Protein Tools
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- What is Ph.D.™ Phage Display?
- What products has NEB developed from ongoing basic research in molecular parasitology?
- Which residues does Endoproteinase AspN cut?
- Are there any amino acid residues that inhibit or reduce the efficiency of digestion of glutamate residues in a peptide sequence with Endoproteinase GluC? The site I want to digest has a glutamate residue followed by a proline residue and some enzymes are inhibited by the presence of a proline after the hydrolysis site.
- How does one do a Trypsin in-gel digest?
- I can’t get Endoproteinase AspN to digest my protein.
- I have a very low concentration of protein and would prefer not to denature as a separate step with buffer exchange before digestion. What denaturants can he use in the Trypsin reaction itself?
- What peptide libraries are available for use with Ph.D.™ Phage Display?
- What is the Proteinase K activity in commonly used buffers?
- Labeling of Escherichia coli Expressed SNAP-tag® Fusion Proteins
- Ph.D.™ Peptide Display Cloning System
- Simultaneous Fluorescent Labeling of Proteins in Living Cells
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT™ Kit
- Comprehensive structural and positional profiling of intact complex O-glycans in biologic drugs using O-Glycoprotease (IMPa)
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Combating Neglected Diseases - a genomic approach to identify potential drug targets
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Parasitic Infections in Humans
Understand the common types of parasitic infections in humans and why they are still increasing in tropical regions.
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Applications of the Ph.D. Phage Display Peptide Libraries
- Glycoproteomics Brochure
- Glycoproteomics Technical Guide
- Glycosylation Poster
- Purification Beads, Columns and Resins Brochure
- A monoclonal antibody for transcriptome-wide N6-methyladenosine analysis (2017)
Feature Articles
Brochures
Posters
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This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.