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FASTKD1 anticorps

L’anticorps Lapin Polyclonal anti-FASTKD1 a été validé pour IHC. Il convient pour détecter FASTKD1 dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7263405

Aperçu rapide pour FASTKD1 anticorps (ABIN7263405)

Antigène

FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

Reactivité

  • 21
  • 14
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 20
  • 1
Lapin

Clonalité

  • 21
Polyclonal

Conjugué

  • 14
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FASTKD1 est non-conjugé

Application

  • 13
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human FASTKD1 (NP_078898.3).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    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

    FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

    Autre désignation

    FASTKD1

    Sujet

    The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

    ID gène

    79675

    UniProt

    Q53R41
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