喜报
IF=9.56，西南大学植物保护学院王进军教授团队近日在《美国科学院院刊》（PNAS）上在线发表题为“The miR-9b microRNA mediates dimorphism and development of wing in aphids”的研究论文，发现小分子RNA介导生物胁迫因子调控蚜虫翅型分化与翅发育的分子机制，研究结果有利于寻获新的小分子RNA控制剂靶标，为蚜虫类害虫防控提供新的思路。（金开瑞合作技术：IP级多克隆抗体制备）
论文链接
（信息来源：西南大学植物保护学院和PNAS杂志官网）
金开瑞抗体定制技术服务
金开瑞抗体定制平台，由多位应用设计专家和工程设计专家合力打造而成，所有技术人员均拥有多年的抗原设计和制备单/多克隆抗体的开发及生产经验。平台建立以来，已成功为客户制备了1000多种高质量抗体，其中部分抗体达到临床应用质量标准。
一站式的抗体服务、多样性的宿主系统、规模化的生产、严格的质控标准，使得金开瑞的定制抗体稳定可靠，深受国内外客户的欢迎。目前金开瑞抗体服务平台提供单/多克隆抗体定制及相关应用型产品的开发和批量生产，真正做到以识别內源性抗原为唯一验收标准，从根本上解决客户的痛点。
服务流程
合作案例回顾
案例一
Comparative proteomics combined with analyses of transgenic plants reveal ZmREM1.3 mediates maize resistance to southern corn rust. Plant Biotechnology Journal.
合作技术：抗体制备
抗体：ZmREM1.3兔多抗
Western blot analysis of ZmREM1.3 in transgenic maize lines 227, 229, 231 and 233 as well as the corresponding non-transgenic sib lines, with b-actin as the loading control.
案例二
In-depth Proteome of the Hypopharyngeal Glands of Honeybee Workers Reveals Highly Activated Protein and Energy Metabolism in Priming the Secretion of Royal Jelly.
合作技术：抗体制备
抗体：多种兔多抗和鼠单抗
Polyclonal rabbit antibodies against 60S ribosomal proteins RpL28, RpL26, and 40S ribosomal protein S4 (RpS4), and the monoclonal mouse antibody against major royal jelly protein 1 (MRJP1) were developed (Genecreate Biological Engineering, Wuhan, China).
案例三
Divergent molecular evolution in glutathione S-transferase conferring malathionresistance in the oriental fruit fly, Bactrocera dorsalis (Hendel).
合作技术：抗体制备
抗体：制备MR、MS特异性抗体
案例四
CRD1, an Xpo1 domain protein, regulates miRNA accumulation and crown root development in rice, plant journal.
合作技术：抗体制备
抗体：抗CRD 1多克隆抗体
(c) Immunostaining of CRD1-GFP (red fluorescence) in cross-sections of root tips of HJ2 (upper panel) and CRD1-GFP lines (lower panel). (d) Validation of CRD1 antibody (Anti-CRD1) using immunoblot analysis. (e) Subcellular localization of CRD1 in HJ2 analyzed by immunoblot analysis.
案例五
Multiplex immunoassay of chicken cytokines via highly-sensitive chemiluminescent imaging array，Analytica Chimica Acta.
合作技术：抗体制备
抗体：CHIL-4和ChIFN-4的单抗、纯化的重组CHIL-4和ChIFN-1抗原
For the first incubation, the surface capture of the cytokines by their respective primary antibodies anti-ChIL-4 and anti-ChIFN-γ, the subsequent CL intensity value increased with increasing incubation time up to a maximum at 30 min (Fig.2a). For the second step, formation of the sandwich via the attachment of the Ab2-AuNP-HRP probe to the exposed Ab1-cytokine-immunocomplex, the maximum CL value was similarly reached with only a 25 min incubation (Fig.2b).