Endo S
$0.00 – $945.00
Buy recombinant Endo S for IgG Fc deglycosylation and antibody glycan analysis. High purity, MS-compatible, research grade enzyme.
| SKU | Options | Price | Quantity | ||
|---|---|---|---|---|---|
| ENDOS-100 | Endo S (Glycerol-free) (18,000 U) | $238.00 | |||
| ENDOS-200 | Endo S (Glycerol-free) (90,000 U) | $945.00 | |||
| ENDOS-OEM | Endo S (Glycerol-free) (Any Size) | Please inquire | |||
| ENDOS-100G | Endo S (10% Glycerol) (18,000 U) | $238.00 | |||
| ENDOS-200G | Endo S (10% Glycerol) (90,000 U) | $945.00 | |||
| ENDOS-OEMG | Endo S (10% Glycerol) (Any Size) | Please inquire |
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Description
Endo S
• Glycerol-free: Cat# ENDOS-100, ENDOS-200, ENDOS-OEM
• 10% glycerol: Cat# ENDOS-100G, ENDOS-200G, ENDOS-OEMG

From left to right: deglycosylated ThT + Endo S, deglycosylated ThT, deglycosylated ThT + biotinylated Endo S. SDS-PAGE shows Mw of deglycosylated ThT decreases slightly after incubation with Endo S or biotinylated Endo S confirming activity of Endo S and biotinylated Endo S.
Description:
IgG-Specific Endoglycosidase with His-tag.
Endo S is a highly specific endoglycosidase that selectively removes N-linked glycans from the chitobiose core of the heavy chain of native IgG. The enzyme hydrolyzes the β-1,4 linkage between the two N-acetylglucosamine residues within Fc N-glycans.
MCLAB’s Endo S is engineered with a His-tag, allowing rapid and efficient removal of the enzyme from deglycosylation reactions using Ni-NTA-based affinity matrices. The enzyme is supplied glycerol-free, making it well suited for HPLC, LC-MS, and other mass spectrometry-intensive workflows.
The enzyme with glycerol as protectant is also available.
Specificity
Endo S exhibits high specificity toward native IgG Fc N-glycans.
Substrate Requirements:
- Active on substrates with or without core α(1-6) fucosylation
- Active on substrates with or without bisecting N-acetylglucosamine
- Does not require a strict peptide sequence for activity
Not Active On:
- Triantennary N-glycans
- Tetraantennary N-glycans
- Highly sialylated complex glycans
Substrate format may include protein, peptide, asparagine-linked glycan, or free glycan.
Applications:
- IgG deglycosylation
- Biotherapeutic characterization
- Antibody structure-function studies
- Glycan sequencing
- Proteomics
- Recombinant glycoprotein analysis
- Expression system validation
Source:
Endo S is cloned from Streptococcus pyogenes and recombinantly expressed in E. coli as a fusion protein with a His-tag.
Recommended Reaction Conditions
Final Reaction Buffer (1X):
- 5 mM CaCl₂
- 50 mM sodium acetate
- pH 5.5 (25°C)
Incubate at 37°C.
Unit Definition (Standard Assay):
One unit is defined as the amount of enzyme required to remove >95% of carbohydrate from 5 μg of native mouse monoclonal IgG in 1 hour at 37°C in a 10 μL total reaction volume.
Unit Assay Conditions
5 μg IgG in 1X reaction buffer is incubated with serial dilutions of Endo S for 1 hour at 37°C. Reaction products are analyzed by SDS-PAGE.
Reagents Supplied with:
Each product configuration includes:
- Endo S enzyme (His-tagged)
- 10X Reaction Buffer
Enzyme Concentration: 200,000 units/mL
Storage Buffer for Endo S (Glycerol Free) Enzyme
20 mM Tris-HCl
50 mM NaCl
1 mM EDTA
pH 7.5 (25°C)
Storage Buffer for Endo S (10% Glycerol) Enzyme
20 mM Tris-HCl
50 mM NaCl
1 mM EDTA
pH 7.5 (25°C)
10% Glycerol
Molecular Weight
Apparent molecular weight: 136 kDa (His-tagged fusion protein)
Heat Inactivation
55°C for 10 minutes
Enzyme Removal
The His-tag enables affinity-based removal using Ni-NTA agarose beads.
* Binding capacity: 1 mg His-tagged protein per mL of Ni-NTA agarose beads
* Removal can be linearly scaled with reaction volume
This feature makes Endo S ideal for workflows requiring clean downstream MS or HPLC analysis.
Related Terms: Endo S2 enzyme, Endo-β-N-acetylglucosaminidase S2, IgG deglycosylation enzyme, Fc glycan removal enzyme, Antibody glycoengineering enzyme, Recombinant Endo S2 protein
Recommended Storage Condition: -20°C, avoid repeated free-thaw
Endo S vs. Endo S2
| ATTRIBUTE | Endo S | Endo S2 |
|---|---|---|
| Enzyme Type | IgG-specific endoglycosidase | Endo-β-N-acetylglucosaminidase S2 |
| Primary Substrate | Native IgG Fc N-glycans | IgG Fc N-glycans + α1-acid glycoprotein |
| Substrate Breadth | IgG-specific | Broader (IgG + non-IgG glycoproteins) |
| Cleavage Site | β-1,4 linkage in chitobiose core of heavy chain | β-1,4 linkage between GlcNAc residues in Fc N-glycans |
| His-Tag (Removable) | YES — Ni-NTA | YES — Ni-NTA |
| Specific Activity | Per unit: >95% removal from 5 μg IgG in 1 hr at 37°C | Stock ≥200,000 U/mL — 1 unit deglycosylates ≥95% of 1 μg IgG in 30 min at 37°C |
| Core Fucosylation Activity | Active (with or without) | Active |
| Bisecting GlcNAc Activity | Active (with or without) | Active |
| Glycerol-Free SKUs | ENDOS-100, ENDOS-200, ENDOS-OEM | ENDOS2-100, ENDOS2-200, ENDOS2-OEM |
| 10% Glycerol SKUs | ENDOS-100G, ENDOS-200G, ENDOS-OEMG | ENDOS2-100G, ENDOS2-200G, ENDOS2-OEMG |
| OEM Quantities | Available | Available |
| Expression Host | E. coli (recombinant) | E. coli (recombinant) |
| Cloned From | Streptococcus pyogenes | Streptococcus pyogenes |
| Storage | -20°C, avoid repeated freeze-thaw | -20°C, avoid repeated freeze-thaw |
| Best For | Standard IgG Fc glycan removal with clean enzyme removal post-reaction | Broader N-glycan analysis, LC-MS, HPLC, ADC synthesis, biotherapeutic characterization |
| Recommended When | Working with native IgG and need clean, removable enzyme | Need broader substrate coverage, HPLC/MS-ready workflow or glycerol-free format |
For Research Use Only
Additional information
| Options | Endo S (Glycerol-free) (18,000 U), Endo S (Glycerol-free) (90,000 U), Endo S (Glycerol-free) (Any Size), Endo S (10% Glycerol) (18,000 U), Endo S (10% Glycerol) (90,000 U), Endo S (10% Glycerol) (Any Size) |
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