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| Catalog: | GBAFP-GPD1-12508 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (GPD1). 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: | GPD1 Gene-specific Break Apart Probe is designed to detect potential GPD1 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 | Glycerol-3-phosphate Dehydrogenase 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that facilitates the transfer of reducing equivalents from the cytosol to mitochondria. Mutations in this gene are a cause of transient infantile hypertriglyceridemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012] |
| Gene Symbol | GPD1 |
| Location | 12q13.12 |
| Chromosome | Chromosome12 |
| Coordinates | This gene maps to 50497800-50505095 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-GPD1-12508-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-GPD1-12508-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-GPD1-12508-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-GPD1-12508-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-GPD1-12508-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-GPD1-12508-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-GPD1-12508-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-GPD1-12508-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-GPD1-12508-REGR | 599nm;515nm | 580nm;491nm |
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