Cat. No. : |
SP1-1159H |
Description : |
Sp1 was first detected in HeLa cells on the basis of its ability to activate the SV40 early promoter transcription. Subsequently it was shown to recognize and bind selectively to a GC-rich consensus sequence (GC-box: GGGCGG or CACCC) that presents in the promoter of several important cellular genes, including SV40 early, HIV-1, PDGF-B etc. Sp1 was the first transcription factor to be cloned and characterized. Analysis of structure and function has revealed that Sp1 can be separated into discrete functional domains. The DNAbinding domain consists of three zinc fingers that specifically bind to the GC-box element. Sp1 contains at least four separate transcriptional activation domains. Two of these domains are glutamine-rich, a wellcharacterized motif found in several other transcription factors. In addition to transcription, Sp1 function has been linked to cell growth, cancer, Huntington disease, and other disorders through transcriptional regulation or specific protein-protein interactions. The function of Sp1 can be regulated by phosphorylation and glycosylation. GST-Sp1was isolated from anE. colistrain that carries the coding sequence of the fused protein under the control of a T7 promoter. |
Source : |
E. coli. |
Form : |
Liquid. Supplied in 20 mM Tris-HCl pH 8.0, 100 mM KCl, 0.2 mM EDTA, 1 mM DTT and 20% glycerol. |
Purity : |
> 95% by SDS-PAGE. |
Activity : |
100 ng are sufficient for a protein-protein interaction assay. |
Application : |
GST-Sp1 has been applied in protein-protein interaction assays. |
Usage : |
For in vitro use only. |
Storage : |
Quality guaranteed for 12 months store at -80°C. Avoid freeze / thaw cycles. |