{"title":"Cloning, Genome Editing \u0026 Expression","description":"\u003cp\u003eDiscover our comprehensive range of tools for cloning, genome editing, and protein expression, covering every step from DNA assembly and CRISPR-based gene editing to cell-free protein synthesis and mRNA production. Our portfolio includes Golden Gate assembly kits, Cas9 and Cas12b nucleases, cell-free expression systems, and RNA synthesis reagents — all engineered for precision, efficiency, and reproducibility.\u003c\/p\u003e\u003cp\u003eWhether you're building synthetic constructs, editing genomic targets, or expressing proteins without a cellular host, our products are validated for high performance across a wide range of experimental conditions. Trusted by researchers in synthetic biology, gene therapy, and molecular engineering, our solutions are designed to accelerate your workflows from design to functional output.\u003c\/p\u003e","products":[{"product_id":"spcas9-nls","title":"SpCas9-NLS","description":"SpCas9-NLS is an RNA-guided endonuclease from Streptococcus pyogenes. Guided by crRNA and tracrRNA (or a sgRNA formed by their fusion), SpCas9-NLS recognizes the region immediately upstream of the PAM sequence (5'-NGG) in double-stranded DNA targets and produces a double-stranded break precisely three nucleotides upstream of the PAM. SpCas9-NLS is commonly employed for gene editing. To enhance cellular editing efficiency, SpCas9-NLS contains a nuclear localization sequence (NLS) derived from Simian virus 40 (SV40) T antigen on N-termini. Additionally, this product can be utilized for the cleavage of target DNA in vitro and gene cloning, etc.","brand":"Cleavion","offers":[{"title":"100 pmol","offer_id":57188440670583,"sku":"CLV-0191","price":74.64,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0191-0-cleavion-product.png?v=1781696383"},{"product_id":"spcas9-nls-1","title":"SpCas9-NLS","description":"SpCas9-NLS is an RNA-guided endonuclease from Streptococcus pyogenes. Guided by crRNA and tracrRNA (or a sgRNA formed by their fusion), SpCas9-NLS recognizes the region immediately upstream of the PAM sequence (5'-NGG) in double-stranded DNA targets and produces a double-stranded break precisely three nucleotides upstream of the PAM. SpCas9-NLS is commonly employed for gene editing. To enhance cellular editing efficiency, SpCas9-NLS contains a nuclear localization sequence (NLS) derived from Simian virus 40 (SV40) T antigen on N-termini. Additionally, this product can be utilized for the cleavage of target DNA in vitro and gene cloning, etc.","brand":"Cleavion","offers":[{"title":"1000 pmol","offer_id":57188440834423,"sku":"CLV-0192","price":252.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0192-0-cleavion-product.png?v=1781696384"},{"product_id":"dna-assembly-mix-mono","title":"DNA Assembly Mix Mono","description":"DNA Assembly Mix Mono is a kind of seamless assembly method, digest, ligate or end repair are not required. This method has been used to assemble different sizes of DNA fragments with varied overlaps (15~30 bp) . And it offers a easy, fast and efficient DNA cloning technique. DNA Assembly Mix Mono is specifically designed for single-fragment DNA assembly. It can complete single-fragment recombination in as fast as 5 minutes with a positive rate of over 95%. Compared with DNA Assembly Mix Ultra (REF: EG24204), DNA Assembly Mix Mono does not rely on ligase, has simpler components, and is more compatible with unpurified PCR products. Meanwhile, DNA Assembly Mix Mono contains no ligase and relies on the repair system of E. coli, thus ensuring higher fidelity.","brand":"Cleavion","offers":[{"title":"50 Reactions","offer_id":57188441620855,"sku":"CLV-0195","price":74.61,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0195-0-cleavion-product.png?v=1781696387"},{"product_id":"dna-assembly-mix-ultra","title":"DNA Assembly Mix Ultra","description":"DNA Assembly Mix Ultra is a kind of seamless assembly methoddigest, ligate or end repair are not required. This method has beenused to assemble different sizes of DNA fragments with variedoverlaps (15~30 bp) . And it offers a easy, fast and efficient DNA cloningtechnique. The DNA Assembly Mix Ultra allows for the assembly of one ormultiple DNA fragments in a single reaction, with single-fragmentinsertion completed in as little as 5 minutes and a positive rateexceeding 95%.This Mix uses HiFi Taq DNA Ligase, which hashigher fidelity compared to wild-type Taq DNA Ligase, significantlyimproving the success rate of seamless cloning. Additionally, the Mixincludes a transformation enhancer, greatly increasing the number oftransformants. While ensuring high fidelity and transformation efficiencythe DNA Assembly Mix Ultra has optimized its components to enhancestability, making it more stable under high temperature or oxidicconditions.","brand":"Cleavion","offers":[{"title":"50 Reactions","offer_id":57188441686391,"sku":"CLV-0176","price":74.61,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0176-0-cleavion-product.png?v=1781696387"},{"product_id":"dna-assembly-mix-mono-1","title":"DNA Assembly Mix Mono","description":"DNA Assembly Mix Mono is a kind of seamless assembly method, digest, ligate or end repair are not required. This method has been used to assemble different sizes of DNA fragments with varied overlaps (15~30 bp) . And it offers a easy, fast and efficient DNA cloning technique. DNA Assembly Mix Mono is specifically designed for single-fragment DNA assembly. It can complete single-fragment recombination in as fast as 5 minutes with a positive rate of over 95%. Compared with DNA Assembly Mix Ultra (REF: EG24204), DNA Assembly Mix Mono does not rely on ligase, has simpler components, and is more compatible with unpurified PCR products. Meanwhile, DNA Assembly Mix Mono contains no ligase and relies on the repair system of E. coli, thus ensuring higher fidelity.","brand":"Cleavion","offers":[{"title":"250 Reactions","offer_id":57188441817463,"sku":"CLV-0196","price":166.25,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0196-0-cleavion-product.png?v=1781696388"},{"product_id":"golden-gate-dna-assembly-kit-with-bpii","title":"Golden Gate DNA Assembly Kit with BpiI","description":"Golden Gate Assembly Kit share the same single-step precision cloning strategy, popularly known as \"Golden Gate Assembly\", that relies on the unique properties of type IIs restriction enzymes to generate compatible ends on DNA fragments that are then joined together by the T4 DNA ligase. The Kit are particularly adept at assembling difficult to-clone sequences such as repetitive and very small sequences (\u0026lt;100 bp), gene variants, and TAL (transcription activator-like) effector genes. Type IIS restriction enzymes bind to their recognition sites but cut the DNA downstream from that site at a positional, not sequence specific, cut site. Thus, a single Type IIS restriction enzyme can be used to generate DNA fragments with unique overhangs. The cloning procedure is as follows: Design recognition sites for type IIS restriction enzymes outside the cleavage sites of the target gene. Assembly of digested fragments proceeds through annealing of complementary four base overhangs on adjacent fragments. The digested fragments and the final assembly no longer contain Type IIS restriction enzyme recognition sites, so no further cutting is possible. The vector contains sticky ends complementary to those of the target gene, enabling ligation without introducing extraneous sequences, thereby achieving seamless cloning. The Golden Gate Assembly Kit (BpiI), based on the above principle, contains all enzymes required for restriction digestion and ligation in a ready-to-use Mix for convenient pipetting. It supports ligation of up to 16 fragments in a single reaction, fully satisfying diverse experimental requirements.","brand":"Cleavion","offers":[{"title":"50 Reactions","offer_id":57188442571127,"sku":"CLV-0281","price":482.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0281-0-cleavion-product.png?v=1781696413"},{"product_id":"aapcas12b-crispr-nuclease","title":"AapCas12b CRISPR Nuclease","description":"AapCas12b is a Type V Cas nuclease, exhibiting good activity across 37~60°C. Guided by crRNA and tracrRNA (or sgRNA), it exhibits cis-cleavage activity against both double-stranded and single-stranded DNA targets. For double-stranded DNA targets, AapCas12b recognizes the site complementary to the crRNA (or sgRNA) spacer sequence downstream of the PAM sequence (5'-TTN) in target DNA, specifically cleaves the target double-stranded DNA to generate sticky ends. For single-stranded DNA targets, its specific cleavage is PAM-independent. After AapCas12b, target DNA and sgRNA form a ternary complex, the enzyme exhibits trans-cleavage activity, namely non-specific cleavage of single-stranded DNA with any sequence. AapCas12b exhibits good activity in common isothermal amplification buffers, making it suitable for rapid nucleic acid detection.","brand":"Cleavion","offers":[{"title":"100 pmol","offer_id":57188442734967,"sku":"CLV-0282","price":137.5,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0282-0-cleavion-product.png?v=1781696415"},{"product_id":"aapcas12b-crispr-nuclease-1","title":"AapCas12b CRISPR Nuclease","description":"AapCas12b is a Type V Cas nuclease, exhibiting good activity across 37~60°C. Guided by crRNA and tracrRNA (or sgRNA), it exhibits cis-cleavage activity against both double-stranded and single-stranded DNA targets. For double-stranded DNA targets, AapCas12b recognizes the site complementary to the crRNA (or sgRNA) spacer sequence downstream of the PAM sequence (5'-TTN) in target DNA, specifically cleaves the target double-stranded DNA to generate sticky ends. For single-stranded DNA targets, its specific cleavage is PAM-independent. After AapCas12b, target DNA and sgRNA form a ternary complex, the enzyme exhibits trans-cleavage activity, namely non-specific cleavage of single-stranded DNA with any sequence. AapCas12b exhibits good activity in common isothermal amplification buffers, making it suitable for rapid nucleic acid detection.","brand":"Cleavion","offers":[{"title":"1000 pmol","offer_id":57188442898807,"sku":"CLV-0283","price":617.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0283-0-cleavion-product.png?v=1781696415"},{"product_id":"t7-rna-polymerase-1","title":"T7 RNA Polymerase","description":"T7 RNA Polymerase is derived from recombinant expression in E.coli. It is a DNA-dependent RNA polymerase that exhibits high specificity for the promoter sequence of bacteriophage T7. T7 RNA Polymerase utilizes double-stranded DNA templates containing the T7 promoter sequence and NTPs as substrates to synthesize singlestranded RNA complementary to the downstream of the promoter.","brand":"Cleavion","offers":[{"title":"25000 U","offer_id":57188444438903,"sku":"CLV-0252","price":309.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0252-0-cleavion-product.png?v=1781696422"},{"product_id":"cell-free-protein-synthesis-kit-lyophilized","title":"Cell-Free Protein Synthesis Kit (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: This product is not suitable for the soluble expression of disulfide-rich proteins, as it does not provide the oxidative environment required for correct disulfide bond folding. If needed, please contact us for other REF NO..","brand":"Cleavion","offers":[{"title":"20 Reactions","offer_id":57188444537207,"sku":"CLV-0233","price":105.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0233-0-cleavion-product.png?v=1781696423"},{"product_id":"high-t7-rna-polymerase","title":"High T7 RNA Polymerase","description":"High T7 RNA Polymerase is a genetically engineered thermostable T7 RNA polymerase, which exhibits high specificity for the bacteriophage T7 promoter sequence. Compared to the wild-type T7 RNA polymerase, High T7 RNA Polymerase enables efficient in vitro transcription (IVT) at temperature from 37 to 52°C.","brand":"Cleavion","offers":[{"title":"5000 U","offer_id":57188444635511,"sku":"CLV-0253","price":128.75,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0253-0-cleavion-product.png?v=1781696423"},{"product_id":"cell-free-protein-synthesis-kit-lyophilized-1","title":"Cell-Free Protein Synthesis Kit (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: This product is not suitable for the soluble expression of disulfide-rich proteins, as it does not provide the oxidative environment required for correct disulfide bond folding. If needed, please contact us for other REF NO..","brand":"Cleavion","offers":[{"title":"100 Reactions","offer_id":57188444766583,"sku":"CLV-0234","price":309.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0234-0-cleavion-product.png?v=1781696423"},{"product_id":"high-t7-rna-polymerase-1","title":"High T7 RNA Polymerase","description":"High T7 RNA Polymerase is a genetically engineered thermostable T7 RNA polymerase, which exhibits high specificity for the bacteriophage T7 promoter sequence. Compared to the wild-type T7 RNA polymerase, High T7 RNA Polymerase enables efficient in vitro transcription (IVT) at temperature from 37 to 52°C.","brand":"Cleavion","offers":[{"title":"25000 U","offer_id":57188444799351,"sku":"CLV-0254","price":390.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0254-0-cleavion-product.png?v=1781696424"},{"product_id":"cell-free-protein-synthesis-kit-pro-lyophilized","title":"Cell-Free Protein Synthesis Kit Pro (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: This product contains the chaperone proteins GroEL (~60 kDa) and GroES (~10 kDa), representing the most extensively characterized chaperone system currently under research. They create a closed folding chamber that provides an optimal environment for unfolded proteins, reducing misfolding and aggregation, thereby increasing the probability of soluble expression. However, protein solubility is influenced by multiple factors (e.g., inherent protein structure, expression system, reaction conditions, etc.) . While this product can significantly improve folding efficiency, soluble expression is not guaranteed for all proteins","brand":"Cleavion","offers":[{"title":"20 Reactions","offer_id":57188444897655,"sku":"CLV-0235","price":140.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0235-0-cleavion-product.png?v=1781696424"},{"product_id":"cell-free-protein-synthesis-kit-pro-lyophilized-1","title":"Cell-Free Protein Synthesis Kit Pro (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: This product contains the chaperone proteins GroEL (~60 kDa) and GroES (~10 kDa), representing the most extensively characterized chaperone system currently under research. They create a closed folding chamber that provides an optimal environment for unfolded proteins, reducing misfolding and aggregation, thereby increasing the probability of soluble expression. However, protein solubility is influenced by multiple factors (e.g., inherent protein structure, expression system, reaction conditions, etc.) . While this product can significantly improve folding efficiency, soluble expression is not guaranteed for all proteins","brand":"Cleavion","offers":[{"title":"100 Reactions","offer_id":57188445061495,"sku":"CLV-0236","price":438.8,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0236-0-cleavion-product.png?v=1781696425"},{"product_id":"cell-free-protein-synthesis-kit-max-lyophilized","title":"Cell-Free Protein Synthesis Kit Max (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: The product is suitable for expressing diverse proteins, particularly disulfide-rich proteins.","brand":"Cleavion","offers":[{"title":"20 Reactions","offer_id":57188445258103,"sku":"CLV-0237","price":170.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0237-0-cleavion-product.png?v=1781696425"},{"product_id":"golden-gate-dna-assembly-kit-with-bpii-1","title":"Golden Gate DNA Assembly Kit with BpiI","description":"Golden Gate Assembly Kit share the same single-step precision cloning strategy, popularly known as \"Golden Gate Assembly\", that relies on the unique properties of type IIs restriction enzymes to generate compatible ends on DNA fragments that are then joined together by the T4 DNA ligase. The Kit are particularly adept at assembling difficult to-clone sequences such as repetitive and very small sequences (\u0026lt;100 bp), gene variants, and TAL (transcription activator-like) effector genes. Type IIS restriction enzymes bind to their recognition sites but cut the DNA downstream from that site at a positional, not sequence specific, cut site. Thus, a single Type IIS restriction enzyme can be used to generate DNA fragments with unique overhangs. The cloning procedure is as follows: Design recognition sites for type IIS restriction enzymes outside the cleavage sites of the target gene. Assembly of digested fragments proceeds through annealing of complementary four base overhangs on adjacent fragments. The digested fragments and the final assembly no longer contain Type IIS restriction enzyme recognition sites, so no further cutting is possible. The vector contains sticky ends complementary to those of the target gene, enabling ligation without introducing extraneous sequences, thereby achieving seamless cloning. The Golden Gate Assembly Kit (BpiI), based on the above principle, contains all enzymes required for restriction digestion and ligation in a ready-to-use Mix for convenient pipetting. It supports ligation of up to 16 fragments in a single reaction, fully satisfying diverse experimental requirements.","brand":"Cleavion","offers":[{"title":"10 Reactions","offer_id":57188445389175,"sku":"CLV-0280","price":150.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0280-0-cleavion-product.png?v=1781696425"},{"product_id":"cell-free-protein-synthesis-kit-max-lyophilized-1","title":"Cell-Free Protein Synthesis Kit Max (Lyophilized)","description":"The Cell-Free Protein Synthesis Kit is a product for in vitro protein synthesis based on E. coli lysate. Coupled transcription\/translation systems contain an RNA polymerase and the necessary cellular machinery needed to direct protein synthesis (e.g., ribosomes, translation factors and tRNAs) . Supplements such as amino acids, an energy source and NTPs complete the system. Proteins are expressed using DNA or RNA as templates. Cell-free protein expression, independent of viable cells, enables rapid, flexible and high-yield protein expression, with numerous advantages over traditional recombinant expression systems: 1. Time saving. Express target proteins in 1~2 hours, with peak yield achieved in 8~24 hours. 2. High protein expression level, up to more than 3 mg\/ml. 3. Easy operation, Add DNA or RNA templates to the reaction system, and the reaction can be performed using 96-well plates or centrifuge tubes. Note: The product is suitable for expressing diverse proteins, particularly disulfide-rich proteins.","brand":"Cleavion","offers":[{"title":"100 Reactions","offer_id":57188445454711,"sku":"CLV-0238","price":568.4,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0238-0-cleavion-product.png?v=1781696426"},{"product_id":"ntp-bundle-25-mm-each","title":"NTP Bundle (25 mM each)","description":"The product is a high-purity NTP Tris-HCl solution, containing 25 mM each of ATP, CTP, GTP, and UTP. It is a colorless and transparent aqueous solution, free from DNase, RNase, and phosphatase contamination. It is primarily used in in vitro transcription (IVT), aptamer, laboratory-developed tests (LDT), analyte-specific reagents (ASR), PCR, and RT-PCR reactions.","brand":"Cleavion","offers":[{"title":"1 mL","offer_id":57188445618551,"sku":"CLV-0259","price":120.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0259-0-cleavion-product.png?v=1781696427"},{"product_id":"n1-methyl-pseudo-utp-100-mm","title":"N1-Methyl-Pseudo-UTP (100 mM)","description":"","brand":"Cleavion","offers":[{"title":"100 µL","offer_id":57188445749623,"sku":"CLV-0260","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0991\/7097\/6119\/files\/CLV-0260-0-cleavion-product.png?v=1781696428"}],"url":"https:\/\/cleavion.com\/collections\/cloning-genome-editing-expression.oembed?page=2","provider":"Cleavion Inc.","version":"1.0","type":"link"}