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Gene-specific Copy Number Variation Probe-COX7A2

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Catalog: CNVFP-COX7A2-03105
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COX7A2). 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: COX7A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COX7A2 genes. This product achieves the purpose of detection by hybridizing with the COX7A2 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 Cytochrome C Oxidase Subunit 7A2
Gene Summary [Provided by RefSeq] Cytochrome c oxidase, the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of three catalytic subunits encoded by mitochondrial genes, and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, while the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 2 (liver isoform) of subunit VIIa, with this polypeptide being present in both muscle and non-muscle tissues. In addition to polypeptide 2, subunit VIIa includes polypeptide 1 (muscle isoform), which is present only in muscle tissues, and a related protein, which is present in all tissues. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4 and 14. [provided by RefSeq, Oct 2009]
Gene Symbol COX7A2
Location 6q14.1
Chromosome Chromosome6
Coordinates This gene maps to 75947390-75953644 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-COX7A2-03105-OR 573nm 548nm
2 RE CNVFP-COX7A2-03105-RE 599nm 580nm
3 GO CNVFP-COX7A2-03105-GO 551nm 525nm
4 GR CNVFP-COX7A2-03105-GR 515nm 491nm
5 AQ CNVFP-COX7A2-03105-AQ 467nm 418nm

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