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Gene-specific Copy Number Variation Probe-FAM99B

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Catalog: CNVFP-FAM99B-05051
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FAM99B). 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: FAM99B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FAM99B genes. This product achieves the purpose of detection by hybridizing with the FAM99B 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 Family With Sequence Similarity 99 Member B (non-protein Coding)
Gene Summary [Provided by RefSeq] The Family With Sequence Similarity 99 Member B (non-protein Coding) (FAM99B) gene is located on chr11:1704499 -1706859 at 11p15.5.
Gene Symbol FAM99B
Location 11p15.5
Chromosome Chromosome11
Coordinates This gene maps to 1704499-1706859 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-FAM99B-05051-OR 573nm 548nm
2 RE CNVFP-FAM99B-05051-RE 599nm 580nm
3 GO CNVFP-FAM99B-05051-GO 551nm 525nm
4 GR CNVFP-FAM99B-05051-GR 515nm 491nm
5 AQ CNVFP-FAM99B-05051-AQ 467nm 418nm

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