Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Size (kb): 5.7810001373291020
Vector: pXC37 (plasmid)
Promoters: Promoter for expression lambda PL
Construction: pXC24, oligo cassette
Construct size (kb): 5.781000137329102
Features: initiation codon: ATG
promoter for expression: lambda PL
replicon: ROP copy number control
restriction site: 3' sites HindIII...BamHI
restriction site: 5' NsiI/NdeI site
ribosome-binding site: synthetic Shine-Dalgarno
spacer sequence: AAAAAA
transcription terminator: partially deleted lambda terminator
translational enhancer: T7 gene 10
coding sequence: 14-3-3
in another host, produces protein
vector useful for cloning PCR products
Restriction digests of the clone give the following sizes (kb): BamHI--5.8; EcoRI--5.8; HindIII--5.8.
The vector contains a 0.7 kb bovine cDNA that can be excised using the 5' and 3' cloning sites and be replaced by a gene of interest. The bovine insert may be used as a positive control for expression.
One of 12 expression vectors (ATCC 86990-87001) designed to maximize expression from the lambda PL promoter and support cloning of PCR products. The vectors differ in cloning sites and in translational enhancer and initiation sequences.
The bovine insert or target sequences cloned into the NsiI/NdeI site are expressed as a Met-His fusion protein.
Cheng X, Patterson TA. Construction and use of lambda PL promoter vectors for direct cloning and high level expression of PCR amplified DNA coding sequences. Nucleic Acids Res. 20: 4591-4598, 1992. PubMed: 1408761
Shipped: Freeze dried Escherichia coli TAP308 containing the plasmid.