Gene-specific Copy Number Variation Probe-CH507-42P11.6

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Catalog:	CNVFP-CH507-42P11.6-02638
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CH507-42P11.6). 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:	CH507-42P11.6 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CH507-42P11.6 genes. This product achieves the purpose of detection by hybridizing with the CH507-42P11.6 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	7-10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name	Uncharacterized CH507-42P11.6
Gene Summary [Provided by RefSeq]	The Uncharacterized CH507-42P11.6 (CH507-42P11.6) gene is located on chr21:6088241 -6084372 at 21p12.
Gene Symbol	CH507-42P11.6
Location	21p12
Chromosome	Chromosome21
Coordinates	This gene maps to 6088241-6084372 in GRCh37 coordinates.
Species	Human

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