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Catalog Number | orb1147034 |
---|---|
Category | Proteins |
Description | Dll4-Notch1 inhibitor; Cell penetrating peptides. |
None | |
H-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Gln-Thr-Leu-Gln-Ala-Glu-Leu-Leu-Val-Val-Tyr-Gly-Ala-OH | |
Nuclear receptor modulators, Protein-protein interactions | |
Form/Appearance | Freeze dried solid |
Purity | > 95% by hplc |
MW | 2946.45 Da |
Formula | C128H221N47O33 |
Solubility (25°C) | Soluble in 50% DMSO and 50% sterile H2O |
Protein Sequence | H-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Gln-Thr-Leu-Gln-Ala-Glu-Leu-Leu-Val-Val-Tyr-Gly-Ala-OH |
Storage | Store dry, frozen and in the dark |
Alternative names | ANK peptideTAT-ANK, YGRKKRRQRRRQTLQAELLVVYGA Read more... |
Background | TAT-ANK is a peptide derived from amino acid residues 179-191 of the G-protein coupled receptor kinase interacting protein-1 (GIT1) ankyrin domain, which are are crucial for GIT1 binding tothe Notch transcription repressor RBP-J. In vitro, application of TAT-ANK significantly inhibits Delta-like 4 (Dll4) expression andNotch 1 activation in human umbilical vein endothelialcells (HUVECs) by competing with activated Notch1 binding to RBP-J, and in mouse models, TAT-ANK reduces tumour size through impairing tumour angiogenesis. |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |