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MRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can alsoIRDYE® 800
IRDyes This product is licensed for sales only for research use. Notwithstanding the foregoing, this product may not be used in diagnostic, therapeutic or human in vivo applications. Commerical Use is prohibited. Commercial Use shall include: 1. resales, lease, license or other transfer of the material or any material derived orproduced from it.
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator. CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink'sMRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can alsoIRDYE® 800
IRDyes This product is licensed for sales only for research use. Notwithstanding the foregoing, this product may not be used in diagnostic, therapeutic or human in vivo applications. Commerical Use is prohibited. Commercial Use shall include: 1. resales, lease, license or other transfer of the material or any material derived orproduced from it.
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. CLEANCAP | TRILINK BIOTECHNOLOGIES CleanCap ® technology is a proprietary, co-transcriptional 5’ capping solution that generates a natural Cap 1 structure. Proper mRNA capping is critical to the production of the most biologically active and least immunogenic mRNA. TriLink scientists developed CleanCap, the next generation of capping technology, as a solution to the low THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: CLEANCAP® FLUC MRNA FLuc is commonly used in mammalian cell culture to measure both gene expression and cell viability. It emits bioluminescence in the presence of the substrate, luciferin. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method, which results in the naturally occuring Cap 1 structure with highcapping efficiency.
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. 5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. PERSPECTIVES ON PLASMIDS FOR IVT MRNA PRODUCTION—PART 1 Plasmids Were Discovered in 1952 as Agents of “Genetic Exchange” Between Bacteria In the Last 50 Years, There Have Been Over 200,000 Plasmid Publications, Averaging 15 Per Day During 1990-2020 Plasmids Provide the Starting Point for IVT mRNA Production TriLink Continuereading →
ENVIRONMENTAL DNA (EDNA) APPLICATIONS—RECENT ADVANCES AND According to a 2020 report by Pathan et al., extracellular eDNA can represent up to 40% of the total soil DNA pool.The interest from the scientific community on eDNA in soil is quite recent; however, according to the researchers, studies have already found that eDNA in soil can act as a constituent of biofilms, as well as a source of nutrients and signaling- or chemoattractant molecules, 2-AMINO-2'-DEOXYADENOSINE-5'-TRIPHOSPHATE Description. Substitution of 2-Amino-2'-deoxyadenosine (also known as 2,6-Diaminopurine-2'-deoxyribose) for adenine in DNA can result in increased stabilization of the DNA duplex. Diaminopurine base pairs with thymine forming three intramolecular hydrogen bonds versus twofor adenine.
THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator. CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink's MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by:MRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can also THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally 5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
PSEUDOURIDINE-5'-TRIPHOSPHATE Pseudouridine (5-ribosyluracil) was the first modified ribonucleoside discovered. It is the most abundant natural modified RNA base, and has been deemed the "fifth nucleoside" in RNA. It can be found in structural RNAs, such as transfer, ribosomal and small nuclear RNA. Pseudouridine has been found to enhance base stacking and translation. N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator.MRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can also CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink's THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. 5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
PSEUDOURIDINE-5'-TRIPHOSPHATE Pseudouridine (5-ribosyluracil) was the first modified ribonucleoside discovered. It is the most abundant natural modified RNA base, and has been deemed the "fifth nucleoside" in RNA. It can be found in structural RNAs, such as transfer, ribosomal and small nuclear RNA. Pseudouridine has been found to enhance base stacking and translation. MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP | TRILINK BIOTECHNOLOGIES CleanCap ® technology is a proprietary, co-transcriptional 5’ capping solution that generates a natural Cap 1 structure. Proper mRNA capping is critical to the production of the most biologically active and least immunogenic mRNA. TriLink scientists developed CleanCap, the next generation of capping technology, as a solution to the low MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: ARCA | TRILINK BIOTECHNOLOGIES Description. Trusted TriLink quality, exceptional price. A key step in cellular mRNA processing is the addition of a 5’ cap structure, which is a 5'-5' triphosphate linkage between the 5' end of the RNA and a guanosine nucleotide. The cap is methylated enzymatically at theN-7
CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
CLEANCAP® CAS9 MRNA (MODIFIED) Cas9 mRNA encodes the Cas9 protein with an N and C terminal nuclear localization signal (NLS). The incorporation of two NLS signals within the mRNA increases the frequency of delivery to the nucleus, thus increasing the rate of DNA cleavage. Additionally, a C terminal HA epitope tag aids detection, isolation, and purification of the Cas9protein.
CLEANCAP® EGFP MRNA (5MOU) The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink'sproprietary co
5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. PERSPECTIVES ON PLASMIDS FOR IVT MRNA PRODUCTION—PART 1 Plasmids Were Discovered in 1952 as Agents of “Genetic Exchange” Between Bacteria In the Last 50 Years, There Have Been Over 200,000 Plasmid Publications, Averaging 15 Per Day During 1990-2020 Plasmids Provide the Starting Point for IVT mRNA Production TriLink Continuereading →
MODIFIED MRNA VACCINE AGAINST AIDS SUPPORTED BY ANTIBODY The United Nations Program on HIV/AIDS released a 2020 fact sheet stating that, in 2019, of the 38.0 million people living with HIV across the globe, 1.7 million of them were newly infected. In addition, it was reported that 690,000 people died from AIDS-related illnesses. As of the end of June 2020, 26.0 million people were accessing antiretroviral therapy, while 12 million people with HIV THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator.MRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can also CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink's THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: PSEUDOURIDINE-5'-TRIPHOSPHATE Pseudouridine (5-ribosyluracil) was the first modified ribonucleoside discovered. It is the most abundant natural modified RNA base, and has been deemed the "fifth nucleoside" in RNA. It can be found in structural RNAs, such as transfer, ribosomal and small nuclear RNA. Pseudouridine has been found to enhance base stacking and translation. 5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator.MRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can also CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink's THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: PSEUDOURIDINE-5'-TRIPHOSPHATE Pseudouridine (5-ribosyluracil) was the first modified ribonucleoside discovered. It is the most abundant natural modified RNA base, and has been deemed the "fifth nucleoside" in RNA. It can be found in structural RNAs, such as transfer, ribosomal and small nuclear RNA. Pseudouridine has been found to enhance base stacking and translation. 5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
CLEANCAP | TRILINK BIOTECHNOLOGIES CleanCap ® technology is a proprietary, co-transcriptional 5’ capping solution that generates a natural Cap 1 structure. Proper mRNA capping is critical to the production of the most biologically active and least immunogenic mRNA. TriLink scientists developed CleanCap, the next generation of capping technology, as a solution to the low MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: ARCA | TRILINK BIOTECHNOLOGIES Description. Trusted TriLink quality, exceptional price. A key step in cellular mRNA processing is the addition of a 5’ cap structure, which is a 5'-5' triphosphate linkage between the 5' end of the RNA and a guanosine nucleotide. The cap is methylated enzymatically at theN-7
CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
CLEANCAP® CAS9 MRNA (MODIFIED) Cas9 mRNA encodes the Cas9 protein with an N and C terminal nuclear localization signal (NLS). The incorporation of two NLS signals within the mRNA increases the frequency of delivery to the nucleus, thus increasing the rate of DNA cleavage. Additionally, a C terminal HA epitope tag aids detection, isolation, and purification of the Cas9protein.
CLEANCAP® EGFP MRNA (5MOU) The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink'sproprietary co
PERSPECTIVES ON PLASMIDS FOR IVT MRNA PRODUCTION—PART 1 Plasmids Were Discovered in 1952 as Agents of “Genetic Exchange” Between Bacteria In the Last 50 Years, There Have Been Over 200,000 Plasmid Publications, Averaging 15 Per Day During 1990-2020 Plasmids Provide the Starting Point for IVT mRNA Production TriLink Continuereading →
PERSPECTIVES ON IN VITRO TRANSCRIPTION (IVT) MRNA SEQUENCE According to Linares-Fernández et al., both the 5’ and 3’ UTRs are important regulators of mRNA decay and translational efficiency, due to RNA-binding proteins.Because of their high stability, the use of globin (α- or β-globin, shown here) UTRs from Xenopus laevis or humans has been the historical standard approach in mRNA vaccination. However, UTR performance is dependent on species MODIFIED MRNA VACCINE AGAINST AIDS SUPPORTED BY ANTIBODY The United Nations Program on HIV/AIDS released a 2020 fact sheet stating that, in 2019, of the 38.0 million people living with HIV across the globe, 1.7 million of them were newly infected. In addition, it was reported that 690,000 people died from AIDS-related illnesses. As of the end of June 2020, 26.0 million people were accessing antiretroviral therapy, while 12 million people with HIV THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator. CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink'sMRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can alsoIRDYE® 800
IRDyes This product is licensed for sales only for research use. Notwithstanding the foregoing, this product may not be used in diagnostic, therapeutic or human in vivo applications. Commerical Use is prohibited. Commercial Use shall include: 1. resales, lease, license or other transfer of the material or any material derived orproduced from it.
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. 2-AMINO-2'-DEOXYADENOSINE-5'-TRIPHOSPHATE Description. Substitution of 2-Amino-2'-deoxyadenosine (also known as 2,6-Diaminopurine-2'-deoxyribose) for adenine in DNA can result in increased stabilization of the DNA duplex. Diaminopurine base pairs with thymine forming three intramolecular hydrogen bonds versus twofor adenine.
THE MODIFIED NUCLEIC ACID EXPERTS TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap ® mRNA capping technology. CLEANCAP® REAGENT AG CleanCap ® Reagent AG is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency. PLEASE NOTE: TriLink recommends using CleanCap AG whenever possible. CleanCap AG requires an AG initiator. CLEANCAP® EGFP MRNA Description. The EGFP mRNA will express an enhanced version of the green fluorescent protein, originally isolated from the jellyfish, Aequorea victoria. EGFP is a commonly used direct detection reporter in mammalian cell culture, yielding bright green fluorescence with an emission peak at 509 nm. This mRNA is capped using CleanCap, TriLink'sMRNA VACCINES
According to Pardi et al., the first advantage is safety: as mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis.Additionally, mRNA is degraded by normal cellular processes, and the in vivo half-life can be regulated through the use of various modifications and delivery methods.The inherent immunogenicity of the mRNA can alsoIRDYE® 800
IRDyes This product is licensed for sales only for research use. Notwithstanding the foregoing, this product may not be used in diagnostic, therapeutic or human in vivo applications. Commerical Use is prohibited. Commercial Use shall include: 1. resales, lease, license or other transfer of the material or any material derived orproduced from it.
CLEANCAP® REAGENT AG (3' OME) CleanCap ® Reagent AG (3' OMe) is TriLink’s proprietary co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency1. CleanCap AG (3' OMe) includes the 5' N7-Methyl-3'-O-Methylguanosine commonly found in mRNA capped using ARCA, whereas CleanCap AG (N-7113) has a naturally CLEANCAP® CRE MRNA (5MOU) NLS-Cre Recombinase mRNA is a capped and polyadenylated messenger RNA encoding Cre recombinase fused to a nuclear localization sequence (NLS). Cre recombinase is a tyrosine recombinase that catalyzes recombination between two loxP sites. This mRNA is capped using CleanCap, TriLink's proprietary co-transciptional capping method,which results in
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. 2-AMINO-2'-DEOXYADENOSINE-5'-TRIPHOSPHATE Description. Substitution of 2-Amino-2'-deoxyadenosine (also known as 2,6-Diaminopurine-2'-deoxyribose) for adenine in DNA can result in increased stabilization of the DNA duplex. Diaminopurine base pairs with thymine forming three intramolecular hydrogen bonds versus twofor adenine.
CLEANCAP | TRILINK BIOTECHNOLOGIES CleanCap ® technology is a proprietary, co-transcriptional 5’ capping solution that generates a natural Cap 1 structure. Proper mRNA capping is critical to the production of the most biologically active and least immunogenic mRNA. TriLink scientists developed CleanCap, the next generation of capping technology, as a solution to the low THERMOSTABLE RNA VACCINE DELIVERY PROMISES ENHANCED Thermostable RNA Vaccine Delivery Promises Enhanced Pandemic Response. RNA-based vaccines offer several advantages over traditional vaccines. These include faster production, simpler scale-up, and more rapid adaptability to new targets. Such factors have proven critical in tackling the ongoing COVID-19 pandemic, allowing vaccines targetingSARS
ARCA | TRILINK BIOTECHNOLOGIES Description. Trusted TriLink quality, exceptional price. A key step in cellular mRNA processing is the addition of a 5’ cap structure, which is a 5'-5' triphosphate linkage between the 5' end of the RNA and a guanosine nucleotide. The cap is methylated enzymatically at theN-7
5-METHYLCYTIDINE-5'-TRIPHOSPHATE Methylation of the 5 position of cytidine is a common, post-transcriptional modification in a number of RNA species, such as mRNA, miRNA and tRNA. 5-Methylcytidine-5'-Triphosphate (5-Methyl-CTP) is a modified nucleoside triphosphate employed to impart desirable characteristics such as increased nuclease stability, increasedtranslation or
MRNA CAPPING ANALOGS, CAPPING ENZYMES & MORE Cap Analogs. 5’ cap structure of messenger RNA (mRNA) prevents degradation of the mRNA in the cytoplasm and promotes ribosome recruitment and protein translation. Cap analogs can be used to initiate transcription which eliminates the need for an additional enzymatic capping step. Sort by: 5-FORMYLCYTIDINE-5'-TRIPHOSPHATE 11,000 Lmol -1 cm -1 at 283 nm. Molecular Formula. C 10 H 16 N 3 O 15 P 3 (free acid) Molecular Weight. 511.10 g/mole (free acid) Salt Form. Li+. Concentration. 100 mM. N 1 -METHYLPSEUDOURIDINE-5'-TRIPHOSPHATE N1-Methyl-Pseudouridine-5'-Triphosphate is a modified NTP for incorporation into messenger RNAs (mRNA) using T7 RNA Polymerase. Incorporation of N1-methylpseudouridine can reduce the immunogenicity of the resulting mRNA. PERSPECTIVES ON PLASMIDS FOR IVT MRNA PRODUCTION—PART 1 Plasmids Were Discovered in 1952 as Agents of “Genetic Exchange” Between Bacteria In the Last 50 Years, There Have Been Over 200,000 Plasmid Publications, Averaging 15 Per Day During 1990-2020 Plasmids Provide the Starting Point for IVT mRNA Production TriLink Continuereading →
MRNA DELIVERY FOR THERAPEUTIC ANTI-HER2 ANTIBODY IN VIVO The remainder of this blog will focus on a recent report by Rybakova et al. that, for the first time, demonstrates the delivery of an IVT-mRNA in vivo to express a fully functional anticancer antibody designed to mimic the monoclonal antibody trastuzumab, sold under the brand name Herceptin.In this instance, unmodified IVT-mRNAs of heavy and light chains were co-delivered in a protective lipid SPECIFICITY ENHANCEMENT OF PCR AND OTHER DNA Following the invention of PCR in 1983 by Kary Mullis (1993 Nobel Prize in Chemistry), dNTPαS analogs were shown to be useful in PCR-based applications such as DNA sequencing by either chemical degradation (Gish and Eckstein), exonuclease digestion (Labeit et al.), or pyrosequencing (Gharizadeh et al.).. In the early literature for polymerase-mediated incorporation of dNTPαS JAVASCRIPT SEEMS TO BE DISABLED IN YOUR BROWSER. For the best experience on our site, be sure to turn on Javascript in your browser. TriLink Biotechnologies is part of Maravai LifeSciences. Learn More* Sign In
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CUSTOM AND STOCKED SOLUTIONS FOR COVID-19 PROGRAMS. CleanCap® mRNA for rapid vaccine development and top-tier oligos to power diagnostic kits Contact Us for Immediate Response CLEANCAP® SETS A NEW STANDARD FOR SUPERIOR MRNA TRANSLATION. Find out how CleanCap® technology reduces cost while increasingefficiency.
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CUSTOM AND STOCKED SOLUTIONS FOR COVID-19 PROGRAMS. CleanCap® mRNA for rapid vaccine development and top-tier oligos to power diagnostic kits Contact Us for Immediate Response CLEANCAP® SETS A NEW STANDARD FOR SUPERIOR MRNA TRANSLATION. Find out how CleanCap® technology reduces cost while increasingefficiency.
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TriLink BioTechnologies is actively responding to the COVID-19 pandemic. Learn More > ABOUT TRILINK BIOTECHNOLOGIES TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap® mRNA capping technology. TriLink continues to expand its cGMP and general mRNA, oligonucleotide & plasmid manufacturing capacity at its new global headquarters to support therapeutic, vaccine and diagnostic customers. CDMO SERVICE SOLUTIONSGMP
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