WNK1-STK38L Fusion FISH Probe
The WNK1-STK38L Fusion FISH Probe is used to confirm a fusion of the WNK1 and STK38L genes. The fusion of the WNK1 and STK38L genes has been associated with Brain Lower Grade Glioma. 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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| WNK1-STK38L-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-RERE | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-REOR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-REGO | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-REGR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-REAQ | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-ORRE | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-OROR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-ORGO | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-ORAQ | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GORE | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GOOR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GOGO | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GOGR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GOAQ | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GRRE | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GROR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GRGO | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GRGR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-GRAQ | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-AQRE | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-AQOR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-AQGO | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-AQGR | 20 (40 μL) | 200 μL |
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| WNK1-STK38L-20-AQAQ | 20 (40 μL) | 200 μL |
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STK38L Gene Summary
The Serine/threonine Kinase 38 Like (STK38L) gene is located on chr12 :27397077-27478890 at 12p11.23.
Gene Name: Serine/threonine Kinase 38 Like
Chromosome: CHR12: 27397077 -27478890
Locus: 12p11.23
WNK1 Gene Summary
This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]
Gene Name: WNK Lysine Deficient Protein Kinase 1
Chromosome: CHR12: 862088 -1020618
Locus: 12p13.33
Gene Diseases
The WNK1 STK38L Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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