CWF19L1-HSPA12A Fusion FISH Probe
The CWF19L1-HSPA12A Fusion FISH Probe is used to confirm a fusion of the CWF19L1 and HSPA12A genes. The fusion of the CWF19L1 and HSPA12A 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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| CWF19L1-HSPA12A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-RERE | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-REOR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-REGO | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-REGR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-REAQ | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-ORRE | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-OROR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-ORGO | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-ORAQ | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GORE | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GOOR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GOGO | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GOGR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GOAQ | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GRRE | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GROR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GRGO | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GRGR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-GRAQ | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-AQRE | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-AQOR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-AQGO | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-AQGR | 20 (40 μL) | 200 μL |
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| CWF19L1-HSPA12A-20-AQAQ | 20 (40 μL) | 200 μL |
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CWF19L1 Gene Summary
This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Gene Name: CWF19 Like 1, Cell Cycle Control (S. Pombe)
Chromosome: CHR10: 101992054 -102027437
Locus: 10q24.31
HSPA12A Gene Summary
The Heat Shock Protein Family A (Hsp70) Member 12A (HSPA12A) gene is located on chr10 :118430702-118502085 at 10q25.3.
Gene Name: Heat Shock Protein Family A (Hsp70) Member 12A
Chromosome: CHR10: 118430702 -118502085
Locus: 10q25.3
Gene Diseases
The CWF19L1 HSPA12A 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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