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                        货号 YXX04901 
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                        描述 Peptide -N-Glycosidase F, also known as PNGase F, is an amidase that cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins 
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                                生物活性 One unit is defined as the amount of enzyme required to remove > 95% of the carbohydrate from 10 μg of denatured RNase B in 1 hour at 37°C in a total reaction volume of 10 μl.
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                                表达系统 E. coli
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                                种属 Elizabethkingia miricola
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                                蛋白长度 PNGase F is cloned from Elizabethkingia miricola and expressed in E.coli.
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                                预测分子量 37.08 kDa
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                                性质 Recombinant
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                                靶标 PNGase F
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                                浓度 80,000 units/ml
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                                内毒素水平 Please contact with the lab for this information.
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                                纯度 >95% as determined by SDS-PAGE.
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                                应用 Removal of high mannose N-glycans from glycoproteins
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                                状态 Liquid
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                                保存溶液 20mM Tris-HCl, pH 7.5, 50mM NaCl, 5mM EDTA, 50% glycerol
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                                实验操作流程 Standard Operating Procedure Denaturing Reaction Conditions: 1. Combine 1-20 µg of glycoprotein, 1 µl of Glycoprotein Denaturing Buffer (10X) and H2O (if necessary) to make a 10 µl total reaction volume. 2. Denature glycoprotein by heating reaction at 100°C for 10 minutes. 3. Chill denatured glycoprotein on ice and centrifuge 10 seconds. 4. Make a total reaction volume of 20 µl by adding 2 µl GlycoBuffer 2 (10X), 2 µl 10% NP-40 and 6 µl H2O. 5. Add 1 µl PNGase F, mix gently. 6. Incubate reaction at 37°C for 1 hour. Note: The simplest method of assessing the extent of deglycosylation is by mobility shifts on SDS-PAGE gels. Note: To deglycosylate different glycoprotein, longer incubation time may be required. Non-Denaturing Reaction Conditions: 1.Combine 1-20 µg of glycoprotein, 2 µl of GlycoBuffer 2 (10X) and H2O (if necessary) to make a 20 µl total reaction volume.2.Add 2-5 µl PNGase F, mix gently. 3.Incubate reaction at 37°C for 4 - 24 hours. Note: To deglycosylate a native glycoprotein, longer incubation time as well as more enzyme may be required. Note: The simplest method of assessing the extent of deglycosylation is by mobility shifts on SDS-PAGE gels. 1X Glycoprotein Denaturing Buffer 
 0.5% SDS
 40 mM DTT
 
 1X NP-40
 1% NP-40 in MilliQ-H2O
 
 1X GlycoBuffer 2
 20 mM Tris,PH 7.5
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                                运输 In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
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                                稳定性和存储 Use a manual defrost freezer and avoid repeated freeze thaw cycles.Store at 2 to 8 °C for one week .Store at -20 to -80 °C for twelve months from the date of receipt.









 
                 
            