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| Catalog: | GBAFP-P4HB-05897 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (P4HB). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | P4HB Gene-specific Break Apart Probe is designed to detect potential P4HB rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| 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 |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-P4HB-05897-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-P4HB-05897-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-P4HB-05897-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-P4HB-05897-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-P4HB-05897-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-P4HB-05897-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-P4HB-05897-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-P4HB-05897-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-P4HB-05897-REGR | 599nm;515nm | 580nm;491nm |
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