PHF21B-CLTCL1 Fusion FISH Probe
The PHF21B-CLTCL1 Fusion FISH Probe is used to confirm a fusion of the PHF21B and CLTCL1 genes. The fusion of the PHF21B and CLTCL1 genes has been associated with Kidney Renal Papillary Cell 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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| PHF21B-CLTCL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-RERE | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-REOR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-REGO | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-REGR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-REAQ | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-ORRE | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-OROR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-ORGO | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GORE | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GOOR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GOGO | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GOGR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GRRE | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GROR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GRGO | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GRGR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-AQRE | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-AQOR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-AQGO | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-AQGR | 20 (40 μL) | 200 μL |
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| PHF21B-CLTCL1-20-AQAQ | 20 (40 μL) | 200 μL |
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CLTCL1 Gene Summary
This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]
Gene Name: Clathrin Heavy Chain Like 1
Chromosome: CHR22: 19166986 -19279239
Locus: 22q11.21
PHF21B Gene Summary
The PHD Finger Protein 21B (PHF21B) gene is located on chr22 :45277042-45405809 at 22q13.31.
Gene Name: PHD Finger Protein 21B
Chromosome: CHR22: 45277042 -45405809
Locus: 22q13.31
Gene Diseases
The PHF21B CLTCL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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