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Gene-specific Copy Number Variation Probe-SLX1A

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Catalog: CNVFP-SLX1A-19023
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLX1A). 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: SLX1A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLX1A genes. This product achieves the purpose of detection by hybridizing with the SLX1A 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 SLX1 Homolog A, Structure-specific Endonuclease Subunit
Gene Summary [Provided by RefSeq] This gene encodes a protein that is an important regulator of genome stability. The protein represents the catalytic subunit of the SLX1-SLX4 structure-specific endonuclease, which can resolve DNA secondary structures that are formed during repair and recombination processes. Two identical copies of this gene are located on the p arm of chromosome 16 due to a segmental duplication; this record represents the more centromeric copy. Alternative splicing results in multiple transcript variants. Read-through transcription also occurs between this gene and the downstream SULT1A3 (sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3) gene. [provided by RefSeq, Nov 2010]
Gene Symbol SLX1A
Location 16p11.2
Chromosome Chromosome16
Coordinates This gene maps to 29465821-29469545 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-SLX1A-19023-OR 573nm 548nm
2 RE CNVFP-SLX1A-19023-RE 599nm 580nm
3 GO CNVFP-SLX1A-19023-GO 551nm 525nm
4 GR CNVFP-SLX1A-19023-GR 515nm 491nm
5 AQ CNVFP-SLX1A-19023-AQ 467nm 418nm

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