SETD7, His, Human
| $370.00 | |
| Z05808-100 | |
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| Ask us a question | |
IVD Raw Materials
| $370.00 | |
| Z05808-100 | |
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| Ask us a question | |
| Species | Human | ||||
| Protein Construction |
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| Purity | > 95% as determined by BisTris PAGE | ||||
| Endotoxin Level | Less than 1EU per μg by the LAL method. | ||||
| Expression System | E.coli | ||||
| Theoretical Molecular Weight | 41.68 kDa | ||||
| Apparent Molecular Weight | The protein migrates to 47-50 kDa based on Bis-Tris PAGE result. | ||||
| Formulation | Lyophilized from 0.22μm filtered solution in PBS (pH 7.4). | ||||
| Reconstitution | Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/ml is recommended. Dissolve the lyophilized protein in distilled water. | ||||
| Storage & Stability | Upon receiving, the product remains stable for 6 months at -20℃ or below. Upon reconstitution, the product should be stable for 3 months at -80℃. Avoid repeated freeze-thaw cycles. |
The purity of SETD7, His, Human is greater than 95% as determined by SEC-HPLC. »
SETD7, His, Human on Bis-Tris PAGE under reduced condition. The purity is greater than 95%. »
| Target Background | SETD7 is a methyltransferase that specifically catalyzes the monomethylation of lysine 4 on histone H3. A variety of studies has revealed the role of SETD7 in posttranslational modifications of non-histone proteins. Aberrant expression of SETD7 has been associated with various diseases, including cancer. As a prognostic marker of breast cancer and a novel antioxidant promoter under oxidative stress in breast cancer, SETD7 is considered a good target for the development of new epigenetic drugs. |
| Synonyms | KIAA1717; KMT7; SET7; SET9; SET7/9 |
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.