Gene-specific Copy Number Variation Probe-TGDS
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| Catalog: |
CNVFP-TGDS-20546 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TGDS). 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: |
TGDS Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TGDS genes. This product achieves the purpose of detection by hybridizing with the TGDS 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 |
TDP-glucose 4,6-dehydratase |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the short-chain dehydrogenases/reductases (SDR) superfamily, and is thought to contain a nicotinamide adenine dinucleotide (NAD) binding domain. This large SDR family of enzymes is involved in the metabolism of a variety of compounds, including prostaglandins, retinoids, lipids, steroid hormones, and xenobiotics. Mutations in this gene have been associated with Catel-Manzke syndrome, which is characterized by Pierre Robin sequence, and radial deviation of the index finger due to the presence of an accessory bone between the index finger and its proximal phalanx. Pierre Robin sequence is defined by an undersized jaw, backwards displacement of the tongue base that causes an obstruction of the airways, and can also be associated with a cleft palate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
TGDS |
| Location |
13q32.1 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 95226307-95248511 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-TGDS-20546-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TGDS-20546-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TGDS-20546-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TGDS-20546-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TGDS-20546-AQ |
467nm |
418nm |
|
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