Bio-Connect
Immunoprecipitation of Rock-2 protein from HeLa whole cell extracts using 5 microg goat IgG isotype control (GTX35039) or Rock-2 Goat pAb. Western blot analysis was performed using Rock-2 goat pAb. Goat IgG HRP (GTX228416-01) was used as a secondary reagent.
Immunoprecipitation of Rock-2 protein from HeLa whole cell extracts using 5 microg goat IgG isotype control (GTX35039) or Rock-2 Goat pAb. Western blot analysis was performed using Rock-2 goat pAb. Goat IgG HRP (GTX228416-01) was used as a secondary reagent.
Immunoprecipitation of Rock-2 protein from HeLa whole cell extracts using 5 microg goat IgG isotype control (GTX35039) or Rock-2 Goat pAb. Western blot analysis was performed using Rock-2 goat pAb. Goat IgG HRP (GTX228416-01) was used as a secondary reagent.

Goat IgG isotype control

GTX35039
GeneTex
ApplicationsFlow Cytometry, ImmunoPrecipitation, ELISA, ImmunoHistoChemistry
Product group Antibodies
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    Goat IgG isotype control
  • Delivery Days Customer
    9
  • Application Supplier Note
    Use at a concentration/dilution equivalent to that of your experimental primary antibody.
  • Applications
    Flow Cytometry, ImmunoPrecipitation, ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Host
    Goat
  • Isotype
    IgG
  • Scientific Description
    Inclusion of an appropriate isotype control is essential for the proper interpretation of experimental results. Because isotype control antibodies have no relevant specificity, they enable the researcher to distinguish non-specific background binding from antigen-specific antibody binding. Non-specific binding of primary antibodies may occur due to either binding of antibody to Fc receptors or non-specific interactions with cellular proteins, lipids, or carbohydrates. Additionally, autofluorescence or endogenous enzyme activity in target cells may give a false positive that could be misinterpreted as antibody binding. These factors vary by target cell type and the isotype of the primary antibody. Therefore, the primary antibody used should be matched to an isotype control of identical species and isotype (including both heavy and light chains).
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

References

  • USP18 enhances dengue virus replication by regulating mitochondrial DNA release.
    Read more
  • SARS-CoV-2 infects an in vitro model of the human developing pancreas through endocytosis. Szlachcic WJ et al., 2022 Jul 15, iScience
    Read more
  • Lipid-based strategies used to identify extracellular vesicles in flow cytometry can be confounded by lipoproteins: Evaluations of annexin V, lactadherin, and detergent lysis. Botha J et al., 2022 Apr, J Extracell Vesicles
    Read more
  • Mitochondrial CMPK2 mediates immunomodulatory and antiviral activities through IFN-dependent and IFN-independent pathways. Lai JH et al., 2021 Jun 25, iScience
    Read more
  • Membrane Protein of Human Coronavirus NL63 Is Responsible for Interaction with the Adhesion Receptor. Naskalska A et al., 2019 Oct 1, J Virol
    Read more
  • Vitrectomy for Diabetic Macular Edema: Optical Coherence Tomography Criteria and Pathology of the Vitreomacular Interface. Hagenau F et al., 2019 Apr, Am J Ophthalmol
    Read more
  • Expression and localization of CRAMP in rat tooth germ and during reparative dentin formation. Horibe K et al., 2018 Sep, Clin Oral Investig
    Read more
  • Different populations of Wnt-containing vesicles are individually released from polarized epithelial cells. Chen Q et al., 2016 Oct 21, Sci Rep
    Read more
  • Melanoma stem cells in experimental melanoma are killed by radioimmunotherapy. Jandl T et al., 2013 Feb, Nucl Med Biol
    Read more