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C19orf54 anticorps (HRP)

Cet anticorps Lapin Polyclonal détecte spécifiquement C19orf54 dans WB et IHC (p). Il présente une réactivité envers Humain.
N° du produit ABIN1421944

Aperçu rapide pour C19orf54 anticorps (HRP) (ABIN1421944)

Antigène

C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))

Reactivité

Humain

Hôte

  • 16
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp C19orf54 est conjugé à/à la HRP

Application

  • 16
  • 13
  • 2
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  •  Réactivité croisée

    Humain

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human C19orf54

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    IHC-P 1:200-400

    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.

    Conseil sur la manipulation

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    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

    C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))

    Autre désignation

    C19orf54

    Sujet

    Synonyms: Chromosome 19 open reading frame 54, FLJ17063, FLJ41131, Hypothetical protein LOC284325, MGC103014, UPF0692 protein C19orf54, CS054_HUMAN.

    Background: C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

    ID gène

    284325
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