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Gene-specific Break Apart Probe-SLC5A7

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Catalog: GBAFP-SLC5A7-17203
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SLC5A7). 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: SLC5A7 Gene-specific Break Apart Probe is designed to detect potential SLC5A7 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 Details

Gene Name Solute Carrier Family 5 Member 7
Gene Summary [Provided by RefSeq] This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
Gene Symbol SLC5A7
Location 2q12.3
Chromosome Chromosome2
Coordinates This gene maps to 108602994-108630443 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-SLC5A7-17203-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-SLC5A7-17203-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-SLC5A7-17203-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-SLC5A7-17203-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-SLC5A7-17203-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-SLC5A7-17203-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-SLC5A7-17203-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-SLC5A7-17203-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-SLC5A7-17203-REGR 599nm;515nm 580nm;491nm

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