Gene-specific Copy Number Variation Probe-CYP3A7-CYP3A51P
Add to Cart
| Catalog: |
CNVFP-CYP3A7-CYP3A51P-03681 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CYP3A7-CYP3A51P). 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: |
CYP3A7-CYP3A51P Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CYP3A7-CYP3A51P genes. This product achieves the purpose of detection by hybridizing with the CYP3A7-CYP3A51P 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 |
CYP3A7-CYP3A51P Readthrough |
| Gene Summary [Provided by RefSeq] |
This locus represents readthrough transcription between the neighboring CYP3A7 (cytochrome P450, family 3, subfamily A, polypeptide 7) and CYP3A51P (cytochrome P450, family 3, subfamily A, polypeptide 51, pseudogene) genes, which are members of the CYP3A gene cluster on chromosome 7. The downstream pseudogene is not known to be independently transcribed. The readthrough transcript includes CYP3A7 exons 1-13 and exons 2 and 13 of the pseudogene. It encodes a CYP3A isoform with a novel C-terminus. This isoform is only expressed in alleles containing a T nucleotide at the -6 position of a splice acceptor in the pseudogene, which enables correct splicing of the upstream CYP3A7 exons to the pseudogene exons. It should be noted that the reference genome sequence represents the CYP3A7_39256 T->A allele, and thus this haplotype is unlikely to produce the readthrough transcript. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
CYP3A7-CYP3A51P |
| Location |
7q22.1 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 99735199-99684678 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-CYP3A7-CYP3A51P-03681-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CYP3A7-CYP3A51P-03681-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CYP3A7-CYP3A51P-03681-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CYP3A7-CYP3A51P-03681-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CYP3A7-CYP3A51P-03681-AQ |
467nm |
418nm |
|
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