Protein Enzymes

Save time at the bench with our complete collection of protein products and reagents.

XJ Autolysis E. coli strains

E. Coli

Chemically competent cells that offer a new alternative for bacterial transformation and lysis that simplify protein expression and purification….

His-Spin Protein Miniprep

P2001, P2002

Fast and simple spin-column method for purifying His-tagged proteins from cell lysates.

Yeast Protein Kit

Y1002

Rapid and thorough lysis of yeast cells for protein and DNA analysis.

Strep-Spin Protein Miniprep Kit

P2004, P2005

Fast and simple spin-column method for purifying Strep-tagged proteins from cell lysates.

Zymolyase

E1004, E1005, E1006

Yeast lytic enzyme for simple and effective digestion of fungal cell walls.

DNase I Set

E1010

Yeast lytic enzyme for simple and effective digestion of fungal cell walls.

ZymoTaq Polymerase

Buffers

ZymoTaq DNA Polymerase contains all the reagents needed to perform “hot-start” PCR. This unique product is specifically designed for the amplification…

DNA Degradase Plus

E2020, E2021

Complete digestion of DNA into individual nucleosides.

MBP-Spin Protein Miniprep Kit

P2006, P2007

Fast and simple spin-column method for purifying MBP-tagged proteins from cell lysates.

Dual Media Set

M3011

Simple, reliable method for high level recombinant protein expression in E. coli.

dsDNA Shearase Plus

E2018-200, E2018-50

Simply control fragment size of dsDNA by adjusting the concentration of dsDNA Shearase Plus.

RNase A

E1008-24, E1008-30, E1008-8

Used for RNA hydrolysis and compatible with a variety of applications.


OVERVIEW – PROTEIN & ENZYMES

Although the expression and purification of recombinant proteins in E. coli is now a routine procedure, high-level expression or over-expression is not always attainable. However, those at Zymo Research have designed products to exploit the fact that high levels of protein expression can be consistently obtained when the processes of cell expansion and protein expression are kept separate. This is easily achieved with the use of the Dual Media Set™ where the over-expression of many proteins can be reliably controlled. In conjunction with the Dual Media Set™, our XJ Autolysis™ expression strains are ideal hosts for recombinant protein expression. With these strains, bacterial cell lysis is complete after a single freeze/thaw cycle. Researchers will find the single step lysis procedure simple, reproducible, and faster than conventional methods.


Culture Media

Expressing recombinant proteins in E.coli is now a routine procedure, though varying levels of protein expression are attainable. Research has proven that high levels of protein expression can be obtained when cell expansion and protein expression are kept separate. The ‘Dual Media Set’ by Zymo Research Corporation takes advantage of this with its two specially prepared mediums. This allows protein overexpression to be easily controlled for many recombinant proteins.


Bacterial Expression Strains

Zymo Research Corporation has produced XJ Autolysis E.Coli Strains, as the ideal hosts for recombinant protein expression. These strains allow complete bacterial lysis after a single freeze/thaw cycle. This single step lysis provides researchers with a fast, reproducible and simple procedure, resulting in high levels of protein expression.

Tag-Spin Protein Purification

The purification of His-tagged proteins is invaluable to the success of downstream applications such as enzymatic assays, protein biochemical analyses and SDS-PAGE. Zymo Research Corporation has produced the ‘His-Spin Protein Miniprep’, ‘MBP-Spin Protein Miniprep’, and ‘Strep-Spin Protein Miniprep’ to provide researchers with a fast and easy to follow procedure for purifying tagged proteins. This kit also allows bacterial colonies to be screened directly on the basis of protein expression vs. plasmid DNA.

Enzymes

Restriction enzymes are an extremely helpful tool in a number of research applications. From molecular cloning to epigenetics, Zymo Research provides a number of restriction enzymes that recognize different cut sites, including methylated and hydroxymethylated modifications of cytosine bases.