Gene-specific Copy Number Variation Probe-P4HB
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| Catalog: |
CNVFP-P4HB-15054 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (P4HB). 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: |
P4HB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to P4HB genes. This product achieves the purpose of detection by hybridizing with the P4HB 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 |
Prolyl 4-hydroxylase Subunit Beta |
| Gene Summary [Provided by RefSeq] |
This gene encodes the beta subunit of prolyl 4-hydroxylase, a highly abundant multifunctional enzyme that belongs to the protein disulfide isomerase family. When present as a tetramer consisting of two alpha and two beta subunits, this enzyme is involved in hydroxylation of prolyl residues in preprocollagen. This enzyme is also a disulfide isomerase containing two thioredoxin domains that catalyze the formation, breakage and rearrangement of disulfide bonds. Other known functions include its ability to act as a chaperone that inhibits aggregation of misfolded proteins in a concentration-dependent manner, its ability to bind thyroid hormone, its role in both the influx and efflux of S-nitrosothiol-bound nitric oxide, and its function as a subunit of the microsomal triglyceride transfer protein complex. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
P4HB |
| Location |
17q25.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 79801033-79818544 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-P4HB-15054-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-P4HB-15054-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-P4HB-15054-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-P4HB-15054-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-P4HB-15054-AQ |
467nm |
418nm |
|
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