Endoglycosidase S2 with Polyhistidine Tag, 50 U/uL (1000 U / 5 x 1000 U)
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Endoglycosidase S2 with Polyhistidine Tag, 50 U/uL (1000 U / 5 x 1000 U)

Cat.No: IVDRM-0302 Datasheet

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Product Name Endoglycosidase S2 with Polyhistidine Tag, 50 U/uL (1000 U / 5 x 1000 U)
Catalog No. IVDRM-0302
Description Endoglycosidase S2 targets a very specific bond: the one between the two innermost N-acetylglucosamine residues of the N-glycan carried by immunoglobulin G. That selectivity is useful because antibody Fc glycosylation is the attribute most often under scrutiny, and S2 handles high-mannose, hybrid and biantennary complex structures with equal efficiency. This preparation is expressed in Escherichia coli, is more than 95% pure by SDS-PAGE, and is specified free of exoglycosidase contamination and free of any proteolytic activity, so the observed change comes only from the intended cleavage. A polyhistidine tag is included so the enzyme can be taken out of the reaction afterwards.
Intended Use Removal of Fc N-glycans from immunoglobulin G subclasses during antibody glycan analysis and glyco-engineering work.
Principle / Technology The endoglycosidase cleaves the glycosidic bond linking the two core N-acetylglucosamine residues, leaving a single GlcNAc optionally bearing fucose on the protein.
Detection Method Released glycan and trimmed antibody are analysed by chromatography, electrophoresis or mass spectrometry.
Sample Type Purified immunoglobulin G from mouse and other species, and Fc-bearing constructs.
Performance Range / Specifications Highly specific for IgG N-glycans; hydrolyses high-mannose, hybrid and biantennary complex structures efficiently; no detectable exoglycosidase contamination; no proteolytic activity; His-tagged for removal.
Specificity Specific activity 50 U/uL; purity above 95% by SDS-PAGE; supplied as 1000 U or 5 x 1000 U with a 10x reaction buffer.
Reaction Conditions / Protocol Mix the antibody with the 10x buffer, add the enzyme, incubate at 37 °C, then remove the histidine-tagged enzyme on nickel resin or proceed directly to analysis.
Components / Formulation Enzyme solution and 10x reaction buffer.
Storage Conditions Store at -25 to -15 °C.
Shelf Life 1 year from receipt when stored as recommended.
Package Specifications Supplied as 1000 U or 5 x 1000 U with matching buffer volumes.
Product Form Clear liquid enzyme with separate concentrated buffer.
Quality Control Released above 95% purity by SDS-PAGE with unit definition verified against native mouse IgG and no detectable exoglycosidase or proteolytic activity.
Key Features - Cleaves specifically between the two core GlcNAc residues of IgG glycans
- Efficient across high-mannose, hybrid and biantennary complex structures
- No detectable exoglycosidase contamination or proteolytic activity
- Above 95% pure by SDS-PAGE
- Polyhistidine tag allows easy removal after digestion
Purity Above 95% by SDS-PAGE.
Concentration 50 U/uL.
Activity / Unit Definition One unit removes more than 95% of carbohydrate from 5 ug of native mouse immunoglobulin G within one hour at 37 °C in a 10 uL reaction.
Molecular Weight Not restated on the source page beyond the purity figure.
Source / Origin Gene from Streptococcus pyogenes, expressed recombinantly in Escherichia coli with a polyhistidine tag.
pH Range / Optimal pH Storage buffer is 20 mM Tris with 100 mM sodium chloride at pH 7.5.
Shipping Conditions Shipped cold.
Expiration Date / Stability Remains usable for the full shelf life provided the temperature recommendation is followed.
Regulatory / Compliance For research use only.
Compatibility Suitable for Fc glycan analysis across high-mannose, hybrid and biantennary complex structures.
Recommended Buffer System 20 mM Tris, 100 mM sodium chloride at pH 7.5 supplied with a 10x reaction concentrate.
Application Notes / Precautions Verify that no exoglycosidase-driven trimming is being read as endoglycosidase activity, and remember the product targets Fc-linked glycans rather than unrelated glycosylation.
Batch-to-Batch Consistency Lot-to-lot consistency is maintained through defined manufacturing specifications; every lot ships with its release record.
Model Type IgG-specific glycan cleavage enzyme
Starting Material / Tissue Site Recombinant endoglycosidase from Escherichia coli with a polyhistidine tag
Delivery Standard Enzyme vial plus 10x buffer vial
Turnaround Time dispatch is arranged at order confirmation.
Readouts / Downstream Assays Mass change of the heavy chain and identity of the residual single GlcNAc.

For in vitro diagnostic use.

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