❞ كتاب Methods in Molecular Biology Min Receptor Protocols ❝ ⏤ Min Li

نبذه عن الكتاب:

Isolation of Receptor Clones
by Expression Screening in Xenopus Oocytes
Fumio Nakamura, Yoshio Goshima,
Stephen M. Strittmatter, and Susumu Kawamoto
1. Introduction
Xenopus laevis oocytes have contributed greatly to the study of glutamate
receptors. The isolation of the first cDNA clone for a glutamate receptor channel, GluR1, was achieved by utilizing an oocyte expression cloning system (1).
In 1991–1992, three groups reported the isolation of cDNA clones encoding of
N-methyl-D-aspartate (NMDA) receptor channel subunit (2–4). Two of the
three groups employed the oocyte system to isolate NMDA receptor clones
(2,3). Furthermore, a metabotropic glutamate receptor (mGluR) clone was also
identified with the oocyte system (5).
This technique was pioneered by Nakanishi’s group to identify a G-proteincoupled substance-K receptor (6). It combines transient protein expression in
oocytes with highly sensitive electrophysiological analysis. Xenopus oocyte
possesses an efficient machinery to translate protein from RNA. Its large size
(~1 mm) allows injection of RNA and two-electrode voltage clamp with relative ease. The voltage-clamp method can detect trace concentrations of channel proteins in cellular membranes. Since the oocyte itself is a living cell, it has
a set of intracellular signal cascades. For example, the phosphatidylinositol
(PI) turnover initiated by G-protein-coupled receptors activates Ca2+-sensitive
Cl– channels in the oocyte membrane, producing a large inward current (6–8).
The combination of these features has facilitated the isolation of dozens of
cDNA clones from voltage-dependent ion channels, to ligand-gated ion channels, to G-protein-coupled receptors, to transporters. A further advantage of
this system is that prior to creating cDNA libraries, poly(A)+ RNA from various tissues can be screened in entire or in fractionated states
Min Li - ❰ له مجموعة من الإنجازات والمؤلفات أبرزها ❞ Methods in Molecular Biology Min Receptor Protocols ❝ ❱
من Biology Books علم الأحياء - مكتبة الكتب العلمية.

اقتباسات من كتاب ❞Methods in Molecular Biology Min .. ❝اقتباسات لـ ❞Min Li❝شارك باقتباسات لهذا الكتاب

نبذة عن الكتاب:

Methods in Molecular Biology Min Receptor Protocols

1999م - 1445هـ
نبذه عن الكتاب:

Isolation of Receptor Clones
by Expression Screening in Xenopus Oocytes
Fumio Nakamura, Yoshio Goshima,
Stephen M. Strittmatter, and Susumu Kawamoto
1. Introduction
Xenopus laevis oocytes have contributed greatly to the study of glutamate
receptors. The isolation of the first cDNA clone for a glutamate receptor channel, GluR1, was achieved by utilizing an oocyte expression cloning system (1).
In 1991–1992, three groups reported the isolation of cDNA clones encoding of
N-methyl-D-aspartate (NMDA) receptor channel subunit (2–4). Two of the
three groups employed the oocyte system to isolate NMDA receptor clones
(2,3). Furthermore, a metabotropic glutamate receptor (mGluR) clone was also
identified with the oocyte system (5).
This technique was pioneered by Nakanishi’s group to identify a G-proteincoupled substance-K receptor (6). It combines transient protein expression in
oocytes with highly sensitive electrophysiological analysis. Xenopus oocyte
possesses an efficient machinery to translate protein from RNA. Its large size
(~1 mm) allows injection of RNA and two-electrode voltage clamp with relative ease. The voltage-clamp method can detect trace concentrations of channel proteins in cellular membranes. Since the oocyte itself is a living cell, it has
a set of intracellular signal cascades. For example, the phosphatidylinositol
(PI) turnover initiated by G-protein-coupled receptors activates Ca2+-sensitive
Cl– channels in the oocyte membrane, producing a large inward current (6–8).
The combination of these features has facilitated the isolation of dozens of
cDNA clones from voltage-dependent ion channels, to ligand-gated ion channels, to G-protein-coupled receptors, to transporters. A further advantage of
this system is that prior to creating cDNA libraries, poly(A)+ RNA from various tissues can be screened in entire or in fractionated states . المزيد..

تعليقات القرّاء:

Biologically

Biology is a natural science that is concerned with the study of life, its various forms and its function, how these organisms interact with each other and with the surrounding environment. The word biology in Greek is made up of two words: bio (βίος) meaning life. And loggia (-λογία) means science or study. Biology: the similarity of vegetation and animal cover on the edges of the African and American states, and the existence of the same fossil.

Branches of biology
Biology is an ancient science thousands of years old and modern biology began in the nineteenth century. This science has multiple branches. Among them are:

Anatomy
Botany
Biochemia
Biogeography
Biofisia
Cytology or cell science
Ecology or environmental science

نبذه عن الكتاب:

Isolation of Receptor Clones
by Expression Screening in Xenopus Oocytes
Fumio Nakamura, Yoshio Goshima,
Stephen M. Strittmatter, and Susumu Kawamoto
1. Introduction
Xenopus laevis oocytes have contributed greatly to the study of glutamate
receptors. The isolation of the first cDNA clone for a glutamate receptor channel, GluR1, was achieved by utilizing an oocyte expression cloning system (1).
In 1991–1992, three groups reported the isolation of cDNA clones encoding of
N-methyl-D-aspartate (NMDA) receptor channel subunit (2–4). Two of the
three groups employed the oocyte system to isolate NMDA receptor clones
(2,3). Furthermore, a metabotropic glutamate receptor (mGluR) clone was also
identified with the oocyte system (5).
This technique was pioneered by Nakanishi’s group to identify a G-proteincoupled substance-K receptor (6). It combines transient protein expression in
oocytes with highly sensitive electrophysiological analysis. Xenopus oocyte
possesses an efficient machinery to translate protein from RNA. Its large size
(~1 mm) allows injection of RNA and two-electrode voltage clamp with relative ease. The voltage-clamp method can detect trace concentrations of channel proteins in cellular membranes. Since the oocyte itself is a living cell, it has
a set of intracellular signal cascades. For example, the phosphatidylinositol
(PI) turnover initiated by G-protein-coupled receptors activates Ca2+-sensitive
Cl– channels in the oocyte membrane, producing a large inward current (6–8).
The combination of these features has facilitated the isolation of dozens of
cDNA clones from voltage-dependent ion channels, to ligand-gated ion channels, to G-protein-coupled receptors, to transporters. A further advantage of
this system is that prior to creating cDNA libraries, poly(A)+ RNA from various tissues can be screened in entire or in fractionated states

Biology
Human biology
Who is the founder of biology?
The importance of biology
Areas of work in the field of biology
Theories of biology
Research on biology for the first grade of secondary school
Human biology

سنة النشر : 1999م / 1420هـ .
حجم الكتاب عند التحميل : 1.23 .
نوع الكتاب : pdf.
عداد القراءة: عدد قراءة Methods in Molecular Biology Min Receptor Protocols

اذا اعجبك الكتاب فضلاً اضغط على أعجبني

و يمكنك تحميله من هنا:

تحميل Methods in Molecular Biology Min Receptor Protocols

شكرًا لمساهمتكم

شكراً لمساهمتكم معنا في الإرتقاء بمستوى المكتبة ، يمكنكم االتبليغ عن اخطاء او سوء اختيار للكتب وتصنيفها ومحتواها ، أو كتاب يُمنع نشره ، او محمي بحقوق طبع ونشر ، فضلاً قم بالتبليغ عن الكتاب المُخالف:

قبل تحميل الكتاب ..
يجب ان يتوفر لديكم برنامج تشغيل وقراءة ملفات pdf
يمكن تحميلة من هنا 'http://get.adobe.com/reader/'

المؤلف:

Min Li -

❰ له مجموعة من الإنجازات والمؤلفات أبرزها ❞ Methods in Molecular Biology Min Receptor Protocols ❝ ❱. المزيد..

كتب Min Li