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Catalog | name | Description | price |
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R-M-2080 | DBCO-PEG4-Val-Cit-PAB-PNP,Cas:2226472-28-0 | DBCO-PEG4-Val-Cit-PAB-PNP is a cleavable ADC linker. The Val-Cit will specifically be cleaved by Cathepsin B. PNP can be substituted by amine-containing payload. DBCO enable click chemistry with azide molecules. | price> |
R-C-4115 | DPPE-PEG350-N3 | 1,2-dipalmitoyl-sn-glycoro-3-phosphoethanolamine-polyethylene glycol azide is applied to medical research,release,nanotechnology and new material research,and cell culture As well as ligand research,peptide synthesis support,grafted polymer compounds,new materials,polyethylene glycol modified functional coatings and other active compounds. | price> |
R-M-1596 | DSIP,CAS :62568-57-4 | A neuropeptide that when infused into the mesodiencephalic ventricle of recipient rabbits induces spindle and delta EEG activity and reduced motor activities. | price> |
R-M-2081 | TCO-PEG4-Val-Cit-PAB-PNP | TCO-PEG4-Val-Cit-PAB-PNP is a cleavable peptide linker. The Val-Cit linker will specifically be cleaved by Cathepsin B. PNP is a good leaving group in nucleophilic reaction. The inverse-electron demand Diels-Alder cycloaddition reaction of TCO with tetrazines is the fastest bioorthogonal reaction with exceptional selectivity. | price> |
R-C-4116 | DPPE-polyethylene glycol550-N3 | 1,2-dipalmitoyl-sn-glycoro-3-phosphoethanolamine-polyethylene glycol azide is applied to medical research,release,nanotechnology and new material research,and cell culture As well as ligand research,peptide synthesis support,grafted polymer compounds,new materials,polyethylene glycol modified functional coatings and other active compounds. | price> |
R-M-1597 | DPDPE,CAS:88373-73-3 | Peptide that performs direct antinociceptive actions via the delta1-opioid receptor, while modulatory via the delta2-opioid receptor. | price> |
R-M-2082 | SPDP-Val-Cit-PAB-PNP | SPDP-Val-Cit-PAB-PNP is a cleavable peptide linker. The Val-Cit linker can bespecifically cleaved by Cathepsin B. Pyridyldithiol reactive group enables disulfide linkage with reduced cysteines and other sulfhydryl molecule. | price> |
R-C-4117 | azide-PEG750-DPPE | 1,2-dipalmitoyl-sn-glycoro-3-phosphoethanolamine-polyethylene glycol azide is applied to medical research,release,nanotechnology and new material research,and cell culture As well as ligand research,peptide synthesis support,grafted polymer compounds,new materials,polyethylene glycol modified functional coatings and other active compounds. | price> |
R-M-1598 | HO-PEG2000-ester-C18 | HO-PEG2000-ester-C18 belongs to a custom compound. Ruixibiotechco.ltd can customize various products according to your needs. | price> |
R-M-2083 | Alkyne-Val-Cit-PAB-FAM | Alkyne-Val-Cit-PAB-FAM,Alkyne-Val-Cit-PAB-fluorescein from ruixi.Alkyne-Val-Cit-PAB-FAM is a cleavable peptide linker. The Val-Cit linker can bespecifically cleaved by Cathepsin B. | price> |
R-C-4118 | DPPE-PEG350-SH | DPPE-PEG-SH,1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Thiol can be conjugated with peptides,antibodies,or proteins which contain Maleimide groups on the surface. | price> |
R-M-1600 | Fusion Inhibitory Peptide,CAS :75539-79-6 | Virus replication inhibitory peptide a potent specific inhibitor of the replication of paramyxovirus and myxovirus, by inhibiting the membrane fusing activity of a viral glycoprotein. | price> |
R-M-2084 | SPDP-Val-Cit-PAB-OH | SPDP-Val-Cit-PAB-OH is a cleavable ADC linker. The Val-Cit was designed specifically be cleaved by Cathepsin B. Pyridyldithiol reactive group enables disulfide linkage with reduced cysteines and other sulfhydryl molecule, providing a stable but cleavable bond. | price> |
R-M-1601 | Galanin, human,CAS :119418-04-1 | Human galanin, originally been isolated from colon and pituitary, that activates the rat galanin receptor and inhibits acetylcholine release, glutamate release and carbachol-stimulated phosphatidylinositol hydrolysis in the hippocampus. Recent studies indicated that galanin is also linked to behavioral and cognitive deficits in Alzheimer’s disease. | price> |
R-M-2085 | Mal-amido-PEG8-Val-Gly,Cas:2353409-54-6 | Mal-amido-PEG8-Val-Gly,Cas:2353409-54-6 from ruixi.Mal-amido-PEG8-Val-Gly is a peptide linker. | price> |
R-C-4120 | Thiol-PEG750-DPPE | DPPE-PEG-SH,1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Thiol can be conjugated with peptides,antibodies,or proteins which contain Maleimide groups on the surface. | price> |
R-M-2086 | Active-Mono-Sulfone-PEG8-acid,Cas:2055048-45-6 | Active-Mono-Sulfone-PEG8-acid is a PEG linker with a sulfone and acid end group. The sulfone group can be conjugated with thiol groups of proteins. The terminal carboxylic acid can react with primary amines in the presence of activators such as EDC and HATU to from stable amide bonds. The hydrophilic PEG chain increases the water solubility of the compound in aqueous media. | price> |
R-C-4121 | DPPE-PEG350-FITC | DPPE-PEG-FITC,1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Fluorescein is Fluorescent-PEG-lipid,Excitation maximum,nm:490,Emission maximum,nm:520. | price> |
R-M-1603 | GEGFLGfL,CAS:61393-34-8 | Inhibitor of cathepsin D, can be used as an affinity ligand for the isolation of cathepsin D. | price> |
R-M-2087 | Azido-PEG4-Ala-Ala-Asn(Trt)-PAB,Cas:2055042-67-4 | Azido-PEG4-Ala-Ala-Asn(Trt)-PAB is a unique peptide cleavable ADC linker for antibody-drug-conjugation, Azido group is very reactive toward DBCO, BCN or other Alkyne groups, called click chemistry. The trt protecting group can be removed under acidic conditions. The hydrophilic PEG linker increases the water solubility of the compound. | price> |