Gene-specific Copy Number Variation Probe-MKKS
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| Catalog: |
CNVFP-MKKS-13400 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MKKS). 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: |
MKKS Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MKKS genes. This product achieves the purpose of detection by hybridizing with the MKKS 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 |
McKusick-Kaufman Syndrome |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family. The encoded protein is a centrosome-shuttling protein and plays an important role in cytokinesis. This protein also interacts with other type II chaperonin members to form a complex known as the BBSome, which involves ciliary membrane biogenesis. This protein is encoded by a downstream open reading frame (dORF). Several upstream open reading frames (uORFs) have been identified, which repress the translation of the dORF, and two of which can encode small mitochondrial membrane proteins. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 6, also known as McKusick-Kaufman syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013] |
| Gene Symbol |
MKKS |
| Location |
20p12.2 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 10385832-10414866 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-MKKS-13400-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MKKS-13400-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MKKS-13400-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MKKS-13400-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MKKS-13400-AQ |
467nm |
418nm |
|
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