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SHANK3 anticorps (AA 1391-1698)

Cet anticorps anti-SHANK3 est un anticorps Lapin Polyclonal détectant SHANK3 dans WB, IHC, ELISA et FACS. Adapté pour Rat, Humain et Souris.
N° du produit ABIN7600006

Aperçu rapide pour SHANK3 anticorps (AA 1391-1698) (ABIN7600006)

Antigène

Voir toutes SHANK3 Anticorps
SHANK3 (SH3 and Multiple Ankyrin Repeat Domains 3 (SHANK3))

Reactivité

  • 53
  • 10
  • 9
  • 2
  • 2
  • 1
  • 1
  • 1
Rat, Humain, Souris

Hôte

  • 31
  • 26
Lapin

Clonalité

  • 31
  • 26
Polyclonal

Conjugué

  • 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
Cet anticorp SHANK3 est non-conjugé

Application

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

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

    Fonction

    Anti-SHANK3 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    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.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human SHANK3 recombinant protein (Position: E1391-H1698).

    Isotype

    IgG
  • Indications d'application

    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.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.01 mg Sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

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

    Autre désignation

    SHANK3

    Sujet

    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.

    Poids moléculaire

    180-190 kDa

    ID gène

    85358

    Pathways

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