LDHB-CTNNA2 Fusion FISH Probe
The LDHB-CTNNA2 Fusion FISH Probe is used to confirm a fusion of the LDHB and CTNNA2 genes. The fusion of the LDHB and CTNNA2 genes has been associated with Uterine Corpus Endometrial 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| LDHB-CTNNA2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-RERE | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-REOR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-REGO | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-REGR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-REAQ | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-ORRE | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-OROR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-ORGO | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-ORAQ | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GORE | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GOOR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GOGO | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GOGR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GOAQ | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GRRE | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GROR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GRGO | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GRGR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-GRAQ | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-AQRE | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-AQOR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-AQGO | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-AQGR | 20 (40 μL) | 200 μL |
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| LDHB-CTNNA2-20-AQAQ | 20 (40 μL) | 200 μL |
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CTNNA2 Gene Summary
The Catenin Alpha 2 (CTNNA2) gene is located on chr2 :79740059-80875988 at 2p12.
Gene Name: Catenin Alpha 2
Chromosome: CHR2: 79740059 -80875988
Locus: 2p12
LDHB Gene Summary
This gene encodes the B subunit of lactate dehydrogenase enzyme, which catalyzes the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+ in a post-glycolysis process. Alternatively spliced transcript variants have been found for this gene. Recent studies have shown that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Mutations in this gene are associated with lactate dehydrogenase B deficiency. Pseudogenes have been identified on chromosomes X, 5 and 13. [provided by RefSeq, Feb 2016]
Gene Name: Lactate Dehydrogenase B
Chromosome: CHR12: 21788274 -21810789
Locus: 12p12.1
Gene Diseases
The LDHB CTNNA2 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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