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CMSS1 anticorps (AbBy Fluor® 750)

Cet anticorps Lapin Polyclonal détecte spécifiquement CMSS1 dans WB. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN4998444

Aperçu rapide pour CMSS1 anticorps (AbBy Fluor® 750) (ABIN4998444)

Antigène

Voir toutes CMSS1 Anticorps
CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Reactivité

  • 16
  • 12
  • 12
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 16
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CMSS1 est conjugé à/à la AbBy Fluor® 750

Application

  • 16
  • 3
Western Blotting (WB)
  •  Réactivité croisée

    Humain

    Homologie

    Mouse,Rat,Horse

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human C3orf26

    Isotype

    IgG
  • Indications d'application

    IF(IHC-P) 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.

    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

    CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

    Autre désignation

    C3orf26

    Sujet

    Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.

    Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.

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