GPCR GPR15 Positive Controlfor Western Blot

  • Catalog number
    PC-GPCR15
  • Price
    Please ask
  • Size
    100 µg
  • Vial description
    purified GPCR GPR15 Positive Control
  • Antibody s or peptide concentration
    ug/ml in stabilization buffer
  • Raised in
    sterile environment
  • Reactivity
    specific antigen
  • Immunogen
    see msds
  • Antigen or peptide
    GPCR GPR15
  • Original name
    GPCR GPR15 Positive Control
  • Phosphorylation
    Non phosphorylated
  • Epitope
    specific sequence
  • Type
    Positive Control
  • Antibody s relevance
    WB
  • Antibody s application
    Western Blot
  • Storage conditions
    -20⁰C for long term storage
  • Genbank number
    see ncbi
  • Protein number
    P49685
  • Test
    Western Blot can be performed on tissues and cell extracts to determine the proteins present in your sample after PAGE electrophoresis and transfer on PVDF or Nitrocellulose. PVDF is more advised. The best detection method is using enhanced chemiluminescence or ECL.
  • Description
    Positive controls are the same as the target vector or antibody or protein and can be spiked to the sample before the analysis starts.
  • Group
    positif
  • Gene target
    GPCR   GPR15   Controlfor  
  • Gene symbol
    GPR15, OXER1, HCAR1, GPBAR1, GPER1
  • Short name
    GPCR GPR15 Positive Controlfor Blot
  • Technique
    Western Blot, Positive, Blot, western Blots
  • Alternative name
    GPCR GPR15 Positive Controlfor Western Blot
  • Alternative technique
    controls, western
Gene info
  • Identity
  • Gene
  • Long gene name
    G protein-coupled receptor 15
  • Locus
  • Discovery year
    1995-08-10
  • Entrez gene record
  • Pubmed identfication
  • Classification
    • G protein-coupled receptors, Class A orphans
  • VEGA ID
Gene info
Gene info
Gene info
Gene info
MeSH Data
  • Name
  • Concept
    Scope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
  • Tree numbers
    • E05.393.620.500
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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