IMPAD1-ZCCHC24 Fusion FISH Probe
The IMPAD1-ZCCHC24 Fusion FISH Probe is used to confirm a fusion of the IMPAD1 and ZCCHC24 genes. The fusion of the IMPAD1 and ZCCHC24 genes has been associated with Breast Invasive Carcinoma. 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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| IMPAD1-ZCCHC24-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-RERE | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-REOR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-REGO | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-REGR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-REAQ | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-ORRE | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-OROR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-ORGO | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-ORAQ | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GORE | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GOOR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GOGO | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GOGR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GOAQ | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GRRE | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GROR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GRGO | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GRGR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-GRAQ | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-AQRE | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-AQOR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-AQGO | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-AQGR | 20 (40 μL) | 200 μL |
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| IMPAD1-ZCCHC24-20-AQAQ | 20 (40 μL) | 200 μL |
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IMPAD1 Gene Summary
This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]
Gene Name: Inositol Monophosphatase Domain Containing 1
Chromosome: CHR8: 57870487 -57906427
Locus: 8q12.1
ZCCHC24 Gene Summary
The Zinc Finger CCHC-type Containing 24 (ZCCHC24) gene is located on chr10 :81142082-81205383 at 10q22.3.
Gene Name: Zinc Finger CCHC-type Containing 24
Chromosome: CHR10: 81142082 -81205383
Locus: 10q22.3
Gene Diseases
The IMPAD1 ZCCHC24 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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