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The vector sequence has been compiled using the information from sequence databases, published literature, and other sources, together with partial sequences obtained by Evrogen. This vector has not been completely sequenced. |
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TurboGFP | ||||
BamH I | ||||
RBS | ATG. | AGA.GGA.TCG. | GGA.TCC. | GAG.AGC.GAC... |
Stop | |||
Hind III | |||
... | TG | A. | AGC.TT |
pTurboGFP-B is a prokaryotic expression vector encoding green fluorescent protein TurboGFP (see reporter description). Reporter codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996].
The vector is primarily intended as a source of TurboGFP coding sequence. Flanking restriction sites are convenient for excision of TurboGFP sequence and its further insertion into other expression vectors of choice. Alternatively, TurboGFP coding sequence can be amplified by PCR.
Note: The plasmid DNA was isolated from dam+-methylated
The vector can be also used for TurboGFP expression in prokaryotes under the control of T5 promoter/lac operator. The vector backbone contains ColE1 origin of replication and ampicillin resistance gene for propagation and selection in
Location of features
T5 promoter/lac operator element: 7-87
T5 transcription start: 61
TurboGFP coding sequence: 132-827
Lambda t0 transcriptional termination region: 848-942
rrnB T1 transcriptional termination region: 1704-1802
ColE1 origin of replication: 2278
beta-lactamase coding sequence: 3896-3036
TurboGFP-related materials (also referred to as "Products") are intended for research use only. The Products are covered by U.S. Pat. 7,678,893; European Pat. 1576157; and other Evrogen Patents and/or Patent applications pending. By use of these Products, you accept the terms and conditions of the applicable Limited Use Label License.
Copyright 2002-2023 Evrogen. All rights reserved. Evrogen JSC, 16/10 Miklukho-Maklaya str., Moscow, Russia, Tel +7(495)988-4084, Fax +7(495)988-4085, e-mail:evrogen@evrogen.com |