Powered by Bioz
How to Optimize Buffer Components for Nickel Agarose Beads
Nickel agarose beads are compatible with a wide range of buffers. However, it is important to limit the amount of metal chelating agents, such as...
Product Specifications
| Catalog ID: | G-211 |
|---|---|
| CAS #: | 50-01-1 |
| MW: | 95.53 g/mol |
| Storage/handling: | Store at room temperature. |
Technical Documentation
P
Protocol
O
Other
C
Certificate of Analysis
S
Safety Data Sheet
CITATIONS
Featured Articles
-
-
An Overview of Hydrophobic Interaction Chromatography
Have you ever felt as if all of your contributions in the lab go unseen and unappreciated? That if only someone would pay attention, they...
-
How Biotinylated Molecules are Purified with Streptavidin Beads
Streptavidin is a bacterial protein that binds to the small molecule biotin with extremely high affinity. This is one of the strongest noncovalent interactions ever...
-
How to Elute Biotinylated Proteins and Nucleic Acids from Streptavidin Beads
Eluting biotinylated proteins and DNA from streptavidin beads requires harsh conditions like enzymatic digestion, extreme pH, organic solvents, and heat with excess biotin. Deciding which...
-
Insoluble Protein Purification: How To Get Proteins Out of Inclusion Bodies?
Proteins are extracted from inclusion bodies using solubilizing salts like guanidine and reducing agents like TCEP. The extracted proteins are then purified and refolded. Functional...
-
Understanding Salting In and Salting Out: Salt as a Protein Purification Tool
Salting in is adding salt to a solution to enhance the solubility of a protein, whereas salting out is adding salt to precipitate a protein....
