Amino Linkers

Proligo® Reagents
 
Product Breadth of Proligo Reagents
 Phosphoramidites :
Pharmadite®
DNA Phosphoramidites
RNA Phosphoramidites
2'O-Methyl RNA Phosphoramidites
 Fast Deprotection Chemistries :
DNA
RNA
 Supports :
Controlled Pore Glass (CPG)
Columns
 Solvents :
Liquid Reagents
Activator 42™
 Modifications :
Fluorescein Phosphoramidite
Biotin Phosphoramidite
Phosphate-ON Phosphoramidite
Non Standard Nucleosides
 Linkers :
Amino Linkers
ssH Linker
Product Breadth of Proligo Reagents


Amino Linkers can be employed to conjugate biotin, fluorescein or other modifiers and reporter groups to the 5’end of oligonucleotides, or to attach oligonucleotides to surfaces. SAFC Proligo Reagents offers monomethoxytrityl-protected amino linkers as well as trifluoroacetyl-protected amino linkers.  
  Download Literature:
  •  User Instructions
MMT-Amino Linker Phosphoramidite
(657k pdf)
  •  User Instructions
TFA-Amino Linker Phosphoramidite
(656k pdf)
  View Structure:
  •  MMT-Amino
hexanol-ß-
Cyanoethyl
phosphoramidite
  •  Trifluoroacetyl-
Aminopentanol-
ß-Cyanoethyl
phosphoramidite
Monomethoxytrityl (MMT)-protected amino linker
The MMT-group can be cleaved on the synthesis instrument with acidic deblock solution to enable on-support labeling protocols. Alternatively, the MMT-amino linker can be attached in the trityl-on mode of the instrument to provide purification handle similar to the DMT-group of the conventional oligonucleotides. The MMT-group is then removed with aqueous acid after purification with either RP-HPLC or a purification cartridge.
Trifluoroacetyl (TFA)-protected amino linker  
  The base-labile TFA-group is easily removed with concentrated ammonia during the cleavage and deprotection step. Additional deprotection steps are not necessary.
   
Key features of Amino Linkers
Completely soluble in acetonitrile
Proligo Reagents offers base-labile or acid-labile protecting groups on the amino linker, depending upon the application
Amino linker products are coupled with standard synthesis protocols, identical to the coupling pf DNA monomer phosphoramidites
No change in auxiliary synthesis reagents is required
The MMT-amino linker features a lipophilic group which aids in purification of the modified oligonucleotide after synthesis
The acid-labile MMT-group permits the colorimetric, determination of the coupling efficiency
It is recommended to deprotect MMT-amino linker oligonucleotides in concentrated ammonia at a lower temperature e.g. at 40°C for 24 hours
The MMT-group can be removed in aqueous solution with 80% acetic acid at room temperature for 24 hours
TFA-amino linker is completely deprotected with concentrated ammonia. Additional deprotection steps are not necessary

Labels and Modifications - Amino Linkers
Compatible with Expedite™ and Polygen® Instruments
Product No. Description Unit
M010282-01 MMT-hexylamine-linker amidite 1 x 0.25g
M010682-01 TFA pentylaminolinker amidite 1 x 0.25g
M010882-01 TFA Hexylaminolinker Amidite 1 x 0.25g
Compatible with ABI™ Instruments
M010232-01 MMT-hexylamine-linker amidite 1 x 0.25g
M010632-01 TFA pentylaminolinker amidite 1 x 0.25g
M010832-01 TFA Hexylaminolinker Amidite 1 x 0.25g
Custom Products Phosphoramidites of non-catalogue linkers, reporters or modifiers are offered as custom synthesis products. Please enquire.

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* Patent pending