MAN1 rabbit pAb

    • 货号:YT7363
    • 应用:WB
    • 种属:Human;Mouse
      • 靶点:
      • MAN1
      • 基因名称:
      • LEMD3 MAN1
      • 蛋白名称:
      • MAN1
      • Human Swiss Prot No:
      • Q9Y2U8
      • Mouse Swiss Prot No:
      • Q9WU40
      • 免疫原:
      • Synthesized peptide derived from human MAN1 AA range: 61-111
      • 特异性:
      • This antibody detects endogenous levels of MAN1 at Human/Mouse
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500-2000
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 分子量:
      • 100kD
      • 背景:
      • This locus encodes a LEM domain-containing protein. The encoded protein functions to antagonize transforming growth factor-beta signaling at the inner nuclear membrane. Two transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.[provided by RefSeq, Nov 2009],
      • 功能:
      • disease:Defects in LEMD3 are a cause of melorheostosis [MIM:155950]. Melorheostosis is a rare mesenchymal dysplasia and one of the sclerosing bone disorders. It is caused by a developmental error, with a sclerotomal distribution, frequently involving one limb. It may be asymptomatic, but pain, stiffness with limitation of motion, leg-length discrepancy and limb deformity may occur.,disease:Defects in LEMD3 are the cause of Buschke-Ollendorff syndrome (BOS) [MIM:166700]; also known as dermatoosteopoikilosis or disseminated dermatofibrosis with osteopoikilosis or dermatofibrosis lenticularis disseminata with osteopoikilosis or osteopathia condensans disseminata. BOS refers to the association of osteopoikilosis with disseminated connective-tissue nevi. Osteopoikilosis is a skeletal dysplasia characterized by a symmetric but unequal distribution of multiple hyperostotic areas in different pa
      • 细胞定位:
      • Nucleus inner membrane ; Multi-pass membrane protein .
      • 组织表达:
      • Heart, brain, placenta, lung, liver and skeletal muscle.
      • 产品图片
      • Western blot analysis of lysates from MCF-7 cells, primary antibody was diluted at 1:1000, 4°over night