Gene-specific Copy Number Variation Probe-BEST1
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| Catalog: |
CNVFP-BEST1-01405 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BEST1). 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: |
BEST1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BEST1 genes. This product achieves the purpose of detection by hybridizing with the BEST1 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 |
Bestrophin 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008] |
| Gene Symbol |
BEST1 |
| Location |
11q12.3 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 61717355-61731935 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-BEST1-01405-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BEST1-01405-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BEST1-01405-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BEST1-01405-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BEST1-01405-AQ |
467nm |
418nm |
|
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