Gene-specific Copy Number Variation Probe-ABCG8
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| Catalog: |
CNVFP-ABCG8-00262 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ABCG8). 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: |
ABCG8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ABCG8 genes. This product achieves the purpose of detection by hybridizing with the ABCG8 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 G 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 White subfamily. The protein encoded by this gene functions to exclude non-cholesterol sterol entry at the intestinal level, promote excretion of cholesterol and sterols into bile, and to facilitate transport of sterols back into the intestinal lumen. It is expressed in a tissue-specific manner in the liver, intestine, and gallbladder. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG5. Mutations in this gene may contribute to sterol accumulation and atherosclerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
ABCG8 |
| Location |
2p21 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 44066102-44105605 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-ABCG8-00262-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ABCG8-00262-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ABCG8-00262-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ABCG8-00262-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ABCG8-00262-AQ |
467nm |
418nm |
|
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