Pro Ligation-Free Cloning Kit (50 reactions)
Cat. No.
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E087
Print
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Name
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Pro Ligation-Free Cloning Kit (50 reactions)
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Unit
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50 Reactions
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Category
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Molecular Biology Enzymes and Kits
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Description
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The Pro Ligation-Free Cloning Kit allows for the robust assembly of multiple DNA fragments in one step. Using a ligation-independent cloning method, as many as six DNA fragments are assembled seamlessly without concern for restriction enzyme site availability. abm’s Pro Ligation-Free cloning is a simple yet highly versatile method to rapidly clone highly complex, multiple component constructs.
Key Kit Features:
- One-step cloning: No more time-consuming, multi-step traditional cloning that depnds on available restrict sites or compatible ends
- Scar-free cloning: No unwanted/extra base pairs in the inserts
- Easy-to-customize: Clone in promoter, gene, tag, multi-fragment or whiole vector constructs in one step
- Ready for downstream applications: Ligase-free reaction, no gel extraction or column purification steps needed
- Robust assembly: Better performance for difficult, multi-fragment assemblies such as CRISPR multiplex sgRNA vector assembly
- Increased thermostability: High colony yields
Testimonial:
"I tried the molecular cloning of inserting two DNA fragments (2Kb & 0.5Kb) into a 4Kb backbone by using the kit. After the transformation, I got about 100 colonies, and when I picked 24 colonies for colony PCR, the bright band from gel running told me that I got 20 potential hits, which is awesome. I sent some plasmids for sequencing, the result I received just now unveiled they are carrying the exact right fragment insertion. Collectively, this is a powerful kit."
- Jianfeng Lan, The Buck Institute
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Application
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- Rapid multi-fragment cloning and assembly of whole vector constructs
- Clone in a promoter, gene, and tag, all in one step
- Rapid assembly of CRISPR multiplex gRNA vectors in one step
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Material Citation
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If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. E087
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Huang, R., Ding, R., Liu, Y., Li, F., Zhang, Z., & Wang, S. A. 2022. GATA transcription factor WC2 regulates the biosynthesis of astaxanthin in yeast Xanthophyllomyces dendrorhous. Microbial Biotechnology, 15(10), 2578-2593.
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Hwang, B.-J., Gonzales, R., Corzine, S., Stenson, E., Pidugu, L., & Lu, A.-L. (2022). DNA binding by the Rad9A subunit of the Rad9-Rad1-Hus1 complex. PLOS ONE, 17(8), e0272645. https://doi.org/10.1371/journal.pone.0272645
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Li, L., Liu, W., Fan, N., Li, F., Huang, B., Liu, Q., ... & Wang, X. (2022). Scallop IKK1 Responds to Bacterial and Virus-Related Pathogen Stimulation and Interacts With MyD88 Adaptor of Toll-Like Receptor Pathway Signaling. Frontiers in Immunology, 13. https://doi.org/10.3389/fimmu.2022.869845
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Huang, B., Wu, Y., Ma, J., Yang, B., Sang, X., Chen, J., Liu, W., Li, F., Li, L., Wang, X., Dong, J., & Wang, X. (2022). The first identified invertebrate LGP2-like homolog gene in the Pacific oyster Crassostrea gigas. Fish & Shellfish Immunology, 128, 238–245. https://doi.org/10.1016/j.fsi.2022.08.005
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Sang, X., Liu, W., Li, F., Huang, B., Li, L., Wang, X., Dong, J., Ma, J., Chen, J., & Wang, X. (2022). Scallop RIG-I-like receptor 1 responses to polyinosinic:polycytidylic acid challenge and its interactions with the mitochondrial antiviral signaling protein. Fish & Shellfish Immunology, 124, 490–496. https://doi.org/10.1016/j.fsi.2022.04.042
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Tettey, C. K., Mu, X.-Q., Ma, H.-Y., Chen, X.-Y., Geng, C., Tian, Y.-P., Yan, Z.-Y., & Li, X.-D. (2023). The role of different innate and environmental factors in Tm-22-mediated resistance to tomato mottle mosaic virus. Phytopathology Research, 5(1). https://doi.org/10.1186/s42483-023-00162-4
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Novak, N., Baumann, M., Friss, A., Cairns, V., DeMaria, C., & Borth, N. (2023). LncRNA analysis of mAb producing CHO clones reveals marker and engineering potential. Metabolic Engineering, 78, 26–40. https://doi.org/10.1016/j.ymben.2023.05.003
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Chen, J., Qu, Y., Dong, J., Xu, W., Zhao, Y., Cui, J., Yu, Z., Bao, Z., Ma, J., Han, Y., Liu, Y., Huang, B., & Wang, X. (2024). A scallop IκB protein involved in innate immunity acts as a key regulator of NF-κB. Fish & Shellfish Immunology, 154, 109897. https://doi.org/10.1016/j.fsi.2024.109897
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Huang, B., Ma, J., Xu, W., Cui, J., Chen, J., Qu, Y., Zhao, Y., Han, Y., Liu, Y., Wang, W., & Wang, X. (2024). A newly identified scallop MyD88 interacts with TLR and functions in innate immunity. Fish & Shellfish Immunology, 151, 109697. https://doi.org/10.1016/j.fsi.2024.109697
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Tao, Y., Wang, J., Xiao, L., Zhang, Q., & Guo, H. (2024). Development and Evaluation of a Shrimp Virus (IHHNV)-Mediated System Used for Efficient Gene Transfer and Expression in Shrimps. https://doi.org/10.20944/preprints202406.2070.v1
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UNIT
500 rxn (4 x 1.25 ml)
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01:04:45"},"info":{"id":18410,"cat_no_base":"E087","parent_id":3195,"description":"\u003Cp\u003EThe Pro Ligation-Free Cloning Kit allows for the robust assembly of multiple DNA fragments in one step. Using a ligation-independent cloning method, as many as six DNA fragments are assembled seamlessly without concern for restriction enzyme site availability.\u0026nbsp;\u003Cstrong\u003Eabm\u003C\/strong\u003E\u0026rsquo;s Pro Ligation-Free cloning is a simple yet highly versatile method to rapidly clone highly complex, multiple component constructs.\u003C\/p\u003E\n\u003Cp\u003E\u003Cstrong\u003EKey Kit Features:\u003C\/strong\u003E\u003C\/p\u003E\n\u003Cul\u003E\n\u003Cli\u003E\u003Cstrong\u003EOne-step cloning:\u003C\/strong\u003E\u0026nbsp;No more time-consuming, multi-step traditional cloning that depnds on available restrict sites or compatible ends\u003C\/li\u003E\n\u003Cli\u003E\u003Cstrong\u003EScar-free cloning:\u003C\/strong\u003E\u0026nbsp;No unwanted\/extra base pairs in the inserts\u003C\/li\u003E\n\u003Cli\u003E\u003Cstrong\u003EEasy-to-customize:\u003C\/strong\u003E\u0026nbsp;Clone in promoter, gene, tag, multi-fragment or whiole vector constructs in one step\u003C\/li\u003E\n\u003Cli\u003E\u003Cstrong\u003EReady for downstream applications:\u003C\/strong\u003E\u0026nbsp;Ligase-free reaction, no gel extraction or column purification steps needed\u003C\/li\u003E\n\u003Cli\u003E\u003Cstrong\u003ERobust assembly:\u003C\/strong\u003E\u0026nbsp;Better performance for difficult, multi-fragment assemblies such as CRISPR multiplex sgRNA vector assembly\u003C\/li\u003E\n\u003Cli\u003E\u003Cstrong\u003EIncreased thermostability:\u003C\/strong\u003E\u0026nbsp;High colony yields\u003C\/li\u003E\n\u003C\/ul\u003E\n\u003Cp\u003E\u003Cstrong\u003ETestimonial:\u003C\/strong\u003E\u003C\/p\u003E\n\u003Cp\u003E\u0022I tried the molecular cloning of inserting two DNA fragments (2Kb \u0026 0.5Kb) into a 4Kb backbone by using the kit. After the transformation, I got about 100 colonies, and when I picked 24 colonies for colony PCR, the bright band from gel running told me that I got 20 potential hits, which is awesome. I sent some plasmids for sequencing, the result I received just now unveiled they are carrying the exact right fragment insertion. 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