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1 IPTG treatment caused parallel increases in the levels o
2 IPTG-induced C/EBPalpha caused inhibition of cell prolif
3 IPTG-induced pilin rescued S motility of the DeltapilA s
4 very low inducer concentrations (3-10microM IPTG) and reached levels significantly higher than in st
5 ive in the Lon and OmpT proteases and allows IPTG-inducible expression of recombinant proteins from t
7 mevalonate pathway genes is regulated by an IPTG (isopropyl-beta-D-thiogalactopyranoside)-inducible
8 of BosR in B. burgdorferi, we constructed an IPTG (isopropyl-beta-d-thiogalactopyranoside)-regulated
10 ichia coli RNA metabolism, we constructed an IPTG-inducible pcnB [poly(A) polymerase I, PAP I] contai
11 corresponds closely to that observed for an IPTG-inducible A14 recombinant whose construction and ch
12 n of the 14 genes in the bfp cluster from an IPTG-inducible promoter, in the absence of pJPN14, is su
14 tants and analyzed their activities using an IPTG (isopropyl-beta-d-thiogalactopyranoside)-inducible
18 lets, we study the diffusion of both AHL and IPTG from inducer-filled reservoirs into bacteria-contai
19 Engineered bacteria that integrate AHL and IPTG signals with a synthetic AND gate gene circuit are
20 ilizes but does not eliminate the loops, and IPTG does not redistribute loops among high-FRET topolog
21 When cells were treated with both Tc and IPTG, full induction of cat was reached in 24 h and main
24 d two-fold when transcription was induced by IPTG, but had no detectable effect on protein yield when
30 cted from the immunoprecipitate demonstrated IPTG (isopropylthiogalactoside)-sensitive binding of GFP
31 lot analysis, we demonstrated dose-dependent IPTG induction of LLO during growth in broth culture.
35 that endogenous p21 mRNA increased following IPTG removal, which may be responsible for the continued
38 lative gene expression changes when RNA from IPTG-induced cells was labeled and compared to RNA from
39 lta virB operon mutant expressing virB7 from IPTG-inducible Pklac and virB9 from an AS-inducible Pvir
40 M isopropyl-1-thio-beta-D-galactopyranoside (IPTG) induced the expression of Ha-Ras(Val12), closely f
43 or isopropyl-beta-D-thio-galactopyranoside (IPTG) can be utilized for the implementation of an artif
44 inhibitor isopropyl thio-beta-D-galactoside (IPTG) requires the mutant enzyme to adopt its less favor
45 dition of isopropyl-beta-D-thio-galactoside (IPTG) destabilizes but does not eliminate the loops, and
47 No free-citrate transport was observed in IPTG (isopropyl-beta-d-thiogalactopyranoside)-induced or
49 d retroviral vector, MSCV-In(S), resulted in IPTG-responsive oncogene expression and cell growth.
51 to increasing concentrations of the inducer IPTG (isopropyl-beta-D-thiogalactopyranoside) and were a
53 biomaterials to present the genetic inducer, IPTG, with different modes of activating genetic circuit
54 recombinant virus in which F18 expression is IPTG (isopropyl-beta-d-thiogalactopyranoside) dependent,
56 her involves isopropylthiogalactopyranoside (IPTG)-induced synthesis of sigma 32 at 30 degrees C from
57 This promoter, LTRo, was shown to mediate IPTG-inducible cat expression in rat cells expressing th
59 ollowing infection of mice in the absence of IPTG or d-alanine, the bacterium survived in vivo for le
60 croscopy of cells infected in the absence of IPTG revealed normal-appearing crescents and immature vi
62 scape into the cytosol following addition of IPTG to the cell culture medium, thus yielding the abili
67 directly correlate with the concentration of IPTG (isopropyl-beta-D-thiogalactopyranoside) in the gro
69 ystem II and system I, both under control of IPTG, we have begun to study the capabilities and charac
72 y inducible trc promoter, the elimination of IPTG, the inclusion of the tetracycline resistance gene,
75 ac-fnr delta resDE mutant in the presence of IPTG indicated that resDE has an additional role in B. s
76 The particles prepared in the presence of IPTG were more infectious than those prepared in its abs
77 te starvation conditions, in the presence of IPTG, all strains containing mutated phoR genes showed a
80 In the absence of an inducer (allolactose or IPTG) this strain, DH1 lackan , cannot grow on kanamycin
83 ion could be alleviated by exposure to Tc or IPTG, which inhibited the binding activities of TTA and
85 sed a fusion of rpoD to the LacI-repressible IPTG-inducible promoter, Pspac, to vary the levels of si
88 Metabolic labelling of newly synthesized IPTG-induced proteins during/absence of proteasomal inhi
90 e consistency in the phenotypes seen for the IPTG- and TET-inducible recombinants confirms the effica
92 ription, fnr was placed under control of the IPTG (isopropyl-beta-D-thiogalactopyranoside)-inducible
93 spx gene was placed under the control of the IPTG (isopropyl-beta-D-thiogalactopyranoside)-inducible
97 of isopropyl beta-D-1-thiogalactopyranoside (IPTG)-inducible mutant T7 promoters of varied strength a
99 er isopropyl beta-D-1-thiogalactopyranoside (IPTG, which inhibits the interaction between the lac rep
100 t on isopropyl-beta-D-thiogalactopyranoside (IPTG) for expression has been inserted into the genome.
101 sing isopropyl beta-D-thiogalactopyranoside (IPTG) in a bacterial strain that harbors the lacIq gene,
102 rief isopropyl-beta-D-thiogalactopyranoside (IPTG) treatment elevated lacZ, lacY, and lacA transcript
104 Isopropyl-beta-D-thiogalactopyranoside (IPTG), an inhibitor of the lac repressor, can prevent de
105 with isopropyl beta-d-thiogalactopyranoside (IPTG), we were able to detect 10 CFU.mL(-1) in drinking
107 d an isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible M. mycoides subsp. mycoides SC biotype p
108 from isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible Plac and other virB genes from acetosyri
109 ated isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible promoter present on a multicopy plasmid.
110 An isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible promoter was constructed in Myxococcus x
112 from isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible promoters for the purpose of continuousl
115 g an isopropyl-beta-D-thiogalactopyranoside (IPTG)-regulated promoter upstream of the ribosomal bindi
122 isopropyl-beta-delta-thiogalactopyranoside (IPTG) inducible promoter, and transfected and then expre
123 inducer isopropyl-beta-D-1-thiogalactoside (IPTG) and the lac repressor complexed with a 21-base pai
125 he inducer isopropyl-beta-D-thiogalactoside (IPTG), iA6 replicated normally, and membrane proteins of
126 ddition to isopropyl-beta-d-thiogalactoside (IPTG), to the growth medium of the E. coli expression ho
127 with the data for isopropyl thiogalactoside (IPTG), but somewhat discrepant with respect to the data
130 macrophages, M. tuberculosis that respond to IPTG with expression of GFP fluorescence, and hence are
131 osis that fail to express GFP in response to IPTG, and hence are metabolically inactive, reside withi
132 otype pyruvate dehydrogenase region, and two IPTG-independent polypeptides, of 29 kDa and 57 kDa, wer
133 nges occur in the R3 dimer-oDNA complex upon IPTG binding, indicative of small adjustments in the ori
138 sform up to 5 mM of phenol and tyrosol using IPTG (isopropyl-beta-D-thiogalactopyranoside) as inducer
144 ne circuits were activated in materials with IPTG embedded within the scaffold walls or chemically li
145 ither native promoter or Pspac promoter with IPTG induction, resulted in a similar level of alkaline
150 biotransformation rate was attained without IPTG, confirming that this fragment encodes for a phenol
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