MYCN CISH Probe

Catalog # CG0022

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Size:400 uL
Price: USD $ 850.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Chromogenic <i>In Situ</i> Hybridization (FFPE Tissue)
Application

Chromogenic In Situ Hybridization (FFPE Tissue)

Normal nuclei each with two MYCN signals

  • Specification

    Product Description

    MYCN CISH Probe is designed for the qualitative detection human MYCN gene in formalin-fixed, paraffin-embedded tissue or cells by chromogenic in situ hybridization (CISH).

    Reactivity

    Human

    Recommend Usage

    The product is ready-to-use. No reconstitution, mixing, or dilution is required. Bring probe to room temperature (18-25°C) and mix briefly before use.

    Supplied Product

    Reagent Provided:

    Digoxigenin-labeled oligonucleotides targeting sequences mapping in 2p24.3* (chr2:15,846,046-16,213,717) harboring the MYCN gene.
    2. Formamide based hybridization buffer.
    *According to Human Genome Assembly GRCh37/hg19

    Probe Position

    Regulatory Status

    For research use only (RUO)

    Storage Instruction

    Store at 2-8°C in an upright position. Return to storage conditions immediately after use.

    Note

    The probe is intended to be used in combination with the CISH Implementation Kit 2 (Catalog #: KA5366), which provides necessary reagents for specimen pretreatment and post-hybridization processing.

    Hybridization signals of digoxigenin-labeled polynucleotides appear as brown- to dark brown colored distinct dots (MYCN gene).
    Normal situation: In interphases of normal cells or cells without an amplification involving the MYCN gene locus, two distinct dot-shaped brown signals per nucleus appear.
    Aberrant situation: In a cell with amplification of the MYCN gene locus or aneuploidy of chromosome 2, multiple copies of the brown signal or brown signal clusters will be observed.

    Interpretation of Result

  • Applications

    Chromogenic In Situ Hybridization (FFPE Tissue)

    Normal nuclei each with two MYCN signals
  • Gene Info — MYCN

    Entrez GeneID

    4613

    Gene Name

    MYCN

    Gene Alias

    MODED, N-myc, NMYC, ODED, bHLHe37

    Gene Description

    v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian)

    Omim ID

    164280 164840 602585

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. [provided by RefSeq

    Other Designations

    N-myc proto-oncogene protein|neuroblastoma MYC oncogene|neuroblastoma-derived v-myc avian myelocytomatosis viral related oncogene|oncogene NMYC|pp65/67|v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived|v-myc myelocytomatosis viral

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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