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Gene-specific Copy Number Variation Probe-HNF4G

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Catalog: CNVFP-HNF4G-06713
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HNF4G). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services.
Application: HNF4G Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HNF4G genes. This product achieves the purpose of detection by hybridizing with the HNF4G gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Category: Copy Number Variation
Probe Kits Volume (µL): 40 μL
Quantity: 20 Tests
Hybridization Solution (µL): 200 μL
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Storage Conditions: Store at -20℃ and avoid light;
Shipping Conditions: -20℃

Gene Details

Gene Name Hepatocyte Nuclear Factor 4 Gamma
Gene Summary [Provided by RefSeq] The Hepatocyte Nuclear Factor 4 Gamma (HNF4G) gene is located on chr8:76452202 -76479061 at 8q21.13.
Gene Symbol HNF4G
Location 8q21.13
Chromosome Chromosome8
Coordinates This gene maps to 76452202-76479061 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-HNF4G-06713-OR 573nm 548nm
2 RE CNVFP-HNF4G-06713-RE 599nm 580nm
3 GO CNVFP-HNF4G-06713-GO 551nm 525nm
4 GR CNVFP-HNF4G-06713-GR 515nm 491nm
5 AQ CNVFP-HNF4G-06713-AQ 467nm 418nm

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