Welcome to Vector Database!
Vector database is a digital collection of vector backbones assembled from publications and commercially available sources. This is a free resource for the scientific community that is compiled by Addgene.
This page is informational only - this vector is NOT available from Addgene - please contact the manufacturer for further details.
This vector is NOT available from Addgene.
Clone pJJS312 was produced by insertion of an Sau3A fragment from clone pJLS1021 (#M10299). The region controlling translation of the cat gene has been varied structurally so that the gene is under control of the lac promoter. Altering the potential for secondary structure formation within the translation control region causes a ten-fold variation in the synthesis of the CAT enzyme, whereas varying the distance between the ribosome binding site and the start codon from 7 to 13 bases does not significantly affect the yield of CAT enzyme. If the Shine Dalgarno sequence is situated in a region of mRNA capable of base pairing, the efficiency of translation is decreased. The start codon can initiate translation efficiently even when located in a segment capable of duplex formation. If translation is initiated upstream of the cat start codon, then out of frame overlapping translation reduces CAT production by 90% and in frame overlapping translation prevents detectable initiation of protein synthesis at the cat gene start codon and yields only fusion proteins. NCBI gi: 208721 Hosts: E.coli. Related vectors: pJLS1021. (Information source: VectorDB ( http://seq.yeastgenome.org/vectordb ).)