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Plasmid rapid extraction kit

Manufactured by Takara Bio
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The Plasmid rapid extraction kit is a laboratory tool designed for the quick and efficient isolation of plasmid DNA from bacterial cultures. The kit utilizes a simple and streamlined protocol to extract plasmid DNA, enabling researchers to obtain high-quality samples for various downstream applications.

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Lab products found in correlation

Restriction endonuclease, by Promega (2 mentions) Dna quick puri cation and recovery kit, by Takara Bio (2 mentions) Insect cell culture medium, by Thermo Fisher Scientific (2 mentions) La taq polymerase, by Takara Bio (2 mentions) Pmd18 t vector, by Takara Bio (2 mentions)

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Plasmid extraction kit (19 citations)

2 protocols using plasmid rapid extraction kit

1

Baculovirus-Mediated Protein Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
Escherichia coli strains Top 10, BL21(DE3) and pET-28a, Pichia receptor strains GS115 and Pichiapastoris expression vector pPIC9-γ, baculovirus transfer vector pVL1393, Bmbacpak-6 virus containing the β-galactosidase gene of Escherichia coli, Bombyx mori cell line, parental virus BmBacmid made from Bombyx mori nucleopolyhedrovirus genome which lacks the ORF1629 gene [16, 17] (link), Bm-N cell and silkworm variety JY-1 were all kept in our own laboratory. Chemical reagents were purchased from Sigma. Restriction endonucleases were purchased from Promega. Vector pMD18-T, LA Taq polymerase, DEPC, DNA quick puri cation and recovery kit, plasmid rapid extraction kit were purchased from TaKaRa.
Insect cell culture medium and FBS were purchased from Invitrogen.
Yi Y., Li J., Zong Z., Liu X., Song H., Wang H., Zhang Z., Zhang H, & Li Y. (2021). Cloning, expression, and characteristic analysis of the novel β-galactosidase from silkworm, Bombyx mori. Genesis (New York, N.Y. : 2000), 59(9).
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2

Baculovirus-Mediated Protein Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
Escherichia coli strains Top 10, BL21(DE3) and pET-28a, Pichia receptor strains GS115 and Pichiapastoris expression vector pPIC9-γ, baculovirus transfer vector pVL1393, Bmbacpak-6 virus containing the β-galactosidase gene of Escherichia coli, Bombyx mori cell line, parental virus BmBacmid made from Bombyx mori nucleopolyhedrovirus genome which lacks the ORF1629 gene [16, 17] (link), Bm-N cell and silkworm variety JY-1 were all kept in our own laboratory. Chemical reagents were purchased from Sigma. Restriction endonucleases were purchased from Promega. Vector pMD18-T, LA Taq polymerase, DEPC, DNA quick puri cation and recovery kit, plasmid rapid extraction kit were purchased from TaKaRa.
Insect cell culture medium and FBS were purchased from Invitrogen.
Yi Y., Li J., Zong Z., Liu X., Song H., Wang H., Zhang Z., Zhang H., & Li Y. (2021). Cloning, Expression, and Characteristic Analysis of the Novel β-Galactosidase from Silkworm,Bombyx Mori.
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