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NOTCH2 anticorps

Cet anticorps anti-NOTCH2 est un anticorps Lapin Polyclonal détectant NOTCH2 dans WB, ELISA et IHC. Adapté pour Humain. Validé indépendamment pour une utilisation dans Western Blotting. Ce Primary Antibody a été cité dans 3+ publications.
Rockland
N° du produit ABIN104899
N° du produit (Fournisseur): 100-401-408

Aperçu rapide pour NOTCH2 anticorps (ABIN104899)

Antigène

Voir toutes NOTCH2 Anticorps
NOTCH2 (Notch 2 (NOTCH2))

Reactivité

  • 74
  • 58
  • 33
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 79
  • 9
  • 4
  • 4
  • 1
Lapin

Clonalité

  • 76
  • 18
  • 2
Polyclonal

Conjugué

  • 49
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NOTCH2 est non-conjugé

Application

  • 52
  • 37
  • 26
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  • 25
  • 19
  • 14
  • 11
  • 9
  • 7
  • 5
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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • N° du produit (Fournisseur)

    100-401-408

    Fournisseur

    Rockland

    Fonction

    NOTCH 2 Antibody

    Réactivité croisée (Details)

    This antiserum is directed against human NOTCH2. The immunogen epitope is only exposed after gamma secretase cleavage and is not accessible in the uncleaved form.

    Attributs du produit

    Synonyms: rabbit anti-Notch2 antibody, AGS2 antibody, hN2 antibody, Notch homolog 2 antibody, neurogenic locus notch homolog protein 2

    Purification

    Antiserum

    Stérilité

    Sterile filtered

    Immunogène

    Immunogen: This whole rabbit serum was prepared by repeated immunizations with a synthetic peptide corresponding to amino acid residues of human Notch 2 located near the N-terminal sequence of the cleaved N intracellular domain (NICD).

    Immunogen Type: Conjugated Peptide

    Informations sur le produit

    A quoi peut servir l'anticorps NOTCH2 ABIN104899 ? Cet anticorps polyclonal non conjugué de lapin anti-NOTCH2 détecte de manière fiable le NOTCH2 humain par ELISA et Western blotting.

    Quelles sont les données de validation disponibles pour cet anticorps NOTCH2 ? Pour le Western blotting, une validation indépendante est actuellement disponible et a été réalisée à l'Université d'Ulm, en Allemagne. Sur la base de la séquence, on peut supposer que l'anticorps NOTCH2 fonctionne également pour les espèces de rat et de souris. L'anticorps a été utilisé dans trois publications à ce jour, qui sont indiquées ci-dessous et peuvent être lues sur PubMed. Il y a 2 images disponibles qui démontrent la performance de l'anticorps NOTCH2 en Western blot. Utilisez notre anticorps NOTCH2 pour détecter de manière fiable le NOTCH2 humain.

    Quelle est la fonction de NOTCH2 ? NOTCH2 fonctionne comme un récepteur pour les ligands membranaires Jagged-1 (JAG1), Jagged-2 (JAG2) et Delta-1 (DLL1) afin de réguler la détermination du statut cellulaire. Lors de l'activation du ligand par le domaine intracellulaire de l'encoche (NICD) libéré, il forme un complexe activateur de transcription avec RBPJ/RBPSUH et active les gènes du locus enhancer of split. Affecte la mise en œuvre des programmes de différenciation, de prolifération et d'apoptose (Par similarité). NOTCH2 semble être impliqué dans le remodelage et l'homéostasie osseuse. En collaboration avec RELA/p65 augmente l'activité du promoteur de NFATc1 et régule positivement la différenciation des ostéoclastes induite par RANKL. (UniProt)

  • Indications d'application

    Immunohistochemistry Dilution: 1:500

    Application Note: Anti-Notch2 has been tested in ELISA, WB, and IHC. Anti-NOTCH-2 has a strong response was detected by ELISA against the immunizing peptide. This product was assayed against the peptide immunogen in a standard capture ELISA using Peroxidase conjugated anti-Rabbit IgG [H&L] (Goat) (code #611-1302) and ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) (code # ABTS-100) as a substrate for 30 minutes at room temperature.  A working dilution of 1:30,000 to 1:90,000 is suggested in ELISA this product.

    Western Blot Dilution: 1:400 - 1:2,000

    ELISA Dilution: 1:20,000 - 1:100,000

    Other: User Optimized

    Restrictions

    For Research Use only
  • Validation #103703 (Western Blotting)
    'Independent Validation' signe
    by
    AG Pancreatic Development and Stem cell differentiation, Universitätsklinikum Ulm
    No.
    #103703
    Date
    16.06.2019
    Antigène
    NOTCH2
    Numéro du lot
    Application validée
    Western Blotting
    Contrôle positif

    pancreatic endoderm cells (day 10)

    pancreatic progenitor cells (day 14)

    Contrôle négative

    human pluripotent stem cells (day 0)

    defnite endoderm cells (day 4)

    Conclusion

    ABIN1043688 reveals two protein bands of the expected size and some weaker extraneous bands in cell lysates of human pluripotent stem cells, definite endoderm cells, pancreatic endoderm cells, and pancreatic progenitor cells.

    'Independent Validation' signe
    Validation Images
    Protocole
    Anticorps primaire
    ABIN1043688
    Anticorps secondaire
    donkey anti-rabbit HRP-conjugated antibody (GE Healthcare, NA9310V)
    Full Protocol
    • Grow HUES8 in mTeSR1 (STEMCELL Technologies, 85850) at 37°C and 5% O2, 5% CO2 in 2ml in a 6-well plate to 90% confluency.
    • Harvest cells using TrypLE (ThermoFisher Scientific, 12604013) following the manufacturer´s instructions.
    • Lyse 2x106 cells in 30µl per well cold RIPA buffer (50mM Tris-HCl pH 8.0, 150mM NaCl, 0.1% SDS, 0.5% deoxycholate, 1% TritonX 100 in ddH2O) supplemented with 1mM PMSF and 1x protease inhibitor (Roche, 11836170001) for 30min on ice with 3x vortexing in 1.5ml microcentrifuge tubes.
    • Centrifuge tubes at 10000xg for 8min at 4°C.
    • Transfer supernatant to a new 1.5ml microcentrifuge tube and store at -80°C.
    • Determine total protein content of the lysates using a Bradford assay (Bio-Rad, 500-0006).
    • Denature 50µg of total protein for 5min at 95°C in 30µl 1x Laemmli SDS sample buffer and subsequently separate them on a denaturing 7.5% polyacrylamide gel (7.5% Acrylamide, 0.375M Tris-HCl pH8.8, 0.1% SDS, 0.1% APS, 0.1% TEMED) for about 120min at 120V.
    • Transfer proteins onto a PVDF membrane (Sigma Aldrich, IPVH00010) with transfer buffer (5.27g Tris, 2.93 g glycerine, 200 ml methanol, fill to 1l ddH2O) in a semidry western blotting system for 80min at 80mA/gel.
    • Check transfer of the separated proteins by Ponceau S staining.
    • Rinse membrane with water.
    • Wash membrane for 5min with TBST (TBS, 0.02% Tween20).
    • Block the membrane with 20ml blocking buffer (TBST, 5% milk) on a shaker for 1h at RT.
    • Rinse membrane 3x with TBST.
    • Wash membrane on a shaker 3x for 5min with TBST.
    • Shrink-wrap and incubate membrane with primary
      • rabbit anti-NOTCH2 antibody (antibodies-online, ABIN1043688) diluted 1:1000 respectively in blocking buffer ON at 4°C or
      • mouse anti-vinculin antibody (SigmaAldrich, V9264) diluted 1:1000 in blocking buffer at RT for 1h.
    • Wash membrane 3x for 5min with TBST.
    • Incubate membrane with secondary
      • donkey anti-rabbit HRP-conjugated antibody (GE Healthcare, NA9310V) diluted 1:5000 in TBST containing 1% milk for 1h at RT or
      • donkey anti-mouse HRP-conjugated antibody (GE Healthcare, NA9340V) diluted 1:5000 in TBST containing 1% milk for 1h at RT.
    • Wash membrane 3x for 5min with TBST.
    • Reveal protein bands using ECL solution (ThermoScientific, 34076) with an exposure time of 40min for the ABIN1043688 and 2min for the vinculin loading control.
    Notes
    • ABIN1043688 revealed some strong unspecific bands. Nevertheless, a band over 250kDa appears to be highly specific, as it is only detected at day 10 (lanes 5 and 6) and day 14 (lanes 7 and 8).

    • Manual exposure had to be performed due to a defect of the fusion detector in our institute.

    • ABIN1043688 was also tested in IHC on 4-5µm FFPE sections of primary human kidney cancer tissue. Epitope retrieval was carried out using Tris-EDTA buffer at pH9.0 (Zytomed, ZUC029-500), EDTA at pH8.0 (Leica, RE7116), or citrate buffer at pH6.1 (Agilent, S169984-2) for 20min in a decloaking chamber.

    • Interpretation of the results was difficult, as the method of antigen retrieval strongly effects the staining pattern. Antigen retrieval using the citrate buffer at pH6 might be ok, but knockout or knockdown studies are necessary to clearly conclusively show specificity.

  • Format

    Liquid

    Concentration

    70 mg/mL

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) 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 vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Date de péremption

    12 months
  • Iervolino, Prosperi, De La Motte, Petrillo, Spagnuolo, DAcierno, Siccardi, Perna, Christensen, Frische, Capasso, Trepiccione: "Potassium depletion induces cellular conversion in the outer medullary collecting duct altering Notch signaling pathway." dans: Scientific reports, Vol. 10, Issue 1, pp. 5708, (2020) (PubMed).

    Gridley: "Notch signaling and inherited disease syndromes." dans: Human molecular genetics, Vol. 12 Spec No 1, pp. R9-13, (2003) (PubMed).

    Bertrand, Eckfeldt, Lysholm, LeBien: "Notch-1 and Notch-2 exhibit unique patterns of expression in human B-lineage cells." dans: Leukemia, Vol. 14, Issue 12, pp. 2095-102, (2001) (PubMed).

  • Antigène

    NOTCH2 (Notch 2 (NOTCH2))

    Autre désignation

    NOTCH2

    Sujet

    Background: Anti-Notch 2 Antibody recognizes Notch2 that is synthesized in the endoplasmic reticulum as an inactive form which is proteolytically cleaved by a furin-like convertase (S1 cleavage) in the trans-golgi network before it reaches the plasma membrane to yield an active, ligand-accessible form. Cleavage results in a C-terminal fragment N(TM) and a N-terminal fragment N(EC). Following ligand binding, it is cleaved (S2 cleavage) by TNF-alpha converting enzyme (TACE) to yield a membrane-associated intermediate fragment called Notch extracellular truncation (NEXT). This fragment is then cleaved by presenilin-dependent gamma-secretase (S3 cleavage) to release the intracellular domain (NICD) from the membrane. Anti-NOTCH2 Antibody is useful for researchers interested in Notch1, Jagged1, Jagged2, and Delta1, as well as neuroscience, transcription and cancer research.

    ID gène

    4853, 24041035

    UniProt

    Q04721

    Pathways

    Signalisation Notch, Stem Cell Maintenance
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