CHD7-TCF7L2 Fusion FISH Probe
The CHD7-TCF7L2 Fusion FISH Probe is used to confirm a fusion of the CHD7 and TCF7L2 genes. The fusion of the CHD7 and TCF7L2 genes has been associated with Colon Adenocarcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CHD7-TCF7L2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-RERE | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-REOR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-REGO | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-REGR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-REAQ | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-ORRE | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-OROR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-ORGO | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-ORAQ | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GORE | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GOOR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GOGO | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GOGR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GOAQ | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GRRE | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GROR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GRGO | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GRGR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-GRAQ | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-AQRE | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-AQOR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-AQGO | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-AQGR | 20 (40 μL) | 200 μL |
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| CHD7-TCF7L2-20-AQAQ | 20 (40 μL) | 200 μL |
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TCF7L2 Gene Summary
This gene encodes a high mobility group (HMG) box-containing transcription factor that plays a key role in the Wnt signaling pathway. The protein has been implicated in blood glucose homeostasis. Genetic variants of this gene are associated with increased risk of type 2 diabetes. Several transcript variants encoding multiple different isoforms have been found for this gene.[provided by RefSeq, Oct 2010]
Gene Name: Transcription Factor 7 Like 2
Chromosome: CHR10: 114710008 -114927436
Locus: 10q25.2-q25.3
CHD7 Gene Summary
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Gene Name: Chromodomain Helicase DNA Binding Protein 7
Chromosome: CHR8: 61591323 -61780586
Locus: 8q12.2
Gene Diseases
The CHD7 TCF7L2 Fusion has been associated with the following diseases:
| Disease Name |
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| Colon Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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