Gene-specific Copy Number Variation Probe-SLC29A1
Add to Cart
| Catalog: |
CNVFP-SLC29A1-18848 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC29A1). 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: |
SLC29A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC29A1 genes. This product achieves the purpose of detection by hybridizing with the SLC29A1 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 |
Solute Carrier Family 29 Member 1 (Augustine Blood Group) |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides used for cancer and viral chemotherapies. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
SLC29A1 |
| Location |
6p21.1 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 44187241-44201888 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-SLC29A1-18848-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC29A1-18848-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC29A1-18848-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC29A1-18848-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC29A1-18848-AQ |
467nm |
418nm |
|
Other Products
