C1S-NXPH4 Fusion FISH Probe
The C1S-NXPH4 Fusion FISH Probe is used to confirm a fusion of the C1S and NXPH4 genes. The fusion of the C1S and NXPH4 genes has been associated with Liver Hepatocellular 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| C1S-NXPH4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-RERE | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-REOR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-REGO | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-REGR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-REAQ | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-ORRE | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-OROR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-ORGO | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-ORAQ | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GORE | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GOOR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GOGO | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GOGR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GOAQ | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GRRE | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GROR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GRGO | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GRGR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-GRAQ | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-AQRE | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-AQOR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-AQGO | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-AQGR | 20 (40 μL) | 200 μL |
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| C1S-NXPH4-20-AQAQ | 20 (40 μL) | 200 μL |
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C1S Gene Summary
This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency. [provided by RefSeq, Mar 2009]
Gene Name: Complement C1s
Chromosome: CHR12: 7167979 -7178335
Locus: 12p13.31
NXPH4 Gene Summary
The Neurexophilin 4 (NXPH4) gene is located on chr12 :57610577-57620232 at 12q13.3.
Gene Name: Neurexophilin 4
Chromosome: CHR12: 57610577 -57620232
Locus: 12q13.3
Gene Diseases
The C1S NXPH4 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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