Gene-specific Copy Number Variation Probe-SLC19A2

Add to Cart

Catalog:	CNVFP-SLC19A2-18603
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC19A2). 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:	SLC19A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC19A2 genes. This product achieves the purpose of detection by hybridizing with the SLC19A2 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 19 Member 2
Gene Summary [Provided by RefSeq]	This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
Gene Symbol	SLC19A2
Location	1q24.2
Chromosome	Chromosome1
Coordinates	This gene maps to 169433148-169455208 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry