1) phosphohydrase
碱性磷酸酯酶(alkaline phosphamonoesterase)
2) Alkaline phosphatase
碱性磷酸酯酶
1.
Expression and purifcation of thermostable alkaline phosphatase produced by genetic engineering;
基因工程耐热碱性磷酸酯酶的表达与分离纯化
2.
The concentration of POS was tested by alkaline phosphatase,this way was proved to be dependable.
用碱性磷酸酯酶法测定土豆淀粉中的磷酸寡糖,具有样品回收率高、相对误差较小、方法简便、仪器廉价、准确性好等优点,适合于磷酸寡糖常规检验。
3.
The susceptibility of Tessaratoma papillosa to trichlorphon was tested with topical application method,and the effect of trichlorphon on carboxylesterase,acid phosphatase and alkaline phosphatase was studied.
采用微量点滴法测定了荔枝蝽对敌百虫的敏感性,并对不同浓度敌百虫处理后荔枝蝽体内羧酸酯酶、酸性磷酸酯酶和碱性磷酸酯酶的活性进行了比较。
3) base phosphastase
碱性磷酸酯酶
1.
Objective To contrast difference between the effect of various concentrations DDVP and nanoemulsion to the acetylcholine esterase(AchE),glutathione-s-transferase(GST) and base phosphastase(BpE) activity of Blattella germanica.
002%时,碱性磷酸酯酶(BpE)的活性受到抑制,而DDVP乳油各施药组与对照组相比,BpE活性无显著性改变。
2.
Objective: To study the relationship between the activities of carboxylesterase、 acid phosphastase、 base phosphastase and pesticide resistance in the German cockroach.
目的 :了解德国小蠊的羧酸酯酶 (β NACarE)、酸性磷酸酯酶 (ApE)和碱性磷酸酯酶 (BpE)与抗药性的关系。
5) Alkaline and acidic phosphatase
碱性和酸性磷酸酯酶
6) Thermostable alkaline phosphatase
耐热碱性磷酸酯酶
1.
In order to determine the functional domain of thermostable alkaline phosphatase(TAPND27),three truncators of pTAPN8,pTAPN16 and pTAPN25 with deletions of 8,16 and 25 amino acids at N\|terminal and two truncators of pTAPC10 and pTAPC30 with deletions of 10 and 30 amino acids at C\|terminal were obtained through PCR\|mediated site\|directed mutagenesis.
为了确定耐热碱性磷酸酯酶 (TAPND2 7)发挥活性所必需的功能结构域 ,通过 PCR介导的诱变缺失 ,得到了 N端分别缺失 8、1 6、2 5个氨基酸的 3个缺失体 p TAPN8、p TAPN1 6和p TAPN2 5以及 C端分别缺失 1 0和 30个氨基酸的两个缺失体 p TAPC1 0和 p TAPC30 。
2.
To reveal the mechanism of protein thermostability, we used in vivo random mutagenesis to generate variants of PTAP503F which contained thermostable alkaline phosphatase (FD-TAP).
为了进一步揭示蛋白质的耐热机制，对含有耐热碱性磷酸酯酶（ＦＤ－ＴＡＰ）的表达质粒ｐＴＡＰ５０３Ｆ进行了随机诱变，用菌落原位显色法从约５０００个转化子中筛选到４个耐热性下降的突变型克隆，并对其中１个克隆（ＴＡＰＭ３）进行了部分酶学性质、ＤＮＡ和氨基酸序列的研究。
3.
The coding sequence of the gene for recombinant thermostable alkaline phosphatase (FD-TAP) was amplified from the pTAP118B by polymerase chain reaction (PCR) using two mutagenic primers incorporating Nde I and Burn H I sites at the 5 termini,respectively.
根据耐热碱性磷酸酯酶（ＦＤ－ＴＡＰ）基因的酶切图谱和ＤＮＡ序列，分别在基因的起始密码子和终止密码子处设计了２个突变引物。
补充资料：碱性磷酸酯酶(alkaline phosphamonoesterase)
分子式：
CAS号：
性质：又称碱性磷酸酯酶(alkaline phosphamonoesterase)。用于催化水解各种磷酸单酯的酶。对磷酸二酯无作用。最适pH值在8附近。二价镁离子为其辅基。
CAS号：
性质：又称碱性磷酸酯酶(alkaline phosphamonoesterase)。用于催化水解各种磷酸单酯的酶。对磷酸二酯无作用。最适pH值在8附近。二价镁离子为其辅基。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条