Labeled FISH probes as chromosomal markers using Fluorescent In Situ Hybridization Technique. (Technology)
Recommend Usage:
The probe is provided in 5x concentrated format, to allow mixing of up to 5 chromosome FISH probes in a single hybridization assay. When used alone, it should be diluted to 1x with FISH Hybridization Buffer (Cat # U0028 or U0029) before use.
Supplied Product:
FISH Hybridization Buffer (80 uL)
Storage Instruction:
Store at 4°C in the dark.
Note:
Hybridization position of the probes on the chromosome:
Probe:Size:Fluorophore:Location:
CEN11pApproximately 630kbFITC11p11.12
Origin:
Human
Source:
Genomic DNA
Notice:
We strongly recommend the customer to use FFPE FISH PreTreatment Kit 1 (Catalog #: KA2375 or KA2691) for the pretreatment of Formalin-Fixed Paraffin-Embedded (FFPE) tissue sections.
Regulation Status:
For research use only (RUO)
Datasheet:
Download
Publication Reference
1.
A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region.Tatyana A Vasilyeva, Andrey V Marakhonov, Marina E Minzhenkova, Zhanna G Markova, Nika V Petrova, Natella V Sukhanova, Philipp A Koshkin, Denis V Pyankov, Ilya V Kanivets, Sergey A Korostelev, Irina A Krynskaya, Nadezhda V Shilova, Sergey I Kutsev, Vitaly V Kadyshev, Rena A Zinchenko.BMC Med Genomics. 2020 Sep 18;13(Suppl 8):130. doi: 10.1186/s12920-020-00790-1.