找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

Titlebook: Differential Display Methods and Protocols; Peng Liang,Arthur B. Pardee Book 19971st edition Humana Press 1997

[復(fù)制鏈接]
41#
發(fā)表于 2025-3-28 16:26:57 | 只看該作者
42#
發(fā)表于 2025-3-28 18:57:52 | 只看該作者
https://doi.org/10.1007/978-1-4939-7108-4tially expressed mRNAs (i.e., using plus/minus screening); but if the quest is to identify the majority of differentially expressed mRNA species, then a method that is not sensitive to mRNA abundance is required. To evaluate how well DD and SH can identify abundant as well as rare differentially exp
43#
發(fā)表于 2025-3-28 23:57:36 | 只看該作者
44#
發(fā)表于 2025-3-29 06:48:20 | 只看該作者
Book 19971st editionmRNAs in a cell or tissue, in particular those with altered expression resulting from diff- ences in transcription or mRNA degradation. In contrast to conventional te- niques, DD can be used to compare mRNA expressions in many samples created under multiple experimental conditions. DD was conceived
45#
發(fā)表于 2025-3-29 07:37:42 | 只看該作者
Differential Displayon and characterization of differentially expressed genes becomes one of the first steps toward the understanding of these important biological questions. Differential display (.) and a related RAP-PCR method (.) were developed to more efficiently identify and isolate these genes.
46#
發(fā)表于 2025-3-29 13:11:14 | 只看該作者
Direct Sequencing of Differential Display PCR Productsnchored primers, T.MN (M = G, A or C; N = G, A, T or C); and (2) PCR amplification of cDNA fragments using arbitrary 10-mer primers (upstream) and anchored downstream primers. One critical feature of this technique is to display most of the mRNA population on a sequencing gel after PCR.
47#
發(fā)表于 2025-3-29 17:04:41 | 只看該作者
A Direct-Sequencing-Based Strategy for Identifying and Cloning cDNAs from Differential Display Gelsther from a variety of sources in a revised order. Methods for the DD reverse transcription-polymerase chain reactions (RT-PCR) and electrophoresis conditions, for which we have used published methods (.) and the GenomyxLR DNA sequencer (.. and ref. .), are not covered here.
48#
發(fā)表于 2025-3-29 19:58:16 | 只看該作者
49#
發(fā)表于 2025-3-30 01:59:54 | 只看該作者
50#
發(fā)表于 2025-3-30 07:36:24 | 只看該作者
RC4D—Restriction Fragment Length Polymorphism-Coupled Domain-Directed Differential Displayreakthrough in molecular biology, because they circumvented some severe limitations of traditional methods, such as differential screening and subtractive hybridization, during the analysis of differential gene expression.
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點評 投稿經(jīng)驗總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機版|小黑屋| 派博傳思國際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-10 07:03
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
原平市| 正安县| 西乌珠穆沁旗| 海南省| 北票市| 沂南县| 濮阳市| 安宁市| 呼和浩特市| 天柱县| 梅河口市| 奉贤区| 买车| 九寨沟县| 天长市| 峨边| 泾川县| 绥滨县| 绿春县| 尚志市| 青浦区| 五常市| 达拉特旗| 南溪县| 五寨县| 南昌市| 开江县| 卓资县| 汕头市| 安宁市| 宁陕县| 无极县| 鹰潭市| 饶河县| 耿马| 永清县| 镇江市| 文山县| 平塘县| 宜宾县| 宣恩县|