动物体内转染试剂,基因敲除和转基因的革命!

动物体内转染试剂,基因敲除和转基因的革命!

价格: ¥1880

品牌:engreen 品牌认证

货号:18668-11-1,18668-11-2

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保存条件 :4度

保质期 :12个月

英文名 :Entranster-in vivo transfection reagent

供应商 :英格恩生物

规格 :0.5ml

主要特点

● 最快3天可以得到结果,核酸+转染试剂,注射动物,完成转染。

● 肝、肾、心、肺,血液系统,神经系统,生殖系统,皮肤…等都可应用。

● 可方便、快捷更换不同的小片断RNA或DNA进行动物试验。

● 方方法先进,抛弃病毒,众多实验室应用,稳定可靠。

● 比使用病毒节省90%以上费用,时间缩短到3天!


应用范围

● 专用于动物体内转染,可直接转染DNA或RNA到动物体内进行。

● 基因治疗的动物体内研究。

● RNA干扰的动物体内研究。

● 蛋白功能的动物体内研究。

方法简单

如图1所示,只需要将核酸和转染试剂分别稀释,混合,无需过滤,即可直接注射动物。

转染效果


将EntransterTM-in vivo与Ambion in vivo siRNA(作用于凝血因子VII)和阴性siRNA通过尾静脉注射成年小鼠,2天后,取动物肝脏检测。在mRNA水平和蛋白水平观察干扰效果。见上图,图中最左侧组为对照组注射阴性siRNA为3mg/kg,后边3组为每kg动物注射阳性siRNA量分别为1mg/kg,2mg/kg和3mg/kg情况。

各器官转染


根据推荐用量注射EntransterTM-in vivo和siRNA(作用于Lamin A/C)和阴性siRNA到成年小鼠。注射后2天收集相应的组织,分离RNA,用qRT-PCR分析Lamin A/C基因的表达水平。图4为尾静脉结果,图5为各器官分别局部注射结果。

应用本产品部分文献

1.Biochemical and Biophysical Research Communications. 2017 May 25. Targeting long non-coding RNA ASBEL with oligonucleotide antagonist for breast cancer therapy.(长链非编码RNA与乳腺癌治疗)

2.Journal of Neurochemistry. 2017 May 24. TRAF6 participates in early brain injury after subarachnoid hemorrhage in rats through inhibiting autophagy and promoting oxidative stress.(大鼠蛛网膜下腔出血与早期脑损伤)

3.Clin Exp Pharmacol Physiol. 2017 May 19. Limb remote ischaemic postconditioning-induced elevation of fibulin-5 confers neuroprotection to rats with cerebral ischaemia/reperfusion injury: Activation of the AKT pathway.(AKT通路与大鼠大脑局部缺血/再灌注损伤)

4.Neurological Research. 2017 May 1. The 15-LO-1/15-HETE system promotes angiogenesis by upregulating VEGF in ischemic brains. (15-LO-1siRNA通过在小鼠缺血性脑中上调VEGF来促进血管生成)

5.Blood. 2017 Apr 27. Osteoblasts support megakaryopoiesis through production of interleukin 9.(IF: 11.841.)(成骨细胞与白介素9研究)

6.Arthritis&Rheumatol, 2016 Apr. In Vivo Therapeutic Success of MicroRNA‐155 (miR‐155) Antagomir in a Mouse Model of Lupus Alveolar Hemorrhage.(IF: 6.009.)(miR‐155拮抗剂体内成功治疗狼疮性肺泡出血模型的小鼠)

7.Canadian Journal of Physiology and Pharmacology. 2016 Nov 24. miR-29b promotes skin wound healing and reduces excessive scar formation by inhibition of TGF-β1/Smad/CTGF signaling pathway.(miR-29b通过抑制TGF-β1/ Smad / CTGF信号通路促进皮肤伤口愈合并减少过度瘢痕形成)

8.Scientific Reports. 2016 Sep 19. Transient receptor potential channel 1/4 reduces subarachnoid hemorrhage-induced early brain injury in rats via calcineurin-mediated NMDAR and NFAT dephosphorylation.(IF: 5.228.)(蛛网膜下腔出血和小鼠大脑损伤)

9.Am J Cancer Res. 2016 Jun 1. BMPR2-pSMAD1/5 signaling pathway regulates RUNX2 expression and impacts the progression of dedifferentiated chondrosarcoma.(BMPR2-pSMAD1 / 5信号通路调节RUNX2表达,并影响去分化软骨肉瘤的进展)

10.Scientific Reports. 2016 Jun 29. Molecular characterization of woodchuck IFI16 and AIM2 and their expression in woodchucks infected with woodchuck hepatitis virus (WHV).(IF: 5.228.)(土拨鼠肝炎病毒感染的土拨鼠中IFI16和AIM2的分子鉴定及表达)

11.Oncotarget. 2016 Sep 26. HMGB2 regulates satellite-cell-mediated skeletal muscle regeneration through IGF2BP2.(IF: 5.008.)(HMGB2通过IGF2BP2调节卫星细胞介导的骨骼肌再生)

12.Journal of Bone and Mineral Research. 2016 Sep 26. TET3 Mediates Alterations in the Epigenetic Marker 5hmC and Akt Pathway in Steroid-Associated Osteonecrosis.(IF: 5.622.)(TET3介导类固醇相关性骨坏死中表观遗传标记5hmC和Akt途径的改变)

13.Journal of Bone and Mineral Research. 2016 Nov 24. The Circadian Gene Clock Regulates Bone Formation via PDIA3.(IF: 5.622.)(昼夜节律基因时钟通过PDIA3调节骨形成)

14.Hepatology, 2015 JUL 3. MicroRNA-125b attenuates epithelial-mesenchymal transitions and targets stem-like liver cancer cells through small mothers against decapentaplegic 2 and 4.((MicroRNA-125b通过small mothers减少Dpp2和4以减弱上皮细胞-间充质细胞转化并作用于肝癌细胞干细胞)(IF: 11.711.)

15.Critical Care Medicine, 2015, June 27. Cyclophilin A/Cluster of Differentiation 147 Interactions Participate in Early Brain Injury After Subarachnoid Hemorrhage in Rats.(大鼠蛛网膜下腔出血早期亲环蛋白A/CD147相互作用)(IF: 7.422.)

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