SERPING1-CHD1 Fusion FISH Probe
The SERPING1-CHD1 Fusion FISH Probe is used to confirm a fusion of the SERPING1 and CHD1 genes. The fusion of the SERPING1 and CHD1 genes has been associated with Skin Cutaneous Melanoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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SERPING1-CHD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-RERE | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-REOR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-REGO | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-REGR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-REAQ | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-ORRE | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-OROR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-ORGO | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-ORAQ | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GORE | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GOOR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GOGO | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GOGR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GOAQ | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GRRE | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GROR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GRGO | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GRGR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-GRAQ | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-AQRE | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-AQOR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-AQGO | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-AQGR | 20 (40 μL) | 200 μL | ||
SERPING1-CHD1-20-AQAQ | 20 (40 μL) | 200 μL |
SERPING1 Gene Summary
This gene encodes a highly glycosylated plasma protein involved in the regulation of the complement cascade. Its protein inhibits activated C1r and C1s of the first complement component and thus regulates complement activation. Deficiency of this protein is associated with hereditary angioneurotic oedema (HANE). Alternative splicing results in multiple transcript variants encoding the same isoform. [provided by RefSeq, Jul 2008]
Gene Name: Serpin Family G Member 1
Chromosome: CHR11: 57365026 -57382326
Locus: 11q12.1
CHD1 Gene Summary
The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. [provided by RefSeq, Jul 2008]
Gene Name: Chromodomain Helicase DNA Binding Protein 1
Chromosome: CHR5: 98190907 -98262238
Locus: 5q15-q21.1
Gene Diseases
The SERPING1 CHD1 Fusion has been associated with the following diseases:
Disease Name |
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Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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