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IHC-P analysis of human lung carcinoma tissue using GTX37416 mGluR1 antibody. Dilution : 1:200
IHC-P analysis of human lung carcinoma tissue using GTX37416 mGluR1 antibody. Dilution : 1:200
IHC-P analysis of human lung carcinoma tissue using GTX37416 mGluR1 antibody. Dilution : 1:200

mGluR1 antibody

GTX37416
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetGRM1
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Overview

  • Supplier
    GeneTex
  • Product Name
    mGluR1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-2000. IHC-P: 1:400-800. *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 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID2911
  • Target name
    GRM1
  • Target description
    glutamate metabotropic receptor 1
  • Target synonyms
    glutamate receptor, metabotropic 1; GPRC1A; metabotropic glutamate receptor 1; MGLU1; MGLUR1; PPP1R85; protein phosphatase 1, regulatory subunit 85; SCA44; SCAR13
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ13255
  • Protein Name
    Metabotropic glutamate receptor 1
  • Scientific Description
    This gene encodes a metabotropic glutamate receptor that functions by activating phospholipase C. L-glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The canonical alpha isoform of the encoded protein is a disulfide-linked homodimer whose activity is mediated by a G-protein-coupled phosphatidylinositol-calcium second messenger system. This gene may be associated with many disease states, including schizophrenia, bipolar disorder, depression, and breast cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of mGluR1/GRM1 using anti-mGluR1/GRM1 antibody (A03049-4). 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 50ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse brain tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-mGluR1/GRM1 antigen affinity purified polyclonal antibody (Catalog # A03049-4) at 0.25 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 1:10000 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 mGluR1/GRM1 at approximately 132KD. The expected band size for mGluR1/GRM1 is at 132KD.
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