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PDE6B Antikörper (AA 25-237)

Dieses Anti-PDE6B-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von PDE6B in WB, IHC, IF, ICC und FACS. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN7600892

Kurzübersicht für PDE6B Antikörper (AA 25-237) (ABIN7600892)

Target

Alle PDE6B Antikörper anzeigen
PDE6B (phosphodiesterase 6B, CGMP-Specific, Rod, beta (PDE6B))

Reaktivität

  • 17
  • 12
  • 10
  • 7
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 16
  • 2
Maus

Klonalität

  • 17
  • 1
Monoklonal

Konjugat

  • 16
  • 1
  • 1
Dieser PDE6B Antikörper ist unkonjugiert

Applikation

  • 15
  • 9
  • 8
  • 7
  • 6
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunocytochemistry (ICC), Flow Cytometry (FACS)

Klon

8I2D7
  • Bindungsspezifität

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 25-237

    Verwendungszweck

    Anti-PDE6 beta/PDE6B Antibody Picoband® (monoclonal, 8I2D7)

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-PDE6 beta/PDE6B Antibody Picoband® (monoclonal, 8I2D7) (ABIN7600892). Tested in Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human PDE6 beta/PDE6B recombinant protein (Position: K25-Q237).

    Isotyp

    IgG2a
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Mouse, Rat
    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x6 cells, Human
    1. Hmani-Aifa, M., Benzina, Z., Zulfiqar, F., Dhouib, H., Shahzadi, A., Ghorbel, A., Rebai, A., Soderkvist, P., Riazuddin, S., Kimberling, W. J., Ayadi, H. Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. Europ. J. Hum. Genet. 17: 474-482, 2009. 2. Tsang, S. H., Woodruff, M. L., Jun, L., Mahajan, V., Yamashita, C. K., Pedersen, R., Lin, C.-S., Goff, S. P., Rosenberg, T., Larsen, M., Farber, D. B., Nusinowitz, S. Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness. Hum. Mutat. 28: 243-254, 2007. 3. Zhao, L., Zabel, M. K., Wang, X., Ma, W., Shah, P., Fariss, R. N., Qian, H., Parkhurst, C. N., Gan, W.-B., Wong, W. T. Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration. EMBO Molec. Med. 7: 1179-1197, 2015.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    PDE6B (phosphodiesterase 6B, CGMP-Specific, Rod, beta (PDE6B))

    Andere Bezeichnung

    PDE6B

    Hintergrund

    Synonyms: Arylsulfatase A, ASA, Cerebroside-sulfatase, Arylsulfatase A component B, Arylsulfatase A component C, ARSA

    Background: Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molekulargewicht

    98 kDa

    Gen-ID

    5158

    UniProt

    P35913

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling, Phototransduction
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