RPGRIP1L-KLHL22 Fusion FISH Probe
The RPGRIP1L-KLHL22 Fusion FISH Probe is used to confirm a fusion of the RPGRIP1L and KLHL22 genes. The fusion of the RPGRIP1L and KLHL22 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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| RPGRIP1L-KLHL22-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-RERE | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-REOR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-REGO | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-REGR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-REAQ | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-ORRE | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-OROR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-ORGO | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-ORAQ | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GORE | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GOOR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GOGO | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GOGR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GOAQ | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GRRE | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GROR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GRGO | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GRGR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-GRAQ | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-AQRE | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-AQOR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-AQGO | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-AQGR | 20 (40 μL) | 200 μL |
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| RPGRIP1L-KLHL22-20-AQAQ | 20 (40 μL) | 200 μL |
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RPGRIP1L Gene Summary
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]
Gene Name: RPGRIP1 Like
Chromosome: CHR16: 53633817 -53737771
Locus: 16q12.2
KLHL22 Gene Summary
The Kelch Like Family Member 22 (KLHL22) gene is located on chr22 :20795805-20850170 at 22q11.21.
Gene Name: Kelch Like Family Member 22
Chromosome: CHR22: 20795805 -20850170
Locus: 22q11.21
Gene Diseases
The RPGRIP1L KLHL22 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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