Gene-specific Copy Number Variation Probe-SPTLC1
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| Catalog: |
CNVFP-SPTLC1-19954 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPTLC1). 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: |
SPTLC1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPTLC1 genes. This product achieves the purpose of detection by hybridizing with the SPTLC1 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 |
Serine Palmitoyltransferase Long Chain Base Subunit 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
SPTLC1 |
| Location |
9q22.31 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 94793426-94877690 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-SPTLC1-19954-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPTLC1-19954-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPTLC1-19954-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPTLC1-19954-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPTLC1-19954-AQ |
467nm |
418nm |
|
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