Gene-specific Break Apart Probe-BHLHE22

Add to Cart

Catalog:	GBAFP-BHLHE22-10188
Classification:	Gene-specific Break Apart Probes
Description:	Our Gene-specific Break Apart Probes usually target the flanks of the target gene (BHLHE22). 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:	BHLHE22 Gene-specific Break Apart Probe is designed to detect potential BHLHE22 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	Basic Helix-loop-helix Family Member E22
Gene Summary [Provided by RefSeq]	This gene encodes a protein that belongs to the basic helix-loop-helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis. [provided by RefSeq, Oct 2016]
Gene Symbol	BHLHE22
Location	8q12.3
Chromosome	Chromosome8
Coordinates	This gene maps to 65492794-65496191 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry