SARS-CoV-2 N Protein Mouse Monoclonal Antibody [Clone ID: OTI1C8]
CAT#: CF814444
Carrier-free (BSA/glycerol-free) SARS-Cov-2 N protein mouse monoclonal antibody, clone OTI1C8
Formulation: Standard
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CNY 3,999.00
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Specifications
Product Data | |
Clone Name | OTI1C8 |
Applications | ELISA |
Recommend Dilution | ELISA 1:5000-10000 |
Reactivity | SARS-CoV-2 |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Full length recombinant SARS-Cov-2 N protein produced in E.coli. |
Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Predicted Protein Size | 47kDa |
Database Link | |
Background | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an enveloped, positive-sense, single-stranded RNA virus that causes coronavirus disease 2019 (COVID-19). Virus particles include the RNA genetic material and structural proteins needed for invasion of host cells. Once inside the cell the infecting RNA is used to encode structural proteins that make up virus particles, nonstructural proteins that direct virus assembly, transcription, replication and host control and accessory proteins whose function has not been determined.~ The structural proteins of SARS-CoV-2 include the envelope protein (E), spike or surface glycoprotein (S), membrane protein (M) and the nucleocapsid protein (N). The nucleocapsid phosphoprotein is a structural protein that binds to, protects the viral RNA genome and is involved in packaging the RNA into virus particles. The N protein has been suggested as an antiviral drug target. |
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