Research
Dynamic instability of the major urinary protein gene family revealed by genomic and phenotypic comparisons between C57 and 129 strain mice
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* Corresponding author: Jonathan M Mudge jm12@sanger.ac.uk
1 Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK
2 Proteomics and Functional Genomics Group, Department of Veterinary Preclinical Science, University of Liverpool, Crown Street and Brownlow Hill, Liverpool, L69 7ZJ, UK
3 Mammalian Behavior and Evolution Group, Department of Veterinary Preclinical Science, University of Liverpool, Leahurst, Neston, CH64 7TE, UK
Genome Biology 2008, 9:R91 doi:10.1186/gb-2008-9-5-r91
Published: 28 May 2008Additional files
Additional data file 1:
Alignment of the B6 and S7 MUPs.
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Additional data file 2:
The point of alignment inversion is seen to correspond to the location of a murine ERV.
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Additional data file 3:
Dot-plot comparison of the mass 18,893-associated duplication from the B6 genome.
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Additional data file 4:
Details of the absence of MUP isoforms in the upper mass range of ESI-MS spectra of inbred mouse urine samples.
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Additional data file 5:
Individual variation in ESI-MS mass spectra of MUP isoforms in urine.
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Additional data file 6:
Increasing the volume of urine loaded onto a native PAGE gel does not change the banding pattern observed once the essential banding pattern has become visible.
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