pRetroX-IRES-ZsGreen1逆转录病毒载体
pRetroX-IRES-ZsGreen1 is a bicistronic, fl uorescent, retroviral vector that allows both a gene of interest and the ZsGreen1 gene to be translated from a single bicistronic mRNA. pRetroXIRES- ZsGreen1 is designed for effi cient delivery and selection (by fl ow cytometry or other methods) of stably transduced mammalian cells expressing the ZsGreen1 fl uorescent protein and the protein of interest. This vector can be used to obtain stable cell lines without timeconsuming drug and clonal selection. ZsGreen1 is derived from the reef coral Zoanthus sp. green fl uorescent protein (ZsGreen) and is easily detected with standard FITC fi lter sets (1).
Bicistronic expression from this vector is facilitated by the encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES). This IRES facilitates cap-independent translation from an internal start site at the IRES/ZsGreen1 junction (2). ZsGreen1 is a human codon optimized ZsGreen variant that encodes the brightest commercially available green fl uorescent protein (1). This retroviral vector is derived from the pMIN series of vectors (3, 4). These optimized vectors have the ability to produce high viral titers, express genes at high levels, and, due to the absence of retroviral coding sequences, exhibit improved safety profi les. The multiple cloning site (MCS) in pRetroX-IRES-ZsGreen1 is between the 5’ MMLV LTR and the IRES sequence. Genes cloned into the MCS are expressed as a bicistronic message transcribed from the 5’ LTR.
pRetroX-IRES-ZsGreen1 contains all of the necessary viral RNA processing elements; these include the 5’ and 3’ LTRs, the packaging signal (ψ), and the tRNA primer-binding site. For safety reasons, however, the vector lacks the structural genes (gag, pol, and env) necessary for retroviral particle formation and replication. pRetroX-IRES-ZsGreen1 contains a ColE1 origin of replication, and an E. coli Ampr gene for propagation and selection in bacteria.
pRetroX-IRES-ZsGreen1 is designed to effi ciently deliver and co-express your gene of interest and ZsGreen1 in any mitotically-active mammalian cell. When cloning into pRetroX-IRES-ZsGreen1, your gene of interest should contain an initiation codon (ATG) and a stop codon. The vector can be infected or transfected into mammalian cells. If required, stable transformants can be selected by fl ow cytometry or limiting dilution.
In order to infect mammalian cells with pRetroX-IRES-ZsGreen1, the vector must be transfected into a packaging cell line, such as the RetroPack? PT67 Cell line (631510), AmphoPack?-293 (631505), EcoPack?2- 293 (631507), Pantropic Expression System (631512), or Retro-X? Universal Packaging System (631530). These cell lines package RNA from the vector into infectious, replication-incompetent, retroviral particles. Such retroviral particles can infect target cells and transmit the gene of interest, but cannot replicate within these cells due to the absence of viral structural genes. The separate introduction and integration of the structural genes into the packaging cell line minimizes the chance of producing replication-competent virus due to recombination events during cell proliferation.
基因搜项目发展历程最早可追溯至2010年01月05日域名注册，项目发起即为促进基因资源共享，避免在基因研究工作中“重复造轮子”，节约广大科研精英的宝贵时间和精力。
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