This gene encodes a member of the S1, or chymotrypsin, family of serine peptidases. This protease catalyzes the cleavage of factor B, the rate-limiting step of the alternative pathway of complement activation. This protein also functions as an adipokine, a cell signaling protein secreted by adipocytes, which regulates insulin secretion in mice. Mutations in this gene underlie complement factor D deficiency, which is associated with recurrent bacterial meningitis infections in human patients. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature protease. [provided by RefSeq, Nov 2015]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
CFDBA-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
CFDBA-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a member of the S1, or chymotrypsin, family of serine peptidases. This protease catalyzes the cleavage of factor B, the rate-limiting step of the alternative pathway of complement activation. This protein also functions as an adipokine, a cell signaling protein secreted by adipocytes, which regulates insulin secretion in mice. Mutations in this gene underlie complement factor D deficiency, which is associated with recurrent bacterial meningitis infections in human patients. Alternative splicing of this gene results in multiple transcript variants. At least one of these variants encodes a preproprotein that is proteolytically processed to generate the mature protease. [provided by RefSeq, Nov 2015]
Gene Symbol : CFD
Gene Name : Complement factor D
Chromosome : CHR 19: 859,658-863,568
Locus : 19p13.3
Alt. Genes : CFM1
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