MSX1 monoclonal antibody, clone 5D11-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
MSX1 monoclonal antibody, clone 5D11

MSX1 monoclonal antibody, clone 5D11

商家询价

产品名称: MSX1 monoclonal antibody, clone 5D11

英文名称: MSX1 monoclonal antibody, clone 5D11

产品编号: MAB10816

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 partial recombinant MSX1.
  • Immunogen:
  • Recombinant protein corresponding to human MSX1.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Isotype:
  • IgG1
  • Storage Buffer:
  • In ascites (0.03% sodium azide)
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Recommend Usage:
  • ELISA (1:10000)
    Western Blot (1:500-1:2000)
    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
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • Western blot analysis using MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816) against NTERA-2 cell lysate.
  • ELISA
  • ELISA
  • ELISA measurement of MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816).
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 4487
  • Gene Name:
  • MSX1
  • Gene Alias:
  • HOX7,HYD1
  • Gene Description:
  • msh homeobox 1
  • Gene Summary:
  • This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000115387,homeobox 7,msh homeo box 1,msh homeobox homolog 1

到Abnova官网查看该产品