-
738415
DE3
(ALR)-deprived E. coli strain BW25113
1
-
738413
DE3
BMBL21-DE3
1
-
738414
DE3
D-F, were expressed in the vector pET 3d/BL21
1
-
738411
DE3
D-hydantoinase gene expression box.The strain pET3a-hyd/BL21
1
-
738412
DE3
D43A and C50A could not be expressed normally; in pET32a(+)/BL21
1
-
738409
DE3
DAB389 IL-2 into the E. coli strain Rosetta-gami
1
-
738410
DE3
DDX3 protein in E. coli BL21
1
-
738407
DE3
DE3 prophage in BL21
1
-
738408
DE3
DE3 region of Escherichia coliBL21
1
-
738397
DE3
deaminase using the pET3c/BL21
1
-
738398
DE3
defective mutant strain, MA1935, was generated from BL21
1
-
738393
DE3
deficient strain E. coli BW25113
1
-
738394
DE3
defined as the use of C43
1
-
738391
DE3
demonstrated that the pET-30a(+)-TP-coreSA/Lemo21
1
-
738392
DE3
demonstrated with selenomethionine using methionine auxotroph E. coli B834
1
-
738395
DE3
derivative C43
1
-
738385
DE3
designated SULT3 ST3, was expressed in and purified from BL21
1
-
738386
DE3
detected only in the pET32a/Origami B
1
-
738389
DE3
detected with Rhodococcus erythropolis NCIMB13064 and Escherichia coli BL21
1
-
738390
DE3
detected with the parental strain BW25113
1
-
738387
DE3
detection wavelength of 254 nm.The specific activity of pET3a-hyd/BL21
1
-
738388
DE3
determined that expression with C43
1
-
738403
DE3
DHAV-1VP3-3VP1 fusion protein expressed in BL21
1
-
738383
DE3
different vectors: pGEX-5X-1, pQE30, ET41a, and expressed in JM109, JM109
1
-
738384
DE3
dificent E. coli HB 351
1
-
738381
DE3
digestion and sequencing, pET-32a(+)-gI was transformed into E.coli BL21
1
-
738382
DE3
directed fractional 13C-labeling for Escherichia coli BL21
1
-
738376
DE3
disrupted the tnaA gene locus of E.coli C43
1
-
738374
DE3
disulfide bonds when hCD83ext was expressed in Origami B
1
-
738375
DE3
diurnal eastward-propagating zonal wave number-3 nonmigrating tide
1
-
738379
DE3
diurnal tide with zonal wavenumber s = -3
1
-
738404
DE3
DNA construct of SmbP_LL-37 was transformed into E. coli BL21
1
-
738380
DE3
domain was expressed in Escherichia coli B834
1
-
738377
DE3
domains E-F, was expressed in the vector pET 3d/BL21
1
-
738378
DE3
double mutant host C43
1
-
738372
DE3
dropped to only 20-30% in strain BL21
1
-
738373
DE3
dsFv PE38 was expressed in E.coli origami
1
-
738401
DE3
DSM 5473 in Escherichia coli Rosetta
1
-
738402
DE3
DSM 5473 in the soluble fraction of Escherichia coli BL21
1
-
738405
DE3
DSM13552 was cloned, sequenced and overexpressed into Escherichia coli BL21
1
-
738396
DE3
DsrP were successfully produced in Escherichia coli C43
1
-
738406
DE3
DT386 fragment, followed by its expression by E. coli BL21
1
-
738371
DE3
duration of HLA-A*0203-BSP fusion protein expressed for E.coli BL21
1
-
738416
DE3
malonyl-CoA-dependent 3-HP biosynthetic pathway were introduced into E. coli BL21
1
-
738417
DE3
pET3a-derived expression vector and transformation into Escherichia coli BL21
1
-
738399
DE3
TS-deficient E. coli strain chi2913recA
1
-
738400
DE3
TS-deficient Escherichia coli strain chi2913recA
1