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TEX43 anticorps (AA 51-134) (AbBy Fluor® 488)

Cet anticorps Lapin Polyclonal détecte spécifiquement TEX43 dans WB, IF (cc) et IF (p). Il présente une réactivité envers Humain.
N° du produit ABIN1695556

Aperçu rapide pour TEX43 anticorps (AA 51-134) (AbBy Fluor® 488) (ABIN1695556)

Antigène

TEX43 (Testis expressed 43 (TEX43))

Reactivité

Humain

Hôte

  • 19
  • 1
Lapin

Clonalité

  • 19
  • 1
Polyclonal

Conjugué

  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TEX43 est conjugé à/à la AbBy Fluor® 488

Application

  • 15
  • 12
  • 12
  • 8
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Épitope

    • 14
    • 6
    AA 51-134

    Homologie

    Human,Mouse,Rat,Dog,Cow,Horse,Rabbit

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human C5orf48

    Isotype

    IgG
  • Indications d'application

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Date de péremption

    12 months
  • Antigène

    TEX43 (Testis expressed 43 (TEX43))

    Autre désignation

    C5orf48

    Sujet

    Synonyms: C5orf48, CE048_HUMAN, Chromosome 5 open reading frame 48, Uncharacterized protein C5orf48.

    Background: C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    ID gène

    389320
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