MID1 polyclonal antibody (A01)-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
MID1 polyclonal antibody (A01)

MID1 polyclonal antibody (A01)

商家询价

产品名称: MID1 polyclonal antibody (A01)

英文名称: MID1 polyclonal antibody (A01)

产品编号: H00004281-A01

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 polyclonal antibody raised against a partial recombinant MID1.
  • Immunogen:
  • MID1 (AAH53626, 441 a.a. ~ 540 a.a) partial recombinant protein with GST tag.
  • Sequence:
  • PNIKQNHYTVHGLQSGTKYIFMVKAINQAGSRSSEPGKLKTNSQPFKLDPKSAHRKLKVSHDNLTVERDESSSKKSHTPERFTSQGSYGVAGNVFIDSGR
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Storage Buffer:
  • 50 % glycerol
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00004281-A01
    Western Blot detection against Immunogen (37 KDa) .
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Recombinant protein)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 4281
  • Gene Name:
  • MID1
  • Gene Alias:
  • BBBG1,FXY,GBBB1,MIDIN,OGS1,OS,OSX,RNF59,TRIM18,XPRF,ZNFXY
  • Gene Description:
  • midline 1 (Opitz/BBB syndrome)
  • Gene Summary:
  • The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Several different transcript variants are generated by alternate splicing; however, the full-length nature of some of the variants has not been determined. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000022896,OTTHUMP00000022898,OTTHUMP00000022900,OTTHUMP00000022901,midline 1,midline 1 ring finger,putative transcription factor XPRF,tripartite motif protein TRIM18,zinc finger on X and Y, mouse, homolog of

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