Gene-specific Copy Number Variation Probe-SCP2
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| Catalog: |
CNVFP-SCP2-18084 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SCP2). 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: |
SCP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SCP2 genes. This product achieves the purpose of detection by hybridizing with the SCP2 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 |
Sterol Carrier Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms.[provided by RefSeq, Aug 2010] |
| Gene Symbol |
SCP2 |
| Location |
1p32.3 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 53392900-53517289 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-SCP2-18084-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SCP2-18084-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SCP2-18084-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SCP2-18084-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SCP2-18084-AQ |
467nm |
418nm |
|
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