w6

RESULTS Six differentially expressed gene fragments ( W1 ~ W6 ) were found and cloned using mRNA differential display technique .

结果采用mRNA差异显示技术从SAM海马内筛选和克隆了6个基因片段（W1～W6）；

W4 and W6 derived from single primer amplification , and had no homology to the known sequences .

W4和W6是单引物扩增产物，与已知序列无同源性。

Monoclonal antibody W6 / 32 ( anti-MHC I ) was prepared and testified to be active .

制备并纯化出具有生物学活性的抗MHCI分子的单克隆抗体W6/32。

The refolded product was detected by ELISA and Western blot with mAb W6 / 32 and rabbit anti-human β _2m antibody .

利用特异性抗体（W6/32及兔抗人β2m抗体）进行免疫印迹及酶联免疫吸附试验，检测稀释复性的折叠产物。

It is proposed that wastewater from W6 should not be discharged directly into biological treatment systems , and wastewater from W1 and W3 should be detoxified before or after the biological treatment .

因此，建议W6工段废水不直接进入好氧生物处理系统，W1和W3工段废水应在好氧生物处理前后采取必要的脱毒措施。

It is proposed that the characteristic of ordered structure is Li + , Fe3 + randomly distribute on B sites , and they orderly arrange with W6 + in alternating { 111 } planes .

提出其有序化结构特点是Li+、Fe3+随机分布，同时它们与W6+相间在〈111〉方向作有序排列。

The refolded and biotinylated products were detected by ELISA and Western blot with monoclonal antibody ( W6 / 32 and rabbit anti-human β _ ( 2 ) m antibody ) and streptavidin .

利用特异单抗（W6/32和兔抗人β2m抗体）及链霉亲合素进行ELISA和westernblot，检测稀释复性和生物素化的折叠产物。

On account of the ESR and XPS results , parts of W6 + in multilayers were reduced to W5 + which exhibited characteristic blue , a possible photo - or thermochromic mechanism can be speculated .

顺磁共振和光电子能谱证实了W6+被还原为W5+而呈现多蓝的特征蓝色。这是由于多金属氧酸盐和聚电解质协同作用的结果。