Biotinylated SARS-CoV-2 (COVID-19) Nucleocapsid protein, His,Avitag™

Proteins and Peptides

貨號 Cat. No.
NUN-C81Q6
規格 Size
25ug
品牌 Brand
ACROBiosystems
Species
SARS-CoV-2
Conjugate
Precision Avi
Expression System
E. coli
Tag
Avi Tag 、 His Tag

Description




Source :


Biotinylated SARS-CoV-2 Nucleocapsid protein, His,Avitag (NUN-C81Q6) is expressed from E.coli cells. It contains AA Met 1 - Ala 419 (Accession # QHO62115.1).


 

Molecule : Nucleocapsid protein


 

Synonyms : Nucleocapsid protein,NP,Protein N,COVID-19


 

Format : Powder


 

Category : MABSol® Biotin Labeled Proteins


 

Accession : QHO62115.1


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 51.1 kDa


 

Characteristics :


This protein carries a polyhistidine tag at the N-terminus, followed by an Avi tag (Avitag™). The protein has a calculated MW of 51.1 kDa. The protein migrates as 52 kDa under reducing (R) condition (SDS-PAGE).


 

Endotoxin Level : Less than 1.0 EU per μg by the LAL method.


 

Buffer : 50 mM Tris, 150 mM NaCl, Arginine, pH7.5


 

Description :


Nucleocapsid protein is a most abundant protein of coronavirus. Nucleocapsid protein is a highly immunogenic phosphoprotein also implicated in viral genome replication and in modulating cell signaling pathways. While screening for ADP-ribosylated proteins during coronavirus (CoV) infection, we identified as the viral nucleocapsid (N) protein. Novel post-translation modification of the CoV N protein that may play a regulatory role for this important structural protein. The array of diverse functional activities accommodated in the hantaviral N protein goes far beyond to be a static structural protein and makes it an interesting target in the development of antiviral therapeutics. Because of the conservation of N protein sequence and its strong immunogenicity, the N protein of coronavirus is chosen as a diagnostic tool.


 

References :


(1) Reuter M, et al. Virus Genes. 2018. 54(1):5-16.
(2) Grunewald ME, et al. Virology. 2018. 517:62-68.
(3) Jeeva S, et al. PLoS One. 2017. 12(9):e0184935.





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