Gene-specific Break Apart Probe-TCF7L2

Add to Cart

Catalog:	GBAFP-TCF7L2-18015
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TCF7L2). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent.
Application:	TCF7L2 Gene-specific Break Apart Probe is designed to detect potential TCF7L2 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	Within 10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name	Transcription Factor 7 Like 2
Gene Summary [Provided by RefSeq]	This gene encodes a high mobility group (HMG) box-containing transcription factor that plays a key role in the Wnt signaling pathway. The protein has been implicated in blood glucose homeostasis. Genetic variants of this gene are associated with increased risk of type 2 diabetes. Several transcript variants encoding multiple different isoforms have been found for this gene.[provided by RefSeq, Oct 2010]
Gene Symbol	TCF7L2
Location	10q25.2-q25.3
Chromosome	Chromosome10
Coordinates	This gene maps to 114710008-114927436 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry