TMLHE-VBP1 Gene Fusion FISH Probe

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Catalog:	GFFP-TMLHE/VBP1-12367
Classification:	Gene Fusion FISH Probes
Description:	The TMLHE-VBP1 Gene Fusion FISH Probecan detect the fusion of TMLHE and VBP1 genes. Our product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We offer a variety of dye color combinations for FISH probes for gene fusions. This product has been verified in both interphase nuclei and metaphase spreads of normal peripheral blood. This is key quality control, you can trust our quality.
Application:	TMLHE-VBP1 Gene Fusion FISH Probe can be used for chromosomal diagnosis to determine gene fusion phenomena associated with diseases such as cancer. You can confirm this in "Associated Diseases" in the product information. This product has been verified in both interphase nuclei and metaphase spreads of normal peripheral blood. This is key quality control, you can trust our quality.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	7-10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name 1	VHL Binding Protein 1
Gene Summary 1	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]
Chromosome 1	Chromosome X
Locus 1	Xq28
Coordinates 1	This gene maps to 154444700-154468098 in GRCh37 coordinates.
Gene Name 2	Trimethyllysine Hydroxylase, Epsilon
Gene Summary 2	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]
Chromosome 2	ChromosomeX
Locus 2	Xq28
Coordinates 2	This gene maps to 154718672-154842622 in GRCh37 coordinates.
Associated Diseases	Adrenocortical Carcinoma
Species	Human

Dye Colors:

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