Skip to main content

Advertisement

Erratum To: Production of recombinant Entamoeba histolyticapyruvate phosphate dikinase and its application in a lateral flow dipstick test for amoebic liver abscess

The original article was published in BMC Infectious Diseases 2014 14:182

Correction

After publication of this article [1], it was brought to our attention that we had failed to make it clear that Figures one (Figure 1 here), two (Figure 2 here) and three (Figure 3 here) were put together by grouping elements from different images. The revised figures, in which this grouping has been made explicit in the arrangement, and figure legends, in which the adjustments are clearly stated, are shown below.

Figure 1
figure1

SDS-PAGE analysis shows the purified rPPDK. Lane 1: Precision Plus Protein™ Unstained Standard Marker (Bio-Rad, USA); Lane 2: Non-induced cell from pET28a/PPDK; Lane 3: Induced cell from pET28a/PPDK; Lanes 4–5: purified rPPDK protein from elution buffer (250 mM imidazole). Arrow indicates the recombinant PPDK protein (~98 kDa). Figure one (Figure 1 here) was made by grouping elements from the original Images 1A and 1B as follows: Lanes 1, 2 and 3 in Figure one (Figure 1 here) came from lanes M, 6 and 8 respectively in Image 1A; while Lanes 4 and 5 in Figure one (Figure 1 here) came from lanes 7 and 8 respectively in Image 1B.

Figure 2
figure2

SDS-PAGE analysis shows the purified rGal/GalNAc lectin. Lane 1: Precision Plus Protein™ Unstained Standard Marker (Bio-Rad, USA); Lane 2: Non-induced cell from pET28a/Gal-GalNAc lectin; Lane 3: Induced cell from pET28a/Gal-GalNAc lectin; Lanes 4–5: purified rGal/GalNAc lectin protein from elution buffer (250 mM imidazole). Arrow indicates the recombinant Gal/GalNAc lectin protein (~53 kDa). Figure two (Figure 2 here) was made by grouping elements from the original image 1A as follows: Lanes 1, 2, 3, 4, and 5 in Figure two (Figure 2 here) came from lanes M, 1, 2, 3 and 4 respectively in Image 1A.

Figure 3
figure3

Representative rPPDK-LFD strips tested with serum samples. Lanes 1–3: Lateral flow test strips tested with serum samples from patients with ALA; Lane 4: strip tested with serum from healthy individual; Lanes 5–6: strips tested with serum samples from other diseases (i.e. malaria and pyogenic liver abscess); C: control line; T: test line. Figure six (Figure 3) was made by grouping elements from original Images 6A and 6B as follows: Dipstick 1 and 2 in Figure six (Figure 3) came from dipsticks 3 and 4 in Image 6A; dipstick 3 in Figure six (Figure 3) came from dipstick 4 in Image 6B; dipsticks 4, 5 and 6 in Figure six (Figure 3) came from dipsticks 5, 6 and 7 respectively in Image 6A.

We regret any inconvenience that this inaccuracy in the figures in the original manuscript might have caused.

References

  1. 1.

    Saidin S, Yunus MH, Zakaria ND, Razak KA, Huat LB, Othman N, Noordin R: Production of recombinant Entamoeba histolytica pyruvate phosphate dikinase and its application in a lateral flow dipstick test for amoebic liver abscess. BMC Infect Dis. 2014, 14: 182-10.1186/1471-2334-14-182.

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/14/533/prepub

Download references

Author information

Correspondence to Rahmah Noordin.

Additional information

The online version of the original article can be found at 10.1186/1471-2334-14-182

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Authors’ original file for figure 3

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark