Ts beads
Ts beads can immobilize His-Tag-introduced proteins site-selectively, which is advantageous for elucidating protein-protein interactions.
Magnetic beads
The lineup of this product is only regular FG beads.
| Beads | FG beads |
|---|---|
| Code | TAS8848N1150 |
| Price | Please contact us |
| Storage conditions | 2-8 ℃ (no freezing) |
| Storage buffer | 1 mM HCl |
| Magnetization | Superparamagnetism (≧10 emu/g) |
| Size of beads | 180±30 nm |
| Concentration | 20 mg/ml |
| Functional groups | Tosyl group |
- Protocol
- SDS
- Papers /
Technical Information - Related Products
- FAQ
Technical Information
Papers
-
Disruption of TBP-2 ameliorates insulin sensitivity and secretion without affecting obesity
Nat. Commun., 1:127 (2010). -
The enteropathogenic E. coli effector EspB facilitates microvillus effeacing and anitiphagocytosis by inhibiting myosin function
Cell Host & Microbe, 2, 383 (2007). -
Preparation of dimerized polypeptide-carrying microspheres and purification of specific proteins bound to these microspheres
Coll. Surf. B., 10, 41 (1997).
- Please tell me how to separate FG beads (magnetic separation and centrifugation).
- Please tell me how to disperse FG beads (ultrasonic method and manual method).
- I mistakenly frozen some beads that were supposed to be stored in the refrigerator. Is it available?
- What is the optimal bead type for binding proteins?
- When binding proteins, what should be done if there is lysine residue at a location related to binding with the target substance?
- What is the efficiency when binding proteins?
- How is the cell extract prepared?
- Is there any problem with using frozen stock homogenate?
- How much protein supply is necessary?
- There are many background bands. how can i reduce it?
- What should be done when a large number of bound protein bands are detected?
- Is it necessary to use the recommended buffer as the binding buffer?
- Why is it that both salt elution and boil elution are performed for elution?
- Does it happen that the band of bound protein becomes thin when the concentration of ligand is increased?
- Why can’t I see any bands of bound proteins?
- How long is the stable period of the ligand-immobilized beads?
- I want to analyze bound proteins with MS, but what should I do if the target protein band is thin?
- How much protein can be analyzed by MS?
