DMT-dG(dmf) Phosphoramidite
configured for MerMade
Manufacturer: Sigma Aldrich
CAS Number: 330628-04-1
Synonym(S): DMT-dG(dmf) Amidite, N-[(dimethylamino)methylene]-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxyguanosine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite], N2-Dimethylformamidine-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 6 X 5 G | G115040-6-X-5-G | In Stock | ₹ 1,64,139.48 |
| 6 X 10 G | G115040-6-X-10-G | In Stock | ₹ 2,71,469.35 |
G115040 - 6 X 5 G
In Stock
Quantity
1
Base Price: ₹ 1,64,139.48
GST (18%): ₹ 29,545.106
Total Price: ₹ 1,93,684.586
type
for DNA synthesis
Quality Level
200
product line
Proligo Reagents
Assay
≥99% (31P-NMR)≥99.0% (reversed phase HPLC)
form
powder
technique(s)
oligo synthesis: suitable
color
white to off-white
λ
conforms (UV/VIS Identity)
compatibility
configured for MerMade
nucleoside profile
base: deoxyguanosinebase protecting group: DMF2' protecting group: none5' protecting group: DMTdeprotection: fast/standard
Other Options
Description
- General description: Proligo′s DNA phosphoramidites lead to high-yield and high-quality oligonucleotides due to their high coupling efficiency. The deprotection step of automated oligonucleotide synthesis is integral to synthesis time and final product quality. The high coupling efficiency of Proligo′s DNA phosphoramidites leads to high-yield and high-quality oligonucleotides.Changing the dG protecting group to the dimethylformamide (dmf) base protecting group enables the rapid synthesis of high-purity, high-yieldoligonucleotide, thus increasing the efficiency of high-throughputproduction.Key Features of dG(dmf)dG(dmf) is deprotected faster than the conventional dG(ib): thedeprotection time in concentrated ammonia is reduced to 2 hours at55 °C or 1 hour at 65 °C The dG(dmf)-monomer is especially suitable for G-rich sequences:incomplete deprotection is greatly reduced in comparison with theconventional dG(ib)-monomerdG(dmf)-phosphoramidite is as stable in solution as the standard dA(bz)-,dC(bz)- and dT-phosphoramiditesdG(dmf)-phosphoramidite can directly substitute for dG(ib)-phosphoramidite No change is required in the reagents commonly used for DNA synthesis(except a low concentration iodine oxidizer i.e., 0.02 M in iodine, should beemployed)DMT-dG(dmf) Phosphoramidite is configured for MerMade Synthesizers.
- Packaging: G115040-6x5G packaged in a 8 oz bottle with a 28-400 capG115040-6x10G packaged in a 8 oz bottle with a 28-400 cap
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable