Ac4ManNAz (Synonyms: N-Azidoacetyl-D-mannosamine, N-Azidoacetylmannosamine-tetraacylated) |
Katalog-Nr.GC60038
One-Click Copy Product Info
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Ac4ManNAz ist ein Azido-haltiges metabolisches Glykoprotein-Markierungsreagenz.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1213701-11-1
Sample solution is provided at 25 µL, 10mM.
Ac4ManNAz (1,3,4,6-tetra-O-acetyl-N-azidoacetylaminomannose) is an azide-containing metabolic glycoprotein labeling reagent that can selectively modify proteins for cell labeling, tracking, and proteomic analysis [1, 2]. Ac4ManNAz is a click chemistry reagent that contains an azide group and can undergo Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) with molecules containing alkyne groups[3]. Ac4ManNAz can also undergo ring strain-driven alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups[4].
Click chemistry is a versatile reaction that can be used for the synthesis of a variety of conjugates. Virtually any biomolecule can be easily labelled with small molecules, such as fluorescent dyes, biotin, etc using click chemistry method.
Click chemistry reaction takes place between two components: azide and alkyne (terminal acetylene). Both azido and alkyne groups are nearly never encountered in natural biomolecules. Hence, the reaction is highly bioorthogonal and specific.
References:
[1] Han S S, Lee D E, Shim H E, et al. Physiological effects of Ac4ManNAz and optimization of metabolic labeling for cell tracking[J]. Theranostics, 2017, 7(5):1164.
[2] Han S S, Shim H E, Park S J, et al. Safety and optimization of metabolic labeling of endothelial progenitor cells for tracking[J]. Scientific reports, 2018, 8(1): 13212.
[3] Singh M S, Chowdhury S, Koley S. Advances of azide-alkyne cycloaddition-click chemistry over the recent decade[J]. Tetrahedron, 2016, 72(35): 5257-5283.
[4] Vidyakina A A, Silonov S A, Govdi A I, et al. Key role of cycloalkyne nature in alkyne-dye reagents for enhanced specificity of intracellular imaging by bioorthogonal bioconjugation[J]. Organic & Biomolecular Chemistry, 2024.
The following general protocol is recommended for chemical labeling of alkyne-modified oligonucleotides or DNA with azides produced by GlpBio. This plan only provides a guide, please modify it to meet your specific needs.
1.Calculate the volumes of reagents required for Click chemistry labeling using the table below. Prepare the required stock solutions(see Appendix).
|
Reagent |
Final concentration in the mixture |
Stock solution concentration |
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Oligonucleotide/DNA, alkyne-modified |
Varies (20 — 200 uM) |
Varies |
|
Azide |
1.5 x (oligonucleotide concentration) |
10 mM in DMSO |
|
DMSO |
50 vol % |
— |
|
Ascorbic acid |
0.5 mM |
5 mM in water |
|
Cu-TBTA complex |
0.5 mM |
10 mM in 55 vol % DMSO |
2.Dissolve alkyne-modified oligonucleotide or DNA in water in a pressure-tight vial.
3.Add 2M triethylammonium acetate buffer, pH 7.0, to final concentration 0.2 M.
4.Add DMSO, and vortex.
5.Add azide stock solution (10 mM in DMSO), and vortex.
6.Add the required volume of 5mM Ascorbic Acid Stock solution to the mixture, and vortex briefly.
7.Degass the solution by bubbling inert gas in it for 30 seconds. Nitrogen, argon, or helium can be used.
8.Add the required amount of 10 mM Copper (II)-TBTA Stock in 55% DMSO to the mixture. Flush the vial with inert gas and close the cap.
9.Vortex the mixture thoroughly. If significant precipitation of azide is observed, heat the vial for 3 minutes at 80°C, and vortex.
10.Keep at room temperature overnight.
11.Precipitate the conjugate with acetone (for oligonucleotides) or with ethanol (for DNA). Mix thoroughly and keep at −20 °C for 20 minutes.
To precipitate an oligonucleotide conjugate: add to the mixture at least a 4-fold excess volume of 3% lithium perchlorate in acetone (if the volume of the mixture is large, split in several vials).
To precipitate a DNA conjugate: add to the mixture sodium acetate to a final concentration of 0.3M; add 2.5 volumes of ethanol (or 0.8 volumes of isopropanol).
12.Centrifuge at 10000 rpm for 10 minutes.
13.Discard the supernatant. Wash the pellet with acetone (1 mL), centrifuge at 10000 rpm for 10 minutes.
14.Discard the supernatant, dry the pellet, and purify the conjugate by RP-HPLC or PAGE.
Appendix. Preparation of stock solutions of the reagents used for click-chemistry labeling and conjugation.
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5 mM Ascorbic Acid Stock |
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Preparation |
Dissolve 18 mg of ascorbic acid in 20 mL of distilled water |
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Storage |
Ascorbic acid is readily oxidized by air. The solution is stable for one day. Use fresh preparations |
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10 mM Copper (II)-TBTA Stock in 55% DMSO |
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|
Preparation |
Dissolve 50 mg of copper (II) sulfate pentahydrate in 10 mL of distilled water. Dissolve 116 mg of TBTA ligand in 11 mL of DMSO. Mix two solutions |
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Storage |
Store at room temperature. The solution is stable for years |
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2M Triethylammonium Acetate Buffer, pH 7.0 |
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Preparation |
Mix 2.78 mL of triethylamine with 1.14 mL of acetic acid. Add water to 10 mL volume, and adjust pH to 7.0 |
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Storage |
Store at room temperature. The solution is stable for years |
| Cas No. | 1213701-11-1 | SDF | |
| Überlieferungen | N-Azidoacetyl-D-mannosamine, N-Azidoacetylmannosamine-tetraacylated | ||
| Canonical SMILES | O=C(N[C@@H]1C(OC(C)=O)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)CN=[N+]=[N-] | ||
| Formula | C16H22N4O10 | M.Wt | 430.37 |
| Löslichkeit | DMSO:100 mg/mL (232.36 mM; Need ultrasonic | Storage | Store at 2-8°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
|
1 mg | 5 mg | 10 mg |
| 1 mM | 2.3236 mL | 11.6179 mL | 23.2358 mL |
| 5 mM | 464.7 μL | 2.3236 mL | 4.6472 mL |
| 10 mM | 232.4 μL | 1.1618 mL | 2.3236 mL |
Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
g
μL
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >98.00% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 13 reference(s) in Google Scholar.)