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TRAPPC2 anticorps (AA 11-39)

L’anticorps Lapin Polyclonal anti-TRAPPC2 a été validé pour WB et ELISA. Il convient pour détecter TRAPPC2 dans des échantillons de Humain.
N° du produit ABIN3029192

Aperçu rapide pour TRAPPC2 anticorps (AA 11-39) (ABIN3029192)

Antigène

Voir toutes TRAPPC2 Anticorps
TRAPPC2 (Trafficking Protein Particle Complex 2 (TRAPPC2))

Reactivité

  • 22
  • 8
  • 8
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 20
  • 2
Lapin

Clonalité

  • 17
  • 5
Polyclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TRAPPC2 est non-conjugé

Application

  • 22
  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 11-39

    Réactivité croisée (Details)

    Expected species reactivity: Mouse, Bovine, Pig, Chicken, Zebrafish

    Purification

    Antigen affinity purified

    Immunogène

    A portion of amino acids 11-39 from the human protein was used as the immunogen for this TRAPPC2 antibody.

    Isotype

    Ig Fraction
  • Indications d'application

    Titration of the TRAPPC2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS pH 7.4 with 0.09 % 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

    Aliquot the TRAPPC2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Antigène

    TRAPPC2 (Trafficking Protein Particle Complex 2 (TRAPPC2))

    Autre désignation

    TRAPPC2

    Sujet

    TRAPPC2 is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT). A processed pseudogene of this gene is located on chromosome 19, and other pseudogenes are found on chromosomes 8 and Y.

    UniProt

    P0DI81
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