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利用碘—三辛胺盐酸盐反应分光光度测定TOA,HCl 总被引:1,自引:0,他引:1
研究了测定三辛胺盐酸盐的一种新方法-碘光谱法。TOA,HCl在四氯化碳溶液中与生成电荷转移化合物,该物质的最大吸收波长为370nm,TOA,HCl在0-4×10^-4mol.L范围内符合比耳定律。该方法准确,简便,快速,其它溶剂的干扰较小,回收率在94.5%-101.9%,能够满足分析的需要。 相似文献
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本文研究我国野生大豆(Glycine soja)种子贮藏蛋白基因的结构,并与栽培大豆进行比较,构建成野生大豆Glycine soja SH1和栽培大豆Glycine max子叶cDNA库。用已知含球蛋白glycinin Gy 4基因的克隆DNA λS 312为探针,从两个cDNA库中分离出6个克隆。其中两个克隆pWS 228与pWS 242含全长cDNA,克隆cDNA的限制酶图谱和cDNA与基因组DNA的Southern法杂交表明它们代表野生大豆球蛋白glycinin Gy 4基因家族的两种表达拷贝。pWS 228 cDNA的部分序列已测定并与栽培大豆相应顺序作比较。分子杂交还证明Ⅱ类glycinin基因家族的组编在野生大豆胚形成过程中的变动。 相似文献
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To study the structure of genes encoding seed storage proteins of the wild variety of soybean (Glycine soja) in comparison with those of the cultivated (Glycine max),cDNA libraries from cotyledon poly(A)~+ RNA of both wild and cultivated soybeans were constructed.Six clones were isolated using the genomic clone λS312 which contains the coding sequence for the glycinin subunit precursor (A_5A_4B_3) as probe for molecular hybridization. Two clones pWS228 and pWS242 contain the full length of cDNA.Restriction mapping of the cloned cDNA and Southern hybridization of the cDNA with genomic DNA showed two expressed copies of glycinin Gy4 gene subfamily in wild soybean Glycine soja SHI. Alteration of DNA arrangement in group-Ⅱ glycinin gene subfamily during embryogenesis was also demonstrated. 相似文献
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沈纬 《理化检验(化学分册)》1999,35(3):117-118
提出了改性炭黑-氯化碳黑的分析方法,即样品在管式炉中通氧灰化,使结合在炭黑有机官能团上的氯转化为可测定的无机氯,用吸收液吸收后,汞量法测定氯含量,方法简便快速,准确度高,回收率在96.8%-101.7%,精密度好,相对标准偏差为1.17%,不需用特殊仪器,适合工业生产中的监控分析。 相似文献
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同时测定三辛妥和三辛胺盐酸盐的双波长分光光度法 总被引:1,自引:0,他引:1
提出了利用双波长分光光度法测定三辛胺及三胺盐酸盐的一种新方法,即TOA和TOA.HCl在CCl4溶液中与I2生成电荷转移化合物,其最大吸收波长分别为293nm和263nm,两组分同时存在时可利用吸光度和加和性得联立方程分别求出两组分的含量。 相似文献
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Two coding sequences for storage protein in Glycine max have been cloned. They were characterized by molecular hybridization and in vitro translation. One sequence happens to hybridize to two sized mRNAs which are translated in vitro to 60 Kd and 42 Kd polypeptides corresponding to a and β subunits of 7S storage protein, and the other is hybridizable with 0.7×10~6 dalton mRNA giving rise to 57 Kd and 49 Kd polypeptides in vitro translation. 相似文献
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