Product Description: The capping enzyme is composed of two subunits: D1 and D12. Eukaryotic RNA must undergo a series of modifications in order to be exported from the nucleus and successfully translated into function proteins, the first mRNA modification is capping.[1][2] 5' capping is essential for mRNA stability, enhancing mRNA processing, mRNA export and translation.[2]
Sequence:
Accession #:
Quality control: Verified by Mass Spectrometry analysis.
Product Source: Both D1 and D12 were produced in E. coli cells transformed with capping. This product is sterile and does not contain any components of animal origin.
Usage: FOR LABORATORY RESEARCH USE ONLY.
References:
Watson J (April 8, 2014). Molecular Biology of the Gene. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press. pp. 429–455. ISBN 9780321762436.
Ghosh A, Lima CD (Jul–Aug 2010). "Enzymology of RNA cap synthesis". Wiley Interdisciplinary Reviews: RNA. 1 (1): 152–72. doi:10.1002/wrna.19. PMC 3962952. PMID 21956912.
Cat No.: | PT-RNA-VCE-CAP |
Product Name: | Capping Enzymes |
Type: | Protein |
Property: | |
Origin: | |
Source: | E.coli |
Application: | Research in mRNA vaccine development |
Formulation: | Sterile filtered through a 0.2 micron filter in 50% glycerol, 10 mM MES buffer at pH 6.5 |
Purity: | >95% by SDS-PAGE gel |
Storage: | Avoid repeated freeze-thaw cycles. 12 months at -20 C to -80 C. 1 month at 2 C to 8 C. |
Limitation: | |
Note: |