CPGs for oligo synthesis

rA (Bz), 2'-OAc CNA (N16) CPG

Description: rA (Bz), 2'-OAc CNA (N16) CPG is a modification reagent used in oligonucleotide synthesis. It incorporates a riboadenosine (rA) residue modified with a benzoyl (Bz) group onto a controlled pore glass (CPG) solid support. This modification enhances stability and functionality. It enables the synthesis of RNA oligonucleotides with improved properties, suitable for various molecular biology and biotechnology applications, including RNA interference and gene expression studies.
CAT: BRP-00506
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Storage: Store at -20 °C
Synonyms: Bz-A-RNA-CPG; 5'-Dimethoxytrityl-N-benzoyl-Adenosine, 2'-acetate-3'-succinoyl-long chain alkylamino-CPG; rA (Bz), 2'-OAc CNA CPG; 2'-OAc Bz-A-RNA-CPG

3'-Azido-modifier CPG

Description: 3'-Azido-modifier CPG is a specialized reagent used in oligonucleotide synthesis. It incorporates an azide group at the 3'-end of the oligonucleotide sequence. This modification allows for further functionalization through click chemistry reactions, enabling the attachment of various molecules or probes to the oligonucleotide. The azido-modified oligonucleotides find applications in bioconjugation, labeling, and imaging studies, as well as in the development of nucleic acid-based therapeutics and diagnostics.
CAT: BRP-00508
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Synonyms: 3'-Azido-modifier CPG 1000A

Native CPG

Description: Natural CPG can be functionalized with a linker and either a base or modifier for solid-supported oligonucleotide synthesis.
CAT: BRP-00511
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2'-OMe-Ac-C-RNA-CPG

Description: 2'-OMe-Ac-C-RNA-CPG is a specialized reagent used in oligonucleotide synthesis. This modification provides enhanced stability and protection against nuclease degradation. The oligonucleotide is immobilized on a controlled pore glass (CPG) solid support, allowing for solid-phase synthesis. Overall, this reagent enables the efficient synthesis of modified RNA oligonucleotides with improved properties, suitable for various molecular biology and biotechnology applications, including gene expression studies and RNA-based therapeutics.
CAT: BRP-00517
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Storage: Store at -20 °C
Synonyms: 2'-OMe-rC(Ac) CPG; 5'-Dimethoxytrityl-N-acetyl-Cytidine, 2'-O-methyl,3'-succinoyl-long chain alkylamino-CPG

2'-OMe-G(dmf)-RNA-CPG

Description: 2'-OMe-G(dmf)-RNA-CPG is a specialized reagent used in oligonucleotide synthesis. It contains a 2'-O-methyl (2'-OMe) modification at the ribose sugar and a dimethylformamide (dmf) group attached to the guanine (G) nucleotide. This modification enhances stability and functionality, making it suitable for various molecular biology applications, including gene expression studies and therapeutic RNA-based treatments. Additionally, the oligonucleotide is immobilized on a controlled pore glass (CPG) solid support, allowing for solid-phase synthesis.
CAT: BRP-00533
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Storage: Store at RT
Synonyms: 2'-OMe-G-RNA-CPG; 5'-Dimethoxytrityl-N-dimethylformamidine-Guanosine, 2'-O-methyl,3'-succinoyl-long chain alkylamino-CPG; 5'-DMT-2'-OMe-G(dmf)-CPG

Bz-A-LNA-CPG

Description: Bz-A-LNA-CPG is a specialized reagent used in the solid-phase synthesis of oligonucleotides. This reagent features a benzoyl (Bz) protecting group on the adenine base, providing stability during the synthesis process. The inclusion of Locked Nucleic Acid (LNA) enhances the binding affinity and specificity of the resulting oligonucleotides to complementary nucleic acid sequences. The reagent is immobilized on a Controlled Pore Glass (CPG) support, which facilitates the step-by-step addition of nucleotides during oligonucleotide synthesis. These oligonucleotides are valuable in various applications, including diagnostics, molecular biology research, and the development of therapeutic agents, particularly in antisense and RNA interference (RNAi) technologies.
CAT: BRP-00550
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Storage: Store at -20 °C
Synonyms: 5'-Dimethoxytrityl-N-benzoyl-(2'-O,4'-C-methylene)-Adenosine, 3'-succinoyl-long chain alkylamino-CPG; Bz-A-LA-CPG 1000Å; Bz-A-LA-CPG; Benzoyl-Adenine-Locked Nucleic Acid-Controlled Pore Glass

Bz-5-Me-C-LNA-CPG

Description: Bz-5-Me-C-LNA-CPG is a specialized reagent used in the synthesis of oligonucleotides. It features a benzoyl (Bz) protecting group on 5-methylcytosine (5-Me-C) and incorporates Locked Nucleic Acid (LNA) for enhanced binding affinity and stability. The reagent is immobilized on Controlled Pore Glass (CPG), facilitating efficient solid-phase synthesis. This combination of modifications results in high-affinity, stable oligonucleotides suitable for applications in molecular diagnostics, therapeutic development, and advanced research.
CAT: BRP-00551
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Storage: Store at -20 °C
Synonyms: 5'-Dimethoxytrityl-N-benzoyl-5-methyl-(2'-O,4'-C-methylene)-Cytidine, 3'-succinoyl-long chain alkylamino-CPG; Bz-5-Me-C-LA-CPG 1000Å; Bz-5-Me-C-LA-CPG

dmf-G-LNA-CPG

Description: dmf-G-LNA-CPG is a specialized reagent utilized in oligonucleotide synthesis. It incorporates dimethylformamidine (dmf) as a protecting group for guanine (G) and Locked Nucleic Acid (LNA) for enhanced binding affinity and stability. Additionally, it is immobilized on Controlled Pore Glass (CPG), facilitating efficient solid-phase synthesis. This combination enables the production of high-affinity, stable oligonucleotides suitable for various molecular biology applications, including diagnostics and therapeutic development.
CAT: BRP-00552
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Storage: Store at -20 °C
Synonyms: dmf-G-LA-CPG 1000Å; dmf-G-LA-CPG; 5'-Dimethoxytrityl-N-dimethylformamidine-(2'-O,4'-C-methylene)-Guanosine, 3'-succinoyl-long chain alkylamino-CPG

5-Me-U-LNA-CPG

Description: 5-Me-U-LNA-CPG is a reagent used in oligonucleotide synthesis. It features 5-methyluridine (5-Me-U) for enhanced binding affinity and stability, Locked Nucleic Acid (LNA) for improved thermal stability and hybridization, and is immobilized on Controlled Pore Glass (CPG) for efficient solid-phase synthesis. This combination produces high-affinity, stable oligonucleotides suitable for molecular diagnostics, therapeutic development, and advanced research.
CAT: BRP-00553
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Storage: Store at -20 °C
Synonyms: 5-Me-U-LA-CPG 1000Å; 5-Me-U-LA-CPG; T-LA-CPG; 5'-Dimethoxytrityl-5-methyl-(2'-O,4'-C-methylene)-Uridine, 3'-succinoyl-long chain alkylamino-CPG

3'-Azido-Modifier Serinol CPG

Description: 3'-Azido-Modifier Serinol CPG is a specialized reagent used in oligonucleotide synthesis. It includes a serinol backbone modification and an azido functional group attached to the 3'-end of the oligonucleotide sequence. This modification allows for further conjugation with other molecules or probes using click chemistry. The Controlled Pore Glass (CPG) support facilitates the solid-phase synthesis of oligonucleotides, providing a stable platform for sequential nucleotide addition. This reagent is valuable for creating customized oligonucleotides for research, diagnostic, and therapeutic applications, particularly those requiring additional functionalization or conjugation for specific downstream assays or targeting purposes.
CAT: BRP-00554
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Storage: Store at 2-8 °C
Synonyms: 3'-Azido-Modifier Serinol CPG 1000Å; 3-Dimethoxytrityloxy-2-(3-(4-azidobutyramido)propanamido)propyl-1-O-succinyl-long chain alkylamino-CPG

3'-Spacer C3 CPG (BRP-02241)

Description: 3'-Spacer C3 CPG can act as a blocker of exonuclease and polymerase activity at the 3' terminal. dSpacer is used to introduce stable racemic sites in oligonucleotides. PC Spacer is a photocracking C3 spacer modifier. Spacer phosphamides C3, C9, C12, and C18 are used to insert spacer arms in oligonucleotides, and these compounds can be added multiple times when longer spacer arms are needed.
CAT: BRP-02241
Appearance: White to off-white powder
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Storage: Store at -20 °C
Shipping: Dry ice
Synonyms: 3'-Spacer C3 CPG 1000; 3'-Spacer C3 CPG (1000 Å); (1-Dimethoxytrityloxy-propanediol-3-succinoyl)-long chain alkylamino-CPG

2'-O-Methyl-A(Bz)-Suc-CPG; 500 Å (RNA) (BRP-02242)

Description: 2'-O-Methyl-A(Bz)-Suc-CPG; 500 Å is a reagent used in the solid-phase synthesis of RNA oligonucleotides, specifically for incorporating 2'-O-methyladenosine residues. It includes a benzoyl-protected adenine base and a succinyl linker that attaches the nucleoside to controlled pore glass (CPG) with a pore size of 500 Å. The 2'-O-methyl modification enhances the stability and resistance to degradation of the RNA, making this reagent ideal for the synthesis of RNA oligonucleotides with improved properties.
CAT: BRP-02242
Appearance: White powder
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Storage: Store at 2-8 °C
Symbol: 2'-OMe-A-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)-N6-benzoyl-2'-O-methyladenosine-3'-Suc-CPG 500 Å; N6-Benzoyl-2'-O-methyl-5'-O-DMT-adenosine-3'-Suc-CPG 500 Å; N6-Benzoyl-2'-O-methyl-5'-O-dimethoxytrityladenosine-3'-Suc-CPG 500 Å

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
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 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
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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

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.
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