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IHC-P analysis of human liver tissue using GTX45800 HBS1L antibody at 1:100. Left to right : DAPI, HBS1L, Merge. Heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.
IHC-P analysis of human liver tissue using GTX45800 HBS1L antibody at 1:100. Left to right : DAPI, HBS1L, Merge. Heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.
IHC-P analysis of human liver tissue using GTX45800 HBS1L antibody at 1:100. Left to right : DAPI, HBS1L, Merge. Heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.

HBS1L antibody, C-term

GTX45800
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetHBS1L
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Overview

  • Supplier
    GeneTex
  • Product Name
    HBS1L antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 2-10 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID10767
  • Target name
    HBS1L
  • Target description
    HBS1 like translational GTPase
  • Target synonyms
    EF-1a; eRF3 family member; eRF3c; ERF3-similar protein; ERFS; HBS1; HBS1-like protein; Hsp70 subfamily B suppressor 1-like protein; HSPC276
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9Y450
  • Protein Name
    HBS1-like protein
  • Scientific Description
    This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203