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CPGs for Oligo Synthesis

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2'-O-Methyl-C(Bz)-Suc-CPG; 500 Å (RNA) (BRP-02243)

Description: 2'-O-Methyl-C(Bz)-Suc-CPG; 500 Å is a reagent used in the solid-phase synthesis of RNA oligonucleotides for incorporating 2'-O-methylcytidine residues. It features a benzoyl-protected cytosine base and a succinyl linker attached to controlled pore glass (CPG) with a 500 Å pore size. The 2'-O-methyl modification enhances the RNA's stability and resistance to enzymatic degradation, making this reagent ideal for synthesizing stable RNA sequences with precise cytosine incorporation.
CAT: BRP-02243
Appearance: White powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Symbol: 2'-OMe-C-RNA-CPG
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1 hour or AMA for 30 minutes. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5 hours. Compatible with the deprotection chemicals used by 2' Fluoro; 2' modified phosphoramidite and TBDMS protected reagents.
Synonyms: 5'-O-(4,4'-Dimethoxytrityl)-N4-benzoyl-2'-O-methylacytosine-3'-Suc-CPG 500 Å; N4-Benzoyl-2'-O-methyl-5'-O-DMT-cytosine-3'-Suc-CPG 500 Å; N4-Benzoyl-2'-O-methyl-5'-O-dimethoxytritylcytosine-3'-Suc-CPG 500 Å

2'-O-Methyl-G(iBu)-Suc-CPG; 500 Å (RNA) (BRP-02244)

Description: 2'-O-Methyl-G(iBu)-Suc-CPG; 500 Å is a reagent used in the solid-phase synthesis of RNA oligonucleotides, specifically for incorporating 2'-O-methylguanosine residues. It includes an isobutyryl-protected guanine base and a succinyl linker attached to controlled pore glass (CPG) with a 500 Å pore size. The 2'-O-methyl modification enhances the RNA's stability and resistance to enzymatic degradation, making this reagent ideal for synthesizing RNA sequences with improved durability and precise guanine incorporation.
CAT: BRP-02244
Appearance: White to off-white powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Symbol: 2'-OMe-G-RNA-CPG
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1 hour or AMA for 30 minutes. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5 hours. Compatible with the deprotection chemicals used by 2' Fluoro; 2' modified phosphoramidite and TBDMS protected reagents.
Synonyms: 2'-OMe-G(iBu) CPG; 2'-OMe-rG(iBu) CPG; 2'-OMe-G-RNA-CPG; 5'-O-(4,4'-Dimethoxytrityl)-N2-isobutyryl-2'-O-methylguanosine-3'-Suc-CPG 500 Å; N2-Isobutyryl-2'-O-methyl-5'-O-DMT-guanosine-3'-Suc-CPG 500 Å; N2-Isobutyryl-2'-O-methyl-5'-O-dimethoxytritylguanosine-3'-Suc-CPG 500 Å

2'-O-Methyl-U-Suc-CPG; 500 Å (RNA) (BRP-02245)

Description: 2'-O-Methyl-U-Suc-CPG; 500 Å is a reagent used in the solid-phase synthesis of RNA oligonucleotides, specifically for incorporating 2'-O-methyluridine residues. It features a succinyl linker that attaches the 2'-O-methyluridine to controlled pore glass (CPG) with a 500 Å pore size. The 2'-O-methyl modification enhances the stability and resistance of the RNA to enzymatic degradation, making this reagent ideal for creating more stable and durable RNA sequences with precise uridine incorporation.
CAT: BRP-02245
Appearance: White to off-white powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Symbol: 2'-OMe-U-RNA-CPG
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 minutes at 25°C or for 30 minutes at 60°C.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1 hour or AMA for 30 minutes. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5 hours. Compatible with the deprotection chemicals used by 2' Fluoro; 2' modified phosphoramidite and TBDMS protected reagents.
Synonyms: 5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyluridine-3'-Suc-CPG 500 Å; 2'-O-methyl-5'-O-DMT-uridine-3'-Suc-CPG 500 Å; 2'-O-methyl-5'-O-dimethoxytrityluridine-3'-Suc-CPG 500 Å

3'-Thiol Modifier C6 SS Glyc CPG; 1000 Å (BRP-02246)

Description: 3'-Thiol Modifier C6 SS Glyc CPG; 1000 Å is a reagent used in the solid-phase synthesis of oligonucleotides to incorporate a protected thiol group at the 3' end. It features a 6-carbon spacer (C6) with a disulfide bond (SS) linked to a glycyl group (Glyc), attached to controlled pore glass (CPG) with a 1000 Å pore size. This setup allows for the introduction of a thiol group, which can be used for further conjugation or cross-linking reactions, while the disulfide bond can be cleaved to reveal the free thiol group after synthesis.
CAT: BRP-02246
Appearance: White to off-white powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Shipping: Room temperature.
Deprotection Conditions: Deprotect the oligo in NH4OH for 2h at 65°C if using fast deprotecting amidites, or 5h at 65°C if using standard amidites. This will remove only the base protecting groups.
Synonyms: 3'-Thiol Modifier C6 S-S Glyc CPG

3'-DMT-dA(Bz)-Suc-CPG; 1000 Å (BRP-02247)

Description: 3'-DMT-dA(Bz)-Suc-CPG; 1000 Å is a reagent used in the solid-phase synthesis of oligonucleotides, specifically for incorporating adenine residues. It features a 3'-DMT protective group, N6-benzoyl protection on the adenine base, and a succinyl linker that attaches the nucleoside to controlled pore glass (CPG) with a pore size of 1000 Å. This setup is ideal for synthesizing longer DNA sequences with high efficiency and precise control over the incorporation of adenine.
CAT: BRP-02247
Appearance: White to off-white powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 3'-O-(4,4'-Dimethoxytrityl)-N6-benzoyl-2'-deoxyadenosine-5'-Suc-CPG 1000 Å; N6-Benzoyl-2'-deoxy-3'-O-DMT-adenosine-5'-Suc-CPG 1000 Å; N6-Benzoyl-2'-deoxy-3'-O-dimethoxytrityladenosine-5'-Suc-CPG 1000 Å

3'-DMT-dC(Ac)-Suc-CPG; 1000 Å (BRP-02248)

Description: 3'-DMT-dC(Ac)-Suc-CPG; 1000 Å is a reagent used in the solid-phase synthesis of oligonucleotides, specifically for incorporating cytosine residues. It includes a 3'-DMT protective group, N4-acetyl protection on the cytosine base, and a succinyl linker that attaches the nucleoside to controlled pore glass (CPG) with a pore size of 1000 Å. This setup is designed for the efficient and accurate synthesis of longer DNA sequences, allowing precise incorporation of cytosine while ensuring easy deprotection and release from the solid support.
CAT: BRP-02248
Appearance: White to off-white powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 3'-O-(4,4'-Dimethoxytrityl)-N4-acetyl-2'-deoxyacytosine-5'-Suc-CPG 1000 Å; N4-Acetyl-2'-deoxy-3'-O-DMT-cytosine-5'-Suc-CPG 1000 Å; N4-Acetyl-2'-deoxy-3'-O-dimethoxytritylcytosine-5'-Suc-CPG 1000 Å

3'-DMT-dG(iBu)-Suc-CPG; 1000 Å (BRP-02249)

Description: 3'-DMT-dG(iBu)-Suc-CPG; 1000 Å is a reagent used in the solid-phase synthesis of oligonucleotides for incorporating guanine residues. It includes a 3'-DMT protective group, N2-isobutyryl protection on the guanine base, and a succinyl linker that attaches the nucleoside to controlled pore glass (CPG) with a 1000 Å pore size. This configuration is optimized for the efficient synthesis of longer DNA sequences, ensuring precise guanine incorporation and easy cleavage after synthesis.
CAT: BRP-02249
Appearance: White to off-white powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: Use concentrated ammonia for 5 hours at 60°C.
Synonyms: 3'-O-(4,4'-Dimethoxytrityl)-N2-isobutyryl-2'-deoxyguanosine-5'-Suc-CPG 1000 Å; N2-Isobutyryl-2'-deoxy-3'-O-DMT-guanosine-5'-Suc-CPG 1000 Å; N2-Isobutyryl-2'-deoxy-3'-O-dimethoxytritylguanosine-5'-Suc-CPG 1000 Å

3'-DMT-T-Suc-CPG; 1000 Å (BRP-02250)

Description: 3'-DMT-T-Suc-CPG; 1000 Å is a reagent used in the solid-phase synthesis of oligonucleotides for incorporating thymine residues. It features a 3'-DMT protective group on the thymine base and a succinyl linker that connects the nucleoside to controlled pore glass (CPG) with a pore size of 1000 Å. This setup is ideal for synthesizing longer DNA sequences with precise thymine incorporation and facilitates efficient deprotection and release of the oligonucleotide from the solid support.
CAT: BRP-02250
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 3'-O-(4,4'-Dimethoxytrityl)-2'-deoxythymine-5'-Suc-CPG 1000 Å; 2'-deoxy-3'-O-DMT-thymine-5'-Suc-CPG 1000 Å; 2'-deoxy-3'-O-dimethoxytritylthymine-5'-Suc-CPG 1000 Å

5'-DMT-T(C6 Amino)-Suc-CPG; 500 Å (BRP-02251)

Description: 5'-DMT-T(C6 Amino)-Suc-CPG is used to introduce an amino function at the 3' end of an oligonucleotide.
CAT: BRP-02251
Appearance: White powder
Size Price Stock Quantity
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Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Before cleavage and deprotection, treat the oligonucleotide linked to the support with 10% DEA (diethylamine) MeCN for 5-10 min to avoid adding acrylonitrile to the amine during the cleavage and deprotection process. After treatment, wash the support with MeCN, and then continue to deprotect and lyse. When using standard amidites, use concentrated ammonia for 90 min at 25°C; when using fast deprotection amidites, use 1:1 ammonia: methylamine (AMA) at 25°C for 25 min.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 5'-DMT-T(C6 Amino)-Suc-CPG; 5'-DMT-T(Hexyl-NH-TFA)-Suc-CPG; 500 Å; 5'-DMT-T(C6 Amino)-Succinate CPG

5'-DMT-A(PAC)-Suc-CPG; 1000 Å (RNA) (BRP-02252)

Description: 5'-DMT-A(PAC)-Suc-CPG is used to incorporate unmodified ribonucleic acid at the 3 end of the oligonucleotide.
CAT: BRP-02252
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Synthesis Conditions: If you use PAC-protected supports or reagents, we recommend using phenoxyacetic anhydride or tert-butylbenzene acetal anhydride (FAST deprotection cap) as the CAPA reagent. Standard acetic anhydride (CAP A) can cause the acetylation of PAC-protected primary amines during the synthesis process.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 5'-O-DMT-2'-OAc-A(Pac)-3'-0-Suc-CPG

5'-DMT-A(PAC)-Suc-CPG; 500 Å (RNA) (BRP-02253)

Description: 5'-DMT-A(PAC)-Suc-CPG is used to incorporate unmodified ribonucleic acid at the 3 end of the oligonucleotide.
CAT: BRP-02253
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
Shipping: Room temperature.
Synthesis Conditions: If you use PAC-protected supports or reagents, we recommend using phenoxyacetic anhydride or tert-butylbenzene acetal anhydride (FAST deprotection cap) as the CAPA reagent. Standard acetic anhydride (CAP A) can cause the acetylation of PAC-protected amines during the synthesis process.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 5'-O-DMT-2'-OAc-A(Pac)-3'-0-Suc-CPG

5'-DMT-C(Ac)-Suc-CPG; 1000 Å (RNA) (BRP-02254)

Description: 5'-DMT-C(Ac)-Suc-CPG is used to incorporate unmodified ribonucleic acid at the 3 end of the oligonucleotide.
CAT: BRP-02254
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 5'-O-DMT-2'-OAc-C(Ac)-3'-0-Suc-CPG

5'-DMT-C(Ac)-Suc-CPG; 500 Å (RNA) (BRP-02255)

Description: 5'-DMT-C(Ac)-Suc-CPG is used to incorporate unmodified ribonucleic acid at the 3 end of the oligonucleotide.
CAT: BRP-02255
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 5'-O-DMT-2'-OAc-C(Ac)-3'-0-Suc-CPG

DABCYL-C3-CPG; 500 Å (BRP-02256)

Description: DABCYL-C3-CPG; 500 Å is a reagent used in oligonucleotide synthesis for incorporating DABCYL, a fluorescence quenching dye, into the oligonucleotide. It features a C3 spacer linking DABCYL to controlled pore glass (CPG) with a 500 Å pore size. DABCYL is used as a quencher in various fluorescence-based assays, where it helps in detecting and quantifying nucleic acids by quenching the fluorescence of a nearby fluorophore. The C3 spacer ensures sufficient distance between the quencher and the fluorophore to achieve effective quenching.
CAT: BRP-02256
Appearance: Orange powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Shipping: Room temperature.
Cleavage Conditions: This support may be cleaved using concentrated NH4OH or t-butylamine/H2O (TAMRA and other rhodamine-based dyes require deprotection with t-butylamine).
Absorption Maximum (Lambda Max): 474
Synonyms: DABCYL-C3-CPG; O-DMT-N-DABCYL-3-aminopropan-1,2-diol-Suc-CPG; 500 Å

dG-CPG; 2000 Å (BRP-02257)

Description: dG-CPG; 2000 Å is a reagent used in the solid-phase synthesis of oligonucleotides for incorporating N2-isobutyryl-deoxyguanosine (dG) residues. It includes a 5'-O-DMT (dimethoxytrityl) protective group, which protects the 5' end of the guanine base during synthesis. The N2-isobutyryl group protects the guanine's exocyclic amino group, and the 3'-suc (succinyl) linker connects the nucleoside to controlled pore glass (CPG) with a 2000 Å pore size. This configuration supports efficient synthesis and loading of long DNA sequences while ensuring precise incorporation and protection of guanine residues.
CAT: BRP-02257
Appearance: White to Off-white Powder
Size Price Stock Quantity
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Storage: Store at -20 °C
Synonyms: dG-CPG 2000; 5'-Dimethoxytrityl-N-isobutyryl-2'-deoxyGuanosine, 3'-succinoyl-long chain alkylamino-CPG 2000; 5'-O-DMT-2'-deoxy-G(iBu)-3'-suc-CPG 2000

5'-DMT-C(Bz)-Suc-CPG; 500 Å (RNA) (BRP-02258)

Description: 5'-DMT-C(Bz)-Suc-CPG; 500 Å (RNA) is a reagent used in the solid-phase synthesis of RNA oligonucleotides for incorporating N4-benzoyl-cytidine (C) residues. It features a 5'-DMT (dimethoxytrityl) protective group to protect the 5' end of the cytidine base, an N4-benzoyl group to protect the cytidine's exocyclic amino group, and a succinyl (Suc) linker that attaches the nucleoside to controlled pore glass (CPG) with a 500 Å pore size. This setup ensures effective incorporation of cytidine into RNA sequences while providing stability and ease of deprotection.
CAT: BRP-02258
Appearance: White powder
Size Price Stock Quantity
-- -- --
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Storage: Store at -20 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotection amidites (such as C-Ac; G-DMF), use concentrated ammonia at 60°C for 1h or AMA for 30 min. When using standard amidites (such as C-Bz; G-iBu), please use concentrated ammonia at 60°C for 5h.
Synonyms: 5'-DMT-2'-OAc-C(Bz)-3'-O-Suc-CPG; 500 Å

5'-DMT-dA(Bz) CPG; 1000 Å (BRP-02259)

Description: 5'-DMT-dA(Bz) CPG is a CPG used for incorporating unmodified dA at the 3' end of an oligonucleotide.
CAT: BRP-02259
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 5'-DMT-dA(Bz)-Suc-CPG; 1000 Å; 5'-O-DMT-2'-deoxy-A(Bz)-3'-O-Suc-CPG; 1000 Å

5'-DMT-dA(Bz) CPG; 1400 Å (BRP-02260)

Description: 5'-DMT-dA(Bz) CPG is a CPG used for incorporating unmodified dA at the 3' end of an oligonucleotide.
CAT: BRP-02260
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 5'-DMT-dA(Bz)-Suc-CPG; 1400 Å; 5'-O-DMT-2'-deoxy-A(Bz)-3'-O-Suc-CPG; 1400 Å

5'-DMT-dA(Bz)-3'-Q Linker-CPG; 1000 Å (BRP-02261)

Description: 5'-DMT-dA(Bz)-3'-Q linker-CPG is a CPG used for incorporating unmodified dA at the 3' end of an oligonucleotide.
CAT: BRP-02261
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Synthesis Conditions: Synthesis can be performed on these supports according to standard procedures with deprotection and cleavage modifications noted.
Cleavage Conditions: Cleavage can be carried out in 2 minutes at room temperature using concentrated NH4OH.
Deprotection Conditions: If fast deprotecting amidites are used; deprotection can be carried out using concentrated NH4OH for 1 hour at 60°C.
Synonyms: 5'-O-DMT-2'-deoxy-A(Bz)-3'-0-Q Linker-CPG; 1000 Å

5'-DMT-dA(Bz)-Suc-CPG; 2000 Å (BRP-02262)

Description: 5'-DMT-dA(Bz)-Suc-CPG is a CPG used for incorporating unmodified dA at the 3' end of an oligonucleotide.
CAT: BRP-02262
Appearance: White powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
Shipping: Room temperature.
Cleavage Conditions: Use concentrated ammonia for 90 min at 25°C or 30 min at 60°C, or 1:1 ammonia:methylamine (AMA) for 25 min at 25°C when using fast deprotecting amidites.
Deprotection Conditions: When using fast deprotecting amidites (e.g., C-Ac; G-DMF; G-PAC), please use concentrated ammonia for 1h or AMA for 30 min at 60°C. When using standard amidites (e.g., C-Bz; G-iBu), please use concentrated ammonia for 5h at 60°C.
Synonyms: 5'-DMT-dA(Bz) CPG; 2000 Å; 5'-O-DMT-2'-deoxy-A(Bz)-3'-O-Suc-CPG; 2000 Å
* Only for research. Not suitable for any diagnostic or therapeutic use.

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