Adrenergic Receptor Kinase, beta 1 (bARK1, B1 AR, ARK1 beta, G Protein Coupled Receptor Kinase 2, GPCR K2, GRK2)[Adrenergic Receptor Kinase, beta 1]

  • Catalog number
    MBS606296
  • Price
    Please ask
  • Size
    NA
  • Products_type
    Antibody
  • Reactivity
    Human, Mammal, Rat
  • Description
    The receptors are ligand binding factors of type 1, 2 or 3 and protein-molecules that receive chemical-signals from outside a cell. When such chemical-signals couple or bind to a receptor, they cause some form of cellular/tissue-response, e.g. a change in the electrical-activity of a cell. In this sense, am olfactory receptor is a protein-molecule that recognizes and responds to endogenous-chemical signals, chemokinesor cytokines e.g. an acetylcholine-receptor recognizes and responds to its endogenous-ligand, acetylcholine. However, sometimes in pharmacology, the term is also used to include other proteins that are drug-targets, such as enzymes, transporters and ion-channels.
  • Gene target
  • Gene symbol
    GRK2, OXER1, HCAR1, GPBAR1, AURKA, GPER1
  • Short name
    Adrenergic Receptor Kinase, beta 1 (bARK1, B1 AR, ARK1 beta, G Protein Coupled Receptor Kinase 2, GPCR K2, GRK2)[Adrenergic Receptor Kinase, beta 1]
  • Host
    Mouse
  • Alternative name
    Adrenergic Receptor phosphorylation catalyst, b 1 (bARK1, B1 AR, ARK1 b, G Protein Coupled Receptor phosphorylation catalyst 2, GPCR K2, GRK2)[Adrenergic Receptor phosphorylation catalyst, b 1]
Gene info
  • Identity
  • Gene
  • Long gene name
    G protein-coupled receptor kinase 2
  • Synonyms gene
  • Synonyms gene name
    • adrenergic, beta, receptor kinase 1
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1992-03-25
  • Entrez gene record
    156
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Pleckstrin homology domain containing
    • AGC family kinases
  • VEGA ID
Gene info
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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