D13S319 FISH Probe
€0.00
In stock
SKU
D13S319-20-
Catalog Number: D13S319-20-
Size: 20 tests (40 μl)
€ 50,00 order handling applies
Size: 20 tests (40 μl)
€ 50,00 order handling applies
The D13S319 FISH Probe is used to detect D13S319 gene aneusomy.
Deletion of chromosome 13q14.2 occurs in multiple myeloma, non-Hodgkins lymphoma, chronic lymphocytic leukemia, myeloproliferative disorders, myelodysplastic syndrome, and acute nonlymphocytic leukemia. The D13S319 Fluorescence In Situ Hybridization (FISH) probe is useful in detecting deletions in a higher percentage of cells than by routine cytogenetic studies. The probe can be used to evaluate complex karyotypes for loss of this critical gene region.
Empire Genomics has developed a D13S319 FISH Probe which can be used to detect D13S319 gene aneusomy. The probe comes labeled in orange, and you may also choose to customize the probe to meet your needs.
Loci: 13q14.2
Deletion of chromosome 13q14.2 occurs in multiple myeloma, non-Hodgkins lymphoma, chronic lymphocytic leukemia, myeloproliferative disorders, myelodysplastic syndrome, and acute nonlymphocytic leukemia. The D13S319 Fluorescence In Situ Hybridization (FISH) probe is useful in detecting deletions in a higher percentage of cells than by routine cytogenetic studies. The probe can be used to evaluate complex karyotypes for loss of this critical gene region.
Empire Genomics has developed a D13S319 FISH Probe which can be used to detect D13S319 gene aneusomy. The probe comes labeled in orange, and you may also choose to customize the probe to meet your needs.
Loci: 13q14.2
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