Il s'agit d'un magasin de démonstration. Aucune commande ne sera honorée.

Introduction: “Suitable for Mass Spectrometry”

Suitable for Mass Spectrometry” (also referred to as MS-grade ) refers to reagents—especially enzymes and chemicals—that meet strict purity and performance criteria for mass spectrometry (MS)-based applications. These reagents are optimized to ensure minimal background noisehigh digestion efficiency, and compatibility with downstream LC-MS/MS workflows.


Key Characteristics

1. High Purity and Low Contaminants

· Free from keratinautolysis fragmentsnucleasesproteasessalts, or other interfering substances.

· Avoidance of reagents that produce signal suppression or non-specific signals in MS analysis.

2. Consistent Performance

· Validated for reproducible enzymatic activity and cleavage specificity.

· Batch-to-batch consistency is critical for quantitative proteomics and sequencing.

3. Stability and Formulation

· Supplied in stabilized lyophilized forms or glycerol-free liquid to be compatible with LC-MS workflows.

· Formulated without additives (e.g., Tris, EDTA, glycerol) that interfere with MS detection.


Common MS-Grade Proteases

Enzyme

Cleavage Specificity

Applications

Trypsin (MS-grade)

After K or R (unless followed by P)

Standard in bottom-up proteomics

Lys-C (Lysine protease)

After K only

Useful for intact or partial digestion

Glu-C (Glutamic acid protease)

After E (sometimes D)

Antibody sequencing, PTM mapping

Asp-N

Before D

N-terminal sequencing

Chymotrypsin

After aromatic residues (F, W, Y)

Complementary to trypsin for full coverage

These enzymes are often referred to collectively as “MS-Grade Proteasesin Chinese when talking about their application in MS workflows.


Typical Applications

1. Proteomics

· Comprehensive analysis of protein expression, modifications, and interactions.

· Label-free or label-based quantification (e.g., TMT, iTRAQ).

2. Protein and Antibody Sequencing

· High-resolution mapping of peptides for de novo or database-driven sequencing.

· Fragmentation mapping of monoclonal antibodies (mAbs).

3. Biopharmaceutical Characterization

· Analysis of biosimilarstherapeutic antibodies, or ADC conjugation sites.

· Post-translational modification (PTM) analysis (e.g., glycosylation, phosphorylation).

4. Biomarker Discovery

· Detecting low-abundance biomarkers in clinical or research settings.


Summary Table ( Chinese version )

project

content

Chinese name

Mass spectrometry grade (suitable for mass spectrometry analysis)

English name

Suitable for Mass Spectrometry / MS-Grade

Features

High purity, low background, elimination of inhibitors, batch consistency

Commonly used enzymes

Trypsin (trypsin), Lys-C (lysyltrypsin), Glu-C (glutamyltrypsin)

Application Areas

Proteomics, antibody sequence analysis, PTM analysis, biopharmaceutical characterization


Selection Tips

· Check vendor certification: Look for terms like "MS-grade," "mass spectrometry validated," or "sequencing-grade."

· Review digestion performance: Validate enzyme efficiency with known proteins before scaling.

· Avoid stabilizers unless clearly MS-compatible.


Sample LC-MS Workflow with Enzymatic Digestion and Cleanup

This is a practical step-by-step protocol for preparing proteins for LC-MS/MS analysis using MS-grade proteases like Trypsin, Lys-C, or Glu-C.


1. Sample Preparation

Step

Description

A. Denaturation

Use 6–8 M Urea or 2–4% SDS to unfold proteins.

B. Reduction

Add 5–10 mM DTT or TCEP, incubate at 37°C for 30–60 min to break disulfide bonds.

C. Alkylation

Add 10–20 mM IAA or CAA, incubate in the dark at room temperature for 20–30 min to prevent reformation.

D. Buffer Exchange

Dilute or desalt to reduce denaturant concentration to <1 M before digestion.


2. Enzymatic Digestion

Parameter

Typical Settings

Enzyme

Trypsin, Lys-C, Glu-C (MS-grade, sequencing-grade)

Enzyme:Protein Ratio

1:20 to 1:100 (w/w)

Buffer

50 mM Ammonium Bicarbonate or Tris-HCl (MS-compatible)

Time/Temp

37°C for 4–16 hours

Optional

Dual digestion: e.g., Lys-C (2 hr) then Trypsin overnight


3. Peptide Cleanup

To remove salts, detergents, or inhibitors before LC-MS:

Method Options:

· C18 Reverse-Phase SPE (Solid Phase Extraction) – e.g., Sep-Pak or OMIX tips

· StageTips – home-packed tips with C18 for small samples

· Magnetic Bead Cleanup – e.g., SP3 method (paramagnetic beads)

Ensure final elution is in LC-MS compatible solvents (e.g., 0.1% FA in water or ACN).


4. LC-MS/MS Analysis

Component

Setup

LC

NanoLC with reverse-phase C18 column (e.g., 75 μm × 15 cm)

Gradient

5%–35% ACN over 60–120 min

MS

Orbitrap, TOF, or Q-Exactive platforms

Scan Mode

DDA (Data-Dependent Acquisition) or DIA (Data-Independent)

Output

.RAW or .mzML files for database search or de novo analysis


View all Suitable for Mass Spectrometry products

Categories: Specifications, Grading and Purity

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.