HOXA10-CSN1S1 Fusion FISH Probe
The HOXA10-CSN1S1 Fusion FISH Probe is used to confirm a fusion of the HOXA10 and CSN1S1 genes. The fusion of the HOXA10 and CSN1S1 genes has been associated with Esophageal 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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| HOXA10-CSN1S1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-RERE | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-REOR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-REGO | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-REGR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-REAQ | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-ORRE | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-OROR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-ORGO | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-ORAQ | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GORE | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GOOR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GOGO | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GOGR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GOAQ | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GRRE | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GROR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GRGO | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GRGR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-GRAQ | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-AQRE | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-AQOR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-AQGO | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-AQGR | 20 (40 μL) | 200 μL |
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| HOXA10-CSN1S1-20-AQAQ | 20 (40 μL) | 200 μL |
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CSN1S1 Gene Summary
The Casein Alpha S1 (CSN1S1) gene is located on chr4 :70796798-70812288 at 4q13.3.
Gene Name: Casein Alpha S1
Chromosome: CHR4: 70796798 -70812288
Locus: 4q13.3
HOXA10 Gene Summary
In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor that may regulate gene expression, morphogenesis, and differentiation. More specifically, it may function in fertility, embryo viability, and regulation of hematopoietic lineage commitment. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the downstream homeobox A9 (HOXA9) gene. [provided by RefSeq, Mar 2011]
Gene Name: Homeobox A10
Chromosome: CHR7: 27210209 -27219880
Locus: 7p15.2
Gene Diseases
The HOXA10 CSN1S1 Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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