PHF21A-CNP Fusion FISH Probe
The PHF21A-CNP Fusion FISH Probe is used to confirm a fusion of the PHF21A and CNP genes. The fusion of the PHF21A and CNP genes has been associated with Pheochromocytoma And Paraganglioma. 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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PHF21A-CNP-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-RERE | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-REOR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-REGO | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-REGR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-REAQ | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-ORRE | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-OROR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-ORGO | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-ORAQ | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GORE | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GOOR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GOGO | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GOGR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GOAQ | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GRRE | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GROR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GRGO | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GRGR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-GRAQ | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-AQRE | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-AQOR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-AQGO | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-AQGR | 20 (40 μL) | 200 μL | ||
PHF21A-CNP-20-AQAQ | 20 (40 μL) | 200 μL |
CNP Gene Summary
The 2',3'-cyclic Nucleotide 3' Phosphodiesterase (CNP) gene is located on chr17 :40118758-40129754 at 17q21.2.
Gene Name: 2',3'-cyclic Nucleotide 3' Phosphodiesterase
Chromosome: CHR17: 40118758 -40129754
Locus: 17q21.2
PHF21A Gene Summary
The PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron-specific genes through the cis-regulatory element known as repressor element-1 (RE1) or neural restrictive silencer (NRS) (Hakimi et al., 2002 [PubMed 12032298]).[supplied by OMIM, Nov 2010]
Gene Name: PHD Finger Protein 21A
Chromosome: CHR11: 45950869 -46142985
Locus: 11p11.2
Gene Diseases
The PHF21A CNP Fusion has been associated with the following diseases:
Disease Name |
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Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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