HAX1 monoclonal antibody, clone 8F9G7-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
HAX1 monoclonal antibody, clone 8F9G7

HAX1 monoclonal antibody, clone 8F9G7

商家询价

产品名称: HAX1 monoclonal antibody, clone 8F9G7

英文名称: HAX1 monoclonal antibody, clone 8F9G7

产品编号: MAB7875

产品价格: null

产品产地: 台湾

品牌商标: Abnova

更新时间: null

使用范围:

亚诺法生技股份有限公司(Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152 点击查看
  • 传真 : 点击查看
  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against synthetic peptide of HAX1.
  • Immunogen:
  • A synthetic peptide corresponding to N-terminus 15 amino acids of human HAX1.
  • Host:
  • Mouse
  • Reactivity:
  • Human, Mouse, Rat
  • Form:
  • Liquid
  • Storage Buffer:
  • In PBS (0.02% sodium azide)
  • Storage Instruction:
  • Store at 4°C for three months. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Recommend Usage:
  • Western Blot (1-2 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
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • Western blot analysis of HAX1 in human brain tissue lysate with HAX1 monoclonal antibody, clone 8F9G7 (Cat # MAB7875) at (A) 1 and (B) 2 ug/mL .
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Gene Name:
  • HAX1
  • Gene Alias:
  • FLJ17042,FLJ18492,FLJ93803,HCLSBP1,HS1BP1,SCN3
  • Gene Description:
  • HCLS1 associated protein X-1
  • Gene Summary:
  • The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • HCLS1 (and PKD2) associated protein,HS1 binding protein,OTTHUMP00000034190
  • Related Disease

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