banner

Gene-specific Break Apart Probe-MYH11

Add to Cart
Catalog: GBAFP-MYH11-05249
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MYH11). 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: MYH11 Gene-specific Break Apart Probe is designed to detect potential MYH11 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 Myosin Heavy Chain 11
Gene Summary [Provided by RefSeq] The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alternative splicing generates isoforms that are differentially expressed, with ratios changing during muscle cell maturation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Symbol MYH11
Location 16p13.11
Chromosome Chromosome16
Coordinates This gene maps to 15796991-15950887 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-MYH11-05249-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-MYH11-05249-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-MYH11-05249-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-MYH11-05249-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-MYH11-05249-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-MYH11-05249-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-MYH11-05249-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-MYH11-05249-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-MYH11-05249-REGR 599nm;515nm 580nm;491nm

Other Products

Products

CONTACT SUPPORT

Online Inquiry

0
Inquiry Basket ( 0 ) Choose Dye*