牛血清蛋白

通过SEM、水接触角、纯水通量、牛血清蛋白截留率、高温条件下性能测试表明超滤膜能够用于高温水的处理并有较好的亲水性和机械性能。

By SEM , the water contact angle , pure water flux , BSA retention rate , performance testing under high temperature conditions that can be used for high temperature ultrafiltration membrane water treatment and better hydrophilicity and mechanical properties .

利用激光光解结合稳态吸收光谱技术，对放线菌素D的模型化合物ADE与DNA和牛血清蛋白的相互作用进行了系统研究。

By use of laser flash photolysis and steady state absorption techniques , a systematic study was carried out on the interaction of ADE , which is a kind of model compound of actinomycin D , with DNA and BSA .

残余牛血清蛋白ELISA检测方法的建立及其初步应用

Development and Primary Application of ELISA Method for Detecting Residual Calf Serum Protein

为验证ELISA法检测病毒性疫苗中残余牛血清蛋白方法的可靠性，由2个部门对12个样品进行4人连续3天的验证。

To validate the reliability of BSP-ELISA method on detecting residual bovine serum contents in virus vaccines .

利用牛血清蛋白合成CdS、ZnS纳米材料

Synthesis of Cadmium Sulfide and Zinc Sulfide Nano-materials by Bovine Serum Albumin Protein

本文把这种理论应用到菁染料检测牛血清蛋白（BSA）体系中。

We applied this method to detect bovine serum albumin ( BSA ) with cyanine dyes .

牛血清蛋白（BSA）的AFM图像表明：BSA在亲水硅片表面是单分子、水平吸附在硅片表面，且呈颗粒状；

These AFM images showed that bovine serum albumin adsorbed flatly in grain shape and mono molecules .

随着PVP含量的增加，水凝胶对鱼精蛋白和牛血清蛋白的吸附减少。

As the PVP content was increased , the absorption of Protamine and was BSA decreased .

绿茶中EGCG提取纯化方法及其与牛血清蛋白相互作用的研究

Purification of EGCG from Green Tea and Its Interaction with Bovine Serum Albumin

以牛血清蛋白（bovineserumalbumin，BSA）及其抗体为检测对象，用常用的硅烷化合物APTES固定蛋白研制石英晶体免疫传感器。

A piesoelectric immunosensor for detection of BSA and anti-BSA antibody , using APTES to immobilize the protein , is described .

同时，壳聚糖海绵对Ca2+和牛血清蛋白（BSA）的吸附能力也随着脱乙酰度的增大而增加。

While adsorptive efficiency of chitosan spoon for Ca2 + and bovine serum albumen ( BSA ) were increased .

牛血清蛋白修饰的CdTe量子点作为铜离子检测探针的实验研究

Experimental Study on Application of Bovine Serum Albumin Modified CdTe Quantum Dots as Detective Probe for Cupric Ions

目的：研究牛血清蛋白（BSA）在聚合物基质中的稳定性及影响因素。

OBJECTIVE : To study the stability of model protein , bovine serum albumin ( BSA ), entrapping in polymer matrices .

研究了PVA含量、过滤压力和过滤时间对BC/PVA共混复合膜过滤牛血清蛋白的影响。

The PVA concentration , filtration pressure and filtration time on the BC / PVA blend composite membrane filtration of bovine serum albumin were studied .

方法：以牛血清蛋白（BSA）为模型药物，以离子凝胶法制备壳聚糖微球（CMs）。

Methods Using Bovine serum album ( BSA ) as model protein , chitosan microspheres ( CMs ) were prepared by inotropic gelation .

主要的研究内容及结论如下：1.以牛血清蛋白（BSA）作为模型蛋白质，研究了其与聚丙烯酸刷（PAA-SPB）的相互作用。

Main work and conclusions as follow : 1 . Bovine serum albumin ( BSA ) is employed as model protein to investigate their interaction with PAA-SPBs .

本论文选择牛血清蛋白（BSA），研究了其与糖胺类表面活性剂、阴离子全氟表面活性剂以及阳离子碳氢表面活性剂的相互作用。

In this paper , we selected bovine serum albumin and studied the effects of one saccharide amide surfactant , one fluorinated surfactant and one cation surfactant on it .

增强的共振光散射强度与牛血清蛋白的浓度在0.08&1.6μg／mL范围内呈良好的线性关系，检出限为18.6ng／mL。

The enhanced RLS intensity is well proportional to the concentration of bovine serum albumin ( BSA ) in the range of 0.08-1.6 μ g / mL , and the detection limit ( 3 σ) is 18.6 ng / mL.

以水为凝固介质，制备了PEI超滤膜，考察了水通量，牛血清蛋白BSA的膜分离性能。

Using water as coagulant , polyetherimide ( PEI ) ultrafitration membranes were prepared . The water permeation fluxes and the separation property of the membranes for BSA were investigated .

本章使用PLGA作为载体材料、牛血清蛋白作为模型药物、选用孔径为2.6μm的SPG膜进行了研究。

This chapter chose 2.6 μ m SPG membrance for research , using PLGA as a carrier materials , bovine serum albumin as model drugs .

用共振光散射光谱（RLS）和紫外-可见电子吸收光谱研究了阿特拉津与牛血清蛋白（BSA）之间的相互作用。

The resonance light scattering ( RLS ) technique and UV-Vis absorption spectra were applied to the investigation of the interaction between atrazine and bovine serum albumin ( BSA ) .

研究了钙红-Cu（Ⅱ）络合物与牛血清蛋白（BSA）作用的共振光散射光谱（RLS）、荧光光谱和电子吸收光谱特征，建立了利用金属配合物作为探针测定痕量蛋白质的方法。

The Resonance light scattering ( RLS ) spectra , fluorescence spectra , and absorption spectra of Cal-Red-Cu (ⅱ) metal complex with bovine serum albumin ( BSA ) were studied .

牛血清蛋白对被胰蛋白酶消化过的叶绿体光还原DCIP的活性有恢复作用。

Bovine serum albumin stimulates the DCIP photoreduction activity of lettuce chloroplasts which has been treated with trypsin .

对膜的牛血清蛋白（BSA）过滤性能和膜污染研究表明：PPgAAc和PPgGly膜对BSA的截留率，即截留效果远远高于未改性的PP膜。

Filtration performances on the bovine serum albumin ( BSA ) and membrane fouling were studied . The results suggested the rate of BSA filtrating for PP g AAc and PP g Gly membrane were higher than for PP membrane .

选择牛血清蛋白（BSA）和β乳球蛋白（BLG）两种等电点相似的蛋白质来研究金纳米粒子对它们的选择性。

Bovine serum albumin ( BSA ) and β - lactoglobulin had a very similar isoelectric point ( pI ), and were chosen to study their selectivity by gold nanoparticles .

用FTIR-ATR、SEM、XPS和表面接触角测定仪对聚砜膜表面结构和性能进行表征，研究了接枝反应的条件的变化对膜的通量和膜的牛血清蛋白（BSA）截留率的影响。

FTIR-ATR , SEM , XPS and Contact angle was used to test the structure and properties of the surface of PSF membrane . The effect of factors of grafting reaction on flux and retention rate of bovine serum albumin was also studied .

固定乙酰胆碱酯酶的合适条件是：戊二醛10%、牛血清蛋白0.1mg/mL、乙酰胆碱酯酶0.1mg/mL。

Proper condition for the fixation of the Acetylcholine Esterase was that : Glutaraldehyde 10 % 、 Bovine Scrum Albumin 0.1mg / mL 、 Acetylcholine Esterase 0.1mg/mL .

采用聚氧乙烯涂层毛细管柱，以牛血清蛋白（BSA）为手性添加剂，运用毛细管电泳电导检测对手性药物沙丁胺醇和多沙唑嗪以及DL组氨酸、色氨酸、苏氨酸进行拆分。

Using polyglycol coated capillary column , the chiral drugs salbutamol and doxazosin , DL-histidine , DL-tryptophan , DL-threonine were separated into two enantiomers by capillary electrophoresis with conductance detection , when bovine serum albumin ( BSA ) was used as a chiral resolving agent .

明胶微球具有较好的缓释能力，其内所载的牛血清蛋白可以持续释放30d，并且在药物释放过程中没有明显的突释现象。

Gelatin microspheres had good release ability : the released process for BSA from the BSA-impregnated gelatin microsphere can be sustained for 30 days , and there was no sudden release phenomenon in the released process for BSA .

在一定范围内，共振光散射强度的增量与蛋白质的浓度成正比，三种蛋白的检测限：牛血清蛋白为1.3ngmL-1，人血清蛋白10ngmL-1，γ-球蛋白5.7ngmL-1。

The enhancement of RLS was proportional to the concentration of the proteins and the detection limits were 1.3 ng mL-1 for BSA , 10 ng mL-1 for HSA and 5.7 ng mL-1 for γ - IgG .