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IQCB1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement IQCB1 dans ELISA et IF. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7115509

Aperçu rapide pour IQCB1 anticorps (ABIN7115509)

Antigène

Voir toutes IQCB1 Anticorps
IQCB1 (IQ Motif Containing B1 (IQCB1))

Reactivité

  • 31
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 28
  • 3
Lapin

Clonalité

  • 31
Polyclonal

Conjugué

  • 16
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp IQCB1 est non-conjugé

Application

  • 20
  • 16
  • 3
  • 2
  • 1
  • 1
  • 1
ELISA, Immunofluorescence (IF)
  • Fonction

    IQCB1 antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    IQ motif containing B1

    Isotype

    IgG
  • Indications d'application

    IF: 1:10-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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 freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    IQCB1 (IQ Motif Containing B1 (IQCB1))

    Autre désignation

    IQCB1

    Sujet

    Synonyms: IQ calmodulin-binding motif-containing protein 1|Nephrocystin-5|p53 and DNA damage-regulated IQ motif protein (PIQ)|IQCB1|KIAA0036|NPHP5

    Background: IQCB1, also known as NPHP5, is a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. It has a central coiled-coil region and two calmodulin-binding IQ domains. Localized to the primary cilia of renal epithelial cells and connecting cilia of photoreceptor cells, IQCB1 is thought to play a role in ciliary function. Mutations in this gene result in Senior-Loken syndrome type 5, a juvenile disorder characterized by defects in the waste filtering system of the kidney, as well as retinal degradation.

    UniProt

    Q15051
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