TMLHE-VBP1 Fusion FISH Probe
The TMLHE-VBP1 Fusion FISH Probe is used to confirm a fusion of the TMLHE and VBP1 genes. The fusion of the TMLHE and VBP1 genes has been associated with Adrenocortical 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. 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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| TMLHE-VBP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-RERE | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-REOR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-REGO | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-REGR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-REAQ | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-ORRE | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-OROR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-ORGO | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GORE | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GOOR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GOGO | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GOGR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GRRE | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GROR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GRGO | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GRGR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-AQRE | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-AQOR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-AQGO | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-AQGR | 20 (40 μL) | 200 μL |
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| TMLHE-VBP1-20-AQAQ | 20 (40 μL) | 200 μL |
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VBP1 Gene Summary
The protein encoded by this gene interacts with the Von Hippel-Lindau protein to form an intracellular complex. The encoded protein functions as a chaperone protein, and may play a role in the transport of the Von Hippel-Lindau protein from the perinuclear granules to the nucleus or cytoplasm. Alternative splicing and the use of alternate transcription start sites results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Jan 2015]
Gene Name: VHL Binding Protein 1
Chromosome: CHRX: 154444700 -154468098
Locus: Xq28
TMLHE Gene Summary
This gene encodes the protein trimethyllysine dioxygenase which is the first enzyme in the carnitine biosynthesis pathway. Carnitine play an essential role in the transport of activated fatty acids across the inner mitochondrial membrane. The encoded protein converts trimethyllysine into hydroxytrimethyllysine. A pseudogene of this gene is found on chromosome X. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Gene Name: Trimethyllysine Hydroxylase, Epsilon
Chromosome: CHRX: 154718672 -154842622
Locus: Xq28
Gene Diseases
The TMLHE VBP1 Fusion has been associated with the following diseases:
| Disease Name |
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| Adrenocortical Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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