Polyclonal antibody preparation against NDRG family.
抗人ndrg家族的多克隆抗体制备。
Polyclonal antibody was prepared by immunizing rabbits.
免疫家兔制备多克隆抗体。
It may be superior to the currently used GP73 polyclonal antibody.
可能优于目前使用的GP73多克隆抗体的检测。
Master the methods of preparation and purification of polyclonal antibody.
⒉ 了解多克隆抗体的制备及纯化的基本方法。
Polyclonal antibody preparation against the peptides of NDRG family proteins.
抗人ndrg家族寡肽的多克隆抗体制备。
The specificity of the polyclonal antibody was good and each parameter was stable.
所制得的多克隆抗体特异性较强，各项参数都较为稳定。
Immunize New Zealand White rabbits to produce polyclonal antibody (rabbit-anti UROC28).
免疫新西兰白兔制备并纯化兔抗uroc28多克隆抗体。
Then polyclonal antibody of nt was acquired from animal immunization of this production.
用此合成产物进行动物体免疫，获得了NT的多克隆抗体。
Objective To develop a method of production of the polyclonal antibody and its preservation.
目的通过鼠痘病毒抗体的制备摸索鼠源性多抗的大量生产方法。
Anti-Acrylamide polyclonal antibody was prepared by immunizing method of artificial antigen.
应用人工抗原免疫成功制备抗丙烯酰胺多克隆抗体。
AIM: To produce high titer PC-1 protein rabbit polyclonal antibody and explore PC-1 function.
目的：获得高效价PC - 1蛋白的兔多克隆抗体，用于PC - 1功能的实验。
Objective To prepare anti-activin receptor-interacting protein 1 (ARIP1) polyclonal antibody.
目的：制备抗激活素受体相互作用蛋白1（ARIP1）抗体并探讨其应用。
The results were compared with those from GP73 polyclonal antibody and alpha-fetoprotein (AFP).
将此结果同多克隆抗体的检测结果及甲胎蛋白（AFP）的诊断结果进行比较。
RESULTS: Polyclonal antibody with higher specificity and higher potency was prepared successfully.
结果成功制备特异性好、效价较高的多克隆抗体。
The specificity of polyclonal antibody of lactoferrin is determined by dot immuno-gold filtration assay(DIGFA).
采用斑点免疫金渗滤法对抗乳铁蛋白多克隆抗体特异性进行检测。
The rabies virus antigen contents were detected by double antibody sandwich ELISA assay using polyclonal antibody.
采用多克隆双抗体夹心elisa法快速检测狂犬病毒抗原含量。
The specificity of the purified polyclonal antibody was identified by indirect fluorescence staining and FCM analysis.
间接免疫荧光染色及流式细胞术鉴定多克隆抗体的特异性。
Methods:Anti-ouabain polyclonal antibody egg yolk(IgY) and anti-ouabain rabbit antibody(IgG) were prepared respectively.
方法：分别制备出鸡蛋黄抗哇巴因多克隆抗体及兔抗体。
Objective: To produce rabbit polyclonal antibody of murine PC 1 protein and detect its expression profile in mouse organs.
目的：获得小鼠pc1蛋白的兔多克隆抗体，检测其在小鼠器官中的表达谱。
The cell culture liquid containing PDGF-BB was active and could be neutralized by the polyclonal antibody of human PDGF-BB.
MTT方法较为稳定，PDGF—BB细胞培养液具有一定活性，并能被抗人PDGF-BB 多克隆抗体中和。
The monoclonal antibody and polyclonal antibody were respectively purified from ascites and serum by affinity chromatography.
亲和层析分别纯化腹水和血清得到单克隆抗体和多克隆抗体。
Purpose To study the value of immunohistochemical stain technique in the diagnosis of tuberculous by using BCG polyclonal antibody.
目的：探讨用卡介苗（BCG）多克隆抗体检测结核性病变组织中BCG抗原对结核病的诊断价值。
Polyclonal antibody against T-2 toxin was produced using T-2 toxin immunity rabbits. It could be used to determine T-2 toxin in corn.
用t - 2毒素免疫家兔，获得了抗t - 2毒素的多克隆抗体，运用该抗体建立了检测玉米中t - 2毒素的间接竞争性酶联免疫吸附测定法。
Objective To investigate the application value of detection of PGL-I antigen by using PGL-I polyclonal antibody in the diagnosis of leprosy.
目的探讨采用酚糖脂- I (PGL - I)多克隆抗体检测皮肤活检标本中PG L - I抗原对麻风诊断和鉴别诊断的价值。
This polyclonal antibody may lay a foundation for the further studies on the biological functions and epitopes of the 3d polymerase of FMDV.
结论制备了具有高亲和性和特异性的3d聚合酶多克隆抗体，为3d聚合酶的生物学功能和抗原表位研究奠定了基础。
Conclusion The recombinant human L-selectin protein can express with high efficiency in E. coli M15. The prepared polyclonal antibody has a high titer.
结论：人l -选择素蛋白可在M15大肠杆菌中高效表达，其多克隆抗体效价较高。
Conclusion The polyclonal antibody against ARIP1 has been successfully prepared and can be used to do immunohistochemical analysis for ARIP1 protein expression.
结论：成功地制备了抗arip1多克隆抗体，该抗体可用于ARIP1成熟蛋白表达的免疫组织化学染色分析。
Objective: To explore the role of BCG polyclonal antibody for early diagnosis of leprosy, assessment of therapeutic efficacy, and detection of the recurrent cases.
目的讨论卡介苗(BCG)多克隆抗体对麻风病的早期诊断，治疗效果评估和复发病人发现的作用。
CONCLUSION: Recombined prokaryotic expression vector, the purified protein and prepared polyclonal antibody were the necessary materials for further study of this protein.
结论：原核表达载体的构建、重组蛋白的表达、纯化及多克隆抗体的制备为今后研究该蛋白的功能提供了良好的基础。
CONCLUSION: Recombined prokaryotic expression vector, the purified protein and prepared polyclonal antibody were the necessary materials for further study of this protein.
结论：原核表达载体的构建、重组蛋白的表达、纯化及多克隆抗体的制备为今后研究该蛋白的功能提供了良好的基础。
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