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IHC-P analysis of human lung tissue using GTX46621 FAM134B antibody at 4.0-8.0μg/ml.
IHC-P analysis of human lung tissue using GTX46621 FAM134B antibody at 4.0-8.0μg/ml.
IHC-P analysis of human lung tissue using GTX46621 FAM134B antibody at 4.0-8.0μg/ml.

FAM134B antibody, Internal

GTX46621
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetRETREG1
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Overview

  • Supplier
    GeneTex
  • Product Name
    FAM134B antibody, Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.2-2.5 ug/ml. IHC-P: 2-10 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID54463
  • Target name
    RETREG1
  • Target description
    reticulophagy regulator 1
  • Target synonyms
    FAM134B, JK-1, JK1, reticulophagy regulator 1, family with sequence similarity 134 member B, protein FAM134B, reticulophagy receptor 1, reticulophagy receptor FAM134B
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9H6L5
  • Protein Name
    Reticulophagy regulator 1
  • Scientific Description
    The protein encoded by this gene is a cis-Golgi transmembrane protein that may be necessary for the long-term survival of nociceptive and autonomic ganglion neurons. Mutations in this gene are a cause of hereditary sensory and autonomic neuropathy type IIB (HSAN IIB), and this gene may also play a role in susceptibility to vascular dementia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Gatz C, Hathazi D, Münchberg U, et al. Identification of Cellular Pathogenicity Markers for SIL1 Mutations Linked to Marinesco-Sjögren Syndrome. Front Neurol. 2019,10:562. doi: 10.3389/fneur.2019.00562
    Read this paper

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