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Merck
CN

SAE0220

Mucinase SmE Protease

cleaves between two glycosylated residues bearing complex O-linked glycans and suitable for mass spec glycoproteomics

别名:

SmEnhancin

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关于此项目

NACRES:
NA.21
Recombinant:
expressed in E. coli
Shelf life:
2 yr (Retest)
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产品名称

Mucinase SmE, mass spec suitable, from Serratia marcescens, recombinant, liquid

recombinant

expressed in E. coli

Quality Level

form

liquid

shelf life

2 yr (Retest)

mol wt

98 kDa

suitability

suitable for mass spectrometry

shipped in

dry ice

storage temp.

-10 to -25°C

General description

Mucinase SmE is a mucin-selective protease that has been engineered to have high activity and and tolerance for site ocupancy and glycoform complexity. Mucinase SmE provides a complementary cleavage profile to Mucinase StcE (Cat No SAE0202). Contrary to StcE digestion that requires an additional tryptic digest prior to MS peptide analysis, when using Mucinase SmE analysis can be done with SmE alone. It is recommended to perform both options to obtain maximal coverage.

Application

Mucinase SmE is useful for glycoproteomics experimentation. It is designed for digestion of densely glycosylated mucin proteins for mass spec based analyses.

Features and Benefits

  • Mucin-selective Protease
  • Cleaves N-terminally to O-link glycosylated Ser/Thr in mucin domains
  • Complimentary cleavage profile to Mucinase StcE
  • Accommodates complex, dense and sialylated glycoforms
  • Recombinant with His-Tag®

Preparation Note

Thaw the Mucinase SmE by brief incubation at 37°C.

The protein solution is stable for 2 weeks at 2-8 °C.

For longer storage, aliquot the protein solution and store at -20 °C.

The enzyme solution should be protected from direct light.

Legal Information

HIS TAG is a registered trademark of Merck KGaA, Darmstadt, Germany


存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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商品

Pretreatment with Mucinase StcE increases glycopeptide identification from mucin samples, enhancing sample preparation efficiency for glycopeptide analysis.