Exact(14)
The following evaluation conditions are listed as below: heated at 60 °C for 24 h without carbon dioxide as test 1; heated at 60 °C for 24 h, and then heated at 70 °C for 24 h without carbon dioxide as test 2; the evaluation experiments for produced water with saturated carbon dioxide heated at 60 °C for 24 h and then heated at 70 °C for 24 h were done as test 3.
For Bayesian analysis, 2 runs with 3 cold chains and 1 heated chain each were done.
Ara h 1 heated without glucose at 60 or 145 °C did not differ in their degree of hydrolysis.
No differences were observed for the electrophoretic analysis of Ara h 1 heated at 37 °C in the presence or absence of glucose.
The significant differences were observed in the effect on the Caco-2 proliferation rate between Ara h 1 heated without glucose and glycated at the temperature of 60 and 145 °C (Fig. 4).
Treatment of Ara h 1 in the presence of glucose for each time/temperature combination resulted in increased levels of bound sugar compared to both non-treated protein and Ara h 1 heated without glucose (Fig. 1b).
Similar(46)
In short, in addition to the normal, unheated chain, n−1 heated chains are started on the CPU cores 2,…, n and states are attempted to swap with a given probability.
Cuttings were treated with 6 g l−1 K-IBA (Indole-3-butiric acid, potassium salt) for 20 s and rooted in vermiculite/perlite 1 1, heated to 24°C under constant 90% humidity in rooting tables.
No additional step is required; for progenies that might be homozygous, each PCR product should be mixed with WT PCR product with a ratio of ∼1 1, heated to 94°C for 3 min and slowly returned to room temperature to form heteroduplexes. for heterozygous founder individuals containing disrupted alleles, heteroduplexes are formed during PCR.
No additional step is required; for progenies that might be homozygous, each PCR product should be mixed with WT PCR product with a ratio of ∼1 1, heated to 94°C for 3 min and slowly returned to room temperature to form heteroduplexes.
CAPAN-1 and CFPAC-1 cells are cultured in Iscove's modified Dulbecco's medium supplemented with 20 and 10% (v v−1) heated-inactivated fetal bovine serum (FBS), 50 U ml−1 penicillin and 50 U ml−1 streptomycin, respectively.
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