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MCFD2 anticorps (AA 27-146)

Cet anticorps anti-MCFD2 est un anticorps Lapin Polyclonal détectant MCFD2 dans WB et IHC. Adapté pour Humain.
N° du produit ABIN6143636

Aperçu rapide pour MCFD2 anticorps (AA 27-146) (ABIN6143636)

Antigène

Voir toutes MCFD2 Anticorps
MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))

Reactivité

  • 25
  • 23
  • 22
Humain

Hôte

  • 29
  • 11
Lapin

Clonalité

  • 30
  • 10
Polyclonal

Conjugué

  • 9
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MCFD2 est non-conjugé

Application

  • 27
  • 15
  • 13
  • 13
  • 7
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 15
    • 7
    • 2
    • 1
    AA 27-146

    Séquence

    EEPAASFSQP GSMGLDKNTV HDQEHIMEHL EGVINKPEAE MSPQELQLHY FKMHDYDGNN LLDGLELSTA ITHVHKEEGS EQAPLMSEDE LINIIDGVLR DDDKNNDGYI DYAEFAKSLQ

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 27-146 of human MCFD2 (NP_644808.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:100 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))

    Autre désignation

    MCFD2

    Sujet

    This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1, also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D), a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms.,MCFD2,F5F8D,F5F8D2,LMAN1IP,SDNSF,Signal Transduction,MCFD2

    Poids moléculaire

    10 kDa/14 kDa/16 kDa

    ID gène

    90411

    UniProt

    Q8NI22
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