Anti-KV2.1 Antibody

KCNB1, DRK1, Delayed rectifier potassium channel 1, Potassium voltage-gated channel subfamily B member 1
    Cat #: APC-012
    Alternative Name KCNB1, DRK1, Delayed rectifier potassium channel 1, Potassium voltage-gated channel subfamily B member 1
  • Lyophilized Powder
  • Antigen Incl.
  • Type: Polyclonal
    Host: Rabbit
    Reactivity: h, m, r
    • Peptide (CY)HMLPGGGAHGSTRDQSI, corresponding to amino acid residues 841-857 of rat KV2.1 (Accession P15387). Intracellular, C-terminus.
    • Anti-KV2.1 Antibody
    Accession (Uniprot) Number P15387
    Gene ID 25736
    Peptide confirmation Confirmed by amino acid analysis and mass spectrometry.
    Homology Mouse - identical; human, rabbit - 15/17 amino acid residues identical.
    RRID AB_2040162.
    Purity IgG fraction purified on immobilized Protein A.
    Form Lyophilized powder. Reconstituted antibody contains phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.05% NaN3.
    Isotype Rabbit IgG.
    Storage before reconstitution The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.
    Reconstitution 50 μl or 0.2 ml double distilled water (DDW), depending on the sample size.
    Antibody concentration after reconstitution 1 mg/ml.
    Storage after reconstitution The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).
    Negative control antigen storage before reconstitution Lyophilized powder can be stored intact at room temperature for 2 weeks. For longer periods, it should be stored at -20°C.
    Negative control antigen reconstitution 100 µl double distilled water (DDW).
    Negative control antigen storage after reconstitution -20°C.
    Preadsorption Control 1 μg peptide per 1 μg antibody.
    Standard quality control of each lot Western blot analysis.
    Applications: ic, if, ih, ip, wb
    May also work in: ifc*
    Western blot
    • Anti-KV2.1 Antibody
      Western blot analysis of rat brain membranes:
      1. Anti-KV2.1 Antibody (#APC-012), (1:500).
      2. Anti-KV2.1 Antibody, preincubated with the control peptide antigen.
    • Xenopus oocyte membranes (MacDonald, P.E. et al. (2002) Mol. Endocrinol16, 2452.).
    • Anti-KV2.1 Antibody
      Expression of KV2.1 channel in rat pancreas
      Immunohistochemical staining of rat paraffin embedded pancreas sections using Anti-KV2.1 Antibody (#APC-012), (1:50), followed by goat anti-rabbit-AlexaFluor-555 secondary antibody. Endocrine (Islets of Langerhans) and exocrine areas of pancreas section are shown. Strong and highly specific KV2.1 staining is evident only in endocrine cells (red). Hoechst 33342 is used as the counterstain (blue).
    • Mouse pancreas sections (10 μg/ml) (MacDonald, P.E. et al. (2002) J. Biol. Chem. 277, 44938.).

      Human brain sections (1:500) (Mezey, E. et al. (2003) Proc. Natl. Acad. Sci. U.S.A. 100, 1364.).
    • Mouse DRGs (Bocksteins, E. et al. (2009) Am. J. Physiol. 296, C1271.).
    1. Albrecht, B. et al. (1993) Receptors Channels 1, 99.
    2. Murakoshi, H. and Trimmer, J.S. (1999) J. Neurosci. 19, 1728.
    3. Archer, S.L. et al. (1998) J. Clin. Invest. 101, 2319.
    4. Escoubas, P. et al. (2002) Mol. Pharmacol. 62, 48.
    Scientific background

    KV2.1 is a member of the voltage-gated K+ channel superfamily. Together with the closely related KV2.2 protein they form the KV2 subfamily also known as Shab.1

    As with all KV channels, KV2.1 possesses the signature structure of the voltage-dependent K+ channels: six membrane-spanning domains with intracellular N and C termini. The functional KV channel is a tetramer that can either be a homotetramer or a heteromer of KV2.1 and KV2.2 subunits.

    Both KV2.1 and KV2.2 channels are known as delayed rectifiers that is, channels that are activated by changes in membrane potential (depolarization) but inactivate very slowly. The current they form is known as IK or IDR. Accessory subunits such as KChaP and the electrically silent a subunits KV8 and KV9 can modulate biochemical and biophysical properties of KV2.1.2

    KV2.1 is widely expressed throughout the body including brain, lung, pancreas, skeletal muscle and pulmonary artery.2 

    The main function of KV2.1 is to maintain membrane potential and to modulate the electrical excitability in neurons and muscle. In rat pulmonary artery it probably mediates hypoxic pulmonary vasoconstriction together with the KV9.3 subunit.3  

    Several toxins from spider venoms are potent blockers (affecting the channels in the nanomolar range) of KV2.1 channels. Among these the most potent and selective are Stromatoxin-1 (#STS-350), (12.7 nM)and Hanatoxin (42 nM).4

    Application key:

    CBE- Cell-based ELISA, FC- Flow cytometry, ICC- Immunocytochemistry, IE- Indirect ELISA, IF- Immunofluorescence, IFC- Indirect flow cytometry, IHC- Immunohistochemistry, IP- Immunoprecipitation, LCI- Live cell imaging, N- Neutralization, WB- Western blot

    Species reactivity key:

    H- Human, M- Mouse, R- Rat
    Last update: 24/01/2020

    Alomone Labs is pleased to offer a highly specific antibody directed against an epitope of the rat KV2.1 channel. Anti-KV2.1 Antibody (#APC-012) can be used in western blot, immunoprecipitation, immunocytochemistry, and immunohistochemistry applications. It has been designed to recognize KV2.1 from rat, human, and mouse samples.

    For research purposes only, not for human use



    Scientific Background


    Western blot citations
    1. Human myometrium tissue lysate.
      Novakovic, R. et al. (2015) Mol. Hum. Reprod. 21, 545.
    2. Rat uterine tissue lysate.
      Novakovic, R. et al. (2013) J. Physiol. Pharmacol. 64, 795.
    3. Rat lung lysate.
      Lv, Y. et al. (2013) Am. J. Physiol. 305, L856.
    4. Mouse heart lysate.
      Huang, H. et al. (2013) J. Mol. Cell. Cardiol. 59, 151.
    Immunoprecipitation citations
    1. Xenopus oocyte membranes.
      MacDonald, P.E. et al. (2002) Mol. Endocrinol. 16, 2452.
    Immunohistochemistry citations
    1. Rat lumbar spinal cord sections.
      Wolff, M. et al. (2016) Neurosci. Res. 109, 16.
    2. Mouse brain sections.
      Peltola, M.A. et al. (2016) Schizophr. Bull. 42, 191.
    3. Human myometrium sections (1:50).
      Novakovic, R. et al. (2015) Mol. Hum. Reprod. 21, 545.
    4. Mouse brain sections (1:250).
      Baver, S.B. et al. (2014) J. Neurosci. 34, 5486.
    5. Human artery tissues (1:50).
      Gojkovic-Bukarica, L. et al. (2011) Eur. J. Pharmacol. 654, 266.
    6. Human brain sections (1:500).
      Mezey, E. et al. (2003) Proc. Natl. Acad. Sci. U.S.A. 100, 1364.
    7. Mouse pancreas sections (10 μg/ml).
      MacDonald, P.E. et al. (2002) J. Biol. Chem. 277, 44938.
    Immunocytochemistry citations
    1. Mouse DRGs.
      Bocksteins, E. et al. (2009) Am. J. Physiol. 296, C1271.
    Neutralization citations
    1. Mouse DRG neurons.
      Regnier, G. et al. (2016) Physiol. Rep. 4, e12731.
    2. Mouse ETV1 cells.
      Bishop, H.I. et al. (2015) J. Neurosci. 35, 14922.
    More product citations
    1. Tiran, Z. et al. (2003) J. Biol. Chem. 278, 17509.
    2. MacDonald, P.E. et al. (2002) Diabetes 51, 443.
    3. Platoshyn, O. et al. (2001) Am. J. Physiol. 280, L801.
    4. Reeve, H.L. et al. (2001) J. Appl. Physiol. 90, 2249.
    5. Trepanier-Boulay, V. et al. (2001) Circ. Res. 89, 437.
    6. Betancourt, L. et al. (2000) J. Neurosci. Res. 61, 646.
    7. Yamashita, T. et al. (2000) Circulation 101, 2007.
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