Gene-specific Copy Number Variation Probe-TRIM6-TRIM34

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Catalog:	CNVFP-TRIM6-TRIM34-21743
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TRIM6-TRIM34). 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:	TRIM6-TRIM34 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TRIM6-TRIM34 genes. This product achieves the purpose of detection by hybridizing with the TRIM6-TRIM34 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	TRIM6-TRIM34 Readthrough
Gene Summary [Provided by RefSeq]	The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This gene represents a readthrough transcript from genes TRIM6 and TRIM34, and it was described as a splice variant of TRIM34. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. [provided by RefSeq, Nov 2009]
Gene Symbol	TRIM6-TRIM34
Location	11p15.4
Chromosome	Chromosome11
Coordinates	This gene maps to 5617864-5665625 in GRCh37 coordinates.
Species	Human

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