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Abnova/DDIT3 Split CISH Probe/1kit/CS0005
  • Abnova/DDIT3 Split CISH Probe/1kit/CS0005

Abnova/DDIT3 Split CISH Probe/1kit/CS0005

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貨號: CS0005
品牌: Abnova
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  • 詳情
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      • Specification
      • Product Description:
      • DDIT3 Split CISH Probe is designed for the qualitative detection of translocations involving the human DDIT3 gene at 12q13.3 in formalin-fixed, paraffin-embedded specimens by chromogenic in situ hybridization (CISH).
      • 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:This Probe is composed of:1. Digoxigenin-labeled polynucleotides, which target sequences mapping in 12q13.3-q14.1* (chr12:58,024,366-58,486,511) distal to the DDIT3 breakpoint region.2. Dinitrophenyl-labeled polynucleotides, which target sequences mapping in 12q13.3* (chr12:57,386,302-57,865,800) proximal to the DDIT3 breakpoint region. 3. Formamide based hybridization buffer.*according to Human Genome Assembly GRCh37/hg19
      • 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.Interpretation of results:Using the CISH Implementation Kit 2 (Cat # KA5366), hybridization signals of Digoxigenin-labeled polynucleotides appear as dark green colored distinct dots (distal to the DDIT3 breakpoint region), and Dinitrophenyl-labeled polynucleotides appear as bright red colored distinct dots (proximal to the DDIT3 breakpoint region).Normal situation: In interphases of normal cells or cells without a translocation involving the DDIT3 gene region, two red/green fusion signals appear.Aberrant situation: One DDIT3 gene region affected by a translocation is indicated by one separate distinct dot-shaped green signal and one separate distinct dot-shaped red signal.Overlapping signals may appear as brown signals. Genomic aberrations due to small deletions, duplications or inversions might result in inconspicuous signal patterns. Other signal patterns than those described above may be observed in some abnormal samples. These unexpected signal patterns should be further investigated.
      • Probe Position:
      • Regulatory Status:
      • For research use only (RUO)
      • Interpretation of Result:
      • Datasheet:
      • PDF DownloadDownload
      • Applications
      • Chromogenic In Situ Hybridization (FFPE Tissue)
      • Chromogenic <i>In Situ</i> Hybridization (FFPE Tissue)
      • Myxoid liposarcoma tissue section with translocation affecting the 12q13.3-q14.1 locus as indicated by one non-rearranged red/green fusion signal, one red signal, and one separate green signal indicating the translocation.
      • Application Image
      • Chromogenic In Situ Hybridization (FFPE Tissue)
      • Chromogenic <i>In Situ</i> Hybridization (FFPE Tissue)
      • enlarge
      • Gene Information
      • Entrez GeneID:
      • 1649
      • Gene Name:
      • DDIT3
      • Gene Alias:
      • CEBPZ,CHOP,CHOP10,GADD153,MGC4154
      • Gene Description:
      • DNA-damage-inducible transcript 3
      • Omim ID:
      • 126337
      • Gene Ontology:
      • Hyperlink
      • Other Designations:
      • C/EBP homologous protein,C/EBP zeta,CCAAT/enhancer-binding protein homologous protein,growth arrest- and DNA damage-inducible
      • Gene Pathway
      • MAPK signaling pathway
      • Related Disease
      • Alzheimer Disease
      • Alzheimer disease
      • Cognition
      • Diabetes Mellitus, Type 2
      • Genetic Predisposition to Disease
      • Kidney Failure, Chronic
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