Using a systematic series of electrophoretic mobility shift assays (EMSA), we have explored the basis for the sequence-specific DNA-binding by FOXP3.
Based on the limited dataset of vertebrate genes, Su et al. [ 15] observed the positive correlation of gene pleiotropy with the number of GO biological processes, as well as the expression broadness provides a biological basis for the sequence-based estimation of gene pleiotropy.
For the PCR the oligonucleotides TriplEx2-5' (from CLONTECH Lab, Palo Alto, CA) and CD3/3' (5'-AAT CTA GAG GCC GAG GCG GCC GAC ATG-3') [ 24], designed on the basis of the CDsequencesequence tag used for library construction, were used as primers.
Then the sequence ({ g^{ k)}(r,s) }_{k inmathbb{N}}) is a Schauder basis for the binomial sequence space (b_{p}^{r,s}), and every (x in b_{p}^{r,s}) has a unique representation of the form x=sum_{k}mu_{k}g^{ k)}(r,s), where (1leq p
In this part, we speak of some inclusion relations and give the Schauder basis for the binomial sequence space (b_{p}^{r,s}), where (1leq p
If a conserved cRE-gene association is the basis for the strong sequence conservation of the HCE, there should be at least one common target gene located on the same chromosome in all of the six genomes where an HCE is found.
Computer-generated random numbers from the uniform (0,1) distribution will form the basis for the allocation sequence.
On the basis of the sequencing result, primers for two rounds of 3′-RACE PCR were designed: first round, 5′-ATGTTCCCCGCGGCACT-3′; and second round, 5′-GGGAGTCTCAGGAGCGGGTT-3′.
This dataset provided the basis for comparative sequence analysis of the transcripts predicted in the Ensembl genome resource.
