KLHL5-SLC16A2 Fusion FISH Probe
The KLHL5-SLC16A2 Fusion FISH Probe is used to confirm a fusion of the KLHL5 and SLC16A2 genes. The fusion of the KLHL5 and SLC16A2 genes has been associated with Head And Neck Squamous 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| KLHL5-SLC16A2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-RERE | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-REOR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-REGO | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-REGR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-REAQ | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-ORRE | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-OROR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-ORGO | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-ORAQ | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GORE | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GOOR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GOGO | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GOGR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GOAQ | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GRRE | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GROR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GRGO | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GRGR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-GRAQ | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-AQRE | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-AQOR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-AQGO | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-AQGR | 20 (40 μL) | 200 μL |
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| KLHL5-SLC16A2-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC16A2 Gene Summary
This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012]
Gene Name: Solute Carrier Family 16 Member 2
Chromosome: CHRX: 73641084 -73753752
Locus: Xq13.2
KLHL5 Gene Summary
The Kelch Like Family Member 5 (KLHL5) gene is located on chr4 :39046450-39127853 at 4p14.
Gene Name: Kelch Like Family Member 5
Chromosome: CHR4: 39046450 -39127853
Locus: 4p14
Gene Diseases
The KLHL5 SLC16A2 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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