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TMEM66 anticorps (Intracellular, Lumenal Region)

Cet anticorps Lapin Polyclonal détecte spécifiquement TMEM66 dans WB, IF et IHC. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7885623
1.466,46 €
Plus frais de livraison 40,00 € et TVA
200 μL
Destination: France
Envoi sous 8 à 9 jours ouvrables

Aperçu rapide pour TMEM66 anticorps (Intracellular, Lumenal Region) (ABIN7885623)

Antigène

Voir toutes TMEM66 Anticorps
TMEM66 (Transmembrane Protein 66 (TMEM66))

Reactivité

  • 19
  • 12
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 21
Lapin

Clonalité

  • 21
Polyclonal

Conjugué

  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Cet anticorp TMEM66 est non-conjugé

Application

  • 14
  • 12
  • 9
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)

Classe de qualité

Carrier-free
  • Épitope

    • 8
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 141-155, Intracellular, Lumenal Region

    Fonction

    A Rabbit Polyclonal Antibody to TMEM66

    Homologie

    15 amino acid residues identical,Mouse - 13, human - 11

    Purification

    Affinity purified on immobilized antigen.

    Immunogène

    (C)ELGLSKLKESGKHQS, corresponding to amino acid residues 141-155 of rat SARAF

    Isotype

    IgG
  • Indications d'application

    WB: 1:500

    FC: The optimal concentration should be determined by the user

    ICC: The optimal concentration should be determined by the user

    IHC: 1:200

    IP: The optimal concentration should be determined by the user

    Commentaires

    Negative Control: (ABIN7237528)

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    0.2 mL double distilled water (DDW)

    Concentration

    1 mg/mL

    Buffer

    PBS pH 7.4

    Agent conservateur

    Without preservative

    Stock

    -20 °C

    Stockage commentaire

    The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
  • Antigène

    TMEM66 (Transmembrane Protein 66 (TMEM66))

    Autre désignation

    Store-operated calcium entry-associated regulatory factor

    Sujet

    Synonyms: Store-operated calcium entry-associated regulatory factor, SOCE-associated regulatory factor, SARAF, Transmembrane protein 66

    Description: TMEM66 (Transmembrane protein 66, also known as SOCE-associated regulatory factor, SARAF) is a regulatory protein of cellular Ca2+ homeostasis, encoded by the TMEM66 gene. TMEM66 is an ER resident protein, which responds to cytosolic Ca2+ elevation after ER Ca2+ refilling.TMEM66 is highly conserved in vertebrates. In mammals it is ubiquitously expressed with high transcript levels in the immune and neuronal tissues. The TMEM66 structure contains validated signal peptide and a putative single membrane spanning domain, a serine-proline rich domain and arginine rich regions followed by a cluster of basic residues at its C-terminal tail1.Store-operated Ca2+ entry (SOCE) is an important Ca2+ influx pathway across plasma membranes in many non-excitable cells. In this pathway, intracellular Ca2+ release through IP3 receptors stimulated by a variety of agonists, results in reduction of Ca2+ concentration in the lumen of the endoplasmic or sarcoplasmic reticulum. SARAF negatively regulates store operated calcium entry into cells and protects cells from calcium overfilling1,2.STIM, Ca2+ sensor, and Orai, the channel pore forming subunit proteins have been identified as the essential components enabling the reconstitution of Ca2+ release-activated Ca2+ channels that mediate SOCE. Knock-out of Orai1 or STIM1 in mice and mutations evoke SOCE in lymphocytes and other cells2,3.Findings show that dysregulation of Ca2+ homeostasis is associated with a plethora of pathological conditions including neurodegenerative diseases, skeletal, muscular and cardiovascular disorders2. Inherited defects in SOCE due to mutations in genes of the Ca2+ release-activated Ca2+ (CRAC) channel complex causes patients to suffer from a severe form of immunodeficiency that is due to defects in the function of T cells, NK cells and potentially other immune cells3.

    ID gène

    290796

    UniProt

    Q6AYN2
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