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New Avantor® J.T.Baker® premium conductive and non-conductive robotic tips deliver superior quality and reliable performance for results you can trust.
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Protein purification systems are intended to isolate one or multiple proteins from a complex mixture. Working with cells, tissues, or whole organisms, the machines purify with predefined start points and editable method templates. With a single click, the compact designed equipment offers real-time run control and visualization. Suitable for even cold-room operations, the products enable you to perform purification of affinity-tagged proteins, antibodies, untagged or native proteins, as well as sample clean-up.
Description:
Alpha1-3,4,6 Galactosidase is a broad specificity exoglycosidase that catalyzes the hydrolysis of alf1-3, alf1-4 & alf1-6 linked D-galactopyranosyl residues from oligosaccharides, Cloned from green coffee bean & expressed in E. coli, Concentration: 8000U/ml, Size: 1000U
Description:
Α1-3, 4 Fucosidase, broad specificity exoglycosidase that catalyzes the hydrolysis of A1-3 and A1-4 linked fucose residues from oligosaccharides and glycoproteins, Reagents Supplied: GlycoBuffer 1, Purified BSA, Size: 200 units
Description:
EnGen Cas9 NLS, S. Pyogenes - 2,000 pmol RNA-guided endonuclease nuclease that catalyzes site- specific cleavage of double stranded DNA. Contains Simian virus 40 (SV40) T antigen nuclear localization sequence (NLS) on the N- and C- termini of the protein.
Description:
Alpha1-3,4,6 Galactosidase is broad specificity exoglycosidase that catalyzes the hydrolysis of alf1-3, alf1-4 & alf1-6 linked D-galactopyranosyl residues from oligosaccharides, Cloned from green coffee bean & expressed in E. coli, Concentration: 8000 U/ml, Size: 200 U
Description:
EnGen Cas9 NLS, S.Pyogenes - 400 pmol RNA-guided endonuclease nuclease that catalyzes site- specific cleavage of double stranded DNA. Contains Simian virus 40 (SV40) T antigen nuclear localization sequence (NLS) on the N- and C- termini of the protein.
Description:
MBP Fusion and Purification System, Reliable E. Coli expression: substantial yields (up to 100 mg/L), Fusion to MBP has been shown to enhance the solubility of proteins expressed in E. Coli, Gentle elution with maltose, harsh denaturants required, 1 set
Description:
Protein Deglycosylation Mix II, most effective enzymatic method for removing almost all N-linked oligosaccharides from glycoproteins. Digestion deaminates the aspargine residue to aspartic acid, and leaves the oligosaccharide intact, Size: 20 reactions