Pax-2 (60-P)

mouse

抗-Pax-2 抗体 60-P 是小鼠单克隆 IgG2a κ，Pax-2抗体, 在5篇文献中引用，规格为100 µg/ml免疫human物种的重组PAX2推荐用于 mouse, rat 和 human 来源的Pax-2 WB 和 IP检测看 Pax (D-7): sc-514352，可查看有标记的 Pax-2 抗体，包括AC, HRP, FITC, PE, Alexa Fluor® 488, 594, 647, 680 和 790关于如何获取Pax-2 (60-P): sc-130387的免费10 µg小样，联系我们技术服务部门 (或者您当地的代理商)了解详情。m-IgG Fc BP-HRP 和 m-IgGκ BP-HRP 是 Pax-2 Antibody (60-P) for WB 的首选应用二抗。这些试剂现在以套装形式提供Pax-2 Antibody (60-P)。 (见下方订购信息). 查看产品引用文献(5) Pax-2 Antibody (60-P) is a high quality monoclonal Pax-2 antibody (also designated PAX2 antibody) suitable for the detection of the Pax-2 protein of mouse, rat and human origin. Pax-2 Antibody (60-P) is available as the non-conjugated anti-Pax-2 antibody. Pax genes contain paired domains with strong homology to genes in Drosophila which are involved in programming early development. The PAX2 gene is expressed in primitive cells of the kidney, ureter, eye, ear, and central nervous system. More specifically, in human embryo sections, PAX2 is expressed in the optic vesicle and later in the retina, in the otic vesicle and later in the semicircular canals of the inner ear, and in mesonephros, metanephros, adrenals, spinal cord, and hindbrain. PAX2 mutations can be responsible for renal hypoplasia, either isolated or associated with various ophthalmologic manifestations ranging from retinal coloboma to microphthalmia. Lesions in the PAX6 gene accounts for most cases of aniridia, a congenital malformation of the eye, chiefly characterized by iris hypoplasia, which can cause blindness. PAX6 is involved in other anterior segment malformations besides aniridia, such as Peters anomaly, a major error in the embryonic development of the eye with corneal clouding with variable iridolenticulocorneal adhesions.For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Replacement monoclonal antibody for: sc-133889.

肾发育及血管生成的重要转绿因子抗体、1.0 ml 磷酸缓冲盐溶液(含 0.1% 叠氮化钠和 0.1% 明胶)

HumanPAX2

5076;18504