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Recombinant PNGase F

规格或纯度: Specific Activity >25 U/mg;Activity 5 U/ml
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库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
R488845-20μl 20μl 期货 Stock Image
R488845-60μl 60μl 期货 Stock Image

基本描述

规格或纯度 Specific Activity >25 U/mg;Activity 5 U/ml
英文名称 Recombinant PNGase F
英文别名 Peptide-N4-(acetyl-?-glucosaminyl)-asparagine amidase, N-Glycosidase F
来源 recombinant gene from Elizabethkingia miricola in E. Coli
储存温度 2-8°C储存
运输条件 冰袋运输
产品介绍


Product Description

Recombinant PNGase F is isolated from a E. coli strain containing a clone of the Elizabethkingia miricola gene. There is no detectable difference in activity or specific activity of the recombinant enzyme from the native enzyme.


PNGase F cleaves asparagine-linked (N-linked) oligosaccharides from glycoproteins. PNGase F deaminates asparagine to aspartic acid, leaving the oligosaccharides intact. Denaturation increases the rate of cleavage up to 100x. Most native proteins can still be completely N-deglycosylated but incubation time must be increased. PNGase F will remain active under incubation conditions for at least 72 hours. PNGase F will not remove oligosaccharides containing Alpha-(1,3)-linked core fucose commonly found on plant glycoproteins; for this purpose, use peptide N-glycosidase A.


Contents

60 μl aliquot of recombinant PNGase F (0.3 U) in 20 mM Tris-HCl, pH 7.5
Included with 20 μL and 60 μL pack sizes
5x PNGase F Reaction Buffer 7.5 for PNGase F – 250 mM sodium phosphate, pH 7.5
PNGase F Denaturation Solution – 2% SDS, 1 M Beta-mercaptoethanol
PNGase F Triton X-100 – 15% solution


Formulation

The enzyme is provided as a sterile-filtered solution in 20 mM Tris-HCl (pH 7.5).


Molecular Weigh

approximately 35 kD.


pH optimum

7.5, active over the range 6-10.


Specific Activity

Specific Activity Defined as the amount of enzyme required to catalyze the release of N-linked oligosaccharides from 1 micromole of RNase B in 1 minute at 37?C, pH 7.5. Cleavage is monitored by SDS-PAGE (cleaved RNase B migrates faster).


Specificity

PNGase F cleaves asparagine-linked (N-linked) oligosaccharides from glycoproteins. PNGase F deaminates asparagine to aspartic acid, leaving the oligosaccharides intact. Denaturation increases the rate of cleavage up to 100x. Most native proteins can still be completely N-deglycosylated but incubation time must be increased. PNGase F will remain active under incubation conditions for at least 72 hours. PNGase F will not remove oligosaccharides containing Alpha-(1,3)-linked core fucose commonly found on plant glycoproteins; for this purpose, use peptide N-glycosidase A.?


Stability

Several days exposure to ambient temperatures will not reduce activity. Stable at least 12 months when stored properly.?


Quality & Purity

PNGase F is tested for contaminating protease as follows: 10 μg of denatured BSA is incubated at 37°C for 24 hours with 2 μl of enzyme. SDS-PAGE analysis of the treated BSA shows no evidence of degradation. The production host strain has been extensively tested and does not produce any detectable glycosidases.


PNGase F Suggested usage

1. Add up to 200 μg of glycoprotein to an Eppendorf tube. Adjust to 35 μl final volume with de-ionized water.

2. Add 10 μl 5x PNGase F Reaction Buffer 7.5 and 2.5 μl of PNGase F Denaturation Solution. Heat at 100?C for 5 minutes.

3. Cool. Add 2.5 μl of PNGase F Triton X-100 and mix.

4. Add 2.0 μl of PNGase F to the reaction. Incubate 3 hours at 37?C.

If SDS or heat denaturation is omitted, increase incubation time to at least 24 hours. Monitor cleavage by SDS-PAGE.

名称和标识符

酶学委员会编号 3.5.1.52

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