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Gene-specific Break Apart Probe-LIMK1

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Catalog: GBAFP-LIMK1-13536
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (LIMK1). 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: LIMK1 Gene-specific Break Apart Probe is designed to detect potential LIMK1 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 LIM Domain Kinase 1
Gene Summary [Provided by RefSeq] There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cognition of Williams syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Feb 2011]
Gene Symbol LIMK1
Location 7q11.23
Chromosome Chromosome7
Coordinates This gene maps to 73498106-73536855 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-LIMK1-13536-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-LIMK1-13536-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-LIMK1-13536-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-LIMK1-13536-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-LIMK1-13536-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-LIMK1-13536-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-LIMK1-13536-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-LIMK1-13536-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-LIMK1-13536-REGR 599nm;515nm 580nm;491nm

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