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Gene-specific Copy Number Variation Probe-PHKA2

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Catalog: CNVFP-PHKA2-15557
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PHKA2). 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: PHKA2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PHKA2 genes. This product achieves the purpose of detection by hybridizing with the PHKA2 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 Phosphorylase Kinase Regulatory Subunit Alpha 2
Gene Summary [Provided by RefSeq] Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, which are encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9A, also known as X-linked liver glycogenosis. Alternatively spliced transcript variants have been reported, but the full-length nature of these variants has not been determined.[provided by RefSeq, Feb 2010]
Gene Symbol PHKA2
Location Xp22.13
Chromosome ChromosomeX
Coordinates This gene maps to 18910415-19002480 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-PHKA2-15557-OR 573nm 548nm
2 RE CNVFP-PHKA2-15557-RE 599nm 580nm
3 GO CNVFP-PHKA2-15557-GO 551nm 525nm
4 GR CNVFP-PHKA2-15557-GR 515nm 491nm
5 AQ CNVFP-PHKA2-15557-AQ 467nm 418nm

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