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In this study, a novel adaptive tabu search approach is proposed for solving buffer allocation problem in unreliable and non-homogeneous production lines.
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This paper investigates the performance of three search algorithms: Myopic Algorithm, Adaptive Tabu Search and Degraded Ceiling to solve the buffer allocation problem in reliable production lines.
In this paper, we present an original methodology to solve a buffer allocation and throughput trade-off problem in single server general queueing networks.
Production line designers often need to solve the Buffer Allocation Problem (BAP), but this can be difficult, especially for large production lines, because the task is currently highly time consuming.
For example, the ability to simultaneously experience both positive and negative emotions when confronted with a high-stress situation increases flexibility of thinking and problem solving and can buffer individuals from developing stress-induced adverse consequences (Fredrickson 2001; Ong et al. 2006).
This paper presents a novel parallel tabu search (PTS) algorithm equipped with a proper adaptive neighborhood generation mechanism to solve the primal buffer allocation problem, which consists of minimizing the total buffer capacity of a serial production system under a minimum throughput rate constraint.
As control for background and non-specific binding 5% bovine serum albumin (BSA) solved in lysis buffer was used.
The obtained film was admixed with fruit extracts solved in phosphate buffer of pH 7.4 and liposomes were formed by mechanical shaking at temperature above the DPPC main phase transition.
Oxytocin samples that were solved in phosphate buffer of pH 4.5, 7.0, and 9.0 and exposed to 70°C for 64 h were also analyzed with CE-MS, showing several degradation products (Fig. 2b d; Table 1).
Control allelic profiles were obtained with DNA extracted from blood cells: after cell lysis and proteinase K degradation, DNA was obtained with phenol chloroform extraction followed by DNA precipitation with ethanol and solved in TE buffer (Tris 10 m M (pH 7.5), EDTA 1 m M) (Muniz et al, 1994).
Because LB shows auto fluorescence, the cells were harvested and washed and solved in TE-buffer (10 mM Tris-HCl, pH 7.5, 1 mM EDTA), physiological solution (0.9% NaCl) or PBS-buffer.
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