WebFrom making transgenic animals, gene targeting and genome modifications to reporter vectors (e.g. pBV-Luc) and gene silencing (e.g. pLKO.1 - TRC cloning vector). Check out our complete guide to empty backbones for …
pAbAi Sequence and Map - SnapGene
WebBackground. When choosing what plasmid backbone to use, you have many elements to consider. Here is a guide to Addgene's empty vector backbones. For the most part, we … This plasmid is available through Addgene. Image: Illustrated plasmid map in PNG … WebThe pLKO.1-puro Control Vector is provided as 10 μg of plasmid DNA in Tris-EDTA (TE) buffer at a concentration of 500 ng/μl. Application MISSION ® pLKO.1-puro Empty Vector Control Plasmid DNA has been used to … shops lye
MISSION ® pLKO.1-puro Empty Vector Control Plasmid DNA
WebMy empty vector contains only eGFP while the modified vector contains my gene of interest fused to eGFP. Transfection efficiency is close to 90% in the first one with cells showing clear green ... WebpEpicVector3mC_Puro-T2A-mCherry-VSVg-StrepTagII-AU1 Citations (1) Plasmid Article: Spatial epitope barcoding reveals subclonal tumor patch behaviors. Rovira-Clavé X, Drainas AP, Jiang S, Bai Y, Baron M, Zhu B, Markovic M, Coles GL, Bassik MC, Sage J, Nolan GP bioRxiv 2024 Journal. WebPopular answers (1) 1) Your plasmid could be self ligating. Try dephosphorylating plasmid and then use for cloning. 2) Your insert may be too big. You can try using stbl2 cells or grow cells at 30 ... shops lyme regis