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CPGs for oligo synthesis

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

Description: 2'-tBDSilyl Guanosine (N-ibu) 3'-lcaa CPG 1000Å is a specialized nucleotide compound utilized in solid-phase oligonucleotide synthesis. It comprises a guanosine nucleoside modified with a 2'-tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position, which protects the hydroxyl group. Additionally, it features an isobutyryl (ibu) group attached to the amine group of the guanosine base, providing additional protection. At the 3'-end, there is a long-chain alkylamine (lcaa) linker, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 1000 angstroms. This compound enables controlled addition during oligonucleotide synthesis, enabling precise customization and design of guanosine-modified oligonucleotides for various molecular biology applications.
CAT: BRP-01479
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Synonyms: 2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG 500Å; 2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG 2000Å; 2'-tBDSilyl Guanosine (n-ibu) 3'-lcaa CPG

2'-tBDSilyl Uridine 3'-lcaa CPG 1000Å

Description: 2'-tBDSilyl Uridine 3'-lcaa CPG 1000Å is a specialized nucleotide used in solid-phase oligonucleotide synthesis. It consists of a uridine nucleoside modified with a 2'-tert-butyldimethylsilyl (tBDSilyl) group at the 2'-position to protect the hydroxyl group. Additionally, it features a long-chain alkylamine (lcaa) linker at the 3' position, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 1000 angstroms. This compound enables controlled addition during oligonucleotide synthesis, allowing for precise customization and design of uridine-modified oligonucleotides for various molecular biology applications.
CAT: BRP-01480
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Synonyms: 2'-tBDSilyl Uridine 3'-lcaa CPG 500Å; 2'-tBDSilyl Uridine 3'-lcaa CPG 2000Å; 2'-tBDSilyl Uridine 3'-lcaa CPG

DMT-C6 Disulfide lcaa CPG 500Å

Description: DMT-C6 Disulfide lcaa CPG 500Å refers to a specialized support matrix used in solid-phase oligonucleotide synthesis. This compound features a long-chain alkylamine (lcaa) linker and is immobilized on Controlled Pore Glass (CPG) with a pore size of 500 angstroms. The support is functionalized with a DMT-C6 disulfide moiety, which allows for the attachment of thiol-containing molecules. This support matrix is particularly useful for the synthesis of oligonucleotides with disulfide modifications, enabling applications such as conjugation to thiol-reactive compounds or surface immobilization in various molecular biology and biotechnology research contexts.
CAT: BRP-01481
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Synonyms: DMT-C6 Disulfide lcaa CPG 1000Å; DMT-C6 Disulfide lcaa CPG

3'-TOM-ribo Uridine 2'-lcaa CPG 1000Å

Description: 3'-TOM-ribo Uridine 2'-lcaa CPG 1000Å is a specialized nucleotide compound utilized in solid-phase oligonucleotide synthesis. It consists of a ribonucleoside with a 3'-TOM (3'-O-tom)-ribo modification, where a TOM (triisopropylsilyl oxy methyl) group is attached to the 3'-hydroxyl of the ribose sugar. Additionally, it features a long-chain alkylamine (lcaa) linker at the 2'-position, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 1000 angstroms. This compound enables controlled addition during oligonucleotide synthesis, allowing for precise customization and design of uridine-modified ribonucleotides for various molecular biology applications.
CAT: BRP-01482
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Synonyms: 3'-TOM-ribo Uridine 2'-lcaa CPG 500Å; 3'-TOM-ribo Uridine 2'-lcaa CPG

3'-TOM-ribo Adenosine (n-acetyl) 2'-lcaa CPG 500Å

Description: 3'-TOM-ribo Adenosine (N-acetyl) 2'-lcaa CPG 500Å is a specialized nucleotide compound used in solid-phase oligonucleotide synthesis. It comprises a ribonucleoside with a 3'-TOM (3'-O-tom)-ribo modification, where TOM (triisopropylsilyl oxy methyl) group is attached to the 3'-hydroxyl of the ribose sugar. Additionally, an acetyl (Ac) group is attached to the amine group of the adenosine base. Moreover, it features a long-chain alkylamine (lcaa) linker at the 2'-position, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 500 angstroms. This compound enables controlled addition during oligonucleotide synthesis, allowing for precise customization and design of adenosine-modified ribonucleotides for various molecular biology applications.
CAT: BRP-01483
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Synonyms: 3'-TOM-ribo Adenosine (n-acetyl) 2'-lcaa CPG 1000Å; 3'-TOM-ribo Adenosine (n-acetyl) 2'-lcaa CPG

3'-TOM-ribo Cytidine (n-acetyl) 2'-lcaa CPG 500Å

Description: 3'-TOM-ribo Cytidine (N-acetyl) 2'-lcaa CPG 500Å is a specialized nucleotide used in solid-phase oligonucleotide synthesis. It comprises a ribonucleoside with a 3'-TOM (3'-O-tom)-ribo modification, where a TOM (triisopropylsilyl oxy methyl) group is attached to the 3'-hydroxyl of the ribose sugar. Additionally, an acetyl (Ac) group is attached to the amine group of the cytidine base. Moreover, it features a long-chain alkylamine (lcaa) linker at the 2'-position, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 500 angstroms. This compound enables controlled addition during oligonucleotide synthesis, allowing for precise customization and design of cytidine-modified ribonucleotides for various molecular biology applications.
CAT: BRP-01484
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Synonyms: 3'-TOM-ribo Cytidine (n-acetyl) 2'-lcaa CPG 1000Å; 3'-TOM-ribo Cytidine (n-acetyl) 2'-lcaa CPG

2'-TOM-ribo Guanosine (n-acetyl) 3'-lcaa CPG 500Å

Description: 2'-TOM-ribo Guanosine (N-acetyl) 3'-lcaa CPG 500Å is a specialized nucleotide used in solid-phase oligonucleotide synthesis. It comprises a ribonucleoside with a 2'-TOM (2'-O-tom)-ribo modification, where a TOM (triisopropylsilyl oxy methyl) group is attached to the 2'-hydroxyl of the ribose sugar. Additionally, an acetyl (Ac) group is attached to the amine group of the guanosine base. Furthermore, it contains a long-chain alkylamine (lcaa) linker at the 3' position, facilitating attachment to a Controlled Pore Glass (CPG) support matrix with a pore size of 500 angstroms. This compound enables controlled addition during oligonucleotide synthesis, allowing for precise customization and design of guanosine-modified ribonucleotides for various molecular biology applications.
CAT: BRP-01485
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Synonyms: 2'-TOM-ribo Guanosine (n-acetyl) 3'-lcaa CPG 1000Å; 2'-TOM-ribo Guanosine (n-acetyl) 3'-lcaa CPG

Universal UnyLinker Support 1000Å

Description: Universal UnyLinker Support 1000Å is a versatile solid-phase support used in oligonucleotide synthesis. It features a Universal UnyLinker, a cleavable linker that allows for the efficient release of synthesized oligonucleotides from the solid support. The support is based on a Controlled Pore Glass (CPG) matrix with a pore size of 1000 angstroms, which provides ample surface area for high-efficiency synthesis. This support is compatible with various oligonucleotide sequences and modifications, making it an ideal choice for a wide range of molecular biology and biotechnology applications.
CAT: BRP-01486
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Synonyms: Universal UnyLinker Support 500Å; Universal UnyLinker Support 2000Å; Universal UnyLinker Support

Universal UnyLinker Support Polystyrene 300Å

Description: Universal UnyLinker Support Polystyrene 300Å is a versatile solid-phase support used in oligonucleotide synthesis. It features a Universal UnyLinker, which is a cleavable linker allowing the efficient release of synthesized oligonucleotides from the solid support. The support is based on polystyrene with a pore size of 300 angstroms, providing a robust and chemically stable matrix. This support is compatible with various oligonucleotide sequences and modifications, making it an ideal choice for diverse molecular biology and biotechnology applications.
CAT: BRP-01487
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Synonyms: Universal UnyLinker Support Polystyrene

2'-Fluoro Guanosine (n-ibu)-3'-succinyl lcaa CPG 1000Å

Description: 2'-Fluoro Guanosine (n-ibu)-3'-succinyl lcaa CPG 1000Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 1000 angstroms. This compound features a 2'-fluoro modification and an N2-isobutyryl (n-ibu) protecting group. The 3'-end is linked via a succinyl linker to the long chain alkylamine (lcaa) CPG, which is commonly used in automated DNA and RNA synthesis. This specific modification enhances the stability and binding properties of synthesized oligonucleotides, making it valuable for research and therapeutic applications.
CAT: BRP-01600
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Synonyms: 2'-Fluoro Guanosine (n-ibu)-3'-succinyl lcaa CPG 500Å; 2'-F-dG(iBu)-3'-Suc-lcaa CPG; 2'-Fluoro Guanosine (n-ibu)-3'-lcaa CPG 1000Å

2'-Fluoro Cytidine (N-Ac) 3'-lcaa CPG 500Å

Description: 2'-Fluoro Cytidine 3'-lcaa CPG 500Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 500 angstroms. The 2'-fluoro modification enhances the stability of nucleic acids by increasing resistance to enzymatic degradation. The 3'-end is linked via a long chain alkylamine (lcaa) linker to the CPG support, which is used in automated DNA and RNA synthesis. This modification is particularly useful in research and therapeutic applications where enhanced nucleic acid stability and binding properties are desired.
CAT: BRP-01601
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Synonyms: 2'-Fluoro Cytidine 3'-lcaa CPG 1000Å; 2'-Fluoro Cytidine 3'-lcaa CPG 500Å; 2'-F-dC(Ac)-3'-Suc-lcaa CPG; 2'-Fluoro Cytidine (N-Ac)-3'-succinyl lcaa CPG

2'-Fluoro Guanosine (N,N-DMF) 3'-lcaa CPG 500Å

Description: 2'-Fluoro Guanosine (N,N-DMF) 3'-lcaa CPG 500Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 500 angstroms. This compound features a 2'-fluoro modification, enhancing stability and resistance to enzymatic degradation. The guanosine is also protected with an N,N-dimethylformamidine (DMF) group. The 3'-end is linked to a long chain alkylamine (lcaa) CPG support, facilitating its use in automated DNA and RNA synthesis. This combination of modifications improves the stability and binding properties of the synthesized oligonucleotides, making it valuable for research and therapeutic applications.
CAT: BRP-01602
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Synonyms: 2'-Fluoro Guanosine (N,N-DMF) 3'-lcaa CPG 1000Å; 2'-F-dG(DMF)-3'-Suc-lcaa CPG; 2'-Fluoro Guanosine (N,N-DMF)-3'-succinyl lcaa CPG

2'-Fluoro Adenosine (N-Bz) 3'-lcaa CPG 1000Å

Description: 2'-Fluoro Adenosine (N-Bz) 3'-lcaa CPG 1000Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 1000 angstroms. It features a 2'-fluoro modification, which enhances the stability of nucleic acids by increasing resistance to enzymatic degradation. The adenosine is protected with an N-benzoyl (N-Bz) group. The 3'-end is linked to a long chain alkylamine (lcaa) CPG support, which is suitable for automated DNA and RNA synthesis. This specific configuration improves the stability and binding properties of the synthesized oligonucleotides, making it beneficial for research and therapeutic applications.
CAT: BRP-01603
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Synonyms: 2'-Fluoro Adenosine (N-Bz) 3'-lcaa CPG 500Å; 2'-F-dA(Bz)-3'-Suc-lcaa CPG; 2'-Fluoro Adenosine (N-Bz)-3'-succinyl lcaa CPG

2'-Fluoro Adenosine (N,N-DMF) 3'-lcaa CPG 1000Å

Description: 2'-Fluoro Adenosine (N,N-DMF) 3'-lcaa CPG 1000Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 1000 angstroms. This compound includes a 2'-fluoro modification, enhancing the stability and resistance of nucleic acids to enzymatic degradation. The adenosine is protected with an N,N-dimethylformamidine (DMF) group. The 3'-end is attached to a long chain alkylamine (lcaa) CPG support, facilitating its use in automated DNA and RNA synthesis. This specific modification improves the stability, binding properties, and overall performance of the synthesized oligonucleotides, making it valuable for research and therapeutic applications.
CAT: BRP-01604
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Synonyms: 2'-Fluoro Adenosine (N,N-DMF) 3'-lcaa CPG 500Å; 2'-F-dA(DMF)-3'-Suc-lcaa CPG; 2'-Fluoro Adenosine (N,N-DMF)-3'-succinyl lcaa CPG

2'-Fluoro Uridine 3'-lcaa CPG 1000Å

Description: 2'-Fluoro Uridine 3'-lcaa CPG 1000Å is a modified nucleoside attached to a controlled pore glass (CPG) solid support with a pore size of 1000 angstroms. It features a 2'-fluoro modification, which enhances the stability of the nucleic acid by increasing resistance to enzymatic degradation. The 3'-end of the nucleoside is linked to a long chain alkylamine (lcaa) CPG support, making it suitable for automated DNA and RNA synthesis. This combination of modifications enhances the stability and binding properties of the synthesized oligonucleotides, making it valuable for various research and therapeutic applications.
CAT: BRP-01605
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Synonyms: 2'-Fluoro Uridine 3'-lcaa CPG 500Å; 2'-Fluoro Uridine-3'-succinyl lcaa CPG; 2'-F-dU-3'-Suc-lcaa CPG

2'-Methyl-guanosine-(iBu)-succinyl-CPG

Description: 2'-Methyl-guanosine-(iBu)-succinyl-CPG is a crucial biomedicine product used for solid-phase synthesis of oligonucleotides. It serves as a key building block for the chemical synthesis of modified nucleic acids. With its unique succinyl modification, this CPG derivative enables efficient incorporation into oligonucleotides for pharmaceutical research and diagnostic applications related to drug screening, target identification, and disease detection.
CAT: BRP-01696
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Synonyms: 2'-O-Methyl Guanosine (n-ibu) 3'-lcaa CPG 1000Å; 2'-O-Methyl Guanosine (n-ibu) 3'-lcaa CPG 500Å; 2'-OMe-rG(iBu) CPG; 2'-O-Methyl Guanosine (n-ibu) 3'-lcaa CPG

2'-Methyl-cytidine-(Bz)-succinyl-CPG

Description: 2'-Methyl-cytidine-(Bz)-succinyl-CPG, an essential entity within the biomedicine realm, serves as a pivotal tool in the intricate process of synthesizing nucleic acids and diverse oligonucleotides. Its significance arises from its multifaceted applicability in drug discovery investigations, specifically focusing on the advancement of antiviral and anticancer medications.
CAT: BRP-01697
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Synonyms: 2'-O-Methyl Cytidine (n-bz) 3'-lcaa CPG 1000Å; 2'-O-Methyl Cytidine (n-bz) 3'-lcaa CPG 500Å; 2'-O-Methyl Cytidine (n-bz) 3'-lcaa CPG

2'-Methyl-adenosine-(benzoyl)-succinyl-CPG

Description: 2'-Methyl-adenosine-(benzoyl)-succinyl-CPG, a highly versatile and pivotal biomedical entity, finds widespread utilization in the realm of pharmaceutical exploration and advancement. This distinctive compound assumes a critical role as an indispensable cornerstone for the synthesis of oligonucleotides and nucleic acid analogs, fostering a promising avenue for combatting an array of diseases such as cancer and viral infections.
CAT: BRP-01698
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Synonyms: 2'-O-Methyl Adenosine (n-bz) 3'-lcaa CPG 1000Å; 2'-O-Methyl Adenosine (n-bz) 3'-lcaa CPG; 2'-O-Methyl Adenosine (n-bz) 3'-lcaa CPG 500Å; 2'-Methyl-adenosine-(Bz)-succinyl-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

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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