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  • 產(chǎn)品名稱(chēng):pGBBAXsiRNAVectorMix

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  • 產(chǎn)品廠(chǎng)商:Biovision
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pGBBAXsiRNAVectorMix
詳情介紹:
Characteristics Small interfering RNAs (siRNAs) are short, double-stranded RNA molecules that can target and degrade specific complementary mRNAs. The target gene-specific degradation is an effective means of gene suppression. GeneBlockertm pGB siRNA vectors are designed to provide efficient, long-term suppression of a target gene in cultured mammalian cells and in vivo. The pGB vectors have been optimized for suppressing expression of target genes using the human U6 promotor (a RNA polymerase III promotor) which generates large amounts of siRNA in mammalian cells. The pGB vectors also provide neomycin resistance marker for the selection of stable cell lines, permitting long-term suppression of the target gene. BioVision offers pGB siRNA vector mix which consists of 4 siRNA vectors for each gene targeted. pGB siRNA negative control vector and pGB cloning vector for cloning in your own insert are also available. Description of the Vectors: pGB expression vectors contain the human U6 RNA polymerase III promoter, which directs constitutive, high-level expression of short RNA transcripts in many cells. Each vector also contains the neomycin/kanamycin-resistance gene to provide kanamycin resistance in bacteria and the G418 resistance in mammalian cells. In addition, pGB Cloning vector which is used to clone your own insert and pGB Negative Control vector which contains an insert that does not have significant homology to mammalian genes expressed in human, mouse, and rat, and therefore can be used as a negative control for pGB-expression vectors. The pGB siRNA vectors are designed to suppress the expression of some of the most important apoptosis genes, individually. The mix of four siRNA vectors for each gene has been proven more efficient for gene suppression.
Application Notes The pGB siRNA vector Mix (1 μ g/ μ l) can be transfected into mammalian cells using Lipofectamine (Invitrogen). For transient transfection, cells can be analyzed in 24-96 hours following transfections, by Western blot analysis or other detection means. For stable transfections, cells can be selected in G418 selection medium to obtain stable cell lines with the specific gene blocked.
Restrictions For Research Use only
Storage -20 °C