Gene-specific Copy Number Variation Probe-TXNL4A
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| Catalog: |
CNVFP-TXNL4A-22620 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TXNL4A). 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: |
TXNL4A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TXNL4A genes. This product achieves the purpose of detection by hybridizing with the TXNL4A 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 |
Thioredoxin Like 4A |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015] |
| Gene Symbol |
TXNL4A |
| Location |
18q23 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 77732866-77748532 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-TXNL4A-22620-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TXNL4A-22620-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TXNL4A-22620-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TXNL4A-22620-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TXNL4A-22620-AQ |
467nm |
418nm |
|
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