Catalog |
name |
Description |
price |
R-CA-011 |
Picolyl-azide-NH2 |
The combination of picolyl-azide-NH2 has considerable potential in several fields:
Bioconjugation: The compound can be used to conjugate biomolecules, such as proteins or peptides, through the azide group in bioorthogonal reactions. Its picolyl group may help in the stabilization of the conjugate or improve solubility.
Drug Development: The amino group and the azide can be used to create targeted drug delivery systems where the drug is attached via a linker that can be cleaved or activated under certain conditions, improving selectivity towards diseased cells.
Chemical Biology: The compound can be a tool in chemical biology to study protein interactions, identify cellular targets of small molecules, or explore metabolic pathways through azide labeling techniques.
Diagnostics: The unique properties of the azide group can be utilized to develop diagnostic reagents, allowing for specific tagging of biomolecules in assays. |
price> |
R-OR-204 |
DBCO-S-S-MAL |
DBCO-S-S-Maleimide DBCO-S-S-MAL from ruixi DBCO-S-S-Maleimide,Dibenzylcyclooctyne(DBCO)-SS-MAL from ruixi.one end of the disulfide bond is linked to DBCO and the other to Maleimide is a new cytosine nucleoside derivative. |
price> |
R-M-411 |
Kdo Azide |
8-Azido-3,8-dideoxy-D-manno-octulosonic acid (Kdo Azide) is an analogue of the natural 3-deoxy-D-manno-octulosonic acid (Kdo) that contains a very small modification, specifically an azido moiety. This molecule can be incorporated by cultured cells (Gram-negative Bacteria, for example) and incorporated into glycans (LPS, for example) during active glycan biosynthesis. Detection utilizes the chemoselective ligation or “click” reaction between an azide and an alkyne or cyclooctyne.Applications:Metabolic Lipopolysaccharide labeling. |
price> |
R-C-811 |
TCO-PEG3-Maleimide |
TCO-PEG3-Maleimide enables simple and efficient incorporation of TCO moiety onto antibodies,cysteine-containing peptides and other thiol-containing molecules.The maleimide group specifically and efficiently reacts with reduced thiols (sulfhydryl groups,-SH) at pH 6.5 to 7.5 to form stable thioether bonds.The hydrophilic polyethylene glycol(PEG)spacer arm improves solubility in aqueous buffers. |
price> |
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-M-3070 |
DBCO-S-S-PEG3-biotin,Cas:1430408-09-5 |
DBCO-S-S-PEG3-biotin is a cleavable reagent for introduction of a biotin moiety to azide-containing biomolecules using copper-free Click Chemistry. PEG spacer arm provides better solubility to the labeled molecules in aqueous media. The disulfide bond in this linker can be cleaved using reducing agents such as DTT, BME and TCEP. |
price> |
R-M-5026 |
Py-Tetrazine-Py-Amide-Butyric acid,cas:1233234-76-8 |
Py-Tetrazine-Py-Amide-Butyric acid,cas:1233234-76-8 from ruixi.Building block for the strain-promoted copper-free click chemistry ligation techniques. Can be attached to the protein, peptide or small molecule via amide or ester bond. |
price> |
R-M-5027 |
Bz-(Me)Tz-NHS,cas:1454558-58-7 |
Bz-(Me)Tz-NHS,5-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)benzylamino)-5-oxopentanoic acid N-succinimidyl ester from ruixi.Bz-(Me)Tz-NHS is a click chemical reaction. |
price> |
R-M-5028 |
Me-Tetrazine-PEG4-O-amine,cas:1704737-07-4 |
Me-Tetrazine-PEG4-O-amine,cas:1704737-07-4 from ruixi.Me-Tetrazine-PEG4-O-amine is a click chemical reaction peg reagent.
|
price> |
R-M-5029 |
Tetrazine-NHBoc,cas:1380500-93-5 |
Tetrazine-NHBoc,tert-butyl 4-(1,2,4,5-tetrazin-3-yl)benzylcarbamate from ruixi.
Tetrazine-NHBoc is a protective click chemical reactant. |
price> |