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Catalog | name | Description | price |
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R-M1-8820 | FITC-Gly-CBT | The CBT-Cys click condensation reaction has found wide applicability in recent years. The reaction is highly biocompatible and controllable and runs under physiological conditions. It is based on the condensation between an N-terminal L- or D-Cysteine with the cyano group of CBT. | price> |
R-M-5368 | SF650-N3 | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4703 | G0-C18 | Synthesis of ionizable lipid-like compounds(G0-Cn).A series of ionizable lipid like compounds termed G0-Cn were synthesized through ring opening of epoxides bearing different alkyl chain lengths by generation 0 of poly(amidoamine)(PAMAM)dendrimers (M1). | price> |
R-M1-8821 | Collagen binding peptide(LHERHLNNN) | Collagen binding peptide (LHERHLNNN) is a short peptide sequence that has been identified to have a high affinity for collagen, which is the main structural protein found in connective tissues.The LHERHLNNpeptide sequence contains specific amino acids that interact with collagen, allowing for the specific recognition and binding to collagen fibers. The peptide binding affinity and specificity for collagen make it a valuable tool in various biomedical and biotechnological applications, particularly those involving the interaction with and modification of collagen-rich tissues or materials. | price> |
R-M-5369 | SF650-DBCO | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4704 | DSPE-PEG-AE105(D-Cha-F-s-r-Y-L-W-S) | 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.It can couple various polypeptide groups.The AE105 peptide (D-Cha-F-s-r-Y-L-W-s) bound to the uPAR domain III ring 3 was coupled with DOTA. After labeling with 64Cu, the tracer was evaluated for microscopic PET imaging of uPAR expression in nurine xenotransplantation model (uPAR positive and uPAR negative). | price> |
R-M1-8806 | NaYF4:Yb,Tm@NaYF4(water-soluble core shell upconversion nanoparticle,980 excitation,blue light) | NaYF4:Yb,Tm@NaYF4 is a Water soluble core-shell upconversion nanoparticles (980 excitation, blue light),material composition: NaYF4:Yb,Tm@NaYF4 .The particle size is 30-40, the concentration is 10mg/ml,the excitation wavelength is 980 nm, the emission wavelength is 365/450/470 nm±15 nm (blue light), and the surface ligand is PAA.Due to the coating of PAA, these nanoparticles are water-soluble.Therefore, high fluorescence efficiency, nano size and hydrophilicity make it a potential application in the field of biological probes. | price> |
R-M-5370 | SF650-NHNH2 | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4705 | DSPE-polyethylene glycol350-AE105(D-Cha-F-s-r-Y-L-W-S) | 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.It can couple various polypeptide groups.The AE105 peptide (D-Cha-F-s-r-Y-L-W-s) bound to the uPAR domain III ring 3 was coupled with DOTA. After labeling with 64Cu, the tracer was evaluated for microscopic PET imaging of uPAR expression in nurine xenotransplantation model (uPAR positive and uPAR negative). | price> |
R-M1-8823 | N3-PEG(3)-NH-Suc | The N3-PEG(3)-NH-Suc molecule can be used in bioconjugation strategies to attach various functional groups or molecules to the azide group using click chemistry or other reactive chemistries. Its structure allows for the modulation of the distance, reactivity, and conjugation properties in the design of bioactive compounds or biomaterials. | price> |
R-M-5371 | SF650-Biotin | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4706 | DSPE-PEG550-AE105(D-Cha-F-s-r-Y-L-W-S) | 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.It can couple various polypeptide groups.The AE105 peptide (D-Cha-F-s-r-Y-L-W-s) bound to the uPAR domain III ring 3 was coupled with DOTA.After labeling with 64Cu, the tracer was evaluated for microscopic PET imaging of uPAR expression in nurine xenotransplantation model (uPAR positive and uPAR negative). | price> |
R-M1-8824 | Biotin-PEG(4)-Gly-CBT | Biotin-PEG(4)-Gly-CBT can be utilized for various applications, including protein labeling, protein immobilization, and the targeted delivery of biotinylated molecules to specific cell types or tissues. | price> |
R-M-5372 | SF680-NHS | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4707 | AE105-PEG750-DSPE | 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.It can couple various polypeptide groups.The AE105 peptide (D-Cha-F-s-r-Y-L-W-s) bound to the uPAR domain III ring 3 was coupled with DOTA. After labeling with 64Cu, the tracer was evaluated for microscopic PET imaging of uPAR expr | price> |
R-M1-8825 | Fmoc-L-Cys(S-DMP)-OH | Fmoc-L-Cys(S-DMP)-OH is a protected form of cysteine suitable for solid-phase peptide synthesis that enables the introduction of cysteine residues into peptide sequences for subsequent modifications or disulfide bonding. | price> |
R-M-5373 | SF680-Mal | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |
R-C-4708 | DSPE-PEG-VSNKYFSNIHWGC | uPA peptide(VSNKYFSNIHWGC)-conjugated,antisense-miR-21 and antisense-miR-10b coloaded PLGA-b-PEG-NPs (called uPA-Anti-miR-21-Anti-miR-10b-NPs) that simultaneously antagonized miR-21-induced inhibition of apoptosis and miR-10b-induced metastasis to achieve TNBC therapy.Our products are only used for scientific research,not for human body. | price> |
R-M1-8826 | Fmoc-L-Dap(Boc-AEEA)-OH | Fmoc-L-Dap(Boc-AEEA)-OH is a protected form of diaminopimelic acid suitable for solid-phase peptide synthesis that enables the introduction of Dap residues into peptide sequences for subsequent modifications or specific structural motifs. | price> |
R-M-5374 | SF680-NH2 | In addition to its superior fluorescence characteristics (such as high brightness and super light stability), the design of SFTM fluorophores also simplifies the fluorescence labeling and detection process. SFTM fluorophores can be directly used in aqueous working buffer without adding any organic solvent.The elimination of organic solvents can not only simplify the labeling and detection process, but also provide additional protection for molecules from some harsh organic solvents.In addition, SFTM fluorophores provide a variety of chemical reactions and / or bioactive parts, which can be directly used to label, image and detect various molecules and particles.These fluorophores range from ultraviolet to near-infrared and can be used for in vitro and in vivo imaging. | price> |