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| Catalog: | GBAFP-GCSH-02802 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (GCSH). 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: | GCSH Gene-specific Break Apart Probe is designed to detect potential GCSH 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 | Glycine Cleavage System Protein H |
| Gene Summary [Provided by RefSeq] | Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.[provided by RefSeq, Jan 2010] |
| Gene Symbol | GCSH |
| Location | 16q23.2 |
| Chromosome | Chromosome16 |
| Coordinates | This gene maps to 81115551-81129980 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-GCSH-02802-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-GCSH-02802-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-GCSH-02802-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-GCSH-02802-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-GCSH-02802-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-GCSH-02802-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-GCSH-02802-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-GCSH-02802-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-GCSH-02802-REGR | 599nm;515nm | 580nm;491nm |
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