|
UPT. PERPUSTAKAAN
Universitas Esa Unggul
Kampus Emas UEU - Jakarta Barat
|
Phone |
: |
021-5674223, ext 282 |
Fax |
: |
|
E-mail |
: |
[email protected] |
Website |
: |
http://library.esaunggul.ac.id
|
Support (Customer Service) :
|
[email protected] |
|
|
Welcome..guys!
|
Have a problem with your access?
Please, contact our technical support below:
|
LIVE SUPPORT
Astrid Chrisafi
|
! ATTENTION !
To facilitate the activation process, please fill out the member application form correctly and completely
Registration activation of our members will process up to max 24 hours (confirm by email). Please wait patiently
Still Confuse?
Please read our User Guide
|
|
UEU » Journal » Bioteknologi Posted by [email protected] at 19/11/2020 15:04:04 • 739 Views
IN-SILICO ANALYSIS FOR CRYI GENE AMPLIFICATION FROM BACILLUS THURINGIENSISCreated by :
Febriana Dwi Wahyuni ( None ) Henny Saraswati Kartika Sari Dewi
Subject: | BIOTEKNOLOGI | Alt. Subject : | BIOTECHNOLOGY | Keyword: | BIOINFORMATICS CRY GENE PCR PRIMER IN SILICO ANALYSIS BACILLUS THURINGIENSIS |
Description:
Bacillus thuringiensis is one type of bacteria that has been used as a microbiological control agent
for pests and a vector of plant disease. The presence of Cry proteins inside the B. thuringiensis can
be acted as a specific insect repellent that only toxic to certain insects. The CryI protein is toxic to
Lepidoptera insects, which can attack various types of plants. Polymerase Chain Reaction (PCR) is a
standard method that can be used to amplify the gene encoding CryI proteins from B. thuringiensis.
This research aimed to design a primer candidate for cryI gene amplification from B.
thuringiensis. In silico analysis for designing cryI primer was carried out using some software, such
as BLAST for searching cryI gene sequence, Bioedit for sequences alignment, and DINAmelt for
analyzing dimer structure of the primers. Ten primer candidates were successfully obtained based on
the result of the primer3 software. A pair of primer was selected to amplify the cryI gene, with a
forward primer 5�- CGGTGAATGCCCTGTTTACT -3� and reverse primer 5�CGGTCTGGTTGCCTATTGAT
-3�. Amplification of the cryI gene by PCR method using selected
primer resulting in a PCR product with a length of approximately 200 bp
Date Create | : | 19/11/2020 | Type | : | Text | Format | : | PDF | Language | : | Indonesian | Identifier | : | UEU-Journal-11_0591 | Collection ID | : | 11_0591 |
Source : Bioedukasi Vol.XVIII No.1 April 2020
Relation Collection: Fakultas Ilmu Kesehatan
Coverage : Civitas Akademika Universitas Esa Unggul
Rights : @2020 Perpustakaan Universitas Esa Unggul
Publication URL : https://digilib.esaunggul.ac.id/insilico-analysis-for-cryi-gene-amplification-from-bacillus-thuringiensis-17334.html
[ Free Download - Free for All ]
- UEU-Journal-17334-11_0591.pdf - 612 KB
[ FullText Content - Please, register first ]
...No Files...
10 Similar Document...
10 Related Document...
|
POLLINGBagaimana pendapat Anda tentang repository kami ?
Visitors Today : 1
Total Visitor : 1970116
Hits Today : 46812
Total Hits : 157671883
Visitors Online: 1
Calculated since 16 May 2012
You are connected from 172.17.121.29 using Mozilla/5.0 AppleWebKit/537.36 (KHTML, like Gecko; compatible; ClaudeBot/1.0; [email protected])
|