FGFR1 Break Apart FISH Probe
€0.00
In stock
SKU
FGFR1BA-20-
Catalog Number: FGFR1BA-20-
Size: 20 tests (40 μl)
€ 50,00 order handling applies
Size: 20 tests (40 μl)
€ 50,00 order handling applies
The FGFR1 Break Apart Probe detects rearrangements of the gene.
The FGFR1 gene, located on chromosome 8p11.2, expresses the frequent t(8;13)(p11;q11-12) translocation that is found in lymphoma and myeloid leukemia cells in stem cell leukemia and lymphoma patients with myeloproliferative syndrome (EMS). Amplification of FGFR1 has been reported in many other cancers including oral squamous cell carcinomas, breast cancer, ovarian cancer, bladder cancer, prostate cancer, and lung cancer. Aberrations of the FGFR1 gene are also commonly expressed in Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and Kallmann syndrome.
Empire Genomics has developed a FGFR1 Break Apart FISH Probe that can be used to detect FGFR1 gene rearrangements. The probe comes labeled in orange and green, and you may also choose to customize the probe to meet your needs.
Loci: 8p11.2
The FGFR1 gene, located on chromosome 8p11.2, expresses the frequent t(8;13)(p11;q11-12) translocation that is found in lymphoma and myeloid leukemia cells in stem cell leukemia and lymphoma patients with myeloproliferative syndrome (EMS). Amplification of FGFR1 has been reported in many other cancers including oral squamous cell carcinomas, breast cancer, ovarian cancer, bladder cancer, prostate cancer, and lung cancer. Aberrations of the FGFR1 gene are also commonly expressed in Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and Kallmann syndrome.
Empire Genomics has developed a FGFR1 Break Apart FISH Probe that can be used to detect FGFR1 gene rearrangements. The probe comes labeled in orange and green, and you may also choose to customize the probe to meet your needs.
Loci: 8p11.2
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