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ITM2B anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement ITM2B dans WB, IHC et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN2723906

Aperçu rapide pour ITM2B anticorps (ABIN2723906)

Antigène

Voir toutes ITM2B Anticorps
ITM2B (Integral Membrane Protein 2B (ITM2B))

Reactivité

  • 27
  • 12
  • 2
  • 1
Humain

Hôte

  • 28
  • 4
  • 1
  • 1
  • 1
Souris

Clonalité

  • 33
  • 2
Monoclonal

Conjugué

  • 19
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ITM2B est non-conjugé

Application

  • 23
  • 17
  • 15
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

1C11
  • Attributs du produit

    Homo sapiens integral membrane protein 2B (ITM2B)

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogène

    Full length human recombinant protein of human ITM2B (NP_068839) produced in HEK293T cell.

    Isotype

    IgG2a
  • Indications d'application

    WB 1:2000, IHC 1:150, FLOW 1:100

    Commentaires

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • Antigène

    ITM2B (Integral Membrane Protein 2B (ITM2B))

    Autre désignation

    ITM2B

    Sujet

    Amyloid precursor proteins are processed by beta-secretase and gamma-secretase to produce beta-amyloid peptides which form the characteristic plaques of Alzheimer disease. This gene encodes a transmembrane protein which is processed at the C-terminus by furin or furin-like proteases to produce a small secreted peptide which inhibits the deposition of beta-amyloid. Mutations which result in extension of the C-terminal end of the encoded protein, thereby increasing the size of the secreted peptide, are associated with two neurogenerative diseases, familial British dementia and familial Danish dementia.

    Poids moléculaire

    30.2 kDa

    ID gène

    9445

    NCBI Accession

    NM_021999

    HGNC

    9445
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