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TMEM184B anticorps (C-Term)

Cet anticorps anti-TMEM184B est un anticorps Lapin Polyclonal détectant TMEM184B dans WB, IF, IHC (p) et EIA. Adapté pour Humain, Souris et Rat.
N° du produit ABIN500976

Aperçu rapide pour TMEM184B anticorps (C-Term) (ABIN500976)

Antigène

Voir toutes TMEM184B Anticorps
TMEM184B (Transmembrane Protein 184B (TMEM184B))

Reactivité

  • 9
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 9
Lapin

Clonalité

  • 9
Polyclonal

Conjugué

  • 5
  • 2
  • 1
  • 1
Cet anticorp TMEM184B est non-conjugé

Application

  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Épitope

    • 5
    • 2
    • 1
    • 1
    C-Term

    Specificité

    This antibody detects TMEM184B near C-term.

    Purification

    Peptide affinity chromatography

    Immunogène

    TMEM184B antibody was raised against a 15 amino acid peptide near the carboxy terminus of human TMEM184B.

    Isotype

    IgG
  • Indications d'application

    ELISA. Western blot.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS containing 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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    TMEM184B (Transmembrane Protein 184B (TMEM184B))

    Autre désignation

    TMEM184B

    Sujet

    TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22, mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.Synonyms: C22orf5, Putative MAPK-activating protein FM08, Transmembrane protein 184B

    ID gène

    25829

    NCBI Accession

    NP_036396
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