Gene-specific Copy Number Variation Probe-C5
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| Catalog: |
CNVFP-C5-01688 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (C5). 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: |
C5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to C5 genes. This product achieves the purpose of detection by hybridizing with the C5 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 |
Complement C5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015] |
| Gene Symbol |
C5 |
| Location |
9q33.2 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 123714613-123812554 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-C5-01688-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-C5-01688-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-C5-01688-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-C5-01688-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-C5-01688-AQ |
467nm |
418nm |
|
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