P4HTM-C16ORF73 Fusion FISH Probe
The P4HTM-C16ORF73 Fusion FISH Probe is used to confirm a fusion of the P4HTM and C16ORF73 genes. The fusion of the P4HTM and C16ORF73 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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| P4HTM-C16ORF73-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-RERE | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-REOR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-REGO | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-REGR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-REAQ | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-ORRE | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-OROR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-ORGO | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-ORAQ | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GORE | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GOOR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GOGO | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GOGR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GOAQ | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GRRE | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GROR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GRGO | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GRGR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-GRAQ | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-AQRE | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-AQOR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-AQGO | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-AQGR | 20 (40 μL) | 200 μL |
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| P4HTM-C16ORF73-20-AQAQ | 20 (40 μL) | 200 μL |
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P4HTM Gene Summary
The product of this gene belongs to the family of prolyl 4-hydroxylases. This protein is a prolyl hydroxylase that may be involved in the degradation of hypoxia-inducible transcription factors under normoxia. It plays a role in adaptation to hypoxia and may be related to cellular oxygen sensing. Alternatively spliced variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Name: Prolyl 4-hydroxylase, Transmembrane
Chromosome: CHR3: 49027340 -49044581
Locus: 3p21.3
Gene Diseases
The P4HTM C16ORF73 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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