Gene-specific Copy Number Variation Probe-BBS7
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| Catalog: |
CNVFP-BBS7-01446 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BBS7). 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: |
BBS7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BBS7 genes. This product achieves the purpose of detection by hybridizing with the BBS7 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 7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy; however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014] |
| Gene Symbol |
BBS7 |
| Location |
4q27 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 122745483-122791652 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-BBS7-01446-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BBS7-01446-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BBS7-01446-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BBS7-01446-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BBS7-01446-AQ |
467nm |
418nm |
|
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