ppcrscript amp sk+ cloning vector (Agilent technologies)
Structured Review
Ppcrscript Amp Sk+ Cloning Vector, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ppcrscript+cloning+vector/pm18466981-52-14-19
Average 90 stars, based on 1 article reviews
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Polymerase Chain Reaction:Article Title: Cloning, expression, and functional characterization of human cyclooxygenase-1 splicing variants: evidence for intron 1 retention. Article Snippet: Recently, a splicing variant of cyclooxygenase (COX)-1, arising via the retention of its intron 1, was identified in canine.. It was called COX-3 and was reported to be differentially sensitive to inhibition by various nonsteroidal anti-inflammatory drugs (NSAIDs) as well as acetaminophen (Chandrasekharan et al., 2002).. However, the existence of an orthologous splicing variant in human tissues has been questioned due to a reading frame shift and premature termination. Cloning:Article Title: Cloning, expression, and functional characterization of human cyclooxygenase-1 splicing variants: evidence for intron 1 retention. Article Snippet: Recently, a splicing variant of cyclooxygenase (COX)-1, arising via the retention of its intron 1, was identified in canine.. It was called COX-3 and was reported to be differentially sensitive to inhibition by various nonsteroidal anti-inflammatory drugs (NSAIDs) as well as acetaminophen (Chandrasekharan et al., 2002).. However, the existence of an orthologous splicing variant in human tissues has been questioned due to a reading frame shift and premature termination. Plasmid Preparation:Article Title: Cloning, expression, and functional characterization of human cyclooxygenase-1 splicing variants: evidence for intron 1 retention. Article Snippet: Recently, a splicing variant of cyclooxygenase (COX)-1, arising via the retention of its intron 1, was identified in canine.. It was called COX-3 and was reported to be differentially sensitive to inhibition by various nonsteroidal anti-inflammatory drugs (NSAIDs) as well as acetaminophen (Chandrasekharan et al., 2002).. However, the existence of an orthologous splicing variant in human tissues has been questioned due to a reading frame shift and premature termination. |
