TBC1D22A-SREBF2 Fusion FISH Probe
The TBC1D22A-SREBF2 Fusion FISH Probe is used to confirm a fusion of the TBC1D22A and SREBF2 genes. The fusion of the TBC1D22A and SREBF2 genes has been associated with Skin Cutaneous Melanoma. 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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| TBC1D22A-SREBF2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-RERE | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-REOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-REGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-REGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-REAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-ORRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-OROR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-ORGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-ORAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GORE | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GOOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GOGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GOGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GOAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GRRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GROR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GRGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GRGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-GRAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-AQRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-AQOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-AQGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-AQGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-SREBF2-20-AQAQ | 20 (40 μL) | 200 μL |
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SREBF2 Gene Summary
This gene encodes a member of the a ubiquitously expressed transcription factor that controls cholesterol homeostasis by regulating transcription of sterol-regulated genes. The encoded protein contains a basic helix-loop-helix-leucine zipper (bHLH-Zip) domain and binds the sterol regulatory element 1 motif. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Gene Name: Sterol Regulatory Element Binding Transcription Factor 2
Chromosome: CHR22: 42229105 -42302375
Locus: 22q13.2
TBC1D22A Gene Summary
The TBC1 Domain Family Member 22A (TBC1D22A) gene is located on chr22 :47158517-47571342 at 22q13.31.
Gene Name: TBC1 Domain Family Member 22A
Chromosome: CHR22: 47158517 -47571342
Locus: 22q13.31
Gene Diseases
The TBC1D22A SREBF2 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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