ライフサイエンスコーパス: counterselection

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1 n H. pylori strain 26695 using sacB-mediated counterselection.

2 s associated with the utilization of sacB in counterselection.

3 ing wild-type rpsL and used streptomycin for counterselection.

4 oved after isolation of recombinants through counterselection.

5 wanted DNA sequences was promoted by sucrose counterselection.

6 Ig alpha-Ig beta, whereas the mechanism for counterselection against D mu has not been determined.

7 Thus, the molecular mechanism for counterselection against D mu in pre-B cells resembles p

8 f the Ig alpha-Ig beta signal transducers in counterselection against D mu using mice that lack Ig be

9 With counterselection against non-engineered cells, eight AEG

10 inant effect on altering autoreactive B cell counterselection before any onset of autoimmunity.

11 tial role in controlling autoreactive B cell counterselection by regulating BCR and TLR functions.

12 strate was used simultaneously with multiple counterselection fluorescent substrates to isolate rare

13 gene of Escherichia coli functioned for the counterselection in the gonococcus, albeit with low effi

14 tion also affected the efficiency of sucrose counterselection in the sucrose-sensitive strains.

15 Reconstruction experiments suggest this counterselection increased cloning specificity by 100-fo

16 propose that scheduled apoptosis provides a counterselection mechanism that keeps the germline stabl

17 ells by Ig membrane mu H chains (mum HC) and counterselection mediated by the truncated HC Dmu depend

18 ted using an allelic replacement and sucrose counterselection method.

19 ting the threshold for B-cell activation and counterselection of autoreactive B cells, making Btk an

20 SAP expression is required for the counterselection of developing autoreactive B cells and

21 TAK1 also promotes counterselection of NF-kappaB-addicted DLBCL lines by a

22 e observed a pervasive pattern of systematic counterselection of nonsynonymous mutations in prophage

23 two additional rounds of transformation and counterselection of the transformation marker.

24 obacterium that relies on both selection and counterselection of ura3 using a uracil dropout medium a

25 exposed to the stress of transformation and counterselection on 5-fluoro-orotic acid.

26 After counterselection, only the desired allele is retained as

27 ng plasmid was subsequently cured by sucrose counterselection, resulting in an unmarked P. aeruginosa

28 This selection-counterselection scheme had acceptable statistics, notwi

29 We used in vitro counterselection/selection to isolate a pool of RNAs tha

30 The rpsL counterselection strategy allows construction of unmarke

31 ted by homologous recombination using a sacB counterselection strategy.

32 dhesion receptor subunit Aga2, selection and counterselection substrate sequences, multiple interveni

33 strain was first isolated, followed by sacB counterselection to isolate the double-crossover strain.

34 A cycloheximide-based counterselection was introduced to increase the specific

35 Cycloheximide counterselection was used in conjunction with 80-bp link

36 To improve the efficiency of the counterselection, we cloned the gonococcal rpsL gene and

37 A third counterselection with 5-fluoroorotic acid (5FOA) against

38 gration event can be followed immediately by counterselection, without the need for growth in permiss

39 describe a high throughput screen based on a counterselection yeast two-hybrid assay, which was used

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