GLRA1 monoclonal antibody (M05), clone 3F1-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
GLRA1 monoclonal antibody (M05), clone 3F1

GLRA1 monoclonal antibody (M05), clone 3F1

商家询价

产品名称: GLRA1 monoclonal antibody (M05), clone 3F1

英文名称: GLRA1 monoclonal antibody (M05), clone 3F1

产品编号: H00002741-M05

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 GLRA1.
  • Immunogen:
  • GLRA1 (NP_000162, 121 a.a. ~ 220 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
  • Sequence:
  • IWKPDLFFANEKGAHFHEITTDNKLLRISRNGNVLYSIRITLTLACPMDLKNFPMDVQTCIMQLESFGYTMNDLIFEWQEQGAVQVADGLTLPQFILKEE
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Isotype:
  • IgG2a Kappa
  • Storage Buffer:
  • In 1x PBS, pH 7.2
  • 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 H00002741-M05
    Western Blot detection against Immunogen (36.74 KDa) .
  • Applications
  • Sandwich ELISA (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • Detection limit for recombinant GST tagged GLRA1 is approximately 0.03ng/ml as a capture antibody.
  • Protocol Download
  • ELISA
  • Application Image
  • Western Blot (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • Sandwich ELISA (Recombinant protein)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2741
  • Gene Name:
  • GLRA1
  • Gene Alias:
  • MGC138878,MGC138879,STHE
  • Gene Description:
  • glycine receptor, alpha 1
  • Gene Summary:
  • The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene
  • Other Designations:
  • OTTHUMP00000160616,glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome),startle disease/hyperekplexia,stiff person syndrome

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