配基

可是，基本的异种化合物活性看来是由配基所决定的。

However , basic Allelochemical activity seems to lie with the aglycone .

配基部分可以来自一个或几个生物合成途径。

The aglycone portion may come from any , or from a combination , of the biosynthetic pathways .

地高辛配基人乳头瘤病毒DNA探针的制备和应用

Preparation of Digoxigenin-HPV DNA Probe and Its Application in Carcinoma of the Cervix

用地高辛配基标记DNA探针及其应用

DNA Probe Labeling with Digoxigenin - dUTP and Its Application in Gene Diagnosis

CD（40）配基化介导B淋巴瘤细胞凋亡机制的研究

Mechanisms of Apoptosis Induced by the Ligation of CD_ ( 40 ) in B-lymphoma-cell

颌间牵引力对成年大鼠髁状突核因子κB受体活化因子配基/骨保护素的调控

Regulation of adult rat condyle receptor activator of nuclear factor kappa B ligand / osteoprotegerin by intermaxillary traction force

微囊藻毒素-LR特异性RNA配基体外筛选探讨

In vitro selection of specific aptamers against microcystin LR

缺血心肌细胞膜β肾上腺素能受体、腺苷酸环化酶和cAMP水平的放射配基分析

Radioligand Assay on β - adrenoreceptor , AC and cAMP Levels During Myocardial Ischemia

IgG配基对肿瘤坏死因子α的吸附机制研究

Studies on Adsorption Mechanism of TNF α with IgG Ligand

急性白血病患者血清中可溶性Fas配基含量的变化

Serum Level of Soluble Fas Ligand in Patients with Acute Leukemia

地高辛配基标记DNA打点杂交和原位杂交检测钩端螺旋体

Marking and Detection of DNA of Leptospires in the Dot - - blot and Situ Hybridization with Digoxigenin - - labelled Probes

急性白血病凋亡因子Fas配基的表达研究

The expression of apoptotic factor Fas ligand in acute leukemia

配基密度为71.4μmol／g。

The ligand density of the macro ligand was 71.4 μ mol / g dextran .

新型阿片受体配基特异性结合μ受体并抑制cAMP生成

Specific binding to μ opioid receptors by new opioid ligands with inhibition of I cAMP production

ERβ蛋白与ERα蛋白有高度的同源性，尤其在DNA结合区和配基结合区。

The ER protein is highly homologous to ER , particularly in the DNA-binding and the ligand binding domains .

结果表明配基密度、pH值、盐浓度和蛋白质特性（等电点和疏水性）对内毒素去除效果均有重要影响。

The results indicated that the ligand density , pH value , salt concentration and protein property all have remarkable effects on endotoxin removal .

FMS样酪氨激酶3受体配基基因的克隆和序列分析

Molecular cloning and sequencing of human c fms-like tyrosine kinase 3 receptor ligand gene

小鼠腹腔巨噬细胞PAF受体放射配基受体结合分析方法

Establishment of PAF receptor radioligand binding assay in mouse peritoneal macrophages

以色氨酸为配基、丁二酸酐为手臂的琼脂凝胶吸附剂吸附动力学实验：吸附剂在37℃对免疫球蛋白E的吸附率为70.73%。

Adsorption dynamics study of adsorbent containing succinic anhydride spacer and tryptophan ligand : The adsorption efficiency to IgE was 70.73 % at 37 ℃ .

雷公藤多苷对佐剂性关节炎模型大鼠关节中核因子κB受体激活剂配基表达的影响

Effect of Glycoside of Tripterygium wilfordii hook . F on Expression of Receptor Activator of Nuclear Factor - κ B Ligand and Osteoprotegerin in Joints of Rat Adjuvant Induced Arthritis

并确定了接间隔臂可以提高载体对HK的选择性.实验证明：以ATP为配基的亲和层析法纯化酵母细胞中的磷酸激酶是可行的。

It is feasible to purify the kinase in yeast by affinity chromatography with ATP as ligand .

随脂蟾毒配基作用浓度和时间的延长，癌细胞核荧光强度减弱，细胞核DNA含量明显降低。

With the prolongation of time and increase of concentration of resibufogenin , fluorescence intensity of cancer cell nucleus reduced and the content of cell nucleus DNA decreased obviously .

D2型多巴胺受体配基的研究进展

Recent advances in the structure activity relationship of dopamine D2-like receptor ligands

用地高辛配基（Digoxigenin）标记的cDNA探针检测登革热病毒

Detection of Dengue Virus with Digoxigenin-labelled cDNA Probes

EB病毒受体的放射配基结合分析

Radioligand Binding Assay of Epstein-Barr Virus Receptor

FTIR和染料释放分析结果表明，亲水层和配基与膜均是共价结合，该膜具有良好的化学稳定性。

FTIR analysis indicates covalent couple of hydrophilic layers and dye release determines the covalent bond of the ligand immobilization .

缓冲液的pH值对BLC与螯合配基的结合影响显著。

The buffer pH notably affect BLC binding to the Cu 2 + chelating membrane adsorbent .

对采用外源基因原核显微注射法生产的基因转移山羊，用一种新的DNA非同位素标记法即地高辛配基标记DNA探针作外源基因整合检测。

Gene transfer goats produced by the method of microinjection foreign gene into pronuclear were made integrated detection with a novel nonradioactive DNA labeling method , namely DNA probe labeling with Digoxigenin .

以卵黄免疫球蛋白（immunoglobulinyolk，IgY）为配基，对小牛肠组织来源的碱性磷酸酶进行免疫亲和纯化。

Immunoglobulin yolk ( IgY ) was employed as immunoaffinity ligand to purify alkaline phosphatase from crude enzyme .

新合成的阿片受体配基对稳定转染μ阿片受体的CHO细胞的受体结合特性

Binding Characteristics of New Synthesized Opioid Receptor Ligands to Cloned μ Opioid Receptors Stably Expressed in CHO Cell