Gene-specific Copy Number Variation Probe-ABCC2
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| Catalog: |
CNVFP-ABCC2-00187 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ABCC2). 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: |
ABCC2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ABCC2 genes. This product achieves the purpose of detection by hybridizing with the ABCC2 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 2 |
| 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 is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ABCC2 |
| Location |
10q24.2 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 101542462-101611662 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-ABCC2-00187-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ABCC2-00187-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ABCC2-00187-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ABCC2-00187-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ABCC2-00187-AQ |
467nm |
418nm |
|
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