NTRK1 Split CISH Probe, Size:100 uL

Detay

Size:100 uL,
Product Description:NTRK1 Split CISH Probe is designed for the qualitative detection of translocations involving the human NTRK1 gene at 1q23.1 in formalin-fixed, paraffin-embedded specimens by chromogenic in situ hybridization (CISH).,
Clone Name:NONE,
Isotype:NONE,
Geneid:NONE,
Gene Name:NONE,
Gene Alias:NONE,
Gene Description:NONE,
Genbank Accession:NONE,
Immunogen:NONE,
Immunogen Sequence Protein Sequence:NONE,
Protein Accession:NONE,
Supplied Product:Reagent Provided:

This Probe is composed of:
1. Digoxigenin-labeled polynucleotides, which target sequences mapping in 1q23.1* (chr1:156,621,188-156,781,745) proximal to the NTRK1 breakpoint region.
2. Dinitrophenyl-labeled polynucleotides, which target sequences mapping in 1q23.1* (chr1:156,854,527-157,186,293) distal to the NTRK1 breakpoint region.
3. Formamide based hybridization buffer.,
Form:Liquid,
Concentration:NONE,
Target Refseq:NONE,
Target Region:NONE,
Plasmid:NONE,
Formulation:NONE,
Lysis Buffer:NONE,
Host Cell:NONE,
Organism:NONE,
Tissue:NONE,
Preparation Method:NONE,
Recommend Dilutions: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. ,
Storage Buffer:NONE,
Storage Instruction:Store at 2-8°C in an upright position. Return to storage conditions immediately after use.,
Quality Control Testing:NONE,
Note:The probe is intended to be used in combination with the CISH Implementation Kit 2 (Catalog #: KA5366 or KA6906 ), which provides necessary reagents for specimen pretreatment and post-hybridization processing.

Interpretation of results:
Using the CISH Implementation Kit 2 (Cat # KA5366 or KA6906), hybridization signals of Digoxigenin-labeled polynucleotides appear as dark green colored distinct dots (proximal to the NTRK1 breakpoint region), and Dinitrophenyl-labeled polynucleotides appear as bright red colored distinct dots (distal to the NTRK1 breakpoint region).
Normal situation:In interphases of normal cells or cells without a translocation involving the NTRK1 gene region, two red/green fusion signals appear.
Aberrant situation: One NTRK1 gene region affected by a translocation is indicated by one separate distinct dot-shaped green signal and one separate distinct dot-shaped red signal. Isolated red signals are the result of deletions proximal to the NTRK1 breakpoint region or are due to unbalanced translocations affecting this chromosomal region.
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.,
Tag:NONE,
Conjugate Tag:NONE,
Type Clonality:DNA/RNA,
Raised In Host Species:NONE,
Antigen Species Target Species:Human,
Specificity:NONE,
Species Reactivity Cross Reactivity:Human,
Application Key:CISH-P

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