Gene-specific Copy Number Variation Probe-PABPN1
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| Catalog: |
CNVFP-PABPN1-15038 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PABPN1). 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: |
PABPN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PABPN1 genes. This product achieves the purpose of detection by hybridizing with the PABPN1 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 |
Poly(A) Binding Protein Nuclear 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails at the 3' ends of eukaryotic transcripts and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. This gene contains a GCG trinucleotide repeat at the 5' end of the coding region, and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene. [provided by RefSeq, Dec 2010] |
| Gene Symbol |
PABPN1 |
| Location |
14q11.2 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 23789396-23795394 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-PABPN1-15038-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PABPN1-15038-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PABPN1-15038-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PABPN1-15038-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PABPN1-15038-AQ |
467nm |
418nm |
|
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