Gene-specific Copy Number Variation Probe-ABCC8
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| Catalog: |
CNVFP-ABCC8-00278 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ABCC8). 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: |
ABCC8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ABCC8 genes. This product achieves the purpose of detection by hybridizing with the ABCC8 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 |
ATP Binding Cassette Subfamily C Member 8 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations and deficiencies in this protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013] |
| Gene Symbol |
ABCC8 |
| Location |
11p15.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 17414431-17498449 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-ABCC8-00278-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ABCC8-00278-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ABCC8-00278-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ABCC8-00278-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ABCC8-00278-AQ |
467nm |
418nm |
|
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