Kim, Hye Ri Kim, Myunghee Kim, Byoung Chan 2024-01-19T14:04:06Z 2024-01-19T14:04:06Z 2022-01-25 2021-07 0003-2654 https://pubs.kist.re.kr/handle/201004/116702 The authors regret that there were errors in the buffer compositions described in section 2.3 of the article. On page 3535, the sentence beginning “Briefly, the DNA library pool…” should be correctly given as “Briefly, the DNA library pool was denatured in binding buffer (25 mM of glucose, 5 mM of MgCl2, 1 mg mL-1 of BSA, and 0.1 mg mL-1 of tRNA in preautoclaved 1X phosphate-buffered saline (PBS)) at 95 °C for 5 min and immediately chilled in an ice-bath before allowing the binding reaction with the target bacteria.” The sentence beginning “After a final partioning step…” should be correctly given as “After a final partioning step, bound ssDNA was eluted from the target bacteria by incubating the sample with 500 ？L of elution buffer (25 mM of glucose, 5 mM of MgCl2, and 1 mg mL-1 of BSA in pre-autoclaved 1X PBS buffer) at 95 °C for 10 min.” The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers. ？ The Royal Society of Chemistry. English Royal Society of Chemistry Specific detection of Cronobacter sakazakii in powdered infant formula using ssDNA aptamer (vol 146, pg 3534, 2021) Article 10.1039/d1an90055b 1 Analyst, v.146, no.14, pp.4708 - 4708 Analyst 146 14 4708 4708 N scie scopus 000661971100001 2-s2.0-85110215261 Chemistry, Analytical Chemistry Correction