Amplification and cloning of taq gene from thermus aquaticus YT-1 strain /
Introduction: DNA polymerase is the crucial enzyme in polymerase chain reaction (PCR). The polymerase derived from Thermus aquaticus was found to be superior to the historical DNA polymerase of Escherichia coli, as it can withstand the extreme denaturation temperature during the PCR procedure. This...
محفوظ في:
المؤلف الرئيسي: | Elsalami, Rabia Mrehil Ali |
---|---|
التنسيق: | أطروحة |
اللغة: | English |
منشور في: |
Kuantan :
Kulliyyah of Medicine, International Islamic University Malaysia,
2011
|
الموضوعات: | |
الوصول للمادة أونلاين: | Click here to view 1st 24 pages of the thesis. Members can view fulltext at the specified PCs in the library. |
الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|
مواد مشابهة
-
Development of a multiplex PCR in the rapid detection of virulence-associated genes in Shigella spp /
بواسطة: Hoe, Susan Ling Ling
منشور في: (2003) -
Multiple domain deletion towards 5’-3’ polymerase activity of DNA polymerase I from Geobacillus sp. strain SK72
بواسطة: Hadrawi, Waqiyuddin Hilmi
منشور في: (2021) -
Improvement of T1 lipase of Geobacillus zalihae by directed evolution
بواسطة: Abdul Rachman, Abdul Rahim
منشور في: (2014) -
Cloning and expression of human globular adiponectin in Pichia Pastoris expression system /
بواسطة: Siddig, Loai Abdelati
منشور في: (2011) -
Validation study on 7500 real time polymerase chain reaction system using plexor HY system /
بواسطة: Siti Mastura Mohamed
منشور في: (2009)