📘 ❞ (Capillary Electrophoresis of Nucleic Acids Volume II Practical App ❝ كتاب ــ Keith R. Mitchelson Jing Cheng

Biology Books - 📖 كتاب ❞ (Capillary Electrophoresis of Nucleic Acids Volume II Practical App ❝ ــ Keith R. Mitchelson Jing Cheng 📖

█ _ Keith R Mitchelson Jing Cheng 0 حصريا كتاب ❞ (Capillary Electrophoresis of Nucleic Acids Volume II Practical App ❝ 2024 App: نبذه عن الكتاب: 1 Introduction Since the first descriptions electrophoresis in small diameter tubes 1970s and 1980s (1,2), capillary (CE) has been recognized for its potential to replace slab gel analysis nucleic acids (3,4) In particular, availability of commercial instrumentation CE over last several years made both size determination and quantitation DNA restriction fragments or polymerase chain reaction (PCR) products amenable automation Due same charge mass ratio, electrophoretic mobility acid molecules free solution is largely independent of their molecular size (5) Therefore, a sieving medium required electrophoretic analysis based on their Typically, two different principal types of separation matrix are used The type high viscosity polymer (e g , polyacrylamide) with well defined crosslinked regard structure of its pores second noncrosslinked linear network materials such as, polyacrylamide, agarose, cellulose, dextran, poly(ethylene oxide), with lower than former more dynamic pore Although the first attached covalently wall may provide better separation (sequencing) fragments, format advantage of being able be replenished after each cycle This typically extends the lifetime capillary, prevents contamination system, avoids sample carryover and allows use temperatures above room temperature Most matrices both systems tolerant addition denaturants Many media useful for the separation have now become commercially available (6) In summary, application related research attractive for numerous reasons: 1 degree cumbersome pouring loading 2 High sensitivity eliminates need label carcinogenic stains, with radioactive precursors Biology Books مجاناً PDF اونلاين Biologically Biology natural science that concerned study life, various forms function, how these organisms interact other surrounding environment word biology Greek up words: bio (βίος) meaning life And loggia ( λογία) means Biology: similarity vegetation animal cover edges African American states, existence fossil Branches biology Biology an ancient thousands old modern began nineteenth century multiple branches Among them are: Anatomy Botany Biochemia Biogeography Biofisia Cytology cell science Ecology environmental science Development Embryology embryology Genetics genetics Histology histology Anthropology anthropology Microbiology bacteriology Molecular Biology Physiology functions organs Taxonemia taxonomy Virology virology Zoology zoology

إنضم الآن وتصفح بدون إعلانات
(Capillary Electrophoresis of Nucleic Acids Volume II Practical App
كتاب

(Capillary Electrophoresis of Nucleic Acids Volume II Practical App

ــ Keith R. Mitchelson Jing Cheng

(Capillary Electrophoresis of Nucleic Acids Volume II Practical App
كتاب

(Capillary Electrophoresis of Nucleic Acids Volume II Practical App

ــ Keith R. Mitchelson Jing Cheng

حول
Keith R. Mitchelson Jing Cheng ✍️ المؤلف
المتجر أماكن الشراء
مناقشات ومراجعات
QR Code
عن كتاب (Capillary Electrophoresis of Nucleic Acids Volume II Practical App:
نبذه عن الكتاب:

1. Introduction
Since the first descriptions of electrophoresis in small diameter tubes in the 1970s and
1980s (1,2), capillary electrophoresis (CE) has been recognized for its potential to replace
slab-gel electrophoresis for the analysis of nucleic acids (3,4). In particular, the availability
of commercial instrumentation for CE over the last several years has made both the size
determination and quantitation of DNA restriction fragments or polymerase chain reaction
(PCR) products amenable to automation. Due to the same charge-to-mass ratio, the electrophoretic mobility of nucleic acid molecules in free solution is largely independent of
their molecular size (5). Therefore, a sieving medium is required for the electrophoretic
analysis of DNA fragments based on their size. Typically, two different principal types of
separation matrix are used. The first type of matrix is of high viscosity polymer (e.g.,
polyacrylamide) with a well-defined crosslinked gel in regard to the structure and size of
its pores. The second type of matrix is a noncrosslinked linear polymer network of materials such as, linear polyacrylamide, agarose, cellulose, dextran, poly(ethylene oxide), with
lower viscosity than the former type and with a more dynamic pore structure. Although the
first type of matrix is attached covalently to the capillary wall and may provide better
separation for small (sequencing) fragments, the second matrix format has the advantage
of being able to be replenished after each electrophoretic cycle. This typically extends the
lifetime of a capillary, prevents contamination of the system, avoids sample carryover and
allows the use of temperatures well above room temperature. Most matrices used in both
systems are tolerant to the addition of DNA denaturants. Many different media useful for
the separation of DNA have now become commercially available (6).
In summary, the application of CE for DNA related research is attractive for
numerous reasons:
1. The high degree of automation avoids cumbersome gel pouring and sample loading.
2. High mass sensitivity eliminates the need to label DNA with carcinogenic stains, or with
radioactive DNA precursors
الترتيب:

#11K

0 مشاهدة هذا اليوم

#20K

17 مشاهدة هذا الشهر

#73K

3K إجمالي المشاهدات
عدد الصفحات: 356.