Human GNB2L1 ELISA Kit

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  • Alternative name

    Guanine nucleotide-binding protein subunit beta-2-like 1 ELISA KIT; Cell proliferation-inducing gene 21 protein ELISA KIT; Guanine nucleotide-binding protein subunit beta-like protein 12.3 ELISA KIT; Human lung cancer oncogene 7 protein ELISA KIT; HLC-7 ELISA KIT; Receptor for activated C kinase ELISA KIT; Receptor of activated protein kinase C 1 ELISA KIT; RACK1GNB2L1 ELISA KIT; HLC7 ELISA KIT; PIG21 ELISA KIT; HLC-7 ELISA KIT; RACK1 ELISA KIT

  • Catalog
    E017732
  • species
    Human
  • GeneGNB2L1
  • Other Species Mouse GNB2L1 ELISA KitMonkey GNB2L1 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of human GNB2L1. No significant cross-reactivity or interference between human GNB2L1 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human GNB2L1 is typically less than 11.75 pg/ml. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the
  • Intended UseHuman GNB2L1 ELISA Kit allows for the in vitro quantitative determination of GNB2L1 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Description
    specifical
    Principle of the assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for GNB2L1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any GNB2L1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for GNB2L1 is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of GNB2L1 bound in the initial step. The color development is stopped and the intensity of the color is measured.


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