第一章 家畜的生殖器官 （ Reproductive Organs of Domestic Animals） 第二章 生殖激素 （ Reproductive Hormone） 第三章 雄性动物生殖生理 (The Physiology of Male Reproduction) 第四章 雌性动物发情周期 （Ｅstrus Ｃycle） 第五章 受精、妊娠和分娩 （Fertilization，Gestation and Parturition） 第六章 人工授精 （Artificial Insemination） 第七章 家畜的繁殖力 （Fertility of Domestic Animals） 第八章 配子与胚胎生物工程 （ Gametal and Embryonic Bioengineering Technology）

第一节 胚胎移植技术 Section 1 Embryo transfer 第二节 体外受精 Section 2 In vitro fertilization 第三节 克隆技术 Section 3 Animal cloning 第四节 转基因技术 Section 4 Transgenic Animal 第五节 性别控制技术 Section 5 Sex control 第六节 胚胎干细胞的分离培养技术 Section 6 Embryonic stem cells technique 第七节 哺乳动物嵌合体的生产 Section 7 Chimera

The introduction of fluidfoil impellers, as shown in Fig. 9a through 9f, give a wide variety of mixing conditions suitable for high flow and low fluid shear rates. Fluidfoil impellers use the principles developed in airfoil work in wind tunnels for aircraft. Figure 10a shows what is desirable, which is no form separation of the fluid, and maximum lift and drag coefficients, which is what one is trying to achieve with the fluidfoil impellers. Figure 10b shows

Fluid mixing is essential in fermentation processes. Usually the most critical steps in which mixers are used are in the aerobic fermentation process. However, mixers are also used in many auxiliary places in the fermentation process and there are places also for agitation in anaerobic fermentation steps

The second edition ofthe Fermentation andBiochemica1 Engineer￾ing Handbook, like the previous edition, is intended to assist the develop￾ment, design and production engineer who is engaged in the fermentation industry. Particular emphasis is give to those unit operations most frequently encountered in the commercial production ofchemicals and pharmaceuticals via fermentation

Copyright 8 1997 by Noyes Publications No part of this book may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording or by any information storage and retrieval system, without permission in writing from the Publisher. Library of Congress Catalog Card Number: 96-29055 Printed in the United States

Capital cost projects begin when a need is defined that cannot be satisfied in existing facilities. Thus begins the life cycle of a capital project (Fig. 1). Once started, the project will progress through all of the following phases or be canceled. It all starts with the recognition of a need that will require capital plant. In the conceptual phase of the project, multiple approaches will be evaluated and one or more plans will be evaluated for meeting these needs

摘要比较了5种固定弗劳地柠檬酸杆菌X05菌体的方法,其中明胶海藻酸钠包埋法为固定菌体的最佳方法。 扫描电子显微镜观察表明,XP05菌体较均匀地分布于包埋基质中。固定化XP05菌体吸附+受吸附时间、固定化菌体浓度、溶液的pH值和P起始浓度的影响。吸附作用是一个快速的过程;吸附A4+的最适pH值为1.5;在50 ~250mgp范围内,吸附量与起始浓度成线性关系,吸附过程符合 Langmuir和 Freundlich吸附等温模型

第1节 概述 1.1 生物材料的概念 1.2 生物材料的发展 1.3 生物材料的基本性能要求 1.4 生物材料的分类 第2节 生物材料的种类 2.1 金属生物材料 2.2 无机非金属生物材料 2.3 高分子生物材料 第3节 组织工程 3.1 组织工程基本概念 3.2 组织工程材料简介 3.3 组织工程材料应用 第4节 蛋白质和细胞在生物材料表面的吸附 4.1 蛋白质结构、性质及对材料表面的吸附 4.2 细胞表面及与材料的相互作用 第5节 蛋白质和细胞在生物材料表面的吸附

一、 生物医学工程的定义 二、 生物医学工程的特点 三、 生物医学工程的研究对象 四、 生物医学工程的发展 五、 中国生物医学工程的发展战略