Labeled FISH probes for identification of gene translocation using Fluorescent In Situ Hybridization Technique. (Technology)
Form:
Liquid
Quality Control Testing:
Representative images of normal human cell (lymphocyte) stain with the dual color FISH probe. The left image is chromosomes at metaphase, and the right image is an interphase nucleus.
Supplied Product:
DAPI Counterstain (1500 ng/mL ) 125 uL for each 100 uL FISH Probe
Storage Instruction:
Store at 4°C in the dark.
Note:
Hybridization position of the probes on the chromosome.
Probe 1:Size:Fluorophore:Location:
AML1Approximately 1340kbFITC21q22.12
Probe 2:Size:Fluorophore:Location:
ETOApproximately 1110kbTexas Red8q21.3
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
Applications
Fluorescent In Situ Hybridization (Cell)
Protocol Download
Fluorescent In Situ Hybridization (Formalin/PFA-fixed paraffin-embedded sections)
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Human lymph node (FFPE) stained with AML1/ETO DY Translocation FISH Probe. Human lymph node cancer showed no AML1/ETO DY Translocation.
Protocol Download
Application Image
Fluorescent In Situ Hybridization (Cell)
Fluorescent In Situ Hybridization (Formalin/PFA-fixed paraffin-embedded sections)
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RUNX1
RUNX1T1
Gene Information
Entrez GeneID:
861
Gene Name:
RUNX1
Gene Alias:
AML1,AML1-EVI-1,AMLCR1,CBFA2,EVI-1,PEBP2aB
Gene Description:
runt-related transcription factor 1
Omim ID:
151385, 180300, 601399, 601626
Gene Ontology:
Hyperlink
Gene Summary:
Core binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
runt-related transcription factor 1; translocated to, 1 (cyclin D-related)
Omim ID:
133435
Gene Ontology:
Hyperlink
Gene Summary:
The protein encoded by this gene is a putative zinc finger transcription factor and oncoprotein. In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5"-region of the RUNX1 gene fused to the 3"-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Several transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq
Other Designations:
acute myelogenous leukemia 1 translocation 1 protein,acute myelogenous leukemia 1 translocation 1, cyclin-D related,core-binding factor, runt domain, alpha subunit 2; translocated to, 1; cyclin D-related,eight twenty one protein,myeloid translocation gene
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