ライフサイエンスコーパス: CBB

1 The dye from a 0.05% CBB staining solution could be removed in 5 to 10 min us

2 Coomassie brilliant blue R-250 (CBB) is a popular and widely used dye for detection of p

3 completely adsorbed the dye released from a CBB-stained mini-gel.

4 acy of various paper adsorbents in adsorbing CBB.

5 The Cord Blood Bank (CBB) contacted the donor's family and established that t

6 s encoding duplicated Calvin-Benson Bassham (CBB) CO2 fixation reductive pentose phosphate cycle stru

7 fixation used in the Calvin-Benson-Bassham (CBB) and reverse tricaboxylic acid (rTCA) cycles.

8 nal regulators of the Calvin-Benson-Bassham (CBB) CO2 fixation pathway (cbbI and cbbII) operons of Rh

9 bonate implicated the Calvin-Benson-Bassham (CBB) cycle in growth-supporting CO2 fixation, as well as

10 n of the genes of the Calvin-Benson-Bassham (CBB) cycle was increased.

11 acteria comprises the Calvin-Benson-Bassham (CBB) cycle, glycolysis, the pentose phosphate (PP) pathw

12 unctional RubisCO and Calvin-Benson-Bassham (CBB) pathway suppressed the deregulation of nitrogenase

13 The absence of the Calvin-Benson-Bassham (CBB) reductive pentose phosphate CO2 fixation pathway re

14 The form I (cbb(I)) Calvin-Benson-Bassham (CBB) reductive pentose phosphate cycle operon of Rhodoba

15 abolic control of the Calvin-Benson-Bassham (CBB) reductive pentose phosphate pathway in Rhodobacter

16 coding enzymes of the Calvin-Benson-Bassham (CBB) reductive pentose phosphate pathway in Rhodobacter

17 the key enzyme of the Calvin-Benson-Bassham (CBB) reductive pentose phosphate pathway, a scheme that

18 ssimilates CO2 by the Calvin-Benson-Bassham (CBB) reductive pentose phosphate pathway.

19 nd shade coffee reduced pest control because CBB was less often profitable prey.

20 ease (CMD) and the cassava bacterial blight (CBB), and MECU72, resistant to cassava white fly.

21 Disease (CMD) and Cassava Bacterial Blight (CBB), drought, and acid soils.

22 Cassava bacterial blight (CBB), incited by Xanthomonas axonopodis pv. manihotis (X

23 he response of the Coomassie Brilliant Blue (CBB) and Pyrogallol Red-molybdate (PRM) protein dye-bind

24 staining following Coomassie Brilliant Blue (CBB) staining involves the use of toxic reagents.

25 chromophore label, Coomassie Brilliant Blue (CBB).

26 e songbirds suppress the coffee berry borer (CBB).

27 n can, therefore, be recycled for destaining CBB-stained gels.

28 sh performance equivalency between different CBB preparations.

29 ain removal with Kimwipes helps in disposing CBB in an environmentally friendly manner and allows rec

30 heaper compared with an available method for CBB disposal.

31 Most genes required for a functional CBB pathway are clustered into the cbbI and cbbII operon

32 However, when cells regained a functional CBB pathway by trans complementation of the deleted gene

33 study suggests that the microbially mediated CBB cycle drives carbon fixation in the Spathi Bay sedim

34 s, compared to the disulfonated structure of CBB, and bind to protein at least 40 times more effectiv

35 We also demonstrated the upregulation of CBB cycle genes upon exposure of CB1190 to these C1 subs

36 at least 40 times more effectively than pure CBB.

37 for quality control testing of the purified CBB lots was also developed.

38 ria contribute significantly to the sediment CBB cycle gene content.

39 ort a sufficient number of birds to suppress CBB in sun coffee; the degree to which trees are dispers

40 The CBB assay was less prone to interference than the PRM as

41 The CBB cycle genes are evolutionarily most related to actin

42 The CBB removed allows its easy disposal as solid waste and

43 The CBB-adsorbed Kimwipes did not release the stain when squ

44 nk between purine recycling pathways and the CBB scheme.

45 e that there is a molecular link between the CBB and nitrogen fixation process, allowing the cell to

46 To complete the CBB pathway, there is a need for an enzyme, i.e., phosph

47 Physiological control of the CBB pathway and regulation of the R. capsulatus cbb gene

48 genes required for CO2 fixation through the CBB pathway and alternative routes.

49 on in vivo under growth conditions where the CBB cycle and CO2 fixation are required.

50 sphosphate or a metabolite derived from this CBB pathway intermediate.

51 a region containing a QTL for resistance to CBB as probe.

52 this procedure to remove the dye from a used CBB staining solution awaiting proper disposal by our In