2′-Deoxy-5′-O-DMT-N2-ethylguanosine 3′-CE phosphoramidite

Reagent Code: #180428
fingerprint
CAS Number 642462-81-5

science Other reagents with same CAS 642462-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 797.88 g/mol
Formula C₄₂H₅₂N₇O₇P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of N2-ethylguanine into DNA strands. The DMT (dimethoxytrityl) group provides 5′-end protection during synthesis, allowing stepwise addition and coupling control. The phosphoramidite moiety ensures efficient and selective phosphite bond formation with the growing DNA chain. This modified nucleoside is particularly valuable in studying DNA damage, epigenetic regulation, and mutagenesis caused by alkylating agents. It is also employed in developing modified aptamers and functional nucleic acids with enhanced stability or binding properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100μg
10-20 days ฿104,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2′-Deoxy-5′-O-DMT-N2-ethylguanosine 3′-CE phosphoramidite
No image available

Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of N2-ethylguanine into DNA strands. The DMT (dimethoxytrityl) group provides 5′-end protection during synthesis, allowing stepwise addition and coupling control. The phosphoramidite moiety ensures efficient and selective phosphite bond formation with the growing DNA chain. This modified nucleoside is particularly valuable in studying DNA damage, epigenetic regulation, and mutagenesi

Used in solid-phase oligonucleotide synthesis, this phosphoramidite building block enables the site-specific incorporation of N2-ethylguanine into DNA strands. The DMT (dimethoxytrityl) group provides 5′-end protection during synthesis, allowing stepwise addition and coupling control. The phosphoramidite moiety ensures efficient and selective phosphite bond formation with the growing DNA chain. This modified nucleoside is particularly valuable in studying DNA damage, epigenetic regulation, and mutagenesis caused by alkylating agents. It is also employed in developing modified aptamers and functional nucleic acids with enhanced stability or binding properties.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...