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CPGs for oligo synthesis

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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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'-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
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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 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
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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
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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
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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
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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
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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
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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
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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

What are CPGs?

Controlled Pore Glasses (CPGs) are made of silica and are widely used in solid phase synthesis reactions of oligonucleotides. CPG spheres have many irregular pore channels and are pore size stable. For spatial reasons, large pore sizes are suitable for the synthesis of long fragments, and short pore sizes are suitable for the synthesis of short fragments. BOC Sciences offers a wide range of CPGs for oligonucleotide synthesis to choose from, with pore sizes ranging from 300 Å-5000 Å. Groups linked to CPGs include TAMRA, DMT-Phosphate, Fluorescein, Aminopropyl, etc.

Different pore size CPGs can be used to synthesize oligonucleotide products with different loadings:

(1) 500 Å/600 Å pore size CPG products are suitable for oligonucleotide synthesis of < 35 mers. For example, therapeutic oligonucleotides can be synthesized at loads up to 100 μmol/g.

(2) 1000 Å pore size CPG products for >35 mers or highly modified oligonucleotide synthesis.

(3) 2000 Å/3000 Å pore size CPG products, suitable for oligonucleotide synthesis on a scale of 80 mers or more, with synthetic loads typically ranging from 10 to 20 μmol/g.

Examples of CPGs

Because tetramethylrhodamine (TAMRA) is not base-stable, procedures for cleaving and deprotecting labeled oligonucleotides must be carefully considered. For example, to simplify the preparation of TAMRA oligonucleotides, 3'-TAMRA CPG for 3' labeling and TAMRA-dT for in-sequence labeling are available.

Fluorescein CPG is traditionally used to add fluorescein labeling to the 3'-end. For example, 3'-(6-FAM) CPG effectively blocks polymerase extension and exonuclease digestion at the 3'-end.

The phosphate functional group on the surface of DMT-Phosphate-CPG usually carries a DMT protecting group. DMT is a commonly used protecting group that protects the phosphate group from non-specific reactions during nucleotide synthesis. The DMT protecting group can be easily removed at the end of the synthesis to expose the phosphate group for further modification. CPGs have a pore size and pore structure that can be tuned similar to that of conventional CPGs. This controllable pore size facilitates efficient solid-phase synthesis of oligonucleotides and ensures good attachment and stability of the phosphate functional groups.

Aminopropyl-CPG is a CPG modified by an aminopropyl functional group, and we can provide products with pore sizes ranging from 300 Å-2000 Å. The products can be used for the amination modification of nucleotides, and by introducing an amino functional group, the chemistry and reactivity of nucleotides can be extended.

Features of CPGs

The pore size and pore structure of CPGs can be tuned as needed, typically in the range of 3-30 nanometers. This controllable pore size and pore structure helps ensure efficient solid phase synthesis of oligonucleotides.

CPGs have a large amount of surface activity, providing enough binding sites to allow nucleotide immobilization and chemical reactions to take place during the synthesis process.

CPGs have good chemical stability and can be used under common nucleotide synthesis reaction conditions. They can tolerate synthesis conditions such as alkaline conditions, organic solvents, and high temperatures, thus ensuring high-quality oligonucleotide synthesis.

CPGs can be scaled and adjusted as needed for both small-scale research and large-scale industrial production.

After years of development, BOC Sciences has the expertise and experience to help you synthesize high-quality CPGs for oligo synthesis and accelerate the achievement of your research goals.

If you have any special requirements for CPGs products, please feel free to contact us. We look forward to working with you on attractive projects.

* Only for research. Not suitable for any diagnostic or therapeutic use.

Our Products

BOC Sciences is a leading provider of DNA and RNA products and services that meet the needs of researchers and pharmaceutical companies worldwide. Its broad product portfolio includes various types of oligonucleotides, DNA/RNA synthesis feedstocks, RNA interference tools, and advanced drug delivery systems, among others. Designed to promote cutting-edge research and innovative therapeutic solutions, at BOC Sciences you are sure to find the right product for you.

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