Scientists are able to determine the levels of the target molecule in solution by measuring the spectral changes.
通过测量光谱变化，科学家们能够确定目标分子在溶液中的浓度。
The Red mediated recombination can be used to insert, delete or substitute DNA sequences at any desired position on a target molecule without the need for restriction enzymes or DNA ligases.
这种技术可在DNA靶标分子的任意位点进行基因敲除、敲入、点突变等操作，无需使用限制性内切酶和连接酶。
Modeling interaction between inhibitor and target molecule is a key step in CADD.
模拟抑制剂与靶标分子的结合作用是计算机辅助药物设计的关键部分。
The structures of the key intermediates and target molecule were confirmed by ESI-MS, IR and NMR.
关键中间体及最终产物的结构经质谱、红外光谱、核磁共振氢谱及碳谱得到确证。
The results predict that the hole transport rate is 30 times of the electron transport rate for the target molecule.
结果显示，该分子的正电荷传输速率为负电荷传输速率的30倍。
The target molecule was synthesized through using chiral reagent, reduction of double bond, hydrogenolysis and hydrolysis of ester group.
之后，经引入手性试剂，双键还原，氢解，水解酯基得到目标产物的合成路线。
Upon binding of the target molecule, the porphyrinogen derivative undergoes a detectable adsorption and emission of electromagnetic radiation.
通过与靶分子的结合，所述卟啉原衍生物发生可探测到的电磁辐射的吸收和发射。
From 2, 6-dichloropyridine as starting material, we can get the target molecule through nitration, substitution, reduction, cyclization, oxidation etc.
以2,6 -二氯吡啶为原料，通过硝化，取代，还原，环化，氧化等几步反应可得到目标化合物。
The measurement target molecule with known concentration is used to perform the measurement, and the measured result is consistent to the added DNA quantity.
用已知浓度的检测靶分子进行测试，测定结果与加入的DNA量是一致的。
They developed a computational method that compares how similar the side effects of different drugs are and predicts how likely the drugs act on the same target molecule.
他们开发了一种计算方法，来比较不同药物产生副作用的相同点，并预测不同药物作用于同一分子靶体的可能性。
Methods: Using the influenza A3 split vaccine as the target molecule, peptides that could bind with target molecule were selected from the phage display 12 peptide library by 3 rounds of biopaning.
方法：以甲三型流感病毒裂解疫苗原液为靶分子，经过3轮生物淘选，从噬菌体随机肽库中筛选与之结合的噬菌体。
Methods: Using the influenza A3 split vaccine as the target molecule, peptides that could bind with target molecule were selected from the phage display 12 peptide library by 3 rounds of biopaning.
方法：以甲三型流感病毒裂解疫苗原液为靶分子，经过3轮生物淘选，从噬菌体随机肽库中筛选与之结合的噬菌体。
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