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TXNL4A anticorps (AA 1-142)

Cet anticorps Lapin Polyclonal détecte spécifiquement TXNL4A dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN6149737

Aperçu rapide pour TXNL4A anticorps (AA 1-142) (ABIN6149737)

Antigène

Voir toutes TXNL4A Anticorps
TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Reactivité

  • 8
  • 2
  • 1
Humain

Hôte

  • 7
  • 1
Lapin

Clonalité

  • 7
  • 1
Polyclonal

Conjugué

  • 4
  • 2
  • 1
  • 1
Cet anticorp TXNL4A est non-conjugé

Application

  • 5
  • 3
  • 1
Western Blotting (WB)
  • Épitope

    AA 1-142

    Séquence

    MSYMLPHLHN GWQVDQAILS EEDRVVVIRF GHDWDPTCMK MDEVLYSIAE KVKNFAVIYL VDITEVPDFN KMYELYDPCT VMFFFRNKHI MIDLGTGNNN KINWAMEDKQ EMVDIIETVY RGARKGRGLV VSPKDYSTKY RY

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human TXNL4A (NP_006692.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Commentaires

    HIGH QUALITY

    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

    TXNL4A (Thioredoxin-Like 4A (TXNL4A))

    Autre désignation

    TXNL4A

    Sujet

    The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants.,TXNL4A,BMKS,DIB1,DIM1,SNRNP15,TXNL4,U5-15kD,Cell Biology & Developmental Biology,Apoptosis,TXNL4A

    Poids moléculaire

    16 kDa

    ID gène

    10907

    UniProt

    P83876

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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