Gene-specific Copy Number Variation Probe-GCSH
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| Catalog: |
CNVFP-GCSH-05995 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GCSH). 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: |
GCSH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GCSH genes. This product achieves the purpose of detection by hybridizing with the GCSH 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 |
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 |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-GCSH-05995-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GCSH-05995-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GCSH-05995-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GCSH-05995-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GCSH-05995-AQ |
467nm |
418nm |
|
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