Gene-specific Copy Number Variation Probe-MSH5
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| Catalog: |
CNVFP-MSH5-13481 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MSH5). 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: |
MSH5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MSH5 genes. This product achieves the purpose of detection by hybridizing with the MSH5 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 |
MutS Homolog 5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011] |
| Gene Symbol |
MSH5 |
| Location |
6p21.33 |
| Chromosome |
Chromosome6_mcf_hap5 |
| Coordinates |
This gene maps to 3087408-3110152 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-MSH5-13481-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MSH5-13481-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MSH5-13481-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MSH5-13481-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MSH5-13481-AQ |
467nm |
418nm |
|
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