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WB analysis of Jurkate cell lysate using GTX85278 SHOC2 antibody in (A) the absence and (B) the presence of blocking peptide. Dilution : 1 microg/ml
WB analysis of Jurkate cell lysate using GTX85278 SHOC2 antibody in (A) the absence and (B) the presence of blocking peptide. Dilution : 1 microg/ml
WB analysis of Jurkate cell lysate using GTX85278 SHOC2 antibody in (A) the absence and (B) the presence of blocking peptide. Dilution : 1 microg/ml

SHOC2 antibody

GTX85278
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetSHOC2
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Overview

  • Supplier
    GeneTex
  • Product Name
    SHOC2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 - 2 microg/mL. IHC-P: 5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID8036
  • Target name
    SHOC2
  • Target description
    SHOC2 leucine rich repeat scaffold protein
  • Target synonyms
    leucine-rich repeat protein SHOC-2; NSLH1; SIAA0862; SOC2; soc-2 suppressor of clear homolog; SUR8
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UQ13
  • Protein Name
    Leucine-rich repeat protein SHOC-2
  • Scientific Description
    SHOC2 protein participates in protein binding / transferase activity in the fibroblast growth factor receptor signaling pathway and Ras protein signal transduction. It is a widely expressed protein composed almost entirely of leucine-rich repeats (LRR), with a lysine-rich sequence at the amino terminus and cytoplasmically localized. SHOC2 acts as a positive modulator of the RAS-MAPK signaling cascade, which is elicited by EGL-15 and LET-23 and mediated by LET-60. SHOC2 together with protein phosphatase 1c (PP1c) forms a highly specific M-Ras effector complex and is essential for activation of the MAPK pathway by growth factors. Furthermore, in tumor cells with Ras gene mutations, inhibition of SHOC2 expression inhibits MAPK, but not PI3K activity. The SHOC2-PP1c holoenzyme provides an attractive therapeutic target for inhibition of the MAPK pathway in cancer. Recent studies show that aberrantly acquired N-myristoylation of SHOC2 causes human disease Noonan-like syndrome with loose anagen hair.
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of Shoc2/Sur8 using anti-Shoc2/Sur8 antibody (A07214-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Shoc2/Sur8 antigen affinity purified polyclonal antibody (Catalog # A07214-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Shoc2/Sur8 at approximately 70 kDa. The expected band size for Shoc2/Sur8 is at 70 kDa.
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Lane 1: Mouse Cerebrum lysates; Lane 2: Mouse Testis lysates; Lane 3: Mouse Esophagus lysates; Lane 4: Mouse Large intestine lysates; Lane 5: Mouse NIH/3T3 cell lysates; Lane 6: Rat Cerebrum lysates; Lane 7: Rat Testis lysates; Lane 8: Rat Esophagus lysates; Lane 9: Rat Large intestine lysates; Lane 10: Human A549 cell lysates; Lane 11: Human U937 cell lysates; Lane 12: Human HL-60 cell lysates probed with SHOC2 Polyclonal Antibody, Unconjugated (bs-7934R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
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