Catalog |
name |
Description |
price |
R-C-4312 |
CTT2-PEG750-DSPE |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.It is a long circulating liposome membrane, formation of micelles in water dispersion,the critical micelle concentration(CMC)ratio of surfactant is 102 times lower,so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors.CCT2 can promote autophagic clearance of toxic protein aggregates related to neurodegenerative diseases.Like traditional aggregate autophagy receptors,CCT2 can bind to LC3 and protein aggregates. |
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R-C-4313 |
DSPE-PEG350-Cell penetrating peptide |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Cell penetrating peptide (CPP)-modified liposome cell penetrating peptide(CPP),also known as protein transduction domain(PTD),is a small peptide fragment with less than 30 amino acids, which can carry macromolecular substances into cells,and its membrane penetrating ability does not depend on classical endocytosis. |
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R-C-4314 |
DSPE-polyethylene glycol550-CPP |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Cell penetrating peptide (CPP)-modified liposome cell penetrating peptide(CPP),also known as protein transduction domain(PTD),is a small peptide fragment with less than 30 amino acids, which can carry macromolecular substances into cells,and its membrane penetrating ability does not depend on classical endocytosis. |
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R-C-4315 |
Cell penetrating peptide-PEG750-DSPE |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Cell penetrating peptide (CPP)-modified liposome cell penetrating peptide(CPP),also known as protein transduction domain(PTD),is a small peptide fragment with less than 30 amino acids, which can carry macromolecular substances into cells,and its membrane penetrating ability does not depend on classical endocytosis. |
price> |
R-C-4316 |
DSPE-PEG350-octreotide |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Octreotide is an octapeptide derivative of synthetic natural somatostatin.Its pharmacological effect is similar to that of somatostatin,but the effect lasts longer.It is only used for scientific research experiments,not for human body. |
price> |
R-C-4317 |
DSPE-polyethylene glycol550-octreotide |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Octreotide is an octapeptide derivative of synthetic natural somatostatin.Its pharmacological effect is similar to that of somatostatin,but the effect lasts longer.It is only used for scientific research experiments,not for human body. |
price> |
R-C-4318 |
octreotide-PEG750-DSPE |
DSPE-PEG,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.Octreotide is an octapeptide derivative of synthetic natural somatostatin.Its pharmacological effect is similar to that of somatostatin,but the effect lasts longer.It is only used for scientific research experiments,not for human body. |
price> |
R-C-4319 |
DSPE-PEG350-R8 |
Membrane penetrating peptide R8 is modified on PEG, and the hydrophilicity of PEG can reduce membrane penetration The peptide is taken up by the reticuloendothelial system. At the same time, after the liposome reaches the tumor site, it directly contacts the cell membrane as a "bridge" to increase the probability of liposome entry. DSPE-PEG-R8 is directly modified in the liposome as a phospholipid material In addition, it can avoid its separation from the surface of liposomes in the process of F blood circulation and increase the stability of CO modified liposomes. |
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R-C-4320 |
DSPE-polyethylene glycol550-R8 |
Membrane penetrating peptide R8 is modified on PEG, and the hydrophilicity of PEG can reduce membrane penetration The peptide is taken up by the reticuloendothelial system. At the same time, after the liposome reaches the tumor site, it directly contacts the cell membrane as a "bridge" to increase the probability of liposome entry. DSPE-PEG-R8 is directly modified in the liposome as a phospholipid material In addition, it can avoid its separation from the surface of liposomes in the process of F blood circulation and increase the stability of CO modified liposomes. |
price> |
R-C-4321 |
R8-PEG750-DSPE |
Membrane penetrating peptide R8 is modified on PEG, and the hydrophilicity of PEG can reduce membrane penetration The peptide is taken up by the reticuloendothelial system. At the same time, after the liposome reaches the tumor site, it directly contacts the cell membrane as a "bridge" to increase the probability of liposome entry. DSPE-PEG-R8 is directly modified in the liposome as a phospholipid material In addition, it can avoid its separation from the surface of liposomes in the process of F blood circulation and increase the stability of CO modified liposomes. |
price> |