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Correction: New fluorescent probe for Zn2+ imaging in living cells and plants

Rong Shen ab, Di Liu ab, Chenchen Hou ab, Ju Cheng abc and Decheng Bai *abc
aInstitute of Integrated Traditional Chinese and Western Medicine, School of Basic Medical Sciences, Lanzhou University, Lanzhou, 730000, Gansu, China. E-mail: shenr12@lzu.edu.cn
bKey Laboratory of Preclinical Study for New Drugs of Gansu Province, Lanzhou University, School of Basic Medical Sciences, 199 West Donggang Road, Lanzhou 730000, Gansu, China. E-mail: bdc@lzu.edu.cn; Tel: +86 13088758222
cInstitute of Operative Surgery, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, Gansu, China

Received 12th February 2016 , Accepted 12th February 2016

First published on 3rd March 2016


Abstract

Correction for ‘New fluorescent probe for Zn2+ imaging in living cells and plants’ by Rong Shen et al., Anal. Methods, 2016, 8, 83–88.


In the original article, there is an error in the x-axis of Fig. 1d. The corrected figure is shown below.
image file: c6ay90030e-f1.tif
Fig. 1 (a) Fluorescent emission spectra of 100 μM other metal ions and 50 μM Zn2+ in the same media. Inset: photograph of L1 and L1 + Zn2+ (20 μM). (b) Fluorescence intensities of L1 (10 μM) upon the addition of various metal ions in H2O/ethanol (8[thin space (1/6-em)]:[thin space (1/6-em)]2, v/v). Yellow bars represent addition of L1 (10 μM) to the other miscellaneous competitive cations (20 μM) including Cd2+, K+, Na+, Fe3+, Cr3+, Ni2+, Mg2+, Ag+, Hg2+, Al3+, Co2+, Mn2+, Pb2+, Li+, Cu2+ and Zn2+. Black bars represent the addition of Zn2+ to the solution of L1 in the presence of different cations. (c) Fluorescence titration spectra of L1 upon the addition of different concentrations of Zn2+ (0–1 equiv.) in H2O/ethanol (8[thin space (1/6-em)]:[thin space (1/6-em)]2, v/v). (d) Fluorescence intensity at 628 nm of L1 as a function of Zn2+ concentration.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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