PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16934821-2	2006	Polymerase chain reaction (PCR), lambda exonuclease digestion combined with (AC)(5)-Sepharose DNA affinity chromatography were used to produce c-jun promoter with a (GT)(5) tail at each 3" end.	Sepharose	84-93	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	143-148	
16934821-4	2006	In solution, tailed c-jun promoter (60 nM) and competitor poly dI:dC (30 ng/microl) was incubated with crude HEK293 nuclear extract to form a large protein-promoter complex, and the complex was then trapped by (AC)(5)-Sepharose by centrifugation or on a column.	Sepharose	218-227	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	20-25	
7702840-4	1995	Complexes containing both ATFa and either c-Jun or c-Fos were specifically retained on glutathione (GSH)-agarose beads as revealed by immunoblot analyses.	Sepharose	105-112	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	42-47	
10880356-2	2000	Here, we show that GSNO-Sepharose mimicks site-specific S-glutathionylation of the transcription factors c-Jun and p50 by free GSNO in vitro.	Sepharose	24-33	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	105-110	
10880356-4	2000	Furthermore, we show that c-Jun, p50, glycogen phosphorylase b, glyceraldehyde-3-phosphate dehydrogenase, creatine kinase, glutaredoxin and caspase-3 can be precipitated from a mixture of purified thiol-containing proteins by the formation of a mixed-disulphide bond with GSNO-Sepharose.	Sepharose	277-286	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	26-31	
18432922-4	2004	Also described is a procedure for preparing GSThyphen;cJun/GSH-Sepharose beads needed in the solid-phase JNK protein kinase activity assay.	Sepharose	63-72	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	54-58	
1608942-5	1992	A c-Jun kinase activity was affinity-purified 5000-fold by using glutathione S-transferase-c-Jun-glutathione-Sepharose beads and was found to phosphorylate the N terminus of c-Jun but not v-Jun or c-Jun containing a 27-amino acid N-terminal deletion found in v-Jun.	Sepharose	109-118	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	2-7	
1608942-5	1992	A c-Jun kinase activity was affinity-purified 5000-fold by using glutathione S-transferase-c-Jun-glutathione-Sepharose beads and was found to phosphorylate the N terminus of c-Jun but not v-Jun or c-Jun containing a 27-amino acid N-terminal deletion found in v-Jun.	Sepharose	109-118	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	91-96	
1608942-5	1992	A c-Jun kinase activity was affinity-purified 5000-fold by using glutathione S-transferase-c-Jun-glutathione-Sepharose beads and was found to phosphorylate the N terminus of c-Jun but not v-Jun or c-Jun containing a 27-amino acid N-terminal deletion found in v-Jun.	Sepharose	109-118	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	91-96	
1608942-5	1992	A c-Jun kinase activity was affinity-purified 5000-fold by using glutathione S-transferase-c-Jun-glutathione-Sepharose beads and was found to phosphorylate the N terminus of c-Jun but not v-Jun or c-Jun containing a 27-amino acid N-terminal deletion found in v-Jun.	Sepharose	109-118	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	91-96	
2648396-4	1989	In Rat-1a cells the expression of human c-jun mRNA was associated with the ability to clone in soft agarose and form tumors in nude mice.	Sepharose	100-107	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	40-45	
2648396-6	1989	However, cotransfection of the c-jun constructs with an activated human c-Ha-ras gene led to foci of transformed cells which gave rise to immortalized cell lines that cloned in soft agarose and formed tumors in nude mice.	Sepharose	182-189	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	31-36