Gene-specific Copy Number Variation Probe-GALE
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| Catalog: |
CNVFP-GALE-05746 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GALE). 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: |
GALE Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GALE genes. This product achieves the purpose of detection by hybridizing with the GALE 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 |
UDP-galactose-4-epimerase |
| Gene Summary [Provided by RefSeq] |
This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and cognitive disability, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). Multiple alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GALE |
| Location |
1p36.11 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 24122088-24127294 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-GALE-05746-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GALE-05746-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GALE-05746-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GALE-05746-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GALE-05746-AQ |
467nm |
418nm |
|
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