ATP6V1H-ST8SIA4 Fusion FISH Probe
The ATP6V1H-ST8SIA4 Fusion FISH Probe is used to confirm a fusion of the ATP6V1H and ST8SIA4 genes. The fusion of the ATP6V1H and ST8SIA4 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ATP6V1H-ST8SIA4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-RERE | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-REOR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-REGO | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-REGR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-REAQ | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-ORRE | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-OROR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-ORGO | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GORE | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GOOR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GOGO | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GOGR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GRRE | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GROR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GRGO | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GRGR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-AQRE | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-AQOR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-AQGO | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-AQGR | 20 (40 μL) | 200 μL |
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| ATP6V1H-ST8SIA4-20-AQAQ | 20 (40 μL) | 200 μL |
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ST8SIA4 Gene Summary
The protein encoded by this gene catalyzes the polycondensation of alpha-2,8-linked sialic acid required for the synthesis of polysialic acid, a modulator of the adhesive properties of neural cell adhesion molecule (NCAM1). The encoded protein, which is a member of glycosyltransferase family 29, is a type II membrane protein that may be present in the Golgi apparatus. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: ST8 Alpha-N-acetyl-neuraminide Alpha-2,8-sialyltransferase 4
Chromosome: CHR5: 100142638 -100238987
Locus: 5q21.1
ATP6V1H Gene Summary
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of intracellular organelles. V-ATPase-dependent organelle acidification is necessary for multiple processes including protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. The encoded protein is the regulatory H subunit of the V1 domain of V-ATPase, which is required for catalysis of ATP but not the assembly of V-ATPase. Decreased expression of this gene may play a role in the development of type 2 diabetes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012]
Gene Name: ATPase H+ Transporting V1 Subunit H
Chromosome: CHR8: 54628114 -54755850
Locus: 8q11.23
Gene Diseases
The ATP6V1H ST8SIA4 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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