Gene-specific Copy Number Variation Probe-SLC35C2

Add to Cart

Catalog:	CNVFP-SLC35C2-18789
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC35C2). 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:	SLC35C2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC35C2 genes. This product achieves the purpose of detection by hybridizing with the SLC35C2 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	Solute Carrier Family 35 Member C2
Gene Summary [Provided by RefSeq]	This gene encodes a member of the triose-phosphate transporter protein family. This gene is regulated by oxygen tension, is induced in hypoxic trophoblast cells, and is overexpressed in ovarian cancer. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Jul 2013]
Gene Symbol	SLC35C2
Location	20q13.12
Chromosome	Chromosome20
Coordinates	This gene maps to 44978176-44993064 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry