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启动子 | CMV |
复制子 | pUC |
终止子 | SV40 poly(A) signal |
质粒分类 | 病毒系列,慢病毒克隆载体 |
质粒大小 | 8892bp |
原核抗性 | Amp |
克隆菌株 | Stbl3 |
培养条件 | 37℃ |
表达宿主 | 哺乳细胞 |
诱导方式 | 无须诱导,瞬时表达 |
5'测序引物 | CMV-F:CGCAAATGGGCGGTAGGCGTG |
3'测序引物 | WPRE-R:CATAGCGTAAAAGGAGCAACA |
质粒宿主 | 哺乳细胞,慢病毒 |
质粒用途 | 蛋白表达 |
原核抗性 | 氨苄青霉素 |
pLVX-IRES-tdTomato is an HIV-1-based,
lentiviral expression vector that allows the simultaneous expression of your
protein of interest and tdTomato in virtually any mammalian cell type,
including primary cells. tdTomato is a member of the family of fruit
fluorescent proteins derived from the Discosoma sp. red fluorescent protein,
DsRed . The vector expresses the two proteins from a bicistronic mRNA
transcript, allowing tdTomato to be used as an indicator of transduction
efficiency and a marker for selection by flow cytometry.Expression of the bicistronic
transcript is driven by the constitutively active human cytomegalovirus
immediate early promoter (PCMV IE) located just upstream of the MCS. An
encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES),
positioned between the MCS and tdTomato, facilitates cap-independent
translation of tdTomato from an internal start site at the IRES/tdTomato
junction .
pLVX-IRES-tdTomato contains all of the viral processing
elements necessary for the production of replication-incompetent lentivirus, as
well as elements to improve viral titer, transgene expression, and overall
vector function. The woodchuck hepatitis virus posttranscriptional regulatory
element (WPRE) promotes RNA processing events and enhances nuclear export of
viral RNA , leading to increased viral titers from packaging cells. In
addition, the vector includes a Rev-response element (RRE), which further
increases viral titers by enhancing the transport of unspliced viral RNA out of
the nucleus . Finally, pLVX-IRES-tdTomato also contains a central polypurine
tract/central termination sequence element (cPPT/CTS). During target cell
infection, this element creates a central DNA flap that increases nuclear
import of the viral genome, resulting in improved vector integration and more
efficient transduction. The vector also contains a pUC origin of replication
and an E. coli ampicillin resistance gene (Ampr ) for propagation and selection
in bacteria.
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