Gene-specific Copy Number Variation Probe-C7
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| Catalog: |
CNVFP-C7-01765 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (C7). 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: |
C7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to C7 genes. This product achieves the purpose of detection by hybridizing with the C7 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 C7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency. [provided by RefSeq, Nov 2016] |
| Gene Symbol |
C7 |
| Location |
5p13.1 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 40909598-40983042 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-C7-01765-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-C7-01765-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-C7-01765-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-C7-01765-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-C7-01765-AQ |
467nm |
418nm |
|
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