Gene-specific Copy Number Variation Probe-SCARB2
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| Catalog: |
CNVFP-SCARB2-17879 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SCARB2). 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: |
SCARB2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SCARB2 genes. This product achieves the purpose of detection by hybridizing with the SCARB2 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 |
Scavenger Receptor Class B Member 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011] |
| Gene Symbol |
SCARB2 |
| Location |
4q21.1 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 77079891-77135052 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-SCARB2-17879-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SCARB2-17879-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SCARB2-17879-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SCARB2-17879-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SCARB2-17879-AQ |
467nm |
418nm |
|
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