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ZNF852 anticorps (AA 65-180) (Cy7)

Cet anticorps anti-ZNF852 est un anticorps Lapin Polyclonal détectant ZNF852 dans IF (cc) et IF (p). Adapté pour Humain.
N° du produit ABIN1413780

Aperçu rapide pour ZNF852 anticorps (AA 65-180) (Cy7) (ABIN1413780)

Antigène

ZNF852 (Zinc Finger Protein 852 (ZNF852))

Reactivité

Humain

Hôte

  • 14
Lapin

Clonalité

  • 14
Polyclonal

Conjugué

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ZNF852 est conjugé à/à la Cy7

Application

  • 12
  • 12
  • 3
  • 3
  • 3
  • 1
Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Épitope

    AA 65-180

    Homologie

    Human

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human ZNF852

    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

    ZNF852 (Zinc Finger Protein 852 (ZNF852))

    Autre désignation

    ZNF852

    Sujet

    Synonyms: Putative zinc finger protein 852,

    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 LOC285346 gene product has been provisionally designated LOC285346 pending further characterization.

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