The product is not tested for endotoxin; however, P1411 may be used to strip endotoxin. The P1411 datasheet includes a suggested protocol for this process. The protocol involves washing the resin, equilibrating the column, dissolving the sample in buffer, eluting with endotoxin-free buffer, and collecting the fractions. The collected fractions containing the protein should then be lyophilized. The polymyxin B agarose can be regenerated at least 10 times, and the resin can be stored in 25% ethanol at 4°C
P1411
Polymyxin B-Agarose
aqueous glycerol suspension
Synonym(s):
PMB
About This Item
Recommended Products
biological source
synthetic (organic)
Quality Level
form
aqueous glycerol suspension
extent of labeling
~1 mg per mL
technique(s)
affinity chromatography: suitable
matrix
Cross-linked 4% beaded agarose
matrix activation
cyanogen bromide
matrix attachment
amino
matrix spacer
1 atom
capacity
200-500 μg/mL binding capacity (lipopolysaccharide)(from Escherichia coli serotype 0128:B12)
suitability
suitable for chromatography
storage temp.
2-8°C
Application
Physical form
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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What methods can be used to remove endotoxin from a product?
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What polypropylene column should the we use according to the protocol to wash the resin prior to use?
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For washing the resin prior to use, the customer can use the following options:
1. C2603 Mini-Columns: These have a capacity of 0.5 mL and an overall height of 1.9 inches.
2. C2728 Mini-Columns: These have a capacity of 2.4 mL and an overall height of 1.5 inches.
The washing procedure using Polymyxin B Agarose (Product No. P1411) can be carried out in a column or in a batch method. For a column, the customer can use disposable mini columns, such as Product Nos. C2603 (0.5 ml) and C2728 (5.0 ml). If a larger column is needed, the customer can use a polypropylene syringe barrel or use the batch method.
In the batch method, the solution is incubated with the polymyxin B agarose for a minimum of 30 minutes with rotation in either a 15 ml or 50 ml polypropylene tube. The tube is then centrifuged, and the supernatant contains the protein of interest with decreased endotoxin that has been bound to the beads and pelleted in the tube.
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