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pRS-shRNA29基因干扰逆病毒质粒载体
Viral Packaging RetroviralFeature The HuSH pRS plasmid vector incorporates all the elements as above two vectors with the absence of a fluorescence marker. The bacterial selection marker for pRS vector is ampicillin and the mammalian selection can still be achieved with puromycin.Product Description: · Plasmid vector for cloning shRNA expression cassettes · Designed for long term gene silencing studies· Ampicillin (100ug/ml) and Puromycin resistance markers for easy selection of transformed or transfected cells· U6 polymerase III promoter for shRNA expression· MMLV LTR sequences for packaging into retroviral particles· EcoRI and HindIII sites convenient for shuttling existing HuSH cassettesQuality Control AssaysDNA Quantitation: The concentration of the purified plasmid was determined at OD260 by a UV spectrometer. DNA Sequence Analysis: The final purified plasmid was sequenced to confirm its identity. Functional Analysis:1. Cloning: the pRS plasmid was digested with BamHI and HindIII and the digested fragment isolated. Multiple shRNA expression cassettes were cloned into this plasmid. 2. Inhibition of target gene: shRNA constructs cloned into pRS were verified for inhibition of target genes. 3. Stable cell lines: pRS was verified to generate stable cell lines using direct transfection
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
Viral Packaging RetroviralFeature The HuSH pRS plasmid vector incorporates all the elements as above two vectors with the absence of a fluorescence marker. The bacterial selection marker for pRS vector is ampicillin and the mammalian selection can still be achieved with puromycin.Product Description: · Plasmid vector for cloning shRNA expression cassettes · Designed for long term gene silencing studies· Ampicillin (100ug/ml) and Puromycin resistance markers for easy selection of transformed or transfected cells· U6 polymerase III promoter for shRNA expression· MMLV LTR sequences for packaging into retroviral particles· EcoRI and HindIII sites convenient for shuttling existing HuSH cassettesQuality Control AssaysDNA Quantitation: The concentration of the purified plasmid was determined at OD260 by a UV spectrometer. DNA Sequence Analysis: The final purified plasmid was sequenced to confirm its identity. Functional Analysis:1. Cloning: the pRS plasmid was digested with BamHI and HindIII and the digested fragment isolated. Multiple shRNA expression cassettes were cloned into this plasmid. 2. Inhibition of target gene: shRNA constructs cloned into pRS were verified for inhibition of target genes. 3. Stable cell lines: pRS was verified to generate stable cell lines using direct transfection
Supplier来源:BioVector NTCC Inc.
TEL电话:400-800-2947
Website网址: http://www.biovector.net
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