Products

Product Description

ERBB2/D17S122 CISH Probe is designed for the qualitative detection of human ERBB2 gene amplifications as well as the detection of the D17S122 locus in formalin-fixed, paraffin-embedded specimens by chromogenic in situ hybridization (CISH).

Reactivity

Human

Form

Liquid

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 17q12** (chr17:37,725,661-37,882,844) harboring the ERBB2 gene region.
2. Dinitrophenyl-labeled polynucleotides, which target sequences mapping in 17p12** (chr17:14,954,785-15,434,017) harboring the D17S122 locus.
3. Formamide based hybridization buffer.

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 or KA6904 ), which provides necessary reagents for specimen pretreatment and post-hybridization processing.

Interpretation of results:
Using the CISH Implementation Kit 2 (Cat # KA5366 or KA6904), hybridization signals of Digoxigenin-labeled polynucleotides appear as dark green colored distinct dots (ERBB2 gene region), and Dinitrophenyl-labeled polynucleotides appear as bright red colored distinct dots (D17S122 locus).
Normal situation:In interphases of normal cells or cells without an amplification involving the ERBB2 gene region, two distinct dot-shaped green and two distinct dot-shaped red signals appear.
Aberrant situation: In cells with an amplification of the ERBB2 gene region, an increased number of green signals or green signal clusters will be observed.
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.

Interpretation of Result