FAM168A-SLC13A2 Fusion FISH Probe
The FAM168A-SLC13A2 Fusion FISH Probe is used to confirm a fusion of the FAM168A and SLC13A2 genes. The fusion of the FAM168A and SLC13A2 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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| FAM168A-SLC13A2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-RERE | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-REOR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-REGO | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-REGR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-OROR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GORE | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GROR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM168A-SLC13A2-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC13A2 Gene Summary
The protein encoded by this gene is a sodium-coupled citrate transporter that is regulated by the chaperone activity of cyclophilin b. The encoded protein may play a role in the formation of kidney stones. [provided by RefSeq, Oct 2016]
Gene Name: Solute Carrier Family 13 Member 2
Chromosome: CHR17: 26800663 -26824798
Locus: 17q11.2
FAM168A Gene Summary
The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.
Gene Name: Family With Sequence Similarity 168 Member A
Chromosome: CHR11: 73117027 -73309228
Locus: 11q13.4
Gene Diseases
The FAM168A SLC13A2 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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