Gene-specific Copy Number Variation Probe-HEXA
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| Catalog: |
CNVFP-HEXA-06594 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HEXA). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
HEXA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HEXA genes. This product achieves the purpose of detection by hybridizing with the HEXA gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Hexosaminidase Subunit Alpha |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I). Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016] |
| Gene Symbol |
HEXA |
| Location |
15q23 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 72635777-72668520 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-HEXA-06594-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HEXA-06594-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HEXA-06594-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HEXA-06594-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HEXA-06594-AQ |
467nm |
418nm |
|
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