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IDE anticorps (AA 491-590)

L’anticorps Souris Polyclonal anti-IDE a été validé pour WB, ELISA, IHC (p) et IHC (fro) et a été validé indépendamment. Il convient pour détecter IDE dans des échantillons de Souris.
N° du produit ABIN723665

Aperçu rapide pour IDE anticorps (AA 491-590) (ABIN723665)

Antigène

Voir toutes IDE Anticorps
IDE (Insulin-Degrading Enzyme (IDE))

Reactivité

  • 77
  • 32
  • 32
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Souris

Hôte

  • 65
  • 12
  • 4
Souris

Clonalité

  • 67
  • 14
Polyclonal

Conjugué

  • 39
  • 6
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp IDE est non-conjugé

Application

  • 62
  • 26
  • 22
  • 14
  • 13
  • 11
  • 9
  • 7
  • 5
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Épitope

    • 15
    • 8
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 491-590

     Réactivité croisée

    Souris

    Homologie

    Human,Rat,Cow,Pig,Chicken

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human IDE

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Validation #104436 (Immunohistochemistry)
    'Independent Validation' signe
    by
    Prof. Merighi, Laboratory of Neurobiology, Department of Veterinary Sciences, University of Turin
    No.
    #104436
    Date
    15.03.2023
    Antigène
    IDE
    Numéro du lot
    9C07M588
    Application validée
    Immunohistochemistry
    Contrôle positif

    Adult mouse liver and brain fixed in 4% paraformaldehyde

    Contrôle négative

    One control slice for each experimental procedure processed omitting the primary antibody; overnight incubation in diluent solution only.

    Conclusion

    Passed. The IDE antibody (AA 491-590) ABIN723665 works in IHC-P at 1:50, 1:100 and 1:300 concentrations with tyramide amplification.

    'Independent Validation' signe
    Validation Images
    Protocole
    Anticorps primaire
    ABIN723665
    Anticorps secondaire
    poly-HRP conjugated goat anti-rabbit antibody
    Full Protocol
    • Perfuse mice with paraformaldehyde 4% in 0.1 M phosphate buffer pH 7.4 and post-fix in the same fixative for an additional 2 h at RT.
    • Wash, dehydrate, and embed samples in paraffin wax.
    • Wash several times with 0.01 M PBS.
    • Cut liver with a microtome into 20 µm sections and mount on glass slides.
    • After paraffin removal, incubate sections for 1 h at RT in PBS containing 1% albumin from chicken egg white (Sigma, A5378) and 0.3% Triton-X-100 (BioRad, 161-0407, lot 00583) to block non-specific binding sites.
    • Incubate sections with primary rabbit anti-IDE (antibodies-online, ABIN723665, lot BB03153570) diluted 1:50, 1:100, 1:200, 1:300, and 1:400 in PBS-BSA-PLL ON at RT in a humid chamber.
    • Wash sections 3x 5 min with 0.01 M PBS.
    • Incubate sections with secondary poly-HRP conjugated goat anti-rabbit antibody from Alexa Fluor 594 Tyramide SuperBoost Kit, goat anti-rabbit IgG (Thermo Fisher Scientific, B40915, lot 2086865) for 1 h at RT.
    • Wash sections 3x 5 min with 0.01 M PBS.
    • I• Incubate sections with Tyramide working solution containing 100X Tyramide stock solution (Alexa 594), 100X H2O2 solution and 1X Reaction buffer for 10 min.
    • Stop the reaction with the Reaction Stop Reagent working solution.
    • Wash sections 3x 5 min with 0.01M PBS.
    • Mount specimens in Fluoroshield (Sigma, F6182, lot MKCB0153V).
    • Acquire images Leica DM 6000B fluorescence microscope equipped with a digital camera at 40x magnification.
    Notes
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Date de péremption

    12 months
  • Antigène

    IDE (Insulin-Degrading Enzyme (IDE))

    Autre désignation

    IDE

    Sujet

    Synonyms: BC2, Insulin degrading enzyme, FLJ35968, insulin protease, insulinase, insulysin, Abeta-degrading protease, FLJ35968, Ide, IDE_HUMAN, Insulin-degrading enzyme, OTTHUMP00000020097.

    Background: Insulysin was identified nearly a century ago as an enzyme responsible for the degradation of insulin in cells, although the precise interactions between insulin and insulysin remain elusive. Human insulysin was cloned in 1988, and shown to be a 118 kDa protein that exists primarily as a homodimer, and perhaps also complexed with other molecules. The sequence is well conserved between humans, rats and mice, and the antibody recognizes these species. Insulysin is a metalloproteinase of the clan ME, family M16, which contains an active site HxxEH, a reversal of the canonical HExxH zinc binding motif. Considered a zinc metalloproteinase, the activity of insulysin can be blocked with EDTA or 1-10 phenanthroline. In addition to the active metalloproteinase domain, insulysin contains a second metalloproteinase site which is considered catalytically inactive, and is thought to assist in substrate binding. Insulysin is most closely related to the bacterial proteinase pitrilysin, (the human orthologue of which appears to be MPRP1) and the mammalian proteinsae nardilysin. Generally thought to be a cytoplasmic protein, insulysin has been isolated from many different tissues and cell lines, and can degrade intact insulin, insulin B chain, glucagon, denatured hemoglobin, alpha amyloid protein, TGF alpha and amylin. Recent work implicates insulysin in clearing beta amyloid plaques from the brain, and has generated much interest in Alzheimer?s disease research. The pH optimum for insulysin is basic, pH 8.5, which also distinguishes it from other metalloproteinases. Insulin degrading enzyme (IDE) has a preferential affinity for insulin such that the presence of insulin will inhibit IDE mediated degradation of other substrates. IDE degrades a variety of other peptides including atrial natriuretic peptide and amylin.

    ID gène

    3416

    Pathways

    SARS-CoV-2 Protein Interactome
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