Gene-specific Copy Number Variation Probe-CHRFAM7A
Add to Cart
| Catalog: |
CNVFP-CHRFAM7A-02580 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CHRFAM7A). 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: |
CHRFAM7A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CHRFAM7A genes. This product achieves the purpose of detection by hybridizing with the CHRFAM7A 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 |
CHRNA7 (exons 5-10) And FAM7A (exons A-E) Fusion |
| Gene Summary [Provided by RefSeq] |
The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The family member CHRNA7, which is located on chromosome 15 in a region associated with several neuropsychiatric disorders, is partially duplicated and forms a hybrid with a novel gene from the family with sequence similarity 7 (FAM7A). Alternative splicing has been observed, and two variants exist, for this hybrid gene. The N-terminally truncated products predicted by the largest open reading frames for each variant would lack the majority of the neurotransmitter-gated ion-channel ligand binding domain but retain the transmembrane region that forms the ion channel. Although current evidence supports transcription of this hybrid gene, translation of the nicotinic acetylcholine receptor-like protein-encoding open reading frames has not been confirmed. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
CHRFAM7A |
| Location |
15q13.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 30653442-30685864 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-CHRFAM7A-02580-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CHRFAM7A-02580-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CHRFAM7A-02580-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CHRFAM7A-02580-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CHRFAM7A-02580-AQ |
467nm |
418nm |
|
Other Products
