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Gene-specific Copy Number Variation Probe-RAX2

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Catalog: CNVFP-RAX2-16958
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAX2). 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: RAX2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAX2 genes. This product achieves the purpose of detection by hybridizing with the RAX2 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 Retina And Anterior Neural Fold Homeobox 2
Gene Summary [Provided by RefSeq] This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Symbol RAX2
Location 19p13.3
Chromosome Chromosome19
Coordinates This gene maps to 3769088-3772219 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-RAX2-16958-OR 573nm 548nm
2 RE CNVFP-RAX2-16958-RE 599nm 580nm
3 GO CNVFP-RAX2-16958-GO 551nm 525nm
4 GR CNVFP-RAX2-16958-GR 515nm 491nm
5 AQ CNVFP-RAX2-16958-AQ 467nm 418nm

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