Protein Expression Eukaryotic cells S. cerevisiae

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Get tips on using ProtoScript® II First Strand cDNA Synthesis Kit to perform cDNA synthesis Yeast

Products New England BioLabs ProtoScript® II First Strand cDNA Synthesis Kit

Get tips on using ProtoScript® II First Strand cDNA Synthesis Kit to perform cDNA synthesis Tissue

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Get tips on using Senescence β-Galactosidase Staining Kit - Beyotime to perform Reporter gene assay β-galactosidase substrates - HepG2

Products Beyotime Senescence β-Galactosidase Staining Kit - Beyotime

Get tips on using Phusion Site-Directed Mutagenesis Kit to perform Site Directed Mutagenesis (SDM) Hamster - Point mutation CHO SGLT1

Products Thermo Fisher Scientific Phusion Site-Directed Mutagenesis Kit

Get tips on using Q5® Site-Directed Mutagenesis Kit to perform Site Directed Mutagenesis (SDM) Dog - Insertion MDCK SLC26A7

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Get tips on using Q5® Site-Directed Mutagenesis Kit to perform Site Directed Mutagenesis (SDM) Dog - Insertion MDCK SLC26A9

Products New England BioLabs Q5® Site-Directed Mutagenesis Kit

Get tips on using Q5® Site-Directed Mutagenesis Kit to perform Site Directed Mutagenesis (SDM) Human - Deletion SKOV3 APRIN

Products New England BioLabs Q5® Site-Directed Mutagenesis Kit

Get tips on using Q5® Site-Directed Mutagenesis Kit to perform Site Directed Mutagenesis (SDM) Dog - Insertion MDCK SLC26A5

Products New England BioLabs Q5® Site-Directed Mutagenesis Kit

DNA isolation and purification is the first critical step in sample preparation that helps ensure optimal performance of downstream assays like PCR, microarrays, and sequencing. Failure in yielding high-quality DNA would be the major reason that DNA doesn't work for the downstream application. To circumvent this, one should follow the recommended storage conditions to minimize DNA degradation by nucleases and shouldn't overload the purification system.

DNA DNA isolation / purification Bacteria Gram negative E.coli

DNA isolation and purification is the first critical step in sample preparation that helps ensure optimal performance of downstream assays like PCR, microarrays, and sequencing. Failure in yielding high-quality DNA would be the major reason that DNA doesn't work for the downstream application. To circumvent this, one should follow the recommended storage conditions to minimize DNA degradation by nucleases and shouldn't overload the purification system.

DNA DNA isolation / purification Bacteria Gram negative Legionella

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