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Anoctamin 5 anticorps (2nd Cytoplasmic Loop)

Cet anticorps anti-Anoctamin 5 Polyclonal Lapin (ABIN7042929) détecte spécifiquement Anoctamin 5 dans WB. L’anticorps est réactif avec des échantillons de Souris.
N° du produit ABIN7042929
854,77 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 8 à 9 jours ouvrables

Aperçu rapide pour Anoctamin 5 anticorps (2nd Cytoplasmic Loop) (ABIN7042929)

Antigène

Voir toutes Anoctamin 5 (ANO5) Anticorps
Anoctamin 5 (ANO5)

Reactivité

  • 17
  • 11
  • 1
Souris

Hôte

  • 12
  • 7
Lapin

Clonalité

  • 12
  • 7
Polyclonal

Conjugué

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Anoctamin 5 est non-conjugé

Application

  • 15
  • 15
  • 10
  • 7
  • 6
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 7
    • 6
    • 6
    • 4
    • 2
    • 1
    • 1
    2nd Cytoplasmic Loop, AA 532-544

    Fonction

    A Rabbit Polyclonal Antibody to Anoctamin-5 Channel

     Réactivité croisée

    Souris, Rat

    Homologie

    Rat - identical, human - 12,13 amino acid residues identical

    Attributs du produit

    Anti-Anoctamin-5 Antibody is directed against an epitope of mouse ANO5. Anti-Anoctamin-5 Antibody (ABIN7042929, ABIN7044135 and ABIN7044136) can be used in western blot analysis. It has been designed to recognize ANO5 from mouse, rat and human samples.

    Purification

    Affinity purified on immobilized antigen.

    Immunogène

    (C)TKMEIPRTHQEYE, corresponding to amino acid residues 532-544 of mouse ANO5

    Isotype

    IgG
  • Indications d'application

    WB: 1:200

    FC: The optimal concentration should be determined by the user

    ICC: The optimal concentration should be determined by the user

    IHC: The optimal concentration should be determined by the user

    IP: The optimal concentration should be determined by the user

    Commentaires

    Negative Control: (ABIN7234743)

    Blocking Peptide: (ABIN7234743)

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    25 μL, 50 μL or 0.2 mL double distilled water (DDW), depending on the sample size.

    Concentration

    0.8 mg/mL

    Buffer

    PBS pH 7.4, 1 % BSA with 0.05 % 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

    Stockage commentaire

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

    Anoctamin 5 (ANO5)

    Autre désignation

    ANO5

    Sujet

    Synonyms: ANO5, Transmembrane protein 16E, TMEM16E, GDD1, LGMD2L

    Description: Anoctamins, also known as TMEM16, is a family of ten proteins involved in a variety of functions including phospholipid scrambling, ion transport and the regulation of other membrane proteins. ANO1 (Anoctamin-1), ANO2 and ANO5 function as Ca2+-activated Cl- channels (CaCCs) and play an important role in calcium dependent chloride secretion. All members of the Anoctamin family present high structural homology and consist of eight transmembrane domains and cytosolic N- and C-termini1.The ANO5 gene is widely distributed and expressed in bone, skeletal muscle, cardiac muscle, brain, lung and kidney and also in the mucosal layer of the GI tract and the skeletal muscle layer of the esophagus of mice2.In phylogenetic analysis ANO5 was found to be a close relative of ANO6. ANO6 has an association with phospholipid scramblase activity. Under both physiological and pathological conditions scramblase dissipates the normal asymmetry of the cell membrane by catalyzing the rapid externalization of phospholipids on the cell membrane and thus promoting apoptosis3.Recessive mutations in the ANO5 gene were found to be linked to limb-girdle muscular dystrophies type 2L (LGMD2L) and non-dysferlin Miyoshi myopathy4. LGMD2L is characterized by proximal weakness, asymmetric quadriceps femoris and atrophy of the biceps brachii muscle5.Mutations in the gene are also linked to the Gnathodiaphyseal dysplasia disease, an unusual generalized autosomal dominant disease. Patients with this syndrome show sclerosis of tubular bones, lesions of jawbones, an increased sensitivity for jaw infection and osteomyeletis and fragile bones6.

    ID gène

    233246

    NCBI Accession

    NM_213599

    UniProt

    Q75UR0
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