Gene-specific Copy Number Variation Probe-GNA11
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| Catalog: |
CNVFP-GNA11-06126 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GNA11). 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: |
GNA11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GNA11 genes. This product achieves the purpose of detection by hybridizing with the GNA11 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 |
G Protein Subunit Alpha 11 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the family of guanine nucleotide-binding proteins (G proteins), which function as modulators or transducers in various transmembrane signaling systems. G proteins are composed of 3 units: alpha, beta and gamma. This gene encodes one of the alpha subunits (subunit alpha-11). Mutations in this gene have been associated with hypocalciuric hypercalcemia type II (HHC2) and hypocalcemia dominant 2 (HYPOC2). Patients with HHC2 and HYPOC2 exhibit decreased or increased sensitivity, respectively, to changes in extracellular calcium concentrations. [provided by RefSeq, Dec 2013] |
| Gene Symbol |
GNA11 |
| Location |
19p13.3 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 3094407-3121454 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-GNA11-06126-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GNA11-06126-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GNA11-06126-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GNA11-06126-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GNA11-06126-AQ |
467nm |
418nm |
|
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