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WB analysis of human breast lysate using GTX89522 SPFH2 antibody, C-term. Dilution : 1microg/ml Loading : 30microg protein in RIPA buffer
WB analysis of human breast lysate using GTX89522 SPFH2 antibody, C-term. Dilution : 1microg/ml Loading : 30microg protein in RIPA buffer
WB analysis of human breast lysate using GTX89522 SPFH2 antibody, C-term. Dilution : 1microg/ml Loading : 30microg protein in RIPA buffer

SPFH2 antibody, C-term

GTX89522
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetERLIN2
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Overview

  • Supplier
    GeneTex
  • Product Name
    SPFH2 antibody, C-term
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is expected to recognise isoform 1 (NP_009106) only.
  • Application Supplier Note
    WB: 0.3-1microg/ml. IHC-P: 3.75microg/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
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID11160
  • Target name
    ERLIN2
  • Target description
    ER lipid raft associated 2
  • Target synonyms
    C8orf2; endoplasmic reticulum lipid raft-associated protein 2; epididymis secretory sperm binding protein; erlin-2; NET32; spastic paraplegia 18 (autosomal dominant); SPFH domain family, member 2; SPFH2; SPG18; stomatin-prohibitin-flotillin-HflC/K domain-containing protein 2
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO94905
  • Protein Name
    Erlin-2
  • Scientific Description
    This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203