PAX-8 (PT0042R) rabbit mAb

  • 货号:YM8013
  • 应用:IHC;ELISA
  • 种属:Human;
    • 靶点:
    • Pax-8
    • 简介:
    • >>Thyroid hormone synthesis;>>Pathways in cancer;>>Transcriptional misregulation in cancer;>>Thyroid cancer
    • 基因名称:
    • PAX8
    • 蛋白名称:
    • Paired box protein Pax-8
    • Human Gene Id:
    • 7849
    • Human Swiss Prot No:
    • Q06710
    • Mouse Swiss Prot No:
    • Q00288
    • 免疫原:
    • Synthesized peptide derived from human protein. AA range:150-250
    • 特异性:
    • endogenous
    • 组成:
    • PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
    • 来源:
    • Monoclonal Rabbit IgG1, Kappa
    • 稀释:
    • IHC 1:100-500 ELISA: 1:20000
    • 纯化工艺:
    • Protein A
    • 储存:
    • -15°C to -25°C/1 year(Do not lower than -25°C)
    • 其他名称:
    • PAX8;Paired box protein Pax-8
    • 背景:
    • This gene encodes a member of the paired box (PAX) family of transcription factors. Members of this gene family typically encode proteins that contain a paired box domain, an octapeptide, and a paired-type homeodomain. This nuclear protein is involved in thyroid follicular cell development and expression of thyroid-specific genes. Mutations in this gene have been associated with thyroid dysgenesis, thyroid follicular carcinomas and atypical follicular thyroid adenomas. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010],
    • 功能:
    • caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,developmental stage:In developing excretory system, during thyroid differentiation and in adult thyroid.,disease:Defects in PAX8 are the cause of congenital hypothyroidism non-goitrous type 2 (CHNG2) [MIM:218700]. CHNG2 is a disease characterized by thyroid dysgenesis, the most frequent cause of congenital hypothyroidism, accounting for 85% of case. The thyroid gland can be completely absent (athyreosis), ectopically located and/or severely hypoplastic. Ectopic thyroid gland is the most frequent malformation, with thyroid tissue being found most often at the base of the tongue.,function:Transcription factor for the thyroid-specific expression of the genes exclusively expressed in the thyroid cell type, maintaining the functional differentiation of such cell
    • 细胞定位:
    • Nuclear
    • 组织表达:
    • Expressed in the excretory system, thyroid gland and Wilms tumors.