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Last updated: 2021/8/8

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LBR monoclonal antibody, clone EDO-12 

  • Catalog # : MAB20437
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against synthetic peptide of human LBR.
  • Immunogen:
  • A synthetic peptide corresponding to human LBR.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 70.703
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Affinity purification
  • Isotype:
  • IgG
  • Recommend Usage:
  • Immunocytochemistry (1:100-1:500)
    Immunofluorescence (1:100-1:500)
    Immunohistochemistry (1:50-1:200)
    Immunoprecipitation (1:30)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).
  • Storage Instruction:
  • Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
  • 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 of Jurkat cell lysate with LBR monoclonal antibody, clone EDO-12 (Cat # MAB20437).
  • Immunohistochemistry
  • Immunocytochemistry
  • Immunofluorescence
  • Immunoprecipitation
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry
  • Immunocytochemistry
  • Immunofluorescence
  • Immunoprecipitation
  • Gene Information
  • Entrez GeneID:
  • 3930
  • Gene Name:
  • LBR
  • Gene Alias:
  • DHCR14B,FLJ43126,LMN2R,MGC9041,PHA
  • Gene Description:
  • lamin B receptor
  • Gene Summary:
  • The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000035631,integral nuclear envelope inner membrane protein
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