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EBP anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-EBP a été validé pour WB. Il convient pour détecter EBP dans des échantillons de Humain. Il y a 3+ publications disponibles.
N° du produit ABIN1881278

Aperçu rapide pour EBP anticorps (C-Term) (ABIN1881278)

Antigène

Voir toutes EBP Anticorps
EBP (Emopamil Binding Protein (Sterol Isomerase) (EBP))

Reactivité

  • 30
  • 13
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 31
Lapin

Clonalité

  • 31
Polyclonal

Conjugué

  • 15
  • 4
  • 4
  • 4
  • 2
  • 2
Cet anticorp EBP est non-conjugé

Application

  • 23
  • 23
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB41564
  • Épitope

    • 8
    • 8
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    AA 201-230, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This EBP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 201-230 amino acids from the C-terminal region of human EBP.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (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

    Date de péremption

    6 months
  • Ausavarat, Tanpaiboon, Tongkobpetch, Suphapeetiporn, Shotelersuk: "Two novel EBP mutations in Conradi-Hünermann-Happle syndrome." dans: European journal of dermatology : EJD, Vol. 18, Issue 4, pp. 391-3, (2008) (PubMed).

    Lu, Dollé, Imholz, van t Slot, Verschuren, Wijmenga, Feskens, Boer: "Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations." dans: Journal of lipid research, Vol. 49, Issue 12, pp. 2582-9, (2008) (PubMed).

    Steijlen, van Geel, Vreeburg, Marcus-Soekarman, Spaapen, Castelijns, Willemsen, van Steensel: "Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome." dans: The British journal of dermatology, Vol. 157, Issue 6, pp. 1225-9, (2007) (PubMed).

  • Antigène

    EBP (Emopamil Binding Protein (Sterol Isomerase) (EBP))

    Autre désignation

    EBP

    Sujet

    The protein encoded by this gene is an integral membrane protein of the endoplasmic reticulum. It is a high affinity binding protein for the antiischemic phenylalkylamine Ca2+ antagonist [3H]emopamil and the photoaffinity label [3H]azidopamil. It is similar to sigma receptors and may be a member of a superfamily of high affinity drug-binding proteins in the endoplasmic reticulum of different tissues. This protein shares structural features with bacterial and eukaryontic drug transporting proteins. It has four putative transmembrane segments and contains two conserved glutamate residues which may be involved in the transport of cationic amphiphilics. Another prominent feature of this protein is its high content of aromatic amino acid residues (>23 % ) in its transmembrane segments. These aromatic amino acid residues have been suggested to be involved in the drug transport by the P-glycoprotein. Mutations in this gene cause Chondrodysplasia punctata 2 (CDPX2, also known as Conradi-Hunermann syndrome).

    Poids moléculaire

    26353

    NCBI Accession

    NP_006570

    UniProt

    Q15125
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