Did you select just the cell content, or did you select the entire cell, including the end-of-cell marker? Since your screen shot shows that the template does not contain any fancy graphics, it would be a lot easier for you to use the built-in label definition in Word.
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On the Mailings tab, in the Create group, click Labels. In the Envelopes and Labels dialog ( Labels tab), click Options. In the Label Options dialog, for 'Label vendor,' select 'Avery US Letter.' . In the 'Product number' box, scroll down to 5520. Note that the numbers are sorted alphabetically rather than numerically, so you have to go down past all the 1s (even five-digit ones), 2s, 3s, and 4s to get to the 5s. Click OK to select the 5520 label.
Back in the Envelopes and Labels dialog, type the text you want on the labels. If you want to change the formatting, you can select the text and right-click to get Font. And Paragraph.
Select the radio button for 'Full page of the same label.' . Click New Document.
You'll get a sheet of labels which you can then further edit as needed. Since you want different content in each column, however, you don't really want a full page of the same label, and the copy/paste technique we have described should work for you provided you select the entire cell before copying.
If I copy just the text without the end-of-cell marker, I do get the same results as you. Microsoft MVP (Word) since 1999 Fairhope, Alabama USA http://ssbarnhill.com.
Full details of the development of a simple, nondestructive, and high-throughput method for establishing DNA binding affinity and sequence selectivity are described. The method is based on the loss of fluorescence derived from the displacement of ethidium bromide or thiazole orange from the DNA of interest or, in selected instances, the change in intrinsic fluorescence of a DNA binding agent itself and is applicable for assessing relative or absolute DNA binding affinities. Enlisting a library of hairpin deoxyoligonucleotides containing all five base pair (512 hairpins) or four base pair (136 hairpins) sequences displayed in a 96-well format, a compound's rank order binding to all possible sequences is generated, resulting in a high-resolution definition of its sequence selectivity using this fluorescent intercalator displacement (FID) assay. As such, the technique complements the use of footprinting or affinity cleavage for the establishment of DNA binding selectivity and provides the information at a higher resolution. The merged bar graphs generated by this rank order binding provide a qualitative way to compare, or profile, DNA binding affinity and selectivity. The 96-well format assay (512 hairpins) can be conducted at a minimal cost (presently ca.
$100 for hairpin deoxyoligonucleotides/assay with ethiduim bromide or less with thiazole orange), with a rapid readout using a fluorescent plate reader (15 min), and is adaptable to automation (Tecan Genesis Workstation 100 robotic system). Its use in generating a profile of DNA binding selectivity for several agents including distamycin A, netropsin, DAPI, Hoechst 33258, and berenil is described. Techniques for establishing binding constants from quantitative titrations are compared, and recommendations are made for use of a Scatchard or curve fitting analysis of the titration binding curves as a reliable means to quantitate the binding affinity.