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Lysozyme Enzyme For Removal Of The Cell Wall Of Gram Positive Bacteria N9021 In Vitro Diagnostic Products
Product Details:
| Place of Origin: | China |
| Brand Name: | GDSBio |
| Certification: | / |
| Model Number: | N9021 |
Payment & Shipping Terms:
| Minimum Order Quantity: | 1 bag |
|---|---|
| Packaging Details: | small package or bulk distribute or OEM |
| Delivery Time: | 8work days |
| Payment Terms: | L/C, D/A, D/P, T/T, Western Union, MoneyGram |
| Supply Ability: | 100 Bag/Bags Per Day |
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Detail Information |
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| Cat. No.: | N9021 | Size: | 1 Ml×5 |
|---|---|---|---|
| Concentration: | 50mg/ml | Appearance: | Colourless Solution |
| Group: | In Vitro Diagnostic Products | Recommend Use Concentration: | 10-20 Mg/ml |
| Logo Printing: | With Logo Printing | Transport Package: | Packing |
| Production Capacity: | 100 Bag/Bags Per Day | Storage Conditions: | Store At -20°C |
| High Light: | 1 ml In Vitro Diagnostic Products,GDSBio In Vitro Diagnostic Products,Lysozyme Enzyme |
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Product Description
Lysozyme
Cat No. N9021 Conc: 50mg/ml
Contents: Lysozyme, 1 ml×5
Recommend use concentration: 10-20 mg/ml
Components
| Component | N9021 |
| Lysozyme | 1 ml×5 |
Store at -20°C
For research use only
Description
Lysozyme is an enzyme used to break down bacterial cell walls to improve protein or nucleic acid extraction efficiency. Lysozyme is a glycoside hydrolase that catalyzes the hydrolysis of 1,4-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in peptidoglycan, which is the major component of gram-positive bacterial cell wall. This hydrolysis in turn compromises the integrity of bacterial cell walls causing lysis of the bacteria. Molecular weight 14.4 kDa.
Applications
•Removal of the cell wall of Gram-positive bacteria
Biochem/physiol Functions
Catalyzes the hydrolysis of 1,4-β-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in peptidoglycans and between N-acetyl-D-glucosamine residues in chitodextrins.
Definition of Activity Unit
1 unit is that amount of enzyme needed to reduce the absorption value of the enzyme solution by 0.001 per minute. The reaction substrate is a 0.2 mg/ml micro-wall lysozyme suspension prepared by phosphoric acid buffer solution (0.05 M, PH 6.1).
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