HOXD13 polyclonal antibody-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
HOXD13 polyclonal antibody

HOXD13 polyclonal antibody

商家询价

产品名称: HOXD13 polyclonal antibody

英文名称: HOXD13 polyclonal antibody

产品编号: PAB18561

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:
  • Goat polyclonal antibody raised against synthetic peptide of HOXD13.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids at internal region of human HOXD13.
  • Sequence:
  • C-KSSFPGDVALNQPD
  • Host:
  • Goat
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Storage Buffer:
  • In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Recommend Usage:
  • ELISA (1:8000)
    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.
  • Applications
  • ELISA
  • Application Image
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 3239
  • Gene Name:
  • HOXD13
  • Gene Alias:
  • BDE,BDSD,HOX4I,SPD
  • Gene Description:
  • homeobox D13
  • Gene Summary:
  • This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq
  • Other Designations:
  • homeo box 4I,homeo box D13

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