Endoglycosidase H (Endo H), 25000 U (for Sugar science related tools enzymes)

Product Information

Product Introduction

Endoglycosidase H is abbreviated as Endo H. It is derived from endoglycosidase H of Streptomyces plicatus and is recombinantly expressed by Escherichia coli. It can specifically cut high-mannose structures and certain hybrid glycoproteins connected by β-1,4-glycosidic bonds to form a glycoprotein structure with an N-acetylglucosamine. The cut protein still has biological activity and does not affect its subsequent research such as function. It is mainly used to remove N-glycosylation of proteins.

Source: Derived from Streptomyces plicatus , recombinantly expressed in E. coli;

Enzyme activity definition: The amount of enzyme required to remove more than 95% of carbohydrates from 10 μg of denatured RNase B at 37°C in 1 h is defined as one unit of enzyme activity;

Purity and concentration: Purity detected by SDS-PAGE>95%; residual endogenous nucleic acid <1 pg/μL (qPCR detection); 500 U/μL;

Inactivation or inhibition: Heating at 75°C for 10 min will inactivate;

Enzyme storage buffer: 20 mM Tris-HCl, 50 mM NaCl, 5 mM EDTA, 50% Glycerol, pH 7.5;

10х Denaturing Buffer: 5% SDS, 400 mM DTT;

10х Native Buffer: 400 mM sodium acetate, pH 6.0;

Figure 1. Deglycosylation effect of substrate RNase B treated with Endo H. After denaturation treatment of substrate RNase B, 10 μg of the substrate was added with different amounts of Endo H (0, 10, 1, 0.5, 0.1 U), incubated at 37 for 1 h, and then all were detected by PAGE electrophoresis.

Storage and transportation

Transported with wet ice; stored at -20, valid for 12 months.

composition

Procedure

1.  Protein deglycosylation under denaturing conditions:

_{Add 1 μL 10х Denaturing Buffer and dH 2} O to 10 μL reaction system in 1-20 μg protein sample , and incubate the system at 100°C for 10 min. Then add 2 μL 10х Native Buffer, 1-5 μL Endo H and appropriate amount of dH ₂ O to 20 μL reaction system, and incubate at 37°C for 1 h.

2.  Protein deglycosylation under non-denaturing conditions:

Add 2 μL 10х Native Buffer, 2-5 μL Endo H and appropriate amount of dH ₂ O to 1-20 μg protein sample to 20 μL reaction system and incubate at 37 for 4-24 h. (Protein deglycosylation under non-denaturing conditions requires longer reaction time or more enzyme)

Precautions

1. SDS does not affect the activity of enzymes.

2. The easiest way to assess the extent of protein deglycosylation is by SDS-PAGE gel electrophoresis.

3. The enzyme should be placed in an ice box and stored at -20 immediately after use.

4. For your safety and health, please wear a lab coat and disposable gloves when operating.

The product is for scientific research purposes only and not for clinical diagnosis!

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