Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Development of SARS-CoV-2 Nucleocapsid Specific Monoclonal Antibodies
by
Schountz, Tony
, Terry, James S
, Scherman, Michael S
, Mcalister, Carley E
, Anderson, Loran Br
, Perera, Rushika
, Geiss, Brian J
in
Coronaviruses
/ COVID-19
/ Enzyme-linked immunosorbent assay
/ Epitope mapping
/ Immunofluorescence
/ Light chains
/ Microbiology
/ Monoclonal antibodies
/ Nucleocapsids
/ Pandemics
/ Proteins
/ Severe acute respiratory syndrome coronavirus 2
2020
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Development of SARS-CoV-2 Nucleocapsid Specific Monoclonal Antibodies
by
Schountz, Tony
, Terry, James S
, Scherman, Michael S
, Mcalister, Carley E
, Anderson, Loran Br
, Perera, Rushika
, Geiss, Brian J
in
Coronaviruses
/ COVID-19
/ Enzyme-linked immunosorbent assay
/ Epitope mapping
/ Immunofluorescence
/ Light chains
/ Microbiology
/ Monoclonal antibodies
/ Nucleocapsids
/ Pandemics
/ Proteins
/ Severe acute respiratory syndrome coronavirus 2
2020
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Development of SARS-CoV-2 Nucleocapsid Specific Monoclonal Antibodies
by
Schountz, Tony
, Terry, James S
, Scherman, Michael S
, Mcalister, Carley E
, Anderson, Loran Br
, Perera, Rushika
, Geiss, Brian J
in
Coronaviruses
/ COVID-19
/ Enzyme-linked immunosorbent assay
/ Epitope mapping
/ Immunofluorescence
/ Light chains
/ Microbiology
/ Monoclonal antibodies
/ Nucleocapsids
/ Pandemics
/ Proteins
/ Severe acute respiratory syndrome coronavirus 2
2020
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Development of SARS-CoV-2 Nucleocapsid Specific Monoclonal Antibodies
Paper
Development of SARS-CoV-2 Nucleocapsid Specific Monoclonal Antibodies
2020
Request Book From Autostore
and Choose the Collection Method
Overview
Abstract The global COVID-19 pandemic has caused massive disruptions in every society around the world. To help fight COVID-19, new molecular tools specifically targeting critical components of the causative agent of COVID-19, SARS-Coronavirus-2 (SARS-CoV-2), are desperately needed. The SARS-CoV-2 nucleocapsid protein is a major component of the viral replication processes, integral to viral particle assembly, and is a major diagnostic marker for infection and immune protection. Currently available antibody reagents targeting the nucleocapsid protein were primarily developed against the related SARS-CoV virus and are not specific to SARS-CoV-2 nucleocapsid protein. Therefore, in this work we developed and characterized a series of new mouse monoclonal antibodies against the SARS-CoV-2 nucleocapsid protein. The anti-nucleocapsid monoclonal antibodies were tested in ELISA, western blot, and immunofluorescence analyses. The variable regions from the heavy and light chains from five select clones were cloned and sequenced, and preliminary epitope mapping of the sequenced clones was performed. Overall, the new antibody reagents described here will be of significant value in the fight against COVID-19. Competing Interest Statement The authors have declared no competing interest.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
This website uses cookies to ensure you get the best experience on our website.