Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System

Malaria rapid diagnostic tests (RDTs) act as important antibody-based immunoassays for prompt malaria diagnosis. Conventional monoclonal antibodies (mAbs) are widely used in RDTs but it can be easily degraded at high ambient temperatures. Hence, the shark VNARS might be good alternatives to mAbs...

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Main Author: Kok, Boon Hui
Format: Monograph
Language:English
Published: Pusat Pengajian Teknologi Industri 2020
Subjects:
Online Access:http://eprints.usm.my/46854/1/PRODUCTION%20OF%20NOVEL%20RECOMBINANT%20ANTIPFHRP%20%28ABSTRACT%29.pdf
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author Kok, Boon Hui
author_facet Kok, Boon Hui
author_sort Kok, Boon Hui
collection USM
description Malaria rapid diagnostic tests (RDTs) act as important antibody-based immunoassays for prompt malaria diagnosis. Conventional monoclonal antibodies (mAbs) are widely used in RDTs but it can be easily degraded at high ambient temperatures. Hence, the shark VNARS might be good alternatives to mAbs due to its higher thermal stability and binding affinity with antigens. In this study, the recombinant antiPfHRP2 VNAR-G1 protein was produced in E. coli expression system through various steps such as recombinant cell isolation, PCR, agarose gel electrophoresis, plasmid extraction, transformation and protein expression.
first_indexed 2024-03-06T15:37:25Z
format Monograph
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institution Universiti Sains Malaysia
language English
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spelling usm.eprints-468542020-08-27T02:09:42Z http://eprints.usm.my/46854/ Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System Kok, Boon Hui T1-995 Technology(General) Malaria rapid diagnostic tests (RDTs) act as important antibody-based immunoassays for prompt malaria diagnosis. Conventional monoclonal antibodies (mAbs) are widely used in RDTs but it can be easily degraded at high ambient temperatures. Hence, the shark VNARS might be good alternatives to mAbs due to its higher thermal stability and binding affinity with antigens. In this study, the recombinant antiPfHRP2 VNAR-G1 protein was produced in E. coli expression system through various steps such as recombinant cell isolation, PCR, agarose gel electrophoresis, plasmid extraction, transformation and protein expression. Pusat Pengajian Teknologi Industri 2020-06 Monograph NonPeerReviewed application/pdf en http://eprints.usm.my/46854/1/PRODUCTION%20OF%20NOVEL%20RECOMBINANT%20ANTIPFHRP%20%28ABSTRACT%29.pdf Kok, Boon Hui (2020) Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System. Project Report. Pusat Pengajian Teknologi Industri. (Submitted) http://ethesis.usm.my:8080/jspui/
spellingShingle T1-995 Technology(General)
Kok, Boon Hui
Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title_full Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title_fullStr Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title_full_unstemmed Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title_short Production Of Novel Recombinant Anti-PFHRP2 VNAR-G1 Protein Using Escherichia COLI BL21(DE3) Expression System
title_sort production of novel recombinant anti pfhrp2 vnar g1 protein using escherichia coli bl21 de3 expression system
topic T1-995 Technology(General)
url http://eprints.usm.my/46854/1/PRODUCTION%20OF%20NOVEL%20RECOMBINANT%20ANTIPFHRP%20%28ABSTRACT%29.pdf
work_keys_str_mv AT kokboonhui productionofnovelrecombinantantipfhrp2vnarg1proteinusingescherichiacolibl21de3expressionsystem