转变具有重要意义。图 4:来源 Nature 5. Nature: 参与 III 型 CRISPR-Cas 系统工作的核酸酶 原核生物有 3 种类型的 CRISPR
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)的分子遗传控制系统。pgSIT 使用一种基于 CRISPR 的方法来产生不能飞行的雌性和不育的雄性。研究结果表明,不育的雄蚊后代在以卵或成虫的形式释放时,可以竞争、抑制甚至消灭多代蚊子种群。同时,本研究还表明,这种系统还适用于许多病媒昆虫,以安全、可控和有效的方式减少疾病传播。图片来源:Nature Communications主要研究内容pgSIT 系统及其设计原理为了在埃及伊蚊中有效使用 pgSIT 系统,研究人员首先通过构建转基因 gRNA 来靶向两个特定基因:β-Tubulin 85
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