LIPN-MINPP1 Gene Fusion FISH Probe

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Catalog:	GFFP-LIPN/MINPP1-06623
Classification:	Gene Fusion FISH Probes
Description:	The LIPN-MINPP1 Gene Fusion FISH Probecan detect the fusion of LIPN and MINPP1 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:	LIPN-MINPP1 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	Multiple Inositol-polyphosphate Phosphatase 1
Gene Summary 1	This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009]
Chromosome 1	Chromosome 10
Locus 1	10q23.2
Coordinates 1	This gene maps to 89264222-89313218 in GRCh37 coordinates.
Gene Name 2	Lipase Family Member N
Gene Summary 2	The gene encodes a lipase that is highly expressed in granular keratinocytes in the epidermis, and plays a role in the differentiation of keratinocytes. Mutations in this gene are associated with lamellar ichthyosis type 4. [provided by RefSeq, Dec 2011]
Chromosome 2	Chromosome10
Locus 2	10q23.31
Coordinates 2	This gene maps to 90521162-90537999 in GRCh37 coordinates.
Associated Diseases	Brain Lower Grade Glioma
Species	Human

Dye Colors:

RE RE RE OR RE GO RE GR RE AQ OR RE OR OR OR GO OR GR OR AQ GO RE GO OR GO GO GO GR GO AQ GR RE GR OR GR GO GR GR GR AQ AQ RE AQ OR AQ GO AQ GR AQ AQ

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