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XP Up Screen

Kit including Crystallization Screen for high TEW concentrations and separate TEW

Cat. No. Amount Price (EUR) Buy / Note
CS-351 1 Kit 756,20 Add to Basket/Quote Add to Notepad

 

For general laboratory use.

Shipping: shipped at ambient temperature

Storage Conditions: store at 8-10 °C

Shelf Life: 12 months

Description:
The additive Anderson-Evans polyoxotungstate (TEW) [TeW6O24]6− has been shown to promote crystal contacts, improve crystal quality, and provide a valuable anomalous signal for phase determination due to its 6 tungsten atoms. It has successfully induced protein crystallization even at low concentrations of 1 mM. However, our own experiments have shown that a higher concentration of 5 or 10 mM TEW can significantly increase crystallizability even further.
The XP Up Screen offers 96 of the most common crystallization conditions that have been proven to be successfully improved with up to 10 mM TEW. To offer complete flexibility in terms of final concentration, TEW is provided in an additional tube and only needs to be added to the protein drop. The solutions are stable in the long term in the presence of up to 10 mM TEW, thus enabling maximum flexibility without compromise.

Content:

  • 96 screening solutions x 1.7 ml each, optimized for high TEW concentrations, Cat.-No. CS-350
  • 20 mg TEW [TeW6O24]6−, dissolve in 93 μl water to achieve a 100 mM stock solution, Cat.-No. X-TEW-20

The exact composition of each buffer is listed under the links “Screen Formulation”.
All solutions are sterile filtered (0.2 μm), filled under sterile conditions and contain 0.1% ProClinTM 950 as preservative to prevent the growth of microbes. (ProClin is a trademark of LANXESS Corp.)

Related products:

BIOZ Product Citations:

Selected References:
[1] Bijelic et al. (2017) Ten Good Reasons for the Use of the Tellurium-Centered Anderson-Evans Polyoxotungstate in Protein Crystallography. Acc. Chem. Res. 50:1441.
[2] Sobala et al. (2020) Structure of human endo-α-1,2-mannosidase (MANEA), an antiviral host-glycosylation target. PNAS 117 (47):29595.
[3] Ames et al. (2020) Identifying a Molecular Mechanism That Imparts Species-Specific Toxicity to YoeB Toxins. Front Microbiol 11:959.