FOXE1 polyclonal antibody-抗體-抗體-生物在線

女人与狗锁死了视频大全|霍金死亡过程恐怖视频|无节社团简谱季免费观看|六间房直播大厅|中文字幕欧美另类精品|久久人人玩人妻潮喷内射人人|亚洲国产一区二区三区在线观看

亞諾法生技股份有限公司(Abnova)
FOXE1 polyclonal antibody

FOXE1 polyclonal antibody

商家詢價

產品名稱: FOXE1 polyclonal antibody

英文名稱: FOXE1 polyclonal antibody

產品編號: PAB6429

產品價格: null

產品產地: 臺灣

品牌商標: Abnova

更新時間: null

使用范圍:

亞諾法生技股份有限公司(Abnova)
  • 聯系人 :
  • 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
  • 郵編 : 11493
  • 所在區域 : 臺灣
  • 電話 : +886-920**1152 點擊查看
  • 傳真 : 點擊查看
  • 郵箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of FOXE1.
  • Immunogen:
  • A synthetic peptide corresponding to human FOXE1.
  • Sequence:
  • C-AYPGGIDRFVSAM
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 38.1
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:8000)
    Immunohistochemsitry (1-3 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • Immunohistochemistry
  • ELISA
  • Application Image
  • Immunohistochemistry
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2304
  • Gene Name:
  • FOXE1
  • Gene Alias:
  • FKHL15,FOXE2,HFKH4,HFKL5,TITF2,TTF-2,TTF2
  • Gene Description:
  • forkhead box E1 (thyroid transcription factor 2)
  • Gene Summary:
  • This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis. Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and hereditary sensory neuropathy type I. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000021756,forkhead box E1,forkhead box E2,forkhead, drosophila, homolog-like 15,forkhead-like 15,thyroid transcription factor-2

到Abnova官網查看該產品