Published TCIMAIL newest issue No.201
Maximum quantity allowed is 999
CAS RN: | Numéro de produit: R0243
rEGCase II assisted by Activator II
Pureté:
- Recombinant Endoglycoceramidase II assisted by Activator II
- Recombinant - Rhodococcus sp. EGCase II expressed in Rhodococcus erythropolis
- Recombinant Endoglycoceramidase II with Activator II
*Stock disponible en Belgique : Expédition le jour même
*Stock disponible au Japon : Veuillez consulter la simulation d'expédition pour une estimation des délais d'expédition (hors articles réglementés et expédition avec Carboglace)
Informations supplémentaires sur le produit:
Product Information
- Quantity : 100 mU per vial (1 mU/μL) and 50 nmol Activator II per vial (0.5 nmol/μL)
- Product Form : Purified recombinant EGCase II and Activator II, Liquid
- Storage buffer : 20 mM sodium phosphate, 50 mM NaCl buffer, pH 7.0
- Preservative : None
- Stabilizer : None
Description
- Endoglycoceramidase II (EGCase II) is a glycolipid-specific hydrolase that cleaves the glycosidic linkage between oligosaccharide and ceramide of various glycosphingolipids (GSLs) under a detergent-containing condition. On the other hand, Activator II is capable of inducing activity of EGCase without any detergent reagents. This product is provided as a mixture-form of EGCase II and Activator II. By using this product, cell-surface glycosphingolipids of living cells are hydrolyzed without cell disruption caused by addition of detergent. The EGCase II gene is derived from Rhodococcus sp. and its recombinant protein is expressed in Rhodococcus erythropolis.
Unit Definition
- One unit (U) of EGCase II is defined as the amount required to hydrolyze 1 μmol of ganglioside GM1 per minute at 37°C under the condition of pH5.5.
Assay Conditions
- Reaction conditions: 50 mM sodium acetate, pH 5.5
The reaction mixture includes the enzyme and 100 nmol of GM1 in 50 μL (without detergent). The mixture is incubated at 37°C for 15 minutes. Quantification of reducing end of released oligosaccharides is measured by the modified Somogyi-Nelson method (see the following reference). - [Reference]
Determination of Glucose by a Modification of Somogyi-Nelson Method
C. Hatanaka, Y. Kobara, Agric. Biol. Chem. 1980, 44, 2943.
- Regarding hydrolysis of cellular GSLs, see the reference (Methods Mol. Biol.) below.
- [Reference]
Assays and Utilization of Enzymes Involved in Glycolipid Metabolism in Bacteria and Fungi
M. Ito, Y. Ishibashi, T. Watanabe, J. Iwaki, T. Kurita, N. Okino, Methods Mol. Biol. 2023, 2613, 229.
Storage
- Store at -20°C. Avoid repetitive freezing and thawing. After thawing the product, it’s recommended to store at 4°C and use it within a few weeks.
Related Products
- G0483 Ganglioside GM1
- P1775 TRITON™ X-100
- Other oligosaccharide-releasing enzymes
- [Endo-type glycoceramidase]
- R0240 rEGCase I
- R0241 rEGCase I assisted by Activator II
- R0242 rEGCase II
- [Endo-type N-glycanase (ENGase)]
- A1651 Endo-M (for hydrolysis of non core-fucosylated biantennary N-glycan)
- E1339 Endo-M-W251N (for hydrolysis of core-fucosylated biantennary N-glycan)
- G0365 Glycosynthase (for transglycosylation of non core-fucosylated biantennary N-glycan)
- [Endo-type O-glycanase]
- A1844 Endo-α (for hydrolysis of core1 O-glycan epitope known as T/TF antigen)
- G0622 O-Glycosidase for core1 (for hydrolysis of sialylated core1 O-glycan epitope)
- [Endo-type glycosaminoglycanase]
- K0069 Keratanase II (for hydrolysis of Keratan sulfate)
| Numéro de produit | R0243 |
| Etat physique (20 ° C) | Liquid |
Condition de stockage
|
Frozen (-20°C) |
| Condition à éviter | Heat Sensitive |
| Appearance | Colorless to Light yellow to Light orange clear liquid |
| Titer | min. 100 mU/Vial |
| N ° SH (import / export) (TCI-E) | 3507909090 |
References
- Purification and characterization of glycosphingolipid-specific endoglycosidases (endoglycoceramidases) from a mutant strain of Rhodococcus sp. Evidence for three molecular species of endoglycoceramidase with different specificities
- Preparation and characterization of EGCase I, applicable to the comprehensive analysis of GSLs, using a rhodococcal expression system
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