英文名称Human Embryonic Kidney Cells ,293T 货号Delf-10618老货号:tings-161813 规格1×10⁶/T25培养瓶 细胞特性贴壁生长,贴壁能力较弱 形态上皮细胞样 来源人;胚胎;肾 传代比例1:2传代 用途仅供科研使用 推荐培养基HEK-293T细胞专用培养基 立即询价说明书 ...
In addition, the results of the DPPH radical scavenging assay showed that RES could effectively scavenge DPPH radicals and had in vitro antioxidant capacity. Conclusion: The major components of resveratrol in peanut red coat have antioxidant effects on HEK293T cells and can ac...
Crocin and quercetin protect HCT116 and HEK293 cells from zearalenone-in- duced apoptosis by reducing endoplasmic reticulum stress. Cell. Stress Chap. http:// dx.doi.org/10.1007/s12192-015-0613-0.Salem I B,Prola A,Boussabbeh M,et al.Crocin and Quercetinprotect HCT116 and HEK293 cells ...
pHEK293 Ultra Expression Vectors enable ultra-high, transient overexpression of a protein of interest in human HEK 293 cells
NPY5R Knockout HEK293T Cells (NPY5R基因敲除HEK293T细胞)是通过同时表达Cas9、目的基因sgRNA和puromycin抗性基因,并实现了目的基因CRISPR敲除的HEK293T细胞。本细胞中目的基因的敲除已经通过T7EI法的验证。本细胞株是多克隆细胞,可用于该目的基因的生物学功能研究,也可以用于该基因相应抗体的验证。
NPY Knockout HEK293T Trizol Lysate (NPY基因敲除HEK293T细胞Trizol裂解液)是通过同时表达Cas9、目的基因sgRNA和puromycin抗性基因,并实现了目的基因CRISPR敲除的多克隆HEK293T细胞的Trizol裂解液。该细胞中目的基因的敲除已经通过T7EI法的验证。本产品可用于该目的基因敲除后其信号通路相关RNA表达的研究。
L00345NPY基因敲除HEK293T细胞Trizol裂解液500µl1258.00元 NPY Knockout HEK293T Cells (NPY基因敲除HEK293T细胞)是通过同时表达Cas9、目的基因sgRNA和puromycin抗性基因,并实现了目的基因CRISPR敲除的HEK293T细胞。本细胞中目的基因的敲除已经通过T7EI法的验证。本细胞株是多克隆细胞,可用于该目的基因的生物学功能...
GCGR/CRE Luciferase Reporter HEK293 Cell Line is a HEK293 cell line that expresses the firefly luciferase reporter, under the control of the cAMP response element (CRE), and human GCGR (Glucagon receptor; NM_000160.5). Activation of GCGR in these cells can be monitored by measuring luciferase...
碧云天同时提供基于CRISPR/Cas9技术的LEP基因敲除的质粒(L28250 pLenti-LEP-sgRNA)、慢病毒(L28251 LEP Knockout Lentivirus)、HEK293T细胞(L28252 LEP Knockout HEK293T Cells)、HEK293T敲除细胞的RIPA裂解液(L28253 LEP Knockout HEK293T RIPA Lysate)、HEK293T敲除细胞的Trizol裂解液(L28254 LEP Knockout HEK...
LEP Knockout HEK293T Cells (LEP基因敲除HEK293T细胞)是通过同时表达Cas9、目的基因sgRNA和puromycin抗性基因,并实现了目的基因CRISPR敲除的HEK293T细胞。本细胞中目的基因的敲除已经通过T7EI法的验证。本细胞株是多克隆细胞,可用于该目的基因的生物学功能研究,也可以用于该基因相应抗体的验证。