Order Center
 
Fluka & Riedel Home

About Fluka and Riedel
Analytical Standards
Drug Discovery
Fluka and Riedel Quality
Analytical Reagents
Bioscience
Biostabilization
Electrophoresis
Fluorescent Probes
Microbiology
Microscopy
Peptide Analysis
Miscellaneous
CBind L-Matrices
Cross Linkers
Cross-linked Dextrans
Lipoprot. Refold. Buffer
Peptidoglycan
Renaturat. Kit for Prot.
Specialties
Fine Chemicals / Bulk
CustomWare / OEM
Literature
Contact Us
Feedback

Bioscience Miscellaneous


Lipoprotein Refolding Buffer (Refolding Buffer for Lipoproteins)


Email Page Link

A buffer specially formulated for the refolding of denatured lipoproteins. Lipoprotein samples are often denaturated after dialysis, lyophilising and refrigerating. This Lipoprotein Refolding Buffer is found to provide the best conditions for the renaturation of all types of lipoproteins.All substances used in the buffer are highly purified, mostly Fluka BioChemika Ultra, and ultra pure water. BioChemika Ultra chemicals have been used successfully for different refolding methods and other applications that are highly sensitive to impurities. The solution is filtered using 0.22 micron filters and is also available in bulk quantities on request.


Table 1: Product List

Catalog No.
Product Name
78658
Lipoprotein Refolding Buffer



Table 2: Composition

Ingredients
Concentration
NaCl150 mM
Tris-Cl30 mM
EDTA1 mM
DTE1 mM
e-Aminocaproic acid1.3 g/l
PMSF200 mM
Sodium azide0.5 g/l
pH7.4±0.2 at 25°C
RNAses, DNAses, Phosphatases and Proteasesnot detected



Directions

It is highly recommended to degas the buffer before every usage (even though the buffer was set under argon at Fluka) to avoid oxidation of the lipoproteins.Rehydrate the lyophilised lipoprotein for example (Fluka 73461 or 80917) at the desired concentration, or add at least one part of buffer to one part of liquid lipoprotein sample. Aerate with argon to protect the lipoproteins against oxidation, mix gently using a pipette, avoid bubbles. Aerate again with argon and incubate the sample for 5-10 minutes.
There should not be any precipitate or the sample is still denatured or oxidised. If a precipitate is present, wait an additional 10 minutes or/and add more buffer.The lipoprotein in the Refolding Buffer is stable for 1-2 days under argon and below 4°C.



Back to Top

Back to Bioscience Miscellaneous


Site Use Terms Terms and Conditions of Sale Privacy Business Development Contact Us
Copyrights © 2008 Sigma-Aldrich Co. All Rights Reserved.
Reproduction of any materials from the site is strictly forbidden without permission.
Sigma-Aldrich brand products are sold exclusively through Sigma-Aldrich, Inc.