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SHANK3 Antikörper (AA 1391-1698)

Dieses Anti-SHANK3-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von SHANK3 in WB, IHC, ELISA und FACS. Geeignet für Ratte, Human und Maus.
Produktnummer ABIN7600006

Kurzübersicht für SHANK3 Antikörper (AA 1391-1698) (ABIN7600006)

Target

Alle SHANK3 Antikörper anzeigen
SHANK3 (SH3 and Multiple Ankyrin Repeat Domains 3 (SHANK3))

Reaktivität

  • 53
  • 10
  • 9
  • 2
  • 2
  • 1
  • 1
  • 1
Ratte, Human, Maus

Wirt

  • 31
  • 26
Kaninchen

Klonalität

  • 31
  • 26
Polyklonal

Konjugat

  • 14
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SHANK3 Antikörper ist unkonjugiert

Applikation

  • 37
  • 37
  • 26
  • 24
  • 17
  • 13
  • 13
  • 13
  • 10
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 14
    • 10
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1391-1698

    Verwendungszweck

    Anti-SHANK3 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-SHANK3 Antibody Picoband® (ABIN7600006). Tested in ELISA, Flow Cytometry, IHC, 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 SHANK3 recombinant protein (Position: E1391-H1698).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.1-0.25 μg/mL, Mouse, Rat
    Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human, Mouse, Rat
    ELISA, 0.1-0.5 μg/mL, -
    1. "Entrez Gene: SHANK3 SH3 and multiple ankyrin repeat domains 3". 2. Boeckers TM, Bockmann J, Kreutz MR, Gundelfinger ED (2002). "ProSAP/Shank proteins - a family of higher order organizing molecules of the postsynaptic absorbance with an emerging role in human neurological disease".J. Neurochem. 81 (5): 903-10.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 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, 0.2 mg Na2HPO4, 0.01 mg Sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store 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 freeze-thaw cycles.
  • Target

    SHANK3 (SH3 and Multiple Ankyrin Repeat Domains 3 (SHANK3))

    Andere Bezeichnung

    SHANK3

    Hintergrund

    Synonyms: Histone deacetylase 5, HD5, Antigen NY-CO-9, HDAC5, KIAA0600

    Tissue Specificity: Ubiquitous.

    Background: SH3 and multiple ankyrin repeat domains 3 (Shank3), also known as proline-rich synapse-associated protein 2 (ProSAP2), is a protein that in humans is encoded by the SHANK3 gene. This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Additionally, Shank proteins play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified.

    Molekulargewicht

    180-190 kDa

    Gen-ID

    85358

    Pathways

    Synaptic Membrane, Tube Formation, Regulation of long-term Neuronal Synaptic Plasticity
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