c-Jun, aa1-79, GST Fusion Protein
Catalog No : USB-C5815-09
489.67€
0.00€
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| Product name | c-Jun, aa1-79, GST Fusion Protein | ||
|---|---|---|---|
| Catalog No | USB-C5815-09 | ||
| Supplier’s Catalog No | C5815-09 | ||
| Supplier | US Biologicals | ||
| Source antigen | E. coli | ||
| Reactivity | |||
| Cross reactivity | |||
| Applications | |||
| Molecular weight | 37 | ||
| Storage | -20°C | ||
|---|---|---|---|
| Other names | |||
| Grade | Affinity Purified | ||
| Purity | Purified by Immunoaffinity chromatography. ≥90% | ||
| Form | Supplied as a liquid in 20mM Tris-HCl, pH 7.5, 50mM sodium chloride, 2mM EDTA, 1mM DTT, 50% glycerol. | ||
| Reactivity life | 12 months | ||
| Note | For reserch purpose only | ||
| Purity | Purified by Immunoaffinity chromatography. ≥90% | ||
| Description | c-Jun is a component of the transcription factor AP-1 that binds and activates transcription at TRE/AP-1 elements. The transcriptional activity of c-Jun is regulated by phosphorylation at Ser63 and Ser73. Extracellular signals including growth factors, transforming oncoproteins, and UV irradiation stimulate phosphorylation of c-Jun at Ser63/73 and activate c-Jun dependent transcription. The MAP kinase homologue, JNK, binds to the N-terminal region of c-Jun and phosphorylates c-Jun at Ser63/73. The activity of JNK is stimulated by the same signals that activates c-Jun. Source: c-Jun fusion protein was expressed in E. coli. It is expressed as a recombinant protein fusion of human c-Jun residue 1-79 and glutathione S-transferase. MOL. WEIGHT: 37kD ACTIVITY: C-Jun fusion protein at a concentration of 2ug/20ul reaction was phosphorylated in an in vitro kinase assay with 200uM ATP. After 30 minutes incubation at 30°C, phosphorylation was detected by Western blot with phospho-specific c-Jun antibodies. Storage and Stability: May be stored at 4°C for short-term only. For long-term storage, store at -20°C. Aliquots are stable for at least 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. | ||
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