Gene-specific Copy Number Variation Probe-BBS2
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| Catalog: |
CNVFP-BBS2-01445 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BBS2). 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: |
BBS2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BBS2 genes. This product achieves the purpose of detection by hybridizing with the BBS2 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 |
Bardet-Biedl Syndrome 2 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014] |
| Gene Symbol |
BBS2 |
| Location |
16q13 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 56518258-56554008 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-BBS2-01445-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BBS2-01445-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BBS2-01445-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BBS2-01445-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BBS2-01445-AQ |
467nm |
418nm |
|
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