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产品介绍 Zaire Ebola Virus (Zebov) glycoprotein 1 (GP1), also known as envelope glycoprotein with a C-terminal His-tag, GenBank Accession No. NP_066246, MW=57.1 kDa, expressed in a HEK293 cell expression system. This protein runs at an apparent higher molecular weight due to glycosylation.
询价背景介绍 POLG is the catalytic subunit of the mitochondrial DNA polymerase. The catalytic subunit contains three enzymatic activities, a DNA polymerase activity, a 3'-5' exonuclease activity that proofreads misincorporated nucleotides, and a 5'-dRP lyase activity required for base excision repair. Mutations in the POLG gene are associated with several mitochondrial diseases, including Alpers' disease, ataxia-neuropathy disorders, and dominant and recessive forms of progressive external ophthalmoplegia. 产品介绍 Human DNA polymerase γ (gamma), also known as Pol gamma and POLG (GenBank Accession No. NM_002693), a.a. 2-1239 (end), with N-terminal His-tag and N-terminal FLAG-tag, MW=141 kDa, expressed in a baculovirus infected Sf9 cell expression system.
询价背景介绍 The Site-Directed Mutagenesis Kit is a simple and highly efficient method to insert any mutation (pint, insert, deletion) into a vector, without time-consuming ligation steps. Multiple mutations can be performed in a single step. The procedure is easy: mutations are generated in the gene of interest using appropriate primers and PCR amplification. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Site-Directed Mutagenesis Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Site Directed Mutagenesis kit allows for the insertion of multiple mutations into the desired vector in a single reaction. No ligation step is required, saving time and effort. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Site-Directed Mutagenesis Kit is a simple and highly efficient method to insert any mutation (pint, insert, deletion) into a vector, without time-consuming ligation steps. Multiple mutations can be performed in a single step. The procedure is easy: mutations are generated in the gene of interest using appropriate primers and PCR amplification. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Site-Directed Mutagenesis Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Site Directed Mutagenesis kit allows for the insertion of multiple mutations into the desired vector in a single reaction. No ligation step is required, saving time and effort. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Site-Directed Mutagenesis Kit is a simple and highly efficient method to insert any mutation (point, insertion, deletion) into a vector, without time-consuming ligation steps. Multiple mutations can be performed in a single step. The procedure is easy: mutations are generated in the gene of interest using appropriate primers and PCR amplification. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Site-Directed Mutagenesis Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Site Directed Mutagenesis kit allows for the insertion of multiple mutations into the desired vector in a single reaction. No ligation step is required, saving time and effort. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Site-Directed Mutagenesis Kit is a simple and highly efficient method to insert any mutation (pint, insert, deletion) into a vector, without time-consuming ligation steps. Multiple mutations can be performed in a single step. The procedure is easy: mutations are generated in the gene of interest using appropriate primers and PCR amplification. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Site-Directed Mutagenesis Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Site Directed Mutagenesis kit allows for the insertion of multiple mutations into the desired vector in a single reaction. No ligation step is required, saving time and effort. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Quick PCR™ Cloning Kit is a simple and highly efficient method to insert any gene or DNA fragment into a vector, without time-consuming ligation steps. Multiple PCR inserts can be added in a single step. The procedure is easy: a primer set homologous to the gene of interest and the vector are used to amplify a PCR product. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Quick PCR™ Cloning Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Quick PCR™ cloning kit allows for the insertion of multiple DNA fragments into the desired vector in a single reaction. No ligation step is required, saving time and effort. The method is fast, simple, and efficient. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Efficiencies of >90% are routinely obtained. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Quick PCR™ Cloning Kit is a simple and highly efficient method to insert any gene or DNA fragment into a vector, without time-consuming ligation steps. Multiple PCR inserts can be added in a single step. The procedure is easy: a primer set homologous to the gene of interest and the vector are used to amplify a PCR product. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Quick PCR™ Cloning Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Quick PCR™ cloning kit allows for the insertion of multiple DNA fragments into the desired vector in a single reaction. No ligation step is required, saving time and effort. The method is fast, simple, and efficient. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Efficiencies of >90% are routinely obtained. Available with or without competent cells for even greater efficiency and flexibility.
询价背景介绍 The Quick PCR™ Cloning Kit is a simple and highly efficient method to insert any gene or DNA fragment into a vector, without time-consuming ligation steps. Multiple PCR inserts can be added in a single step. The procedure is easy: a primer set homologous to the gene of interest and the vector are used to amplify a PCR product. This purified PCR product is incubated with restriction enzyme-digested vector and Reagent A of the Quick PCR™ Cloning Kit. Following a brief (5 minute) incubation with Reagent B, the annealed vector is ready for transformation. 产品介绍 The BPS Bioscience Quick PCR™ cloning kit allows for the insertion of multiple DNA fragments into the desired vector in a single reaction. No ligation step is required, saving time and effort. The method is fast, simple, and efficient. Go from PCR product to transforming cells in under an hour! Simply mix the purified PCR product with the vector in a 1:1 molar ratio (Total DNA : Vector) and follow the protocol. Efficiencies of >90% are routinely obtained. Available with or without competent cells for even greater efficiency and flexibility.
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