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.
Created by Moore, July 1995, under contract with NCBI. The nucleotides remaining in the codon after cutting the vector with the given enzyme are:BamHI-1, ClaI-?, EcoRI-1, HindIII-1, KpnI-2, PstI-2, SacI-2, SalI-1, SmaI-1, SphI-2, XbaI-1, XmaI-2. Restriction digests of the clone give the following sizes (kb): BamHI--3.85; EcoRI--3.85; HindIII--3.85. (ATCC staff) Nucleotide 1 is the first in the trp fragment, at the beginning of a PvuII site 261 nucleotides upstream of the transcription start site. The multiple cloning site follows codon 323 of trpE. To prevent recircularization of the vector, the depositors recommend including 30 - 50 U of calf alkaline phosphatase in the restriction enzyme digestion used to prepare the vector. E. coli containing pATH vectors should be grown on medium supplemented with tryptophan to prevent expression. Storage as DNA at -20C is preferred; long term storage as cells may result in selection of non-expressing promoter mutations. Fusion proteins are produced in E.coli usually in an insoluble form which facilitates purification.Hybrid proteins larger than 90 kDa are not expressed as efficiently as shorter ones. This is one of a series of vectors (ATCC 37695-37703) designed to facilitate expression of an open reading frame as a trpE fusion protein. Medium is -1 1065 plus ampicillin (50 ug/ml) & tryptophan (10 ug/ml). Hosts: E.coli RR1, E.coli. Related vectors: pATH1, pUC18, pUC8. (Information source: VectorDB ( http://seq.yeastgenome.org/vectordb ).)