Gene-specific Copy Number Variation Probe-ABCB11
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| Catalog: |
CNVFP-ABCB11-00198 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ABCB11). 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: |
ABCB11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ABCB11 genes. This product achieves the purpose of detection by hybridizing with the ABCB11 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 B Member 11 |
| Gene Summary [Provided by RefSeq] |
The membrane-associated 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ABCB11 |
| Location |
2q31.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 169779448-169887833 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-ABCB11-00198-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ABCB11-00198-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ABCB11-00198-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ABCB11-00198-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ABCB11-00198-AQ |
467nm |
418nm |
|
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