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CPGs for oligo synthesis

6-FAM Glyceryl Support 500Å

Description: 6-FAM Glyceryl Support CPG 500Å is a controlled pore glass (CPG) with a pore size of 500 angstroms, functionalized with a glyceryl linker and 6-carboxyfluorescein (6-FAM). This support material is used for synthesizing oligonucleotides that are fluorescently labeled with 6-FAM, facilitating applications in molecular biology such as fluorescence-based detection, quantitative PCR (qPCR), and fluorescence resonance energy transfer (FRET) assays. The glyceryl linker ensures efficient attachment of the fluorophore to the oligonucleotide, providing strong and reliable fluorescence signals.
CAT: BRP-01364
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Synonyms: 6-FAM Glyceryl Support CPG; 6-FAM Glyceryl Support CPG 500Å

DMT-5-FAM lcaa CPG 500Å

Description: DMT-5-FAM lcaa CPG 500Å is a controlled pore glass (CPG) with a pore size of 500 angstroms, featuring a 5-carboxyfluorescein (5-FAM) fluorophore linked through a long chain alkylamine (lcaa) spacer and protected by a dimethoxytrityl (DMT) group. This support is designed for the synthesis of 3'-fluorescein-labeled oligonucleotides. The DMT protecting group allows for efficient incorporation and subsequent deprotection during synthesis, while the lcaa linker enhances the accessibility and performance of the fluorophore. This material is commonly used in fluorescence-based detection, quantitative PCR (qPCR), and fluorescence resonance energy transfer (FRET) assays due to its strong and reliable fluorescence signals.
CAT: BRP-01367
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Synonyms: DMT-5-FAM lcaa CPG

8-Bromo Adenosine (n,n-dibuf) 3'-tBDSilyl 2'-lcaa CPG 500Å

Description: 8-Bromo Adenosine (n,n-dibuf) 3'-tBDSilyl 2'-lcaa CPG 500Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 8-bromo adenosine into oligonucleotides. The modifications include a 3'-tert-butyldimethylsilyl (tBDSilyl) group for protecting the 3'-hydroxyl, and an n,n-dibutylformamidine (dibuf) protection on the adenosine base. The long chain alkylamine (lcaa) linker and the controlled pore glass (CPG) with 500Å pores ensure efficient solid-phase synthesis. The resulting oligonucleotides are useful in biochemical research for studying nucleic acid interactions and for therapeutic applications requiring enhanced stability and specific binding properties.
CAT: BRP-01369
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Synonyms: 8-Bromo Adenosine (n,n-dibuf) 3'-tBDSilyl 2'-lcaa CPG 1000Å; 8-Bromo Adenosine (n,n-dibuf) 3'-tBDSilyl 2'-lcaa CPG

5-Bromo Uridine 3'-tBDSilyl 2'-lcaa CPG 500Å

Description: 5-Bromo Uridine 3'-tBDSilyl 2'-lcaa CPG 500Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 5-Bromo uridine into oligonucleotides. It features a 3'-tert-butyldimethylsilyl (tBDSilyl) group protecting the 3'-hydroxyl, and a long chain alkylamine (lcaa) linker attached to controlled pore glass (CPG) with 500Å pores. The modification with 5-Bromo uridine provides enhanced stability and unique properties to the synthesized oligonucleotides, which are useful for various research applications, including studies of nucleic acid interactions and the development of therapeutic agents.
CAT: BRP-01370
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Synonyms: 5-Bromo Uridine 3'-tBDSilyl 2'-lcaa CPG 1000Å; 5-Bromo Uridine 3'-tBDSilyl 2'-lcaa CPG

5-Fluoro Uridine 3'-tBDSilyl 2'-lcaa CPG 1000Å

Description: 5-Fluoro Uridine 3'-tBDSilyl 2'-lcaa CPG 1000Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 5-fluoro uridine into oligonucleotides. It features a 3'-tert-butyldimethylsilyl (tBDSilyl) group protecting the 3'-hydroxyl, and a long chain alkylamine (lcaa) linker attached to controlled pore glass (CPG) with 1000Å pores. The modification with 5-fluoro uridine provides enhanced stability and unique properties to the synthesized oligonucleotides, which are useful for various research applications, including studies of nucleic acid interactions and the development of therapeutic agents.
CAT: BRP-01371
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Synonyms: 5-Fluoro Uridine 3'-tBDSilyl 2'-lcaa CPG 500Å; 5-Fluoro Uridine 3'-tBDSilyl 2'-lcaa CPG

5-Bromo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 1000Å

Description: 5-Bromo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 1000Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 5-bromo cytidine into oligonucleotides. It includes a 5-bromo modification on the cytidine base, a benzoyl (n-bz) protecting group on the exocyclic amino group, a 3'-tert-butyldimethylsilyl (tBDSilyl) group protecting the 3'-hydroxyl, and a long chain alkylamine (lcaa) linker attached to controlled pore glass (CPG) with 1000Å pores. This setup ensures efficient solid-phase synthesis and provides the resulting oligonucleotides with enhanced stability and unique properties for various biochemical and therapeutic research applications.
CAT: BRP-01372
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Synonyms: 5-Bromo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 500Å; 5-Bromo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG

5-Iodo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 500Å

Description: 5-Iodo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 500Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 5-iodo cytidine into oligonucleotides. It includes a 5-iodo modification on the cytidine base, a benzoyl (n-bz) protecting group on the exocyclic amino group, a 3'-tert-butyldimethylsilyl (tBDSilyl) group protecting the 3'-hydroxyl, and a long chain alkylamine (lcaa) linker attached to controlled pore glass (CPG) with 500Å pores. This setup ensures efficient solid-phase synthesis and provides the resulting oligonucleotides with enhanced stability and unique properties for various biochemical and therapeutic research applications.
CAT: BRP-01373
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Synonyms: 5-Iodo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG 1000Å; 5-Iodo Cytidine (n-bz) 3'-tBDSilyl 2'-lcaa CPG

5-Iodo Uridine 3'-tBDSilyl 2'-lcaa CPG 1000Å

Description: 5-Iodo Uridine 3'-tBDSilyl 2'-lcaa CPG 1000Å is a specialized solid support used in the synthesis of modified oligonucleotides. It facilitates the incorporation of 5-Iodo uridine into oligonucleotides. It features a 3'-tert-butyldimethylsilyl (tBDSilyl) group protecting the 3'-hydroxyl, and a long chain alkylamine (lcaa) linker attached to controlled pore glass (CPG) with 1000Å pores. The modification with 5-Iodo uridine provides enhanced stability and unique properties to the synthesized oligonucleotides, which are useful for various research applications, including studies of nucleic acid interactions and the development of therapeutic agents.
CAT: BRP-01375
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Synonyms: 5-Iodo Uridine 3'-tBDSilyl 2'-lcaa CPG 500Å; 5-Iodo Uridine 3'-tBDSilyl 2'-lcaa CPG

isoGuanosine (n,n-isobudmf) 2'-lcaa CPG 1000Å

Description: isoGuanosine (n,n-isobudmf) 2'-lcaa CPG 1000Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified guanosine, isoGuanosine, into nucleic acid sequences. This modification provides unique chemical properties, enabling tailored customization of oligonucleotides for diverse research and therapeutic applications.
CAT: BRP-01377
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Synonyms: isoGuanosine (n,n-isobudmf) 2'-lcaa CPG 500Å; isoGuanosine (n,n-isobudmf) 2'-lcaa CPG

IsoCytidine (n,n-diisobutylformamidine) 2'-lcaa CPG 1000Å

Description: IsoCytidine (n,n-diisobutylformamidine) 2'-lcaa CPG 1000Å is a specialized solid support used in oligonucleotide synthesis to introduce modified cytidine, IsoCytidine, into nucleic acid sequences. This modification offers unique chemical properties, allowing for customized oligonucleotide design for various research and therapeutic applications.
CAT: BRP-01379
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Synonyms: IsoCytidine (n,n-diisobutylformamidine) 2'-lcaa CPG 500Å; IsoCytidine (n,n-diisobutylformamidine) 2'-lcaa CPG

Beta-L-2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG 1000Å

Description: Beta-L-2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG 1000Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified guanosine, specifically Beta-L-2'-tBDSilyl Guanosine, into nucleic acid sequences. This modification involves a Beta-L configuration at the 2'-position of the ribose sugar, a tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position, and an n-ibu (n-isobutyryl) group at the nucleobase. Additionally, it features a long-chain alkylamine linker with controlled pore glass (CPG) having 1000 angstrom pores. This reagent facilitates the synthesis of oligonucleotides with unique structural and chemical properties for various research and therapeutic applications.
CAT: BRP-01380
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Synonyms: Beta-L-2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG 500Å; Beta-L-2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG

Beta-L-2'-tBDSilyl Adenosine (n-bz) 3'-lcaa CPG 1000Å

Description: Beta-L-2'-tBDSilyl Adenosine (n-bz) 3'-lcaa CPG 1000Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified adenosine, specifically Beta-L-2'-tBDSilyl Adenosine, into nucleic acid sequences. This modification involves a Beta-L configuration at the 2'-position of the ribose sugar, a tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position, and a benzoyl (n-bz) group at the nucleobase. Additionally, it features a long-chain alkylamine linker with controlled pore glass (CPG) having 1000 angstrom pores. This reagent facilitates the synthesis of oligonucleotides with unique structural and chemical properties for various research and therapeutic applications.
CAT: BRP-01381
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Synonyms: Beta-L-2'-tBDSilyl Adenosine (n-bz) 3'-lcaa CPG 500Å; Beta-L-2'-tBDSilyl Adenosine (n-bz) 3'-lcaa CPG

Beta-L-2'-tBDSilyl Cytidine (n-bz) 3'-lcaa CPG 500Å

Description: Beta-L-2'-tBDSilyl Cytidine (n-bz) 3'-lcaa CPG 500Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified cytidine, specifically Beta-L-2'-tBDSilyl Cytidine, into nucleic acid sequences. This modification involves a Beta-L configuration at the 2'-position of the ribose sugar, a tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position, and a benzoyl (n-bz) group at the nucleobase. Additionally, it features a long-chain alkylamine linker with controlled pore glass (CPG) having 500 angstrom pores. This reagent facilitates the synthesis of oligonucleotides with unique structural and chemical properties for various research and therapeutic applications.
CAT: BRP-01383
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Synonyms: Beta-L-2'-tBDSilyl Cytidine (n-bz) 3'-lcaa CPG 1000Å; Beta-L-2'-tBDSilyl Cytidine (n-bz) 3'-lcaa CPG

Beta-L-2'-tBDSilyl Uridine 3'-lcaa CPG 1000Å

Description: Beta-L-2'-tBDSilyl Uridine 3'-lcaa CPG 1000Å is a specialized solid support utilized in oligonucleotide synthesis to introduce modified uridine, specifically Beta-L-2'-tBDSilyl Uridine, into nucleic acid sequences. This modification involves a Beta-L configuration at the 2'-position of the ribose sugar, with a tert-butyldimethylsilyl (tBDSilyl) group attached. Additionally, it features a long-chain alkylamine linker with controlled pore glass (CPG) having 1000 angstrom pores. This reagent facilitates the synthesis of oligonucleotides with unique structural and chemical properties, suitable for various research and therapeutic applications.
CAT: BRP-01384
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Synonyms: Beta-L-2'-tBDSilyl Uridine 3'-lcaa CPG 500Å; Beta-L-2'-tBDSilyl Uridine 3'-lcaa CPG

Beta-L-2'-tBDSilyl Cytidine (n-acetyl) 3'-lcaa CPG 500Å

Description: Beta-L-2'-tBDSilyl Cytidine (n-acetyl) 3'-lcaa CPG 500Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified cytidine, specifically Beta-L-2'-tBDSilyl Cytidine, into nucleic acid sequences. This modification includes a Beta-L configuration at the 2'-position of the ribose sugar, a tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position, and an acetyl (n-acetyl) group at the nucleobase. Additionally, it features a long-chain alkylamine linker with controlled pore glass (CPG) having 500 angstrom pores. This reagent facilitates the synthesis of oligonucleotides with unique structural and chemical properties, suitable for various research and therapeutic applications.
CAT: BRP-01385
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Synonyms: Beta-L-2'-tBDSilyl Cytidine (n-acetyl) 3'-lcaa CPG 1000Å; Beta-L-2'-tBDSilyl Cytidine (n-acetyl) 3'-lcaa CPG

5-Methyl Cytidine (n,n-dmf) 2'-O-Methyl lcaa CPG 1000Å

Description: 5-Methyl Cytidine (n,n-dmf) 2'-O-Methyl lcaa CPG 1000Å is a specialized solid support used in oligonucleotide synthesis to incorporate modified cytidine, specifically 5-methyl cytidine, into nucleic acid sequences. This modification introduces a methyl group at the 5-position of the cytidine base and features a long-chain alkylamine linker with controlled pore glass (CPG) having 1000 angstrom pores. This reagent enables the tailored synthesis of oligonucleotides with enhanced stability and specific chemical properties for diverse research and therapeutic applications.
CAT: BRP-01393
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Synonyms: 5-Methyl Cytidine (n,n-dmf) 2'-O-Methyl lcaa CPG 500Å; 5-Methyl Cytidine (n,n-dmf) 2'-O-Methyl lcaa CPG

2'-O-Methyl Inosine lcaa CPG 500Å

Description: 2'-O-Methyl Inosine lcaa CPG 500Å is a solid support reagent used in oligonucleotide synthesis. It features 2'-O-methyl inosine linked to long chain alkylamine (lcaa) on Controlled Pore Glass (CPG) with a pore size of 500 angstroms. This modification enhances the stability and nuclease resistance of synthesized oligonucleotides, making it suitable for various research and therapeutic applications.
CAT: BRP-01395
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Synonyms: 2'-O-Methyl Inosine lcaa CPG 1000Å; 2'-O-Methyl Inosine lcaa CPG

5-Bromo Uridine 2'-O-Methyl lcaa CPG 500Å

Description: 5-Bromo Uridine 2'-O-Methyl lcaa CPG 500Å is a reagent utilized in oligonucleotide synthesis. It contains 5-Bromo Uridine, where a bromine atom is attached to the 5-position of the uridine nucleoside, along with a methyl group at the 2'-position of the ribose sugar. The nucleoside is linked to a solid support using a long-chain alkylamine (lcaa) linker, and the support material is Controlled Pore Glass (CPG) with a pore size of 500 angstroms. This reagent is instrumental in the creation of oligonucleotides with enhanced stability and resistance to degradation, crucial for diverse research and diagnostic applications in molecular biology.
CAT: BRP-01398
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Synonyms: 5-Bromo Uridine 2'-O-Methyl lcaa CPG 1000Å; 5-Bromo Uridine 2'-O-Methyl lcaa CPG

5-Iodo Uridine 2'-O-Methyl lcaa CPG 500Å

Description: 5-Iodo Uridine 2'-O-Methyl lcaa CPG 500Å is a reagent used in oligonucleotide synthesis. It contains 5-Iodo Uridine, where an iodine atom is attached to the 5-position of the uridine nucleoside, along with a methyl group at the 2'-position of the ribose sugar. The nucleoside is linked to a solid support using a long-chain alkylamine (lcaa) linker, and the support material is Controlled Pore Glass (CPG) with a pore size of 500 angstroms. This reagent facilitates the synthesis of oligonucleotides with enhanced stability and resistance to degradation, important for various molecular biology applications.
CAT: BRP-01399
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Synonyms: 5-Iodo Uridine 2'-O-Methyl lcaa CPG 1000Å; 5-Iodo Uridine 2'-O-Methyl lcaa CPG

2-Amino Purine Riboside 3'-tBDSilyl 2'-lcaa CPG 1000Å

Description: 2-Amino Purine Riboside 3'-tBDSilyl 2'-lcaa CPG 1000Å is a modified nucleoside which is used as a building block for the synthesis of oligonucleotides. It contains a 2-amino purine base, a ribose sugar, and a protecting group at the 3'-position. The 2'-lcaa CPG refers to the controlled pore glass (CPG) support with a linker attached to the 2'-position of the ribose sugar. The 1000Å designation refers to the pore size of the CPG support, indicating the size of molecules that can be efficiently synthesized on this support. This compound is commonly used in the field of molecular biology and nucleic acid research for the synthesis of modified oligonucleotides with specific properties.
CAT: BRP-01403
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Synonyms: 2-Amino Purine Riboside 3'-tBDSilyl 2'-lcaa CPG 500Å; 2-Amino Purine Riboside 3'-tBDSilyl 2'-lcaa CPG

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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