EML1 monoclonal antibody (M01A), clone 5G3-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
EML1 monoclonal antibody (M01A), clone 5G3

EML1 monoclonal antibody (M01A), clone 5G3

商家询价

产品名称: EML1 monoclonal antibody (M01A), clone 5G3

英文名称: EML1 monoclonal antibody (M01A), clone 5G3

产品编号: H00002009-M01A

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 a partial recombinant EML1.
  • Immunogen:
  • EML1 (NP_001008707, 1 a.a. ~ 99 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
  • Sequence:
  • MEDGFSSYSSLYDTSSLLQFCNDDSASAASSMEVTDRIASLEQRVQMQEDDIQLLKSALADVVRRLNITEEQQAVLNRKGPTKARPLMQTLPLRTTVNN
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Isotype:
  • IgM Kappa
  • Storage Buffer:
  • In ascites fluid
  • 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 H00002009-M01A
    Western Blot detection against Immunogen (36.63 KDa) .
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • EML1 monoclonal antibody (M01A), clone 5G3 Western Blot analysis of EML1 expression in HepG2 ( Cat # L019V1 ).
  • Protocol Download
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Recombinant protein)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2009
  • Gene Name:
  • EML1
  • Gene Alias:
  • ELP79,EMAP,EMAPL,FLJ45033,HuEMAP
  • Gene Description:
  • echinoderm microtubule associated protein like 1
  • Gene Summary:
  • Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • echinoderm microtubule-associated protein-like

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