BPTF-ABCC3 Fusion FISH Probe
The BPTF-ABCC3 Fusion FISH Probe is used to confirm a fusion of the BPTF and ABCC3 genes. The fusion of the BPTF and ABCC3 genes has been associated with Breast Invasive Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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BPTF-ABCC3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-RERE | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-REOR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-REGO | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-REGR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-REAQ | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-ORRE | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-OROR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-ORGO | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-ORAQ | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GORE | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GOOR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GOGO | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GOGR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GOAQ | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GRRE | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GROR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GRGO | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GRGR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-GRAQ | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-AQRE | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-AQOR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-AQGO | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-AQGR | 20 (40 μL) | 200 μL | ||
BPTF-ABCC3-20-AQAQ | 20 (40 μL) | 200 μL |
BPTF Gene Summary
This gene was identified by the reactivity of its encoded protein to a monoclonal antibody prepared against brain homogenates from patients with Alzheimer's disease. Analysis of the original protein (fetal Alz-50 reactive clone 1, or FAC1), identified as an 810 aa protein containing a DNA-binding domain and a zinc finger motif, suggested it might play a role in the regulation of transcription. High levels of FAC1 were detected in fetal brain and in patients with neurodegenerative diseases. The protein encoded by this gene is actually much larger than originally thought, and it also contains a C-terminal bromodomain characteristic of proteins that regulate transcription during proliferation. The encoded protein is highly similar to the largest subunit of the Drosophila NURF (nucleosome remodeling factor) complex. In Drosophila, the NURF complex, which catalyzes nucleosome sliding on DNA and interacts with sequence-specific transcription factors, is necessary for the chromatin remodeling required for transcription. Two alternative transcripts encoding different isoforms have been described completely. [provided by RefSeq, Jul 2008]
Gene Name: Bromodomain PHD Finger Transcription Factor
Chromosome: CHR17: 65821779 -65980494
Locus: 17q24.2
ABCC3 Gene Summary
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. The specific function of this protein has not yet been determined; however, this protein may play a role in the transport of biliary and intestinal excretion of organic anions. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]
Gene Name: ATP Binding Cassette Subfamily C Member 3
Chromosome: CHR17: 48712217 -48769063
Locus: 17q21.33
Gene Diseases
The BPTF ABCC3 Fusion has been associated with the following diseases:
Disease Name |
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Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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